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Currently, atmospheric emission inventory that includes multi-type pollutants and sources is still limited at the city level. This study developed a high-resolution emission inventory of eight pollutants based on detailed investigated data for Wuxi city in 2015. Results show that the total emissions of sulfur dioxide (SO2), nitrogen oxides (NOx), total suspended particulates (TSP), particulate matter with an aerodynamic diameter of 10 μm or less (PM10), particulate matter with an aerodynamic diameter of 2.5 μm or less (PM2.5), carbon monoxide (CO), ammonia (NH3), and volatile organic compounds (VOCs) were 36.9 kt, 95.2 kt, 287.3 kt, 127.8 kt, 46.0 kt, 626.4 kt, 10.9 kt, and 104.9 kt, respectively. Power plants were the major contributors of SO2 and NOx, accounting for 34.6% and 36.3% of the total emissions, respectively. Road dust was the dominant source of particulate matter, contributing 63.1%, 57.8% and 38.2% to the total TSP, PM10 and PM2.5 emissions, respectively. Around 67.0% of CO emissions were from iron and steel plants, while 50.1% of NH3 emissions were from livestock and poultry sectors. VOCs emissions largely came from oil refinery and chemical industry, with a share of 41.3%. High NH3 emissions were found in the southwest and northeast of Wuxi where high-intensity agriculture was located, while other pollutants were mainly concentrated on the eastern Wuxi where heavy industries, crowded traffic and highly dense population were located. Most pollutants from the industrial source exhibited the lowest value in February due to the Chinese Spring Festival with the exception of CO and NH3. This study helps to formulate the targeted air pollution control measures for Wuxi city by providing detailed information regarding the spatial-temporal distribution of multi-type air pollutants.

The phosphorus footprint (PF) is a novel concept to analyze human burdens on phosphorus resources. However, research on PF approach is still limited, and current several PF studies include incomplete phosphorus sources and have limited quantitative interpretation about the drivers of PF changes, which can help understand future trends of PF. This study develops a more comprehensive PF model by considering crop, livestock and aquatic food, and non-food goods, which covers the mainly phosphorus containing products consumed by human. The model is applied to quantify China's PF from 1961 to 2014, and the results of the model are also used to analyze the factors driving the PF changes and explored China's PF scenarios for 2050 using an econometric analysis model (STIRPAT). The result shows that China's PF increased over 11-fold, from 0.9 to 10.6 Tg between 1961 and 2014. The PF of livestock food dominated China's PF, accounting for 57% of the total in 1961 and 45% in 2014. The key factors driving the increase in China's PF are the increase in population and urbanization rate, with contributions of 38% and 33%, respectively. We showed that in the baseline scenario, China's PF would increase by 70% during 2014–2050 and cause the depletion of China's phosphate reserves in 2045. However, in the best case scenario, China's PF would decrease by 15% in 2050 compared with that in 2014, and it would have 50% of current phosphate reserve remaining by 2050. Several mitigation measures are then proposed by considering China's realities from both production and consumption perspective, which can provide valuable policy insights to other rapid developing countries to mitigate the P footprint.

As the largest producer of coal chemical products in the world, China faces tremendous pressure to reduce its carbon emission. An accurate quantification of the carbon dioxide (CO2) emission of coal chemical industry in China is therefore necessary. However, due to the variety of coal chemical products and limitations of CO2 emission factors, the total CO2 emission of coal chemical industry has yet to be determined. In this study, local CO2 emission factors of coal chemical products in China are published based on first hand data from twenty-three coal chemical enterprises and the total CO2 emission of China's coal chemical industry is extrapolated. The provincial-level spatial distribution of the CO2 emission of coal chemical industry is presented to assist the government in identifying key emission reduction areas. Additionally, scenario analysis of CO2 emission for China’s modern coal chemical industry in 2020 is conducted to determine whether the development of the modern coal chemical industry will have a significant impact on future CO2 emission, as well as the effect of carbon capture, utilization and storage technologies on the reduction in carbon emission. The estimate shows that the total CO2 emission of the coal chemical industry in 2015 was 607 million tonnes (Mt), accounting for approximately 5.71% of China’s total CO2 emission. The figure is higher than the total annual CO2 emission of a country such as Canada (555 Mt) or Brazil (486 Mt). Quantifying the emission of the coal chemical industry is therefore critical to understand the global carbon budget. The spatial distribution shows that Shandong, Inner Mongolia and Shanxi release one-third of the coal chemical industry’s total CO2 emission. Considering the development of the modern coal chemical industry, its CO2 emission is predicted to be as high as 416.52 million tonnes in 2020. However, the CO2 emission could be reduced by 317.98 million tonnes when carbon capture, utilization and storage are applied to process and energy systems simultaneously. This paper quantifies the CO2 emission of the coal chemical industry in China for the first time, identifies key chemical products and the provinces in which they are produced, explores the carbon reduction potential by scenario analysis, and provides specific data to support the assessment of effective CO2 reduction policy.

Rapid increase in accumulation of phosphorus (P) relative to nitrogen (N) has been observed in human-impacted regions, but the reasons are largely unknown. We developed an Integrated Nutrient Flow Analysis (INFA) model in order to assess the changes in nutrient flows of the Chaohu Lake basin from 1978 to 2015. Results show that the increase in total N input is slower than that of P (3.5-fold versus 4.2-fold) during 1978–2015, while total N loss increases much faster than that of P (3.1-fold versus 2.3-fold). We found a decline trend in the N:P ratio of nutrient input and accumulation since the mid-1990s. The decline in N:P ratio of nutrient loss to waterbodies in the basin is correlated (p

The phosphorus (P) cycle is an important Earth system process. While natural P mobilization is slow, humans have been altering P cycle by intensifying P releases from lithosphere to ecosystems. Here, we examined magnitudes of which humans have altered the P cycles by integrating the estimates from recent literatures, and furthermore illustrated the consequences. Based on our synthesis, human alterations have tripled the global P mobilization in land-water continuum and increased P accumulation in soil with 6.9 ± 3.3 Tg-P yr–1. Around 30% of atmospheric P transfer is caused by human activities, which plays a significant role than previously thought. Pathways involving with human alterations include phosphate extraction, fertilizers application, wastes generation, and P losses from cropland. This study highlights the importance of sustainable P supply as a control on future food security because of regional P scarcity, food demand increase and continuously P intensive food production. Besides, accelerated P...

Intensified human activities have generated a large amount of phosphorus-containing waste (P waste). Unrecycled P waste is lost to the environment and causes eutrophication, while the increasing phosphate consumption risks the depletion of phosphorus resources. The management of P waste is critical to solving these problems. In this study, we quantified the historic trends of P waste generation and recycling in China. From 1900 to 2015, the annual generation of P waste increased from 1 Mt P to 12 Mt P. Crop farming was the largest P waste source in most years, while P waste from phosphate mining and phosphorus chemical production increased the fastest. The total recycled P waste increased 5-fold, but phosphorus loss increased 26-fold. In 2015, 28% of the P waste was lost on cultivated land, and 21% was lost on nonarable land. The largest phosphorus contributor to inland water changed from crop farming to aquaculture. The full recycling of P waste would have reduced phosphate consumption by more than one-third in 2015. The results of a scenario analysis showed that a healthier diet would greatly increase the generation and loss of P waste, but balanced fertilization could reduce the generation of P waste by 17% and promoting waste recycling could reduce the phosphorus loss by 35%.

Life-cycle assessment (LCA) emphasizes obtaining primary data from an on-site process to reduce uncertainties. However, data of the upstream process from secondary sources also yield significant uncertainties, which have not been drawn enough attention. This study aims to explore the importance of primary data of the upstream process in LCAs. Here, we choose lithium, a key component of lithium-ion (Li-ion) battery, as a case to present a cradle-to-gate LCA for its production by rock-based technology (LRT). Then, we compare the environmental impacts of lithium by LRT with that by brine-based technology (LBT) and the Li-ion battery using lithium by the two methods. The result shows that the impacts of rock-based lithium production are dominated by the leaching process, which has the highest levels of impacts for 8 of 10 environmental categories. Besides, all 10 impact categories of lithium produced by LRT are much larger than that by LBT, with differences up to 60.4 -fold. We also find that the Li-ion battery pack by rock-based lithium offers a 17-32% increase in acidification and global warming potential relative to that by brine-based lithium. Our results contribute by providing the first mass-produced life-cycle inventory of rock-based lithium and showing the importance of primary data of the upstream process in LCAs.

The flavon luteolin has various health-promoting activities including cardiovascular protection, anti-inflammatory activity and anticancer activity. A serum concentration of about 100 nM luteolin is reached by dietary habit. However, little is known about the function of luteolin over its physiological concentration range. In this study, we investigated whether a physiological concentration of luteolin could activate nuclear factor-erythroid-2-related factor 2 (Nrf2)-mediated expression of phase II drug-metabolizing enzymes in human hepatoma HepG2 cells. Interestingly, less than 1 nM of luteolin could induce phase II drug-metabolizing enzymes, such as GSTs, HO-1, and NQO1. Both 1 and 100 nM luteolin increased expression and activity of ALDH2, which metabolized toxic acetaldehyde into nontoxic acetic acid. Luteolin increased nuclear accumulation of Nrf2 and enhanced the ARE-binding complex through increasing the stability of the Nrf2 protein. Luteolin increased phosphorylation of Nrf2 at Ser40, and MEK inhibitors (U0126 and PD98059) canceled luteolin-induced phosphorylation of Nrf2. Furthermore, luteolin increased modified Keap1. In conclusion, a physiological concentration of luteolin induces the expression of phase II drug-metabolizing enzymes by enhancement of Nrf2 nuclear accumulation through MEK1/2-ERK1/2-mediated phosphorylation of Nrf2, increasing Nrf2 stability and inducing a conformational change of Keap1.

Identifying the key nodes of the phosphorus flows in animal raising system is fundamental to improve P utilization efficiency and reduce the P contamination. This study established a phosphorus flow analysis model for livestock and poultry raising, depicted P flows for major livestock and poultry under two raising modes, and further analyzed their spatial and temporal distributions. We find that around 15% of P input was transferred into the products, and in P output around 40% lost into the environment in 2015. The P flows have been increasing since 2000, and the main contributor is pigs followed by beef cattle. It should be noticed that P loss from livestock and poultry raising is huge with extensive prospect of recycling in some central provinces of China, and western region where ecological environment is fragile, has a higher P loss rate which need to change the dietary preference and adjust raising structure. As for diets, pork and eggs are better choices than milk or other kinds of meat in terms of reducing the P load, when producing per unit protein or energy. This study contributes to the understanding of P management in husbandry industry, the quantification of environmental loads of animal-based food and the identification of the potential of reducing P loss to realize sustainable utilization of P.

Understanding historical patterns of phosphorus (P) cycling is critical for sustainable P management and eutrophication mitigation in watersheds. This study built a bottom-up model using the substance flow analysis approach to quantify P cycling in the Chaohu watershed during 1978-2012. We found that P flows have been intensified, with a 5-fold increase of annual P inputs to sustain the expanding intensive agriculture. Annually, most P inputs (75%) were stored within the watershed, which caused accelerating buildup of legacy P in cultivated land (from 4.9 Gg to 6.5 × 10(2) Gg), uncultivated land (from 2.1 Gg to 1.3 × 10(2) Gg) and surface water (from 3.7 Gg to 2.6 × 10(2) Gg) during 1978-2012. The main legacy P sources include fertilizer application for cultivated land, phosphogypsum abandonment for uncultivated land, respectively. The animal husbandry contributed about 63-66% of total P inputs to surface water. The contribution of animal food-P increased greatly during 1978-2012, from 7% to 24% and from 1% to 8% for urban and rural residents, respectively. This work demonstrates principle for the buildup of legacy P at the watershed-scale, and advances the knowledge of sustainable P management, such as improving agricultural technologies to reduce fertilizer application.

Drugs, xenobiotics including environmental pollutants, and certain food components modulate expression of drug-metabolizing enzymes. An aryl hydrocarbon receptor (AhR) possesses possible expression of phase I and phase II enzymes directly by binding of its ligands such as 2,3,7,8-tetrachlorodibenzo- p -dioxin (TCDD) and indirectly by regulating expression of nuclear factor-erythroid-2-related factor 2 (Nrf2). Previous our result demonstrated that luteolin, a natural flavonoid existing in vegetables and herbs, competed the binding of TCDD to AhR. In the present study, we investigated the effect of luteolin on the expression of drug-metabolizing enzymes through the AhR and Nrf2 pathways. Luteolin inhibited TCDD-induced protein expression of phase I enzyme cytochrome P450 1A1 (CYP1A1), phase II enzymes NAD(P)H:quinone oxidoreductase-1 (NQO1) and glutathione- S -transferase P1 (GSTP1) in HepG2, Hepa1c1c7 and RL-34 cells in a dose-dependent manner. Luteolin suppressed TCDD- and tert -butylhydroquinone-induced Nrf2 protein by decreasing its stability in HepG2 cells. In tert -butylhydroquinone treated cells, luteolin dose-dependently inhibited NQO1, GSTP1 and aldo–keto reductases (AKRs). Of these, protein expression of CYP1A1 and GSTP1 was mainly dominated by the AhR pathway, while that of NQO1 and AKRs was by the Nrf2 pathway. In conclusion, luteolin inhibits expression of phase I and phase II drug-metabolizing enzymes by modulating the AhR and Nrf2 pathways.

Black soybean seed coat is a rich source of polyphenols that have been reported to have various physiological functions. The present study investigated the potential protective effects of polyphenolic extracts from black soybean seed coat on DNA damage in human hepatoma HepG2 cells and ICR mice. The results from micronucleus (MN) assay revealed that black soybean seed coat extract (BE) at concentrations up to 25μg/mL was non-genotoxic. It is noteworthy that BE (at 4.85μg/mL) and its main components, procyanidins (PCs) and cyanidin 3-glucoside (C3G), at 10μM significantly reduced the genotoxic effect induced by benzo[a]pyrene [B(a)P]. To obtain insights into the underlying mechanism, we investigated BE and its main components on drug-metabolizing enzyme expression. The results of this study demonstrate that BE and its main components, PCs and C3G, down-regulated B(a)P-induced cytochrome P4501A1 (CYP1A1) expression by inhibiting the transformation of aryl hydrocarbon receptor. Moreover, they increased expression of detoxifying defense enzymes, glutathione S-transferases (GSTs) via increasing the binding of nuclear factor-erythroid-2-related factor 2 to antioxidant response elements. Collectively, we found that PCs and C3G, which are the main active compounds of BE, down-regulated CYP1A1 and up-regulated GST expression to protect B(a)P-induced DNA damage in HepG2 cells and ICR mice effectively.