Bioindication of volatile elements emission by the Puyehue-Cordón Caulle (North Patagonia) volcanic event in 2011

The emission of volatile pollutants from the volcanic eruption of the Puyehue-Cordón Caulle complex (North Patagonia Andean Range) that started in June 4th, 2011, was investigated by bioindication means with the epyphytic fruticose lichen Usnea sp. The elemental composition of pooled samples made up with 10 lichen thalli were analysed by Instrumental Neutron Activation Analysis. Eleven sampling sites were selected within the impacted region at different distance from the volcanic source. Five sites were selected as they were already sampled in a previous study prior to the eruption. Two other new sampling sites were selected from outside the impacted zone to provide non-impacted baseline sites.The elements associated with the lichen incorporation of particulate matter (PM) of geological origin were identified by linear correlation with a geochemical tracer (Sm concentrations). The elements associated with PM uptake were Ce, Eu, Fe, Hf, La, Lu, Na, Nd, Sb, Sc, Se, Ta, Tb, Th, U, and Yb. Arsenic and Cs concentrations showed contributions exceeding the PM fraction in sites near the volcanic centre, also higher than the baseline concentrations, which could be associated with permanent emissions from the geothermal system of the Puyehue-Cordón Caulle complex. The lichen concentrations of Ba, Ca, Co, Hg, K, Rb, Sr, and Zn were not associated with the PM, not showing higher concentrations in the sites nearby the volcanic source or respect to the baseline values either. Therefore, there is no indication of the emission of volatile forms of these elements in the lichen records. The lichen records only identified Br volatile emissions associated with the Puyehue-Cordón Caulle complex eruption in 2011.     

长白山天池火山的研究现状与展望

较详细地介绍了近年来长白山天池火山喷发历史、火山形成机制、火山系统的探测和火山灾害的研究现状，指出了当前研究中存在的一些主要问题。建议今后应加强火山活动历史研究；探测岩浆作用及其动态变化，限定火山失稳条件；研究岩浆作用和火山触发机制；开展火山作用的试验模拟和火山灾害区划的定量模拟研究；建立火山灾害预警系统，制定火山灾害应急预案，以达到减轻火山灾害的目的。     

基于分步热解技术的沉积岩形态汞同位素分析方法

沉积岩中的汞及其同位素常被用于指示大规模火山活动、海洋氧化还原演变等古环境演化事件,但现有研究主要聚焦总汞含量及相应的总汞同位素组成,缺少形态汞含量及其同位素组成数据,因此无法精准判别古环境中汞的来源、沉积环境和沉积过程。本研究开发了基于热解技术的沉积岩中不同形态汞的分离和同位素分析方法。首先通过沉积岩中典型形态汞（有机质、硫化物和粘土矿物结合态汞）单一标准建立热解温度曲线,然后将上述单一标准物质混合,通过调整升温速率以及形态汞采集的温度范围和时间优化热解分离方法,收集不同温度下析出的气态单质汞进行同位素分析。结果表明,分离的有机质结合态及硫化物结合态汞的δ²⁰²Hg和Δ¹⁹⁹Hg值同参考值的平均差值分别小于0.20‰和0.03‰,因此该分离方法能有效分离上述形态汞并进行汞同位素组成分析。上述方法被进一步应用于分析天然标准物质（黄红壤、水系沉积物、海相沉积岩）的汞形态及其同位素组成,验证了该方法在自然样品中的广泛适用性。     

Environmental Radioactivity and Volcanological Features of Three Islands of the Mediterranean Sea (Pantelleria, Ustica and Vulcano)

The Mediterranean Sea is an area of great interest for its volcanic activities. This paper presents a comparative study of radiometric and chemical data regarding three volcanic islands located in southern Italy (Pantellena, Ustica, and Vulcano) characterized by different magmatic histories. Measurements of radionulide contents and chemical composition of rock samples belonging to the main lithologies present in the three islands were carried out the observed correlations among radiometric, chemical and mineralogical data reflect the differences in the volcanological genesis and suggest some hypotheses on the magmatic evolution.     

Mechanism of lead immobilization by oxalic acid-activated phosphate rocks

Lead (Pb) chemical fixation is an important environmental aspect for human health. Phosphate rocks (PRs) were utilized as an adsorbent to remove Pb from aqueous solution. Raw PRs and oxalic acid-activated PRs (APRs) were used to investigate the effect of chemical modification on the Pb-binding capacity in the pH range 2.0-5.0. The Pb adsorption rate of all treatments above pH 3.0 reached 90%. The Pb binding on PRs and APRs was pH-independent, except at pH 2.0 in activated treatments. The X-ray diffraction analysis confirmed that the raw PRs formed cerussite after reacting with the Pb solution, whereas the APRs formed pyromorphite. The Fourier Transform Infrared spectroscopy analysis indicated that carbonate (CO₃^2-) in raw PRs and phosphate (PO₄^3-) groups in APRs played an important role in the Pb-binding process. After adsorption, anomalous block-shaped particles were observed by scanning electron microscopy with energy dispersive spectroscopy. The X-ray photoelectron spectroscopy data further indicated that both chemical and physical reactions occurred during the adsorption process according to the binding energy. Because of lower solubility of pyromorphite compared to cerussite, the APRs are more effective in immobilizing Pb than that of PRs.     

黑龙江二克山及其邻区富钾火山岩系的地球化学探讨

基于12个微量元素、10个稀土元素和24个同位素分析结果,作者认为本区钾质火山岩系中超基性岩和极大多数基性岩有接近原生岩浆的成分,岩浆都是地幔岩石低程度部分熔融形成的,其源岩成分为受流体交代的金云母石榴石二辉橄榄岩。综地球化学、地球物理及地质三方面资料分析,论证本区火山活动的构造背景是大陆裂谷。     

软质岩边坡挂网植草绿化防护技术研究

挂网植草解决了红砂岩、紫砂岩等软质岩石坡面因没有土层而不能绿化的难题。在经平整的软质岩石边坡上,铺粘10～15cm厚的泥浆层,满植规格为40×40cm狗牙根(Cynodon dactylon)、假俭草(Eremochloa ophiuroides)、结缕草(Zoysia japonica)等具有匍匐枝茎、耐瘠薄土壤、有良好的水土保持力等特性的草皮,草层上盖2.5×30m高强度的专用塑料网,用钢钉和竹签加以固定,造价为28～30元/m~2,是混凝土喷射、窗式护面墙等其它防护方法成本的1/3～1/5。在京珠、潭邵等高速上推广了近400 000 m~2,能在最短的时间内恢复植被,形成优美的景观,又能发挥较好的生态防护作用。该技术材料来源广、工艺操作易、实用性强,可广泛应用于公路、铁路、水库、堤坡等软质岩石地段的景观绿化与生态防护。     

岩溶生态系统的土壤

岩溶生态系统的土壤是岩溶地区岩石、大气、水、生物等四大圈层相互作用的产物，成土速率较慢，土壤剖面和空间分布受地貌演化阶段和岩溶双层空间结构的控制。在碳酸盐岩的差异侵蚀和土壤丧失的作用下，岩溶生态系统的土壤逐渐向裂隙和低洼部位退缩，形成景观中的土壤资源斑块，成为岩溶生态系统的养分库、水库和种子库，这种自然演替形成的小尺度上的土壤斑块和生境异质性对于维持岩溶景观的健康状况是非常重要的。今后的研究应着重从岩溶表层生态系统的运行过程中来把握岩溶生态系统土壤的动态特征和相互间的反馈关系。     

Effect of low-molecular weight organic acids on phosphorus release and phytoavailabilty of phosphorus in phosphate rocks added to soils

Phosphorus (P) is critically needed to improve soil fertility in many parts of the world. The use of water-soluble P fertilizers, e.g., single super-phosphate and triple super-phosphate in developing countries to improve crop production has been limited primarily by their high cost. The presence of indigenous phosphate deposits in some countries provides an incentive for direct application or local chemical treatment at low cost to improve the solubility of low reactive phosphate rocks (PRs). The use of naturally occurring low-molecular weight organic acids (LMWOAs) that are produced in soil as microbial metabolites or plant exudates from dead or living cells represents a new perspective in PR research. The LMWOAs contain various functional groups that may play a significant role in PR dissolution. Little information is available, however, about the potential of LMWOAs in releasing P from PRs. This study reports P release from 12 PRs, four each of low, medium, and high reactivity, obtained from various deposits (Kodjari, Tahoua, North Carolina, Gafsa, Khouribga, Tilemsi Valley, Central Florida, Sechura, Minjingu, North Florida, Hahotoe, and Parc W) using nine LMWOAs containing mono-, di-, and tri-carboxylic groups and a mineral acid (H₂SO₄). Laboratory studies showed that the organic acids are effective in releasing P from low and medium reactive PRs, but very ineffective in releasing P from high reactive PRs. The average amounts of P released by all the organic acids from the three types of PRs were 65.5 mmol kg⁻¹ PR from the low reactive PRs, 55.1 mmol kg⁻¹ from the medium, and 11.1 mmol kg⁻¹ from the high; those released from across all the PRs were 21.9 by the mono-carboxylic acid group, 54.2 by the di-carboxylic acid group, and 57.0 mmol P kg⁻¹ by the tri-carboxylic acid group. The P released was negatively correlated with the equilibrium pH, but positively correlated with Ca released from the PRs. Laboratory incubation studies on the release of P from PRs added to soils with or without organic acids and incubated at 25 °C for 15, 30, and 45 days showed that the percentage of plant-available P released varied considerably from 0.95 in the Kodjari PR to 40.1% in the North Carolina PR and was related to PR reactivity. A greenhouse study with corn (Zea mays L.) grown for 60 days on soils treated with PRs or with PRs mixed with organic acids showed that corn response to addition of oxalic or citric acid varied with P rates and PR sources, suggesting that organic acids have potential as amendments for increasing plant-available P in PR-treated soils.     

火山岩填料曝气生物滤池的SNAD工艺启动特性及功能菌丰度演替

为研究同步亚硝化、厌氧氨氧化耦合反硝化(SNAD)工艺在浸没式生物滤池反应器(SBAF)内的运行特性,同时接种亚硝化污泥和富集ANAMMOX的填料启动SNAD反应器.结果表明在60 mg·L~(-1)有机物浓度下,自养脱氮和反硝化实现较好的耦合,并在该浓度下稳定运行了67 d,其总氮去除率最高可达92.0%,COD去除率最高达82.9%,最高总氮去除负荷为2.3 kg·(m~3·d)~(-1).与全程自养脱氮(CANON)工艺相比,SNAD工艺的平均总氮去除率提高了12.6%.荧光定量PCR结果显示,系统启动后AOB菌的丰度有所增长,ANAMMOX菌的丰度增长了1个数量级,而NOB菌和反硝化菌的数量维持在较低水平(小于10~7 copies·g~(-1)),表明以火山岩为填料的浸没式生物滤池反应器有利于ANAMMOX和AOB的协同生长,可快速实现SAND工艺的启动.