Greenhouse gas and NH3 emissions are exacerbated by the inappropriate timing and excessive application of nitrogen (N) fertilizers in wheat cultivation in China. In this study, the impacts on N2O, CO2, and NH3 emissions of a delayed and reduced N application regime on the Huang-Huai-Hai Plain were investigated. The treatments comprised the control (N0), conventional N at 270 kg N ha−1 (N270) and optimized N application of 180 kg N ha−1 (N180), N180 + biochar at 7.5 t ha−1 (N180B7.5), N180 + biochar at 15 t ha−1 (N180B15), N180 + DMPP (a nitrification inhibitor; N180D), N180D + biochar at 7.5 t ha−1 (N180DB7.5), and N180D + biochar at 15 t ha−1 (N180DB15). Reduced N application (N180) lowered N2O and NH3 emissions. Biochar application resulted in a 4–25% and 12–16% increase in N2O and NH3 emissions, respectively. Application of DMPP significantly decreased N2O emissions by 32% while concurrently inducing a 9% increase in NH3 emissions. Co-application of DMPP and biochar significantly reduced the activity of nitrification enzymes (HAD, NOO), resulting in a reduction of 37–38% in N2O emissions and 13–14% in NH3 emissions. No significant differences in CO2 emissions were observed among the various N treatments except the N0 treatment. Application of DMPP alone did not significantly affect grain yield. However, biochar, in combination with DMPP, effectively increases grain yield. The findings suggest that the N180DB15 treatment has the potential to reduce emissions of N2O and NH3 while concurrently enhancing soil fertility (pH, SOC) and wheat yield.
Selenium is an important indicator for the evaluation of tea quality. However, the relationship between selenium uptake by tea plants (Camellia sinensis) and soil properties, as well as selenium transport and distribution in a tea plantation soil–tea plant–tea infusion production system, remain unclear. In this study, 12 tea plantations situated in a typical selenium-rich area of China were selected, and the characteristics and crucial factors influencing the uptake and transport of selenium were analyzed using a plantation soil–tea plant–tea infusion production system. The soil total selenium content ranged from 1.12 to 6.67 mg kg−1, with an average of 2.57 mg kg−1. The average available selenium content was 53.56 µg kg−1, and the activation rate of soil selenium was 2.27%. Soil-available selenium was significantly positively correlated with total selenium, available potassium, and soil organic matter contents, and was significantly negatively correlated with soil pH. The selenium content in old leaves ranged from 0.29 to 2.73 mg kg−1, which met the standard for selenium-rich tea, whereas only 33% of young leaves met this standard. The selenium enrichment factor was highest in the fibrous root and lowest in the young leaves. The average selenium transport factors from fibrous roots to main roots, from main roots to main stems, from main stems to lateral stems, from lateral stems to young leaves, and from lateral stems to old leaves were 0.53, 0.92, 0.67, 0.97, and 2.30, respectively. The selenium concentration of tea infusion ranged from 1.88 to 12.49 μg L−1, and the average selenium dissolution rate was 22.62% after one brewing. This study identified critical factors that influence soil-selenium availability. The selenium content in tea plant organs is indicated to be strongly associated with the selenium content in the main roots.
Tea trees (Camellia sinensis) growing on selenium (Se)-rich soils often exhibit the phenomenon of cadmium (Cd) accumulation. However, the transport of Cd in the soil–tea tree–tea infusion continuum in such areas, as well as the impact of Se on Cd in this system, remains enigmatic. In this study, we investigated the migration of Cd from soil to tea tree and from tea tree to tea infusion, as well as the influence of Se on the Cd. The Cd content of the soil was 0.37 mg kg−1, which was approximately 3.81 times higher than the background value. The average activation rate of soil Cd was 20.93%, and was significantly negatively correlated with soil pH and significantly positively correlated with available potassium. The Cd enrichment coefficients in tea tree organs showed a gradually decreasing trend from fibrous roots to taproots, lateral stems, main stems, old leaves, and young leaves. The Cd transport coefficients from fibrous roots to taproots, taproots to main stems, and main stems to lateral stems progressively increased, whereas from lateral stems to old and young leaves significantly decreased. The maximum potential carcinogenic health risk from Cd in the tea infusion was 1.60 × 10−7 to 5.03 × 10−7, thus drinking Se-enriched tea had a low health risk from Cd intake. Our findings revealed a notable threshold effect on the accumulation of Cd in fibrous roots. The primary factor contributing to the low Cd concentration in tea leaves lies in the reduced Cd transport efficiency from fibrous roots to taproots and from lateral stems to young leaves.