[Effects of different amounts of straw return and nitrogen fertilizer application on soil CO2 emission from maize fields.] / ä¸åŒç§¸ç§†è¿˜ç”°é‡å’Œæ°®è‚¥é æ–½å¯¹çŽ‰ç±³ç”°åœŸå£¤CO2排放的影响.

Understanding the effects of different amounts of straw returning and nitrogen fertilizer application on soil CO2 emission from maize field can provide theoretical support for carbon sequestration and CO2 emission reduction and the implementation of black soil region conservation plan. Three rates of straw returning were set up in the semi-arid area of northwest Liaoning Province, China, i.e. 3000 (S1), 6000 (S2) and 9000 kg·hm-2(S3, full amount of straw returned to the field); crossed with three nitrogen fertilizer application rates in the sub-region, respectively, i.e. 105 (N1), 210 (N2, conventional nitrogen application rate) and 420 kg N·hm-2(N3). In addition, there was a control treatment (CK) without nitrogen fertilizer and straw returning. Soil samples were collected after 4 years field experiment with maize plantation. The influence of different treatments on maize field soil CO2 emission and the relationship between CO2 emission and soil dissolved organic carbon (DOC) and microbial biomass carbon (MBC) were investigated in an incubation experiment. The results showed that both of straw returning and nitrogen fertilizer application promoted soil CO2 emission in maize field, which were increased significantly with the increases of straw returning amount and nitrogen application amount. Nitrogen fertilizer application was the most important factor promoting soil CO2 emission in maize field. Straw returning combined with nitrogen fertilizer promoted soil CO2 emission by increasing microbial biomass and increasing DOC consumption. MBC and DOC stimulated soil CO2 emission significantly in maize field, and were mainly affected by their contents in the early stage of incubation. From the perspective of ensuring the fertilization of straw return to the field while reducing CO2 emissions, results from our experiment showed that 210 kg N·hm-2 conventional nitrogen application in combination with 6000 kg N·hm-2 straw returning (N2S2) was the most promising mode in the semi-arid area of northwest Liaoning Province.

Transcriptome alterations in zebrafish gill after exposure to different sizes of microplastics.

Most studies on microplastics (MPs) focused on gut, liver, and brain, and MPs toxicity was size-dependent, but less has been reported on gill. Here, zebrafish were exposed to three sizes of MPs (45-53 µm, 90-106 µm, and 250-300 µm). Next, comparative transcriptome analysis and determination of physiological indices were performed in zebrafish gills to elucidate the size-associated toxicity of MPs to fish gills. Compared with the control, 60, 344, and 802 differentially expressed genes (DEGs) were identified after exposure to 45-53 µm, 90-106 µm, and 250-300 µm MPs for 5 days, respectively. More DEGs in treatment with bigger MPs suggested that bigger MPs might induce more changes in zebrafish gills than smaller ones. These DEGs were significantly enriched in the FoxO signaling, cellular senescence, circadian rhythm and p53 signaling pathways. Besides, 90-106 µm and 250-300 µm MPs treatments inhibited the cell cycle and prevented the apoptosis. The GSH content significantly increased after MPs exposure, suggesting the induction of oxidative stress. AChE and Na+/K+-ATPase activities were significantly lowered in all MPs treatments than in the control, suggesting the inhibition of neurotransmission and ion regulation. These changes might negatively influence the normal functioning of gills, such as osmoregulation, ion regulation, and respiration.

The time-dependent variations of zebrafish intestine and gill after polyethylene microplastics exposure.

Microplastics (MPs) are common environmental contaminants that present a growing health concern due to their increasing presence in aquatic and human systems. However, the mechanisms behind MP effects on organisms are unclear. In this study, zebrafish (Danio rerio) were used as an in vivo model to investigate the potential risks and molecular mechanisms of the toxic effects of polyethylene MPs (45-53 µm). In the zebrafish intestine, 6, 5, and 186 genes showed differential expression after MP treatment for 1, 5, and 10 days, respectively. In the gills, 318, 92, and 484 genes showed differential expression after MP treatment for 1, 5, and 10 days, respectively. In both the intestine and the gills, Gene Ontology (GO) annotation showed that the main enriched terms were biological regulation, cellular process, metabolic process, cellular anatomical entity, and binding. KEGG enrichment analysis on DEGs revealed that the dominant pathways were carbohydrate metabolism and lipid metabolism, which were strongly influenced by MPs in the intestine. The dominant pathways in the gills were immune and lipid metabolism. The respiratory rate of gills, the activity of SOD and GSH in the intestine significantly increased after exposure to MPs compared with the control (p < 0.05), while the activity of SOD did not change in the gills. GSH activity was only significantly increased after MP exposure for 5 days. Also, the MDA content was not changed in the intestine but was significantly decreased in the gills after MP exposure. The activity of AChE significantly decreased only after MPs exposure for 5 days. Overall, these results indicated that MPs pollution significantly induced oxidative stress and neurotoxicity, increased respiratory rate, disturbed energy metabolism and stimulated immune function in fish, displaying an environmental risk of MPs to aquatic ecosystems.

Algal density affects the influences of polyethylene microplastics on the freshwater rotifer Brachionus calyciflorus.

Most previous researches focused on the toxicity of polystyrene microplastics (MPs) to marine organisms, but less on polyethylene MPs and freshwater zooplanktons. The present study aims to elucidate the toxicity of polyethylene (PE) MPs (diameter = 10-22 µm) to the typical freshwater rotifer Brachionus calyciflorus. Firstly, fluorescent microscope observation showed that rotifers could ingest PE MPs and accumulate them in their digestive tracts. Life-table experiments revealed that exposure to 0.5 × 103, 2.5 × 103, and 1.25 × 104 particles/mL PE MPs significantly reduced net reproductive rate and intrinsic rate of pollution increase of rotifers under algal densities (Scenedesmus obliquus) of 0.1 × 106, and 0.5 × 106 cells/mL, but no significant effects were observed under 2.5 × 106 cells/mL algal density. These results showed that PE MPs suppressed the reproduction of rotifer and this negative effect could be alleviated by increasing food supply. The swimming linear speed of rotifers significantly decreased with increasing MP concentrations. The activities of superoxide dismutase and Na+-K+-ATPase significantly decreased in treatments with high concentration of PE MPs under 0.1 × 106 cells/mL algal density, but did not change significantly in MP treatments under 0.5 × 106 and 2.5 × 106 cells/mL, compared to the control. Glutathione peroxidase activity significantly increased in treatments with 1.25 × 104 particles/mL and 2.5 × 103 particles/mL under 0.1 × 106 and 0.5 × 106 cells/mL algal density, respectively, but did not change significantly in all MP treatments under 2.5 × 106 cells/mL. Exposure to PE MPs might lower the gathering capacity of algae, induce oxidative stress, trigger cell membrane damages and disturb energy metabolism in rotifers, which can explain the PE MPs toxicity to rotifer reproduction.