Carbon balance analysis of agricultural production systems in oasis areas.

China is the biggest emitter of greenhouse gases (GHGs) in the world, and agricultural GHG emission accounts for nearly a fifth of the total emission in China. To understand the carbon absorption and emission characteristics of agricultural production systems in those arid oasis areas, a typical representative city in northwestern China, Zhangye City, was selected for study.The emission factor method was used to analyze and calculate the characteristics of changing carbon emission dynamics in the whole agricultural production system in Zhangye city region (38,592 km2) from 2010 to 2021.The results revealed that carbon emissions during agricultural planting mainly come from fertilizers, which account for the highest proportion (47.9%) of total carbon emissions in agricultural planting. Animal enteric fermentation emissions from local livestock farming are the main contributor (86%) to GHG emissions. The annual average carbon absorption intensity is 4.4 t C-eq ha-1 for crop and 2.6 t C-eq ha-1 for the agricultural production system. The ratio of total carbon emissions from agricultural production to carbon sequestration of crops is 1:1.7. We find that the total carbon sequestration slightly exceeds its total carbon emissions in the study region, with an annual average of 41% for its sustainable development index. Carbon emissions of the agricultural production system in this oasis area are mainly driven by the livestock industry, mostly CH4 emissions from cattle raising.Reducing the local carbon emissions from the livestock industry, typically the cattle raising, will play a crucial role in reducing carbon emissions from this local agricultural production system and maintaining its net positive carbon balance.

Analysis of the characteristics of major pollutants discharged from wastewater in China's provinces.

In recent years, the discharge of major pollutants in China's wastewater has been decreasing but remains at a high level. Controlling the discharge of pollutants in sewage is of great importance for protecting water quality and maintaining ecological balance. Based on data collected from 31 provinces in China from 2011 to 2020 (except 2018), this study analyzes the spatiotemporal variation emissions of the wastewater pollutants: chemical oxygen demand (COD), ammonia nitrogen (NH3-N), total nitrogen (TN), and total phosphorus (TP). The entropy method was used to evaluate the effectiveness of water pollution control in different provinces. Our results revealed that the total emission per gross domestic product (GDP) for COD, NH3-N, TN and TP in China decreased by 50.7%, 81.9%, 65.4% and 70.8%, respectively. In terms of regional annual emission differences, the Northwest region was the lowest compared with other regions, accounting for 4.87%-6.59% of the national pollutant emissions, and the Central China region was the highest, accounting for 22.4%-26.05% of the national pollutant emissions. The average value of pollutant emissions per unit of GDP decreased year-to-year overall, but Guangxi and Tibet showed a trend of first decreasing and then increasing. The correlation results indicated a significant correlation (0.977) between TN and TP emissions in wastewater in China during 2011-2020. Through clustering and Multidimensional Scaling model (MDS) analysis, Beijing and Shanghai have been performing well in controlling water pollution discharge, while the provinces of Tibet and Guangxi must still increase their efforts in water pollution control. Furthermore, these results demonstrate the experience and achievements of the Chinese government in the treatment of wastewater pollution and provide a useful reference for treatment of wastewater pollution in the world.

An evaluation of the spatial rationality of provincial territory: a case study of Gansu Province.

In China, utilization and evaluation of territorial space have become national strategic issues. Evaluating the rationality of urban, ecological, and agricultural space is significant in the development of territorial space and provides a theoretical basis for the optimization of provincial territorial space. The strategic positioning of Gansu Province as a national ecological environment safety barrier is significant to the protection of the ecological environment of northwest China. This study used the entropy method to evaluate the rationality of territorial space development in 14 cities in Gansu Province in 2019, using 50 indicators of urban, ecological, and agricultural space. Results reveal that in the evaluation of these three spaces, the most important influencing indicators are water supply penetration rate, proportion of desert area, and proportion of agricultural population, respectively. In the total evaluation of territorial space rationality, the city with the highest comprehensive index is Qingyang (2.0521), followed by Zhangye (1.5635), while Lanzhou (1.1553) has the lowest evaluation. In Gansu, cities with the best territorial spatial conditions are concentrated in the east, whereas those with poor territorial spatial environmental security are located in central Gansu and the Hexi Corridor. Collectively, these findings suggest that the equity and rationality of urban, ecological, and agricultural space in territorial space should be considered in territorial space planning strategies. The balance and harmony of these three spaces play a positive role in the sustainable development of the economy, society, and the environment in urban areas.

[Atmospheric Pollution Characteristics and Inhalation Exposure Risk of Nitrated Polycyclic Aromatic Hydrocarbons in PM2.5 at the Ningdong Energy and Chemical Industry Base, Northwest China].

Atmospheric PM2.5 samples were collected by using the active sampling method to investigate the pollution characteristics of nitrated polycyclic aromatic hydrocarbons (NPAHs) at the Ningdong Energy and Chemical Industry Base, Northwest China. Furthermore, the primary sources and the contributions of secondary formation sources as well as the inhalation exposure risks were identified. The main results were as follows. The concentration levels of ∑12NPAHs in PM2.5 ranged from 2.06 ng·m-3 to 37.14 ng·m-3 at the Ningdong Energy and Chemical Industry Base. The average concentrations of ∑12NPAHs were (25.57±5.76) ng·m-3 in winter and (6.22±1.74) ng·m-3 in summer for the Baofeng sampling site associated with the energy industry. The average concentrations of ∑12NPAHs were (7.13±1.44) ng·m-3 in winter and (2.58±0.39) ng·m-3 in summer for the Yinglite sampling site associated with chemical and electricity industries. The levels of ∑12NPAHs in PM2.5 were higher in winter than those in summer because of the increased heating in winter. Atmospheric pollution levels of NPAHs at the Baofeng sampling site were generally higher than those at the Yinglite sampling because of the higher primary NPAHs emissions from coal mining and coke production in Baofeng compared with those from the chemical industry in Yinglite. The calculated nocturnal/diurnal ratios revealed that the concentrations of ∑12NPAHs in PM2.5 during the summer season were higher in the daytime than those in the nighttime, but the opposite trend occurred in winter, thus indicating that secondary formation processes made more contributions to NPAHs during summer in the daytime. The congener profiles of NPAHs were mainly composed of primary emission markers such as 2-nitrofluorene (2N-FLO) and 6-nitrochrysene (6N-CHR), which were the predominant ones in winter and summer for both the Baofeng and Yinglite sampling sites. Total proportions of 2N-FLO and 6N-CHR were 46% in winter and 73% in summer for Baofeng and 59% in winter and 55% in summer for Yinglite, respectively. Meanwhile, 3N-PHE, which is a marker compound of secondary formation processes, accounted for a higher percentage in summer especially at Yinglite. This finding revealed that the chemical production at Yinglite was associated with higher precursor emissions than that of Baofeng, and thus, more NPAHs were derived from secondary formation processes. Moreover, ∑12NPAHs/∑16PAHs ratios were calculated to identify the potential sources of NPAHs across the city. The results indicated that higher environmental temperatures in summer promoted the degradation of PAHs and secondary formation of NPAHs, and thus, secondary formation contributed more to NPAHs in summer than in winter. Furthermore, lung cancer risks induced by inhalation exposures to ∑5NPAHs were assessed based on the BaP equivalent toxicity factor. The results showed that the lung cancer risk values of ∑5NPAHs were (3.06×10-5±1.36×10-5) in winter and (1.79×10-5±0.80×10-5) in summer for the Baofeng sampling site, while the risk values were (2.85×10-5±1.20×10-5) in winter and (1.86×10-5±0.83×10-5) in summer for the Yinglite sampling site. Notably, the lung cancer risk values in our study for both sampling sites were higher than the standard limit value (1.00×10-5) of the California Environmental Protection Agency, which indicates that the local population at the Ningdong Energy and Chemical Industry Base has been subjected to potentially elevated lung cancer risks due to inhalation exposures to PM2.5-bound NPAHs.

Spatiotemporal variation of atmospheric nitrated polycyclic aromatic hydrocarbons in semi-arid and petrochemical industrialized Lanzhou City, Northwest China.

Polyurethane foam-based passive air sampler (PUF-PAS) and passive dry deposition sampler (PAS-DD) were adopted, for the first time ever in China, to investigate the atmospheric levels and spatial-temporal distributions of air burdens and dry deposition fluxes of 12 nitrated polycyclic aromatic hydrocarbons (NPAHs) during winter and summer seasons in a multiple site field campaign in a petrochemical industrialized capital city in Northwest China. The results showed that the highest air concentration and dry deposition fluxes of ∑12NPAHs occurred at a heavy traffic site among 18 sampling sites in both winter and summer season. The lowest air concentration and dry deposition fluxes were observed at the background site. The mean concentrations of ∑12NPAHs in the ambient air were 8.6 ± 8.1 ng m-3 in winter and 15 ± 11 ng m-3 in summer. The mean dry deposition fluxes of ∑12NPAHs were 1.8 × 103 ± 1.9 × 103 ng (m2 day)-1 in winter and 1.4 × 103 ± 1.3 × 103 ng (m2 day)-1 in summer, respectively. The total concentration of 12 NPAHs was mainly dominated by 1-nitro-naphthalene (1N-NAP) and 2-nitro-naphthalene(2N-NAP) in air, accounting for 32% in winter and 45% in summer of ∑12NPAHs. 7-Nitro-benzo [a] anthracene (7N-BaA) made the largest contribution to dry deposition fluxes of ∑12NPAHs, accounting for 28% in winter and 24% in summer. The ratios of ∑12NPAHs/∑15pPAHs (parent polycyclic aromatic hydrocarbons) were calculated to identify potential sources of NPAHs across the city. The results revealed that the main atmospheric air concentration and dry deposition fluxes of 12 NPAHs could be attributed to the primary emissions in winter and the secondary reaction formation in summer. The sources of primary emissions could be traced back to petrochemical, steel mills, as well as aluminum industries in winter and vehicle exhaust in summer. Higher ∑12NPAH/∑15pPAH concentration ratios in summer indicated that the oxidation of pPAHs contributed to the secondary formation of NPAHs via atmospheric chemical reactions in this petrochemical industrialized mountain-valley city.

[Atmospheric Dry Deposition Fluxes and Sources of Polycyclic Aromatic Hydrocarbons in Lanzhou Valley, Northwest China].

The atmospheric dry deposition flux pollution levels were determined and the sources apportioned for 15 US EPA priority polycyclic aromatic hydrocarbons (PAHs) collected at 13 sampling sites in the Lanzhou valley using passive sampling techniques. The results are as follows. The annual atmospheric dry deposition fluxes ranged from 7.48 to 53.94 µg·(m2·d)-1, with a mean of 18.65 µg·(m2·d)-1. The highest flux levels for both the heating and non-heating seasons, 60.85 µg·(m2·d)-1 and 47.03 µg·(m2·d)-1, respectively, appeared at the traffic site (Donggang Bridge), where the heaviest traffic in the Lanzhou valley occurs. The lowest flux levels of 8.16 µg·(m2·d)-1 and 6.80 µg·(m2·d)-1 for the heating and non-heating seasons, respectively, were found at Baita Mountain, which has a higher percentage of vegetation cover. Meanwhile, the flux levels at the background site (Guantangou Mountain) were significantly lower than those of the other sampling sites. For dry deposition, the PAH components Phe, Flua, Flu, and Pyr were dominant in the heating and non-heating periods, and the sums of the percentages of 3- and 4-ring PAHs were 87.53% for the heating season and 82.73% for the non-heating season. Moreover, the percentage of 5- and 6-ring PAHs for the non-heating period was higher than that for the heating period, which may be because the lighter PAHs were easily volatilized, and thus escaped. Furthermore, the sources of atmospheric dry deposition were identified by principal component analysis (PCA). The results of source apportionment showed that the main atmospheric PAH dry deposition in the Lanzhou valley were from vehicle exhaust emissions, coal combustion, and the coking industry. In further detail, coal combustion and the coking industry contributed most of the PAH dry deposition emissions during the heating period except for the traffic area site of Donggang Bridge, whereas vehicle exhaust was the dominant contributor during the non-heating season. In addition, the annual average dry deposition velocities of atmospheric PAHs were calculated using the dry deposition model for three sites: 0.20 cm·s-1 downtown (Environmental Protection Agency of Lanzhou; JCZ), 0.15 cm·s-1 in an industrial area (Lanyuan Hotel of Xigu; LLH), and 0.17 cm·s-1 in a traffic area (the Staff Hospital of Gansu Province; ZGH), of which the latter two were relatively lower because of comprehensive meteorological factors such as wind speed, temperature, and land use categories. Regarding the dry deposition flux values of the 3- and 4-ring PAHs, the simulated values were a bit larger than the observed values, but all were at the same level of magnitude. However, the simulated flux values were closer to their observed values for 4-ring PAHs than for 3-ring PAHs, which indicated that 3-ring PAHs were lost more easily than 4-ring PAHs were during monitoring.

Dechlorination and decomposition of chloroform induced by glow discharge plasma in an aqueous solution.

In this study, efficient dechlorination and decomposition of chloroform (CF) induced by glow discharge plasma (GDP) in contact with a sodium sulfate solution was investigated. Intermediate byproducts were determined by ionic chromatography and headspace gas chromatography, respectively. Results showed that CF can be effectively dechlorinated and decomposed under the action of GDP. Both removal and dechlorination of CF increased with increasing pH and with addition of hydroxyl radical scavengers to the solution. Addition of H2O2 to the solution slightly decreased the CF removal. Formic acid, oxalic acid and dichloromethane were determined as the major intermediate byproducts. Final products were carbon dioxide and hydrochloric acid. Hydrated electrons were the most likely active species responsible for initiation of the dechlorination, and hydroxyl radicals may be the ones for the oxidation of the organic intermediate byproducts. Hydrolyses of the chloromethyl radicals contributed much in the mineralization of the organic chlorine. Reaction mechanism was proposed based on the dechlorination kinetics and the distribution of intermediate byproducts.