|
|
|
题名
|
作者
|
年代
|
出处
|
被引量
|
| 1 | Kinetics and mechanism of hexavalent chromium removal by basic oxygen furnace slag显示文摘Basic oxygen furnace slag(BOFS) has the potential to remove hexavalent chromium(Cr(VI))from wastewater by a redox process due to the presence of minerals containing Fe2+. The effects of the solution p H, initial Cr(VI) concentration, BOFS dosage, BOFS particle size, and temperature on the removal of Cr(VI) was investigated in detail through batch tests. The chemical and mineral compositions of fresh and reacted BOFS were characterized using scanning electron microscope(SEM) equipped with an energy dispersive spectrometer(EDS)system and X-ray diffractometer(XRD). The results show that Cr(VI) in wastewater can be efficiently removed by Fe2+released from BOFS under appropriate acidic conditions. The removal of Cr(VI) by BOFS significantly depended on the parameters mentioned above. The reaction of Cr(VI) with BOFS followed the pseudo-second-order kinetic model. Fe2+responsible for Cr(VI) removal was primarily derived from the dissolution of Fe O and Fe3O4 in BOFS. When H2SO4 was used to adjust the solution acidity, gypsum(Ca SO4·2H2O)could be formed and become an armoring precipitate layer on the BOFS surface, hindering the release of Fe2+and the removal of Cr(VI). Finally, the main mechanism of Cr(VI) removal by BOFS was described using several consecutive reaction steps. | Chong Han Yanan Jiao Qianqian Wu Wangjin Yang He Yang Xiangxin Xue | 2016 | Journal of Environmental Sciences2016，28，8： | 4 |
| 2 | Auxin response factor 6A regulates photosynthesis,sugar accumulation,and fruit development in tomato显示文摘Auxin response factors(ARFs)are involved in auxin-mediated transcriptional regulation in plants.In this study,we performed functional characterization of SlARF6A in tomato.SlARF6A is located in the nucleus and exhibits transcriptional activator activity.Overexpression of SlARF6A increased chlorophyll contents in the fruits and leaves of tomato plants,whereas downregulation of SlARF6A decreased chlorophyll contents compared with those of wild-type(WT)plants.Analysis of chloroplasts using transmission electron microscopy indicated increased sizes of chloroplasts in SlARF6A-overexpressing plants and decreased numbers of chloroplasts in SlARF6A-downregulated plants.Overexpression of SlARF6A increased the photosynthesis rate and accumulation of starch and soluble sugars,whereas knockdown of SlARF6A resulted in opposite phenotypes in tomato leaves and fruits.RNA-sequence analysis showed that regulation of SlARF6A expression altered the expression of genes involved in chlorophyll metabolism,photosynthesis and sugar metabolism.SlARF6A directly bound to the promoters of SlGLK1,CAB,and RbcS genes and positively regulated the expression of these genes.Overexpression of SlARF6A also inhibited fruit ripening and ethylene production,whereas downregulation of SlARF6A increased fruit ripening and ethylene production.SlARF6A directly bound to the SAMS1 promoter and negatively regulated SAMS1 expression.Taken together,these results expand our understanding of ARFs with regard to photosynthesis,sugar accumulation and fruit development and provide a potential target for genetic engineering to improve fruit nutrition in horticulture crops. | Yujin Yuan Xin Xu Zehao Gong Yuwei Tang Mengbo Wu Fang Yan Xiaolan Zhang Qian Zhang Fengqing Yang Xiaowei Hu Qichen Yang Yingqing Luo Lihua Mei Wenfa Zhang Cai-Zhong Jiang Wangjin Lu Zhengguo Li Wei Deng | 2019 | Horticulture Research2019，6，1： | 3 |
| 3 | Significant influences of TiO_(2)crystal structures on NO_(2)and HONO emissions from the nitrates photolysis显示文摘The emissions of NO_(2)and HONO from the KNO_(3)photolysis in the presence of TiO_(2)were measured using a round-shape reactor coupled to a NO_(x)analyzer.TiO_(2)played important roles in the emission flux density of NO_(2)(R_(NO_(2)))and HONO(R HONO),depending on crystal structures and mass ratios of TiO_(2).R NO_(2)and R HONO significantly decreased with increasing the rutile and anatase mass ratios from 0 to 8 and 0.5 wt.%,respectively.Nevertheless,with further increasing the anatase mass ratio to 8 wt.%,there was an increase in R_(NO_(2))and R HONO.R NO_(2)on KNO_(3)/TiO_(2)/SiO_(2)had positive correlation with the KNO_(3)mass(1–20 wt.%),irradiation intensity(80–400 W/m^(2))and temperature(278–308 K),while it had the maximum value at the relative humidity(RH)of 55%.R HONO on KNO_(3)/TiO_(2)/SiO_(2)slightly varied with the KNO_(3)mass and temperature,whereas it increased with the irradiation intensity and RH.In addition,the mechanism for NO_(2)and HONO emissions from the nitrates photolysis and atmospheric implications were discussed. | Wenwen Xu Wangjin Yang Chong Han He Yang Xiangxin Xue | 2021 | Journal of Environmental Sciences2021，33，4： | 0 |
| 4 | Mitogen-activated protein kinase 14-mediated phosphorylation of MaMYB4 negatively regulates banana fruit ripening显示文摘Mitogen-activated protein kinase(MAPK/MPK)cascades play crucial parts in plant growth,development processes,immune ability,and stress responses;however,the regulatory mechanism by which MAPK affects fruit ripening remains largely unexplored.Here,we reported that MaMPK14 cooperated with MaMYB4 to mediate postharvest banana fruit ripening.Transient overexpression of individual MaMPK14 and MaMYB4 in banana fruit delayed fruit ripening,confirming the negative roles in the ripening.The ripening negative regulator MaMYB4 could repress the transcription of genes associated with ethylene biosynthesis and fruit softening,such as MaACS1,MaXTH5,MaPG3,and MaEXPA15.Furthermore,MaMPK14 phosphorylated MaMYB4 at Ser160 via a direct interaction.Mutation at Ser160 of MaMYB4 reduced its interaction with MaMPK14 but did not affect its subcellular localization.Importantly,phosphorylation of MaMYB4 by MaMPK14 enhanced the MaMYB4-mediated transcriptional inhibition,binding strength,protein stability,and the repression of fruit ripening.Taken together,our results delineated the regulation pathway of MAPK module during banana fruit ripening,which involved the phosphorylation modification of MaMYB4 mediated by MaMPK14. | Yingying Yang Chaojie Wu Wei Shan Wei Wei Yating Zhao Jianfei Kuang Jianye Chen Yueming Jiang Wangjin Lu | 2023 | Horticulture Research2023，10，1： | 0 |
您所在的机构暂未开通此部分的功能，请联系管理员