基于余震序列分布信息的地震极灾区快速判断方法研究

利用震级加权标准差椭圆法研究了基于震后短期内(24 h)余震序列判定地震极灾区的方法,研究结果表明:1利用该方法判断宏观震中是一种比较可行的方法,不同震源破裂方式的震例利用该方法判断宏观震中的精度不同,倾滑-近倾滑型破裂方式的震例利用余震序列判定宏观震中的精度最高;2整体上看,利用该方法判断极灾区长轴方向的准确性低于利用距震中最近活动断裂判断的准确性,但对于倾滑-近倾滑型破裂方式的震例,利用该方法的准确性高于利用断层数据判定的准确性。     

Microcystis aeruginosa/Pseudomonas pseudoalcaligenes interaction effects on off-flavors in algae/bacteria co-culture system under different temperatures

We conducted an experiment to study the interaction effects of Microcystis aeruginosa and Pseudomonas pseudoalcaligenes on off-flavors in an algae/bacteria co-culture system at three temperatures (24, 28 and 32°C). Gas chromatography–mass spectrometry was applied to measure off-flavor compounds dimethyl sulfide (DMS), dimethyl trisulfide (DMTS), 2-methylisoborneol, geosmin (GEO) and β-cyclocitral. During the lag phase of co-cultured M. aeruginosa (first 15 days), P. pseudoalcaligenes significantly increased the production of DMS, DMTS and β-cyclocitral at all three temperatures. In the exponential phase of co-cultured M. aeruginosa (after 15 days), M. aeruginosa became the main factor on off-flavors in the co-culture system, and β-cyclocitral turned to the highest off-flavor compound. These results also indicated that DMS, DMTS and β-cyclocitral were the main off-flavor compounds in our M. aeruginosa/P. pseudoalcaligenes co-culture system. Univariate analysis was applied to investigate the effects of M. aeruginosa and P. pseudoalcaligenes on the production of off-flavors. The results demonstrated that both M. aeruginosa and P. pseudoalcaligenes could increase the production of DMS and DMTS, while β-cyclocitral was mainly determined by M. aeruginosa. Our results also provide some insights into understanding the relationship between cyanobacteria and heterotrophic bacteria.     

Bioreduction of vanadium (V) in groundwater by autohydrogentrophic bacteria: Mechanisms and microorganisms

As one of the transition metals, vanadium (V) (V(V)) in trace amounts represents an essential element for normal cell growth, but becomes toxic when its concentration is above 1 mg/L. V(V) can alter cellular differentiation, gene expression, and other biochemical and metabolic phenomena. A feasible method to detoxify V(V) is to reduce it to V(IV), which precipitates and can be readily removed from the water. The bioreduction of V(V) in a contaminated groundwater was investigated using autohydrogentrophic bacteria and hydrogen gas as the electron donor. Compared with the previous organic donors, H₂ shows the advantages as an ideal electron donor, including nontoxicity and less production of excess biomass. V(V) was 95.5% removed by biochemical reduction when autohydrogentrophic bacteria and hydrogen were both present, and the reduced V(IV) precipitated, leading to total-V removal. Reduction kinetics could be described by a first-order model and were sensitive to pH and temperature, with the optimum ranges of pH 7.5–8.0 and 35–40°C, respectively. Phylogenetic analysis by clone library showed that the dominant species in the experiments with V(V) bioreduction belonged to the β-Proteobacteria. Previously known V(V)-reducing species were absent, suggesting that V(V) reduction was carried out by novel species. Their selective enrichment during V(V) bioreduction suggests that Rhodocyclus, a denitrifying bacterium, and Clostridium, a fermenter known to carry out metal reduction, were responsible for V(V) bioreduction.     

Mobility and sulfidization of heavy metals in sediments of a shallow eutrophic lake,Lake Taihu,China

The technique of DGT (diffusive gradients in thin films) using three diffusive gel thicknesses was applied to estimate the mobility and bioavailability of heavy metals in sediments and porewater of Lake Taihu, China. The DGT results showed significantly positive correlations between Co, Pb, Cd and Mn, and Ni and Fe concentrations in porewater. Cu and Zn showed a significantly negative correlation with Mn, due to Cu combination with carbonates and Zn derived from agricultural pollution, respectively. The rank order of average concentrations of Co, Ni and Cd at each station was DGT_1.92 > DGT_0.78 > DGT_0.39, suggesting stronger resupply from sediments to porewater when using thicker diffusive gels. Comparing centrifugation and DGT measurements, Co, Ni and Cd are highly labile; Mn and Fe are moderately labile; and Cu, Zn and Pb are slightly labile. The variations of AVS concentrations in sediment cores indicate that metal sulfides in deeper layers are easily diffused into surface sediments.     

Microcystis aeruginosa/Pseudomonas pseudoalcaligenes interaction effects on off-flavors in algae/bacteria co-culture system under different temperatures

We conducted an experiment to study the interaction effects of Microcystis aeruginosa and Pseudomonas pseudoalcaligenes on off-flavors in an algae/bacteria co-culture system at three temperatures(24, 28 and 32℃). Gas chromatography–mass spectrometry was applied to measure off-flavor compounds dimethyl sulfide(DMS), dimethyl trisulfide(DMTS),2-methylisoborneol, geosmin(GEO) and β-cyclocitral. During the lag phase of co-cultured M. aeruginosa(first 15 days), P. pseudoalcaligenes significantly increased the production of DMS, DMTS and β-cyclocitral at all three temperatures. In the exponential phase of co-cultured M. aeruginosa(after 15 days), M. aeruginosa became the main factor on off-flavors in the co-culture system, and β-cyclocitral turned to the highest off-flavor compound. These results also indicated that DMS, DMTS and β-cyclocitral were the main off-flavor compounds in our M. aeruginosa/P. pseudoalcaligenes co-culture system. Univariate analysis was applied to investigate the effects of M. aeruginosa and P. pseudoalcaligenes on the production of off-flavors. The results demonstrated that both M. aeruginosa and P. pseudoalcaligenes could increase the production of DMS and DMTS, while β-cyclocitral was mainly determined by M. aeruginosa. Our results also provide some insights into understanding the relationship between cyanobacteria and heterotrophic bacteria.     

酸浸法回收制革污泥中的铬

利用硫酸酸浸提取制革污泥中的金属铬,研究了固液比、酸浓度、浸出时间、温度和搅拌速度等因素对浸出效率的影响,并获得最优浸出条件。结果表明,最优浸出条件为:固液比10g/L,硫酸浓度0.5mol/L,浸出温度50℃,浸出时间1.5h。搅拌速度对硫酸浸出铬影响较小。经硫酸二次浸出铬的效率达到90.95%。因此,用硫酸酸浸的方法提取制革污泥中的铬是可行的。     

运用正弦扫频实现电动振动台模型的频域辨识

目的研究以电动振动台为典型设备的相关振动试验装置的频域辨识技术。方法通过分析电动振动台数学模型,采用正弦扫频试验方法,进行全频带振动台空台面正弦扫频,并对所获得的时域正弦扫频数据进行频谱分析,进而获得系统的频率数据,再运用复数域上的最小二乘拟合算法,完成振动台模型传递函数的辨识。结果通过某型电动台空台面试验,对一组实测数据进行辨识,辨识出的电动振动台模拟与真实模拟一致。结论通过该方法并合理选取模型结构,能够很好地辨识出振动试验装置的模型。     

甘肃南部典型城镇PM2.5浓度及水溶性离子特征分析

为研究甘肃南部城镇PM_2.5及水溶性离子（WSIIs）浓度水平,于2019年4月—2020年2月在甘肃成县按季度进行PM_2.5样品采集,分析了其变化特征,并运用相关和主成分分析法进行来源解析.结果表明：采样期间甘肃成县PM_2.5年平均质量浓度为（57.2±26.9） μg·m^-3,表现为冬季>春季>秋季>夏季的季节变化特征,冬季质量浓度约为夏季的1.9倍,全年空气质量优良率为81%,其中夏季达100%.WSIIs质量浓度呈现SO₄^2->NO₃^->Na⁺>NH₄⁺>Ca²⁺> K⁺>Cl^->Mg²⁺的特征.SNA是浓度水平最高的3种水溶性离子,占8种主要水溶性离子浓度的70.1%.ρ（NO₃^-）/ρ（SO₄^2-）平均值为0.6,表明工农业生产及化石燃料燃烧排放等固定源是颗粒物污染的主要来源.新型冠状病毒疫情期间人员管控对PM_2.5和水溶性离子中SNA质量浓度影响显著,PM_2.5平均质量浓度降幅达44.2%.源解析表明,PM_2.5中WSIIs主要来自化石燃料燃烧、生物质燃烧及二次源和道路建筑扬尘等.     

Year-round observation of atmospheric inorganic aerosols in urban Beijing: Size distribution, source analysis, and reduction mechanism

To investigate particle characteristics and find an effective measure to control severe particle pollution, year-round observation of size-segregated inorganic aerosols was conducted in Beijing from January to December, 2016. The sampled atmospheric particles all presented bimodal size distribution at four pollution levels (clear, slight pollution, moderate pollution and severe pollution), and peak values appeared at the size range of 0.7-2.1 μm and >9.0 μm, respectively. As dominant particle compositions, NO₃⁻, SO₄²⁻, and NH₄⁺ in four pollution levels all showed significant peaks in fine mode, especially at the size range of 1.1-2.1 μm. Secondary inorganic aerosols accounted for about 67.6% (36.3% (secondary sulfates) + 31.3% (secondary nitrates)) of the total sources of fine particles in urban Beijing. Severe pollution of fine particles was mainly caused by the air masses transported from nearby western and southern areas, which are industrial and densely populated region, respectively. Sensitivity tests further revealed that the control measures focusing on ammonium emission reduction was the most effective for particle pollution mitigation, and fine particles all showed nonlinear responses after reducing ammonium, nitrate, and sulfate concentrations, with the fitting curves of y = -120.8x - 306.1x² + 290.2x³, y = -43.5x - 67.8x², and y = -25.8x - 110.4x² + 7.6x³, respectively (y and x present fine particle mass variation (μg/m³) and concentration reduction ratio (CRR)/100 (dimensionless)). Overall, our study presents useful information for understanding the characteristics of atmospheric inorganic aerosols in urban Beijing, as well as offers policy makers with effective measure for mitigating particle pollution.     

河北省某大型焦化厂地下水中多环芳烃的污染特点、源解析及生态风险评价

为研究焦化厂地下水中美国EPA优先控制的16种多环芳烃(PAHs)的分布特点和污染来源,本研究联合使用统计技术、正定矩阵因子分析(PMF)模型和风险商值法,深入分析了焦化厂地下水中PAHs的分布规律,定量解析了PAHs的污染来源,并且对其生态风险进行了科学评价.结果表明,焦化厂地下水中16种PAHs的总检出率较高,达到46.7%.地下水中∑₁₆PAHs的浓度范围是n.d.～444.9μg·L^-1,均值为1.88μg·L^-1.不同生产车间地下水中PAHs的浓度存在明显差异,其中污染最重的车间位于焦油精制区,地下水中∑₁₆PAHs的浓度为444.92μg·L^-1.应用PMF源解析模型,识别出该焦化厂地下水中PAHs有二类污染源：一是石油的燃烧源,二是煤和生物质燃烧以及石油类的泄漏,二种污染源对焦化厂地下水中PAHs的贡献率分别为38.6%和61.4%.焦化厂地下水中∑₁₆PAHs处在高生态风险等级,且有53.4%的地下水采样点单体PAHs的生态风险处在高风险等...