太湖表层沉积物多环芳烃的空间分布、来源及其风险

随着太湖流域社会与经济的发展,多环芳烃(PAHs)在各种环境介质中逐渐累积,污染日益严重,可能对太湖生态环境及周边人体健康构成威胁。为探究太湖沉积物PAHs的来源及生态风险,于2021年12月在太湖采集30个表层沉积物样品,利用气相色谱-质谱联用仪(GC-MS)检测样品中16种PAHs含量;利用受体模型和苯并[a]芘(BaP)毒性当量法进行来源解析及生态风险评估,并将各来源贡献与毒性当量浓度相结合,量化源风险。结果表明,太湖表层沉积物中16种PAHs总含量介于124~592 ng/g之间,平均值为294 ng/g,中值为279 ng/g;高环多环芳烃(HMW PAHs)为主要组分,占∑PAHs的67%。高含量区域位于竺山湾、梅梁湾、贡湖湾和西太湖,与国内外其他湖泊沉积物相比,太湖沉积物PAHs含量处于较低水平。源解析的结果表明,太湖表层沉积物中PAHs交通排放源贡献率为29.1%、煤炭燃烧源贡献率为26.7%、生物质燃烧源贡献率为28.7%、石油源贡献率为15.6%。生态风险评价结果表明,交通排放源、生物质燃烧源、煤炭燃烧源和石油源的BaP毒性当量含量(TEQ_BaP)均值分别为19.34、17.81、16.33和9.1 ng/g,均小于70 ng/g,几乎处于无风险水平。西太湖、贡湖湾和梅梁湾的部分区域ΣTEQ_BaP大于70 ng/g属于潜在风险区,具有一定潜在毒性。在后续的污染治理中应重点关注太湖西北部地区污染物的排放。本研究可为沉积物中PAHs污染的研究提供数据支撑,为地方政府精准、高效地管控PAHs污染提供理论依据。     

建国前中国共产党获取群众支持经验浅析

从1921年中国共产党的成立到1949年中华人民共和国成立前,是中国共产党创建与局部执政时期。这时期,中国共产党及其领导下的军队为了获取群众支持,积累了丰富的经验。这些经验可以概括为:关心群众利益,让群众拥护党和政府;实行精兵简政,让群众理解党和政府;严惩贪污腐败,让群众相信党及其领导下的地方政府。     

自动建模客观分型方法在非汛期人工增雨中的应用

根据安徽省人工影响天气业务系统需要,利用NCEP 500 hPa高度场和风场格点资料及安徽省81站10年非汛期逐日降水资料,在客观分析天气形势基础上,结合预报员实践经验给出的不同系统影响安徽省时的关键区,计算机自动建模,形成逐日天气型日历,实现环流分型客观化。此方法识别条件实用,模型物理意义明确,自动化程度高,自动生成的逐日天气型日历,为安徽省非汛期人工增雨作业指挥系统提供了很好的天气预报参考依据。     

Conditions of pocket formation in the Oktyabrskaya tourmaline-rich gem pegmatite (the Malkhan field, Central Transbaikalia, Russia)

Coexisting melt (MI), fluid-melt (FMI) and fluid (FI) inclusions in quartz from the Oktaybrskaya pegmatite, central Transbaikalia, have been studied and the thermodynamic modeling of PVTX-properties of aqueous orthoboric-acid fluids has been carried out to define the conditions of pocket formation. At room temperature, FMI in early pocket quartz and in quartz from the coarse-grained quartz–oligoclase host pegmatite contain crystalline aggregates and an orthoboric-acid fluid. The portion of FMI in inclusion assemblages decreases and the volume of fluid in inclusions increases from the early to the late growth zones in the pocket quartz. No FMI have been found in the late growth zones. Significant variations of solid/fluid ratios in the neighboring FMI result from heterogeneous entrapment of coexisting melts and fluids by a host mineral. Raman spectroscopy, SEM EDS and EMPA indicate that the crystalline aggregates in FMI are dominated by mica minerals of the boron-rich muscovite–nanpingite CsAl₂[AlSi₃O₁₀](OH,F)₂ series as well as lepidolite. Topaz, quartz, potassium feldspar and several unidentified minerals occur in much lower amounts. Fluid isolations in FMI and FI have similar total salinity (4–8 wt.% NaCl eq.) and H₃BO₃ contents (12–16 wt.%). The melt inclusions in host-pegmatite quartz homogenize at 570–600 °C. The silicate crystalline aggregates in large inclusions in pocket quartz completely melt at 615 °C. However, even after those inclusions were significantly overheated at 650±10 °C and 2.5 kbar during 24 h they remained non-homogeneous and displayed two types: (i) glass+unmelted crystals and (ii) fluid+glass. The FMI glasses contain 1.94–2.73 wt.% F, 2.51 wt.% B₂O₃, 3.64–5.20 wt.% Cs₂O, 0.54 wt.% Li₂O, 0.57 wt.% Ta₂O₅, 0.10 wt.% Nb₂O₅, 0.12 wt.% BeO. The H₂O content of the glass could exceed 12 wt.%. Such compositions suggest that the residual melts of the latest magmatic stage were strongly enriched in H₂O, B, F, Cs and contained elevated concentrations of Li, Be, Ta, and Nb. FMI microthermometry showed that those melts could have crystallized at 615–550 °C.

Crystallization of quartz–feldspar pegmatite matrix leads to the formation of H₂O-, B- and F-enriched residual melts and associated fluids (prototypes of pockets). Fluids of different compositions and residual melts of different liquidus–solidus P–T-conditions would form pockets with various internal fluid pressures. During crystallization, those melts release more aqueous fluids resulting in a further increase of the fluid pressure in pockets. A significant overpressure and a possible pressure gradient between the neighboring pockets would induce fracturing of pockets and “fluid explosions”. The fracturing commonly results in the crushing of pocket walls, formation of new fractures connecting adjacent pockets, heterogenization and mixing of pocket fluids. Such newly formed fluids would interact with a primary pegmatite matrix along the fractures and cause autometasomatic alteration, recrystallization, leaching and formation of “primary–secondary” pockets.     

珍珠陶石的夹层化合物法鉴定

应用联氨、使珍珠陶石形成其夹层物，然后再用水洗获是水合珍珠陶石，这种水合珍珠陶石具有十分特征的０．８３５ｎｍＸ射线衍射峰，而高岭石族的其它矿物却保持不变，利用这一明显的特征，可以容易地区分出混合在高岭石中的少量珍珠陶石。     

山西义兴寨金矿床地球化学研究

晋东北地区以唐河大断裂为核心的一组早燕山期 NW向张剪性断裂与区域 NE向复向斜复合部位 ,控制着区内燕山期中酸性浅成侵入体及其与之有关的铁、金、铜矿化 ,义兴寨金矿是该地区具代表性的典型矿床。金矿床为热液型脉状金 -多金属矿床 ,矿体受岩体和断裂构造控制。金矿床分 4个成矿期 ,8个亚期。对金矿床的矿床地质特征、成矿流体成分、性质、成矿物理化学条件及成矿时代的研究表明 ,成矿溶液的 p H值为 6 .1 6～ 6 .5 3:Eh值为 -0 .2 81～-0 .2 80 ;lgf O2 =-3.6～ -2 9,lgf CO2 =4 .3～ 5 .2 ;成矿温度为 1 90～ 349℃ ;成矿压力为 2 0 .0～ 76 .0 MPa;矿床主成矿期石英的 40 Ar— 3 9Ar坪年龄为 ( 1 31 .4± 3.1 ) Ma。     

山西高家山铝土矿稀土元素地球化学特征及意义

山西沁源县高家山铝土矿床是山西省地质调查院于2013年发现的大型铝土矿床。本文通过对高家山铝土矿的研究,分析并研究铝土矿样品的稀土元素含量和地球化学特征,探讨稀土元素对于本区铝土矿成因和环境的指示意义。研究表明:该区铝土矿体的ΣREE总量较大,轻稀土元素相对富集,具有明显的Eu负异常;利用稀土元素图解大致反映出底板碳酸盐岩是本区铝土矿床的主要物质来源,铝土矿形成于被动大陆边缘地带海相或海陆过渡相环境。ΣREE与Al2O3含量相关性不大。本区矿床稀土元素含量达到或超过综合利用标准,具有巨大的潜在经济价值。     

中国区域地壳稳定性定量化评价与分区

中国地处环太平洋构造带与地中海构造带交接部位,地质构造复杂,活动性较为强烈,各种内动力地质灾害比较严重,总体看来中国区域地壳稳定性相对较差。为了使区域地壳稳定性评价与分区获得定量化认识,更好地服务于经济建设和减灾防灾,本文在分析中国现今活动的主要构造体系与内动力地质灾害的分布规律的基础上,首先进行区域地壳稳定性定量化评价待评区的划分;其次进行定量化评价指标的选定、取值、权重分配及评价标准的确定;最后运用模糊数学进行中国区域地壳稳定性定量化评价与分区。      

居室氡的影响因素及分布特点

氡是天然放射性系列铀系中唯一的气态元素,它对人体健康的影响尤其是氡与肺癌的关系已引起人们的高度重视,已成为环境保护研究的一个重要对象.本文就地壳中放射性元素的分布规律及氡的迁移进行介绍,并着重讨论了居室氡的影响因素,以期利于今后氡危害防治工作的进行.