Applying mineral phosphorus (P) fertilizers introduces a considerable input of the toxic heavy metal cadmium (Cd) into arable soils. This study investigates the fate of P fertilizer derived Cd (Cddff) in soil-wheat systems using a novel combination of enriched stable Cd isotope mass balances, sequential extractions, and Bayesian isotope mixing models. We applied an enriched ¹¹¹Cd labeled mineral P fertilizer to arable soils from two long-term field trials with distinct soil properties (a strongly acidic pH and a neutral pH) and distinct past mineral P fertilizer application rates. We then cultivated wheat in a pot trial on these two soils. In the neutral soil, Cd concentrations in the soil and the wheat increased with increasing past mineral P fertilizer application rates. This was not the case in the strongly acidic soil. Less than 2.3% of freshly applied Cddff was taken up by the whole wheat plant. Most of the Cddff remained in the soil and was predominantly (>95% of freshly applied Cddff) partitioned into the easily mobilizable acetic acid soluble fraction (F1) and the potentially mobile reducible fraction (F2). Soil pH was the determining factor for the partitioning of Cddff into F1, as revealed through a recovery of about 40% of freshly applied Cddff in F1 in the neutral pH soil compared with about 60% in the strongly acidic soil. Isotope mixing models showed that F1 was the predominant source of Cd for wheat on both soils and that it contributed to over 80% of the Cd that was taken up by wheat. By tracing the fate of Cddff in entire soil-plant systems using different isotope source tracing approaches, we show that the majority of Cddff remains mobilizable and is potentially plant available in the subsequent crop cycle.

Since the urbanization and industrialization are wildly spread in recent decades, the concentration of Zn in soil has increased in various regions. Although the interactions between P and Zn has long been recognized, the effect of high level of Zn on P uptake, translocation and distribution in rice and its molecular mechanism are not fully understood. In this study, we conducted both hydroponic culture and field trial with different combined applications of P and Zn to analyze the rice growth and yield, the uptake, translocation and distribution of P and Zn, as well as the P- and Zn-related gene expression levels. Our results showed that high level of Zn decreased the rice biomass and yield production, and inhibited the root-to-shoot translocation and distribution of P into new leaves by down-regulating P transporter genes OsPT2 and OsPT8 in shoot, which was controlled by OsPHR2-OsmiR399-OsPHO2 module. High Zn supply triggered P starvation signal in root, thereafter increased the activities of both root-endogenous and -secreted acid phosphatase to release more Pi, and induced the expression OsPT2 and OsPT8 to uptake more P for plant growth. On the other hand, high level of P significantly decreased the Zn concentrations in both root and shoot, and the root uptake ability of Zn through altering the expression levels of OsZIPs, which were further confirmed by the P high-accumulated mutant osnla1-2 and OsPHR2-OE transgenic plant. Taken together, we revealed the physiological and molecular mechanisms of P–Zn interactions, and proposed a working model of the cross-talk between P and Zn in rice plants. Our results also indicated that appropriate application of P fertilizer is an effective strategy to reduce rice uptake of excessive Zn when grown in Zn-contaminated soil.

Overuse of phosphorus (P) fertilizer and the resulting soil P accumulation in vegetable production increases the risk of P runoff and leaching. However, P transformations under continuous fertilization and their effects on environmental risk are unclear. The current study examined the effects of long-term P fertilizer application on P fractions in different soil layers, and assessed the correlations between P fractions and environmental risks in intensive vegetable production in a subtropical region. A total of 32 fields were studied, including 8 uncultivated fields and 24 fields continuously used for vegetable production for 1–3, 4–9, or 10–15 years. The results showed that excessive P fertilizer input caused soil P surpluses ranging from 204.6 to 252.4 kg ha⁻¹ yr⁻¹. Compared to uncultivated fields, vegetable fields contained higher levels of labile P, moderately labile P, sparingly labile P, and non-labile P. The combined percentage of labile P and moderately labile P increased from 55.2% in fields cultivated for 0–3 year to 65.5% in fields cultivated for 10–15 years. The concentrations of soil P fractions were higher at 0–20 cm soil depth than at 20–40 and 40–60 cm soil depth. Soil available P was positively correlated with all soil P fractions except diluted HCl-Pᵢ or concentrated HCl-Pₒ. Long-term vegetable production increased CaCl₂–P downward movement, which was positively correlated with levels of labile and moderately labile P. The P index indicated a high risk of P losses from the vegetable fields. The P index was on average 3.27-fold higher in the vegetable fields than in uncultivated fields, and was significantly correlated with soil available P and organic and inorganic P fertilizer input. The environmental risk caused by P in vegetable production should be reduced by reducing P fertilizer input so as to maintain soil available P within an optimal range for vegetable production.

Huelva is a highly industrialized city in SW Spain hosting, among others, a Cu smelter, a phosphate fertilizer plant, a power plant, and oil refineries. This study aims to evaluate metal concentrations in lichens as bioindicators of atmospheric pollution in the impacted urban areas. Xanthoria parietina species from Huelva and nearby villages, as well as reference samples from remote, non-contaminated urban areas, were analyzed for trace elements (V, Cr, Mn, Co, Ni, Cu, Zn, Sr, As, Cd, Sb, Cs, Ba, La, Ce, Pr, Nd, Sm, Er, Tm, Yb, Lu, Pb, Th, U) using Inductively Coupled Plasma-Mass Spectrometry; and for major elements (Ca, K, Mg, P, and S) by Inductively Coupled Plasma-Optical Emission Spectrometry after acid digestion.The metal composition of X. parietina exhibits spatial distribution patterns with extremely elevated concentrations (Co, Ni, Cu, Zn, As, Cd, Sb, Ba, Pb, U, and S) in the surroundings of the industrial estates to <1 km distance. Mean concentrations were significantly lower in the urban areas >1 km from the pollution sources. However, air pollution persists in the urban areas up to 4 km away, as the mean concentrations of Cu, Zn, As, Cd, Sb and S remained considerably elevated in comparison to the reference samples. Though rigorous source apportionment analysis was not the aim of this study, a good positive correlation of our results with metal abundances in ambient particulate matter and in pollution sources points to the Cu smelter as the main source of pollution. Hence, the severe air pollution affecting Huelva and nearby urban areas may be considered a serious health risk to local residents.

Mineral phosphorus fertilizers are regularly applied to agricultural sites, but their uranium (U) content is potentially hazardous to humans and the environment. Fertilizer-derived U can accumulate in the soil, but might also leach to ground-, spring and surface waters. We sampled 19 mineral fertilizers from the canton of Bern and soils of three arable and one forest reference sites at each of four locations with elevated U concentrations (7–28 μg L⁻¹) in nearby drinking water wells. The total U concentrations of the fertilizers were measured. The soils were analysed at three depth intervals down to 1 m for general soil parameters, total Cd, P, U and NaHCO₃-extractable U concentrations, and ²³⁴/²³⁸U activity ratios (AR). The U concentrations and AR values of the drinking water samples were also measured. A theoretical assessment showed that fertilizer-derived U may cause high U concentrations in leaching waters (up to approx. 25 μg L⁻¹), but normally contributes only a small amount (approx. 0–3 μg L⁻¹). The arable soils investigated showed no significant U accumulation compared to the forest sites. The close positive correlation of AR with NaHCO₃-extractable U (R = 0.7, p < 0.001) indicates that application of fertilizer can increase the extractable U pool. The lack of depth gradients in the soil U concentrations (1.5–2.7 mg kg⁻¹) and AR (0.90–1.06) ratios are inconsistent with the accumulation of U in the surface soil, and might indicate some leaching of fertilizer-derived U. The AR values in the water samples were close to 1, possibly suggesting an influence of fertilizer-derived U. However, based on findings from the literature and considering the heterogeneity of the catchment area, the agricultural practices, and the comparatively long distance to the groundwater, we conclude that fertilizer-derived U makes only a minor contribution to the elevated U concentrations in the water samples.

Mineral phosphorus (P) fertilizers contain contaminants that are potentially hazardous to humans and the environment. Frequent mineral P fertilizer applications can cause heavy metals to accumulate and reach undesirable concentrations in agricultural soils. There is particular concern about Cadmium (Cd) and Uranium (U) accumulation because these metals are toxic and can endanger soil fertility, leach into groundwater, and be taken up by crops. We determined total Cd and U concentrations in more than 400 topsoil and subsoil samples obtained from 216 agricultural sites across Switzerland. We also investigated temporal changes in Cd and U concentrations since 1985 in soil at six selected Swiss national soil monitoring network sites. The mean U concentrations were 16% higher in arable topsoil than in grassland topsoil. The Cd concentrations in arable and grassland soils did not differ, which we attribute to soil management practices and Cd sources other than mineral P fertilizers masking Cd inputs from mineral P fertilizers. The mean Cd and U concentrations were 58% and 9% higher, respectively, in arable topsoil than in arable subsoil, indicating that significant Cd and U inputs to arable soils occurred in the past. Geochemical mass balances confirmed this, indicating an accumulation of 52% for Cd and 6% for U. Only minor temporal changes were found in the Cd concentrations in topsoil from the six soil-monitoring sites, but U concentrations in topsoil from three sites had significantly increased since 1985. Sewage sludge and atmospheric deposition were previously important sources of Cd to agricultural soils, but today mineral P fertilizers are the dominant sources of Cd and U. Future Cd and U inputs to agricultural soils may be reduced by using optimized management practices, establishing U threshold values for mineral P fertilizers and soils, effectively enforcing threshold values, and developing and using clean recycled P fertilizers.

Archived samples from the Park Grass Experiment, established in 1856, were analysed to determine the impacts of long-term phosphate fertiliser applications on arsenic concentrations in soil and herbage. In plots receiving 35 kg P ha−1 annually (+P), topsoil As concentrations almost doubled from an initial value of ∼10 mg kg−1 during 1888–1947 and remained stable thereafter. The phosphate fertilisers used before 1948 contained 401–1575 mg As kg−1, compared to 1.6–20.3 mg As kg−1 in the later samples. Herbage samples from the +P plots collected during 1888–1947 contained significantly more As than those from the −P plots, but later samples did not differ significantly. Mass-balance calculations show that the increase in soil As can be explained by the As input from P fertiliser applications before 1948. The results demonstrate that the P fertilisers used on the Park Grass Experiment before 1948 caused substantial As contamination of the soil.

Application of phosphate fertilizer can be a significant contributor of potentially hazardous trace elements such as arsenic, cadmium, and lead in croplands. These trace elements have the potential to accumulate in soils and be transferred through the food chain. We articulated the environmental risks of trace elements associated with long-term phosphate fertilizer applications by combining data from the literature and results from model simulations. Results illustrate that under normal cropping practice, the impact of phosphate fertilizers applications on trace element accumulation in receiving soils has been limited and localized. Their plant uptake varied greatly depending on the fertilizer application rates, soil and plant characteristics. This has led to a great deal of uncertainty in characterizing soil distribution coefficients, Kd, and plant uptake factors, PUF, two of the most used parameters in assessing the risks of accumulations. Therefore, the risks may be more appropriately assessed based on the probabilistic distributions of Kd and PUF.

Both eutrophication and SO₄ pollution can lead to higher availability of nutrients and potentially toxic compounds in wetlands. To unravel the interaction between the level of eutrophication and toxicity at species and community level, effects of SO₄ were tested in nutrient-poor and nutrient-rich fen mesocosms. Biomass production of aquatic and semi-aquatic macrophytes and colonization of the water layer increased after fertilization, leading to dominance of highly competitive species. SO₄ addition increased alkalinity and sulphide concentrations, leading to decomposition and additional eutrophication. SO₄ pollution and concomitant sulphide production considerably reduced biomass production and colonization, but macrophytes were less vulnerable in fertilized conditions. The experiment shows that competition between species, vegetation succession and terrestrialization are not only influenced by nutrient availability, but also by toxicity, which strongly interacts with the level of eutrophication. This implies that previously neutralized toxicity effects in eutrophied fens may appear after nutrient reduction measures have been taken. Interspecific competition, vegetation succession and terrestrialization in fens depend on the interacting effects of SO₄ pollution, sulphide toxicity and nutrient availability.

Phytoextraction using hyperaccumulator, Pteris vittata, to extract arsenic (As) from soil has been applied to large areas to achieve an As removal rate of 18% per year. However, remarkable difference among different studies and field practices has led to difficulties in the standardization of phytoextraction technology. In this study, data on As concentration in P. vittata and related environmental conditions were collected through literature search. A conceptual framework was proposed to guide the improvement of phytoextraction efficiency in the field. The following influencing factors of As concentration in this hyperaccumulator were identified: total As concentration in soil, soil available As, organic matter in soil, total potassium (K) concentration in soil, and annual rainfall. The geodetection results show that the main factors that affect As concentration in P. vittata include soil organic matter (q = 0.75), soil available As (q = 0.67), total K (q = 0.54), and rainfall (q = 0.42). The predictive models of As concentration in P. vittata were established separately for greenhouse and field conditions through multivariate linear stepwise regression method. Under greenhouse condition, soil available As was the most important influencing factor and could explain 41.4% of As concentration in P. vittata. Two dominant factors were detected in the field: soil available As concentration and average annual rainfall. The combination of these two factors gave better prediction results with R² = 0.762. The establishment of the model might help predict phytoextraction efficiency and contribute to technological standardization. The strategies that were used to promote As removal from soil by P. vittata were summarized and analyzed. Intercropping with suitable plants or a combination of different measures (e.g., phosphate fertilizer and water retention) was recommended in practice to increase As concentration in P. vittata.