Addressing transboundary conservation challenges through marine spatial prioritization

The Adriatic and Ionian Region is an important area for both strategic maritime development and biodiversity conservation in the European Union (EU). However, given that both EU and non‐EU countries border the sea, multiple legal and regulatory frameworks operate at different scales, which can hinder the coordinated long‐term sustainable development of the region. Transboundary marine spatial planning can help overcome these challenges by building consensus on planning objectives and making the trade‐offs between biodiversity conservation and its influence on economically important sectors more explicit. We address this challenge by developing and testing 4 spatial prioritization strategies with the decision‐support tool Marxan, which meets targets for biodiversity conservation while minimizing impacts to users. We evaluated these strategies in terms of how priority areas shift under different scales of target setting (e.g., regional vs. country level). We also examined the trade‐off between cost‐efficiency and how equally solutions represent countries and maritime industries (n = 14) operating in the region with the protection‐equality metric. We found negligible differences in where priority conservation areas were located when we set targets for biodiversity at the regional versus country scale. Conversely, the prospective impacts on industries, when considered as costs to be minimized, were highly divergent across scenarios and biased the placement of protection toward industries located in isolation or where there were few other industries. We recommend underpinning future marine spatial planning efforts in the region through identification of areas of national significance, transboundary areas requiring cooperation between countries, and areas where impacts on maritime industries require careful consideration of the trade‐off between biodiversity conservation and socioeconomic objectives.     

脱硫渣废弃物对盐碱地油葵根际微生物数量及土壤酶活性的影响

通过大田实验,研究了不同脱硫渣废弃物对油葵（Helianthus annuus）根际微生物数量和酶活性的影响。结果表明：随着生育期的进行,微生物总量在苗期和花期数量较少,成熟期是数量较多。脱硫渣施用量对油葵根际微生物数量及酶活性均产生影响,微生物总量和油葵根际土壤酶活性均随着脱硫渣施用量的增加呈现出先升高后下降的趋势,同一生育期内,微生物总量以C（1.5 t/hm2）或D（2.25 t.hm-2）处理的微生物数量较高,B（0.75 t.hm-2）处理时的微生物数量较少;表明施用适量的脱硫渣有益于油葵根际微生物数量和酶活性的提高,过高则导致微生物数量和酶活性下降。     

Application of permanganate in the oxidation of micropollutants: a mini review

As a green oxidant, permanganate has received considerable attention for the removal of micropollutants in drinking water treatment. To provide a better understanding of the oxidation of organic micropollutants with permanganate, the oxidation kinetics of 32 micropollutants were compiled. The pollutants include algal toxins, endocrine disrupting chemicals (EDCs), and pharmaceuticals. The oxidation kinetics of micropollutants by permanganate were found to be first order with respect to both contaminant and permanganate concentrations from which second-order rate constants (k″) were obtained. Permanganate oxidized the heterocyclic aromatics with vinyl moiety (i.e., microcystins, carbamazepine, and dichlorvos) by the addition of double bonds. For the polycyclic aromatic hydrocarbons (PAHs) with alkyl groups, permanganate attacked the benzylic C-H through abstraction of hydrogen. The mechanism for the oxidation of phenolic EDCs by permanganate was a single electron transfer and aromatic ring cleavage. The presence of background matrices could enhance the oxidation of some phenolic EDCs by permanganate, including phenol, chlorinated phenols, bisphenol A, and trichlosan. The toxicity of dichlorvos solution increased after permanganate oxidation, and the estrogenic activity of bisphnol A/estrone increased significantly at the beginning of permanganate oxidation. Therefore, the toxicity of degradation products or intermediates should be determined in the permanganate oxidation processes to better evaluate the applicability of permanganate. The influence of background ions on the permanganate oxidation process is far from clear and should be elucidated in the future studies to better predict the performance of permanganate oxidation of micropollutants. Moreover, methods should be employed to catalyze the permanganate oxidation process to achieve better removal of micropollutants.     

市政污泥焚烧过程中重金属迁移转化行为研究进展

焚烧已成为市政污泥处置或资源化利用的重要手段.焚烧过程会改变市政污泥中重金属的化合态和价态,从而影响其迁移转化行为.目前,国内外已对市政污泥焚烧过程中重金属的迁移转化行为开展了大量研究.梳理和归纳了市政污泥特性以及焚烧炉炉型、焚烧温度、停留时间、反应气氛和添加物等工况对重金属迁移转化行为影响的研究进展,并提出了未来仍需...     

气候变化对澜沧江-湄公河上中游径流的影响研究

将区域气候模式RegCM3与水循环模拟模型WACM进行单向耦合,对澜沧江-湄公河流域未来气候变化和流域上中游主要控制水文站径流响应进行了模拟和分析。区域气候预估表明,相对于现状(1980—2009年),A1B情景下未来(2010—2039年)流域年平均温度和降水均有增加趋势,分别增加了0.65 ℃和1.87%,但降水增加不明显;流域北部温度增幅比南部明显,而降水区域差异较大,变化较为复杂。径流模拟结果表明,未来气候变化情景下,清盛和琅勃拉邦站多年平均径流量与天然情景相比均有减少趋势,分别减少了1.23%和3.69%,但变化不明显;未来径流年际变化呈不显著的减少趋势,而温度变化对径流影响作用要强于降水;未来春季和夏季(3—6月)径流增减相对明显,局部区域有洪涝和水文干旱的风险,而其它月份径流变化不显著。     

热解工艺参数和污泥理化性质对污泥残渣特性的影响

研究了热解工艺参数和污泥理化性质对热解残渣特性的影响,着重分析了不同热解工艺参数和污泥理化性质下,污泥热解残渣的吸附性能与内部孔结构.研究表明,当热解终温Tend在300℃—550℃之间,污泥热解残渣的碘值在450℃时最大,亚甲基蓝值在500℃时最小.热解残渣的碘值随着RT的延长先增大,当停留时间RT=75 min时达到最大值;亚甲基蓝值的最小值随着RT的延长逐渐往低温区移动.污泥热解残渣的碘值随着升温速率β的增大而减小,无论Tend的高低,亚甲基蓝值的最小值都出现在β=3℃.min-1.污泥热解残渣的比表面积随着颗粒粒径d的增大迅速减小,但d对残渣吸附性能的影响却不大.当含水率M=10%—40%,热解残渣的吸附性能基本不受M的影响;继续提高含水率,热解残渣的碘值迅速减小,而亚甲基蓝值却随M的增大而增大.Tend为450℃、RT为75 min和β为3℃.min-1是较佳的污泥热解工艺参数.     

难降解有机污染物与葡萄糖的光电催化协同氧化作用

利用薄层反应器研究了典型的难降解有机污染物——三环癸胺在二氧化钛纳米管阵列电极表面的光电催化降解性能,重点考察了三环癸胺与葡萄糖的光电催化协同氧化作用.研究表明,三环癸胺作为一种化学性质稳定的化合物,在薄层反应器中难以在二氧化钛纳米管阵列电极光电催化中实现完全降解.在三环癸胺COD浓度50—400 mg.L-1条件下,其降解效率均低于30%,且随着三环癸胺浓度的增加降解效率下降.三环癸胺与葡萄糖之间存在着明显的光电催化协同氧化作用,且随着葡萄糖浓度的增加协同作用增强,当葡萄糖与三环癸胺浓度比值大于2时,可以实现三环癸胺的完全降解.在光电催化协同氧化过程中,三环癸胺与葡萄糖的降解并非同步进行,易降解的多羟基葡萄糖所产生的大量羟自由基,可能促进了三环癸胺或三环癸胺中间产物的氧化.该研究也为难降解的有机物的光电催化处理提出了一条新的途径.     

A GC method to determine o‐chloroacetophenone residual in soil and vegetable substrates

o‐Chloroacetophenone (CAF) is a peripheral sensory irritant used in open air situations giving rise to human and environmental exposure. An analytical GC method has been developed to determine CAF residual in soil and vegetable substrates at low ppm levels.     

甲草胺热裂解气相色谱-质谱分析

甲草胺是一种广泛用于农作物上的酰胺类除草剂.本文利用裂解气相色谱与质谱联用(Py-GC-MS)研究了甲草胺在热裂解温度200℃、400℃、600℃、800℃下的降解产物和热降解机理.实验结果表明,共有60种裂解产物被分离鉴定,随着温度的升高甲草胺显著分解,当裂解温度超过600℃时,大量的芳烃类、喹啉类、吲哚类化合物在高温裂解中产生,温度越高他们的相对含量也越高.基于对裂解产物的定性和它们含量的变化提出了甲草胺的热降解机理.