湖北九宫山甜槠群落结构与优势种的空间分布格局研究

通过对湖北九宫山国家级自然保护区甜槠群落建立的1ha固定森林样地进行植物群落调查,分析了样地内木本植物物种组成、区系成分、种群径级结构和空间分布格局,结果表明:(1)样地内木本植物(DBH≥1 cm)共有132种,隶属于42科78属,其中,杜鹃花科、壳斗科、樟科、蔷薇科、冬青科等是优势科,短柄袍、鹿角杜鹃、青冈、长叶石栎、甜槠等是优势种.(2)样地内植物科、属的分布类型均以泛热带分布类型为主,分别为30.95％和20.51％.(3)样地内所有木本植物个体的径级结构均呈倒"J"型,幼龄个体数量大,森林群落更新状况良好.(4)样地内木本植物个体的空间分布格局以聚集分布为主,部分优势物种在小尺度上呈聚集分布,而在较大尺度上则为随机分布.     

Lithium extraction from salt lake brines with high magnesium/lithium ratio: a review

Environmental Chemistry Letters - The demand for lithium is growing rapidly with the increase in electric vehicles, batteries and electronic equipments. Lithium can be extracted from brines, yet...     

A combined radical and non-radical oxidation processes for efficient degradation of Acid Orange 7 in the homogeneous Cu(II)/PMS system: important role of chloride

Environmental Science and Pollution Research - Trace copper ion (Cu(II)) in water and wastewater can trigger peroxymonosulfate (PMS) activation to oxidize organic compounds, but it only works under...     

原子荧光法测定水中汞的原子化条件研究

分别采用热原子化原子荧光法(热汞法)和冷原子化原子荧光法(冷汞法)测定水中汞,比较了两种方法的检出限、线性相关系数、准确度和精密度的差异。冷汞法和热汞法的检出限分别为0.003和0.01μg/L,标准曲线相关系数分别为0.999 9和0.999 7,加标回收率范围分别为102%~106%和106%~113%。结果表明,冷汞法比热汞法具有更低的检出限,灵敏度和准确度也略优于热汞法。对于冷汞法,提高负高压有利于提高方法的灵敏度、准确度,并具有更低的方法检出限。     

Approach to the management of magnesium slag via the production of Portland cement clinker

Journal of Material Cycles and Waste Management - This work aims to develop another approach to the management of magnesium slag (MS) via the production of Portland cement clinker. Thus, 0, 10, 20,...     

利用毒代动力学模型研究氟虫腈在夹杂带丝蚓体内的手性选择性积累过程

农药的生物积累直接影响其毒性,但是手性农药在生物体内的选择性积累过程仍不明确.本文在恒定环境水浓度的条件下,开展手性农药氟虫腈的外消旋体及其对映体在底栖无脊椎动物夹杂带丝蚓体内的生物积累实验.在96 h和72 h的吸收和消除实验过程中,测定生物体内的氟虫腈的外消旋体和对映体浓度随时间的变化情况,构建毒代动力学模型,获取吸收和消除速率常数.结果表明夹杂带丝蚓对R-氟虫腈的生物浓缩因子(1981 L·kg~(-1)脂肪)比对S-氟虫腈(1748 L·kg~(-1)脂肪)更大.R-氟虫腈和S-氟虫腈的吸收速率常数相当,分别为311±11 L·kg~(-1)脂肪·h~(-1)和313±13 L·kg~(-1)脂肪·h~(-1),而R-氟虫腈的消除速率常数小于S-氟虫腈,分别为0.157±0.006 h~(-1)和0.179±0.008 h~(-1),因此相对较慢的消除是导致R-氟虫腈在夹杂带丝蚓体内更高生物积累的主要原因.研究说明毒代动力学参数可有效阐释手性外源物质在生物体内选择性积累的差异.     

电化学开关表面活性剂对芘的可逆增溶作用

表面活性剂增强修复技术(SER)是目前行之有效的有机污染土壤修复技术,但SER技术存在表面活性剂与污染物分离困难、易导致二次污染、成本高等问题.基于此,提出采用具有电化学开关特性的表面活性剂(N,N-二甲基二茂铁甲基十二烷基溴化铵,Fc12)代替SER技术中的常规表面活性剂,发展基于开关表面活性剂的可逆增强修复技术(RSER).选取芘作为目标物,研究了Fc12在氧化和还原态对芘的增溶作用以及常见环境因素,如pH和温度对Fc12可逆增溶的影响.结果表明,相对于氧化态Fc12,还原态Fc12在其临界胶束浓度(CMC)以上时对芘表现出显著的增溶作用,且增溶能力随表面活性剂浓度增大而增强.温度对Fc12的增溶作用影响显著,例如,还原态Fc12在浓度为3 mmol·L~(-1)、25℃条件下时,芘的表观溶解度为0.779 mg·L~(-1),当温度增加到40℃时,芘的表观溶解度为0.971 mg·L~(-1),其表观溶解度增加了24.6%;但氧化态条件下,芘的表观溶解度仅增加了6.5%;芘的解吸率(芘在还原和氧化态Fc12的表观溶解度差值与还原态Fc12增溶芘的比值)由63.67%增加到71.27%.pH也显著影响Fc12的增溶,当pH值在6—10范围变化时,还原态Fc12的增溶作用呈现先增加后减小的趋势,且在pH 9附近增溶能力最强,而pH 8时芘的解吸果最好.     

土壤中挥发性芳香烃的顶空前处理方法研究

本方法针对土壤中挥发性芳香烃顶空前处理条件进行了研究,优化了顶空密封垫的选择、顶空平衡温度、加热平衡时间、进样时间和顶空瓶压力等顶空前处理条件,测定条件科学、准确,完全能够满足土壤中挥发性芳香烃监测分析的灵敏度和准确度相关的技术要求。该方法精密度为1.7%~9.8%,准确度为34.3%~83.7%,检出限为2.0~4.2μg/kg。为制订土壤中挥发性芳香烃监测分析方法提供了技术支持。     

Combined toxicity of imidacloprid,acetochlor, and tebuconazole to zebrafish ( Danio rerio ): acute toxicity and hepatotoxicity assessment

Compound pollution refers to two or more kinds of pollutants with different properties, a pollutant from different sources, or the simultaneous existence of two or more different types of pollutants in the same environment. In this study, we aimed to investigate the individual and combined toxicity of the insecticide imidacloprid (IMI), the herbicide acetochlor (ACT), and the fungicide tebuconazole (TBZ) to zebrafish. The acute toxicity test results showed that the 96-h LC50 values of IMI, ACT, and TBZ were 276.84 (259.62–294.35) mg active ingredient (a.i.) L−1, 1.52 (1.34–1.74) mg a.i. L−1, and 8.16 (7.7–8.6) mg a.i. L−1, respectively. The combinations of IMI, ACT, and TBZ with toxicity ratios of 1:2:2, 1:4:4, 2:4:1, and 4:1:4 displayed synergistic toxic effects on zebrafish, while the toxicity ratios of 1:1:1, 1:1:2, 2:1:2, 2:2:1, and 4:2:1 of IMI, ACT, and TBZ, respectively, exhibited antagonistic toxic effects on zebrafish. The following experiments were performed with a toxicity ratio of 1:4:4 (IMI:ACT:TBZ). The activities of four enzyme biomarkers related to oxidative stress in the liver, catalase (CAT), superoxide dismutase (SOD), glutathione S-transferase (GST), and malondialdehyde (MDA) content were evaluated in each exposure group on days 7, 14, 21, and 28. Compared with those of the control group, the activities of CAT, SOD, and GST and the MDA content were significantly altered at different time points in the individual and combined exposure groups. Additionally, the activities of CAT, SOD, and GST and the MDA content were significantly altered in the combined group compared with those of the individual group after 14 days or 21 days of exposure. Therefore, it was confirmed that combined toxicity studies are indispensable in risk assessment.     

Comparison on surface properties and desulfurization of MnO2 and pyrolusite blended activated carbon by steam activation

In this study, MnO₂ and pyrolusite were used as the catalysts to prepare modified activated carbon, that is, AC-Mn and AC-P, respectively, from coals by blending method and steam activation. The Brunauer–Emmett–Teller (BET) results indicated that the AC-P had higher surface areas and micropore volumes than the AC-Mn with the same blending ratio. The relative contents of basic functional groups (i.e., C = O, π-π*) on AC-P were slightly lower than those on AC-Mn, while both contained the same main metal species, namely, MnO. The desulfurization results showed that with 3 wt% of blending ratio, AC-Mn3 and AC-P3 had higher sulfur capacities at 220 and 205 mg/g, respectively, which were much higher than for the blank one (149.6 mg/g). Moreover, the AC-P had relatively higher sulfur capacity than the AC-Mn with the same contents of Mn, which might be attributed to the existence of other metals in pyrolusite. After the desulfurization process, MnO were gradually transferred into MnSO₄, and the relative contents of basic functional groups decreased evidently for both AC-Mn3 and AC-P3. The results demonstrated that pyrolusite could be one good alternative to MnO₂ to prepare modified activated carbon for desulfurization.

Implications: MnO₂ and pyrolusite were used as the additives to prepare modified activated carbon from coals by a blending method and by steam activation, that is, AC-Mn and AC-P, respectively. The AC-P had higher surface areas and micropore volumes than the AC-Mn with the same blending ratio. The AC-Mn and AC-P had higher sulfur capacities than a blank one. Moreover, the AC-P had relatively higher sulfur capacity than the AC-Mn with the same contents of Mn. The results demonstrated that pyrolusite could be one good alternative to MnO₂ to prepare modified activated carbon for desulfurizatio.