四川黄龙沟天然水中的深源CO_2与大规模的钙华沉积

在有大规模钙华沉积的四川黄龙沟中,使用化学成分数据以及碳氧稳定同位素组成对其水文地球化学特征进行了分析研究。研究区钙华沉积的地表溪流水质基本上受到两种水混合的制约,即断层泉水和山区的融雪(冰)水。泉水中含有高浓度的经由断层提供的CO2,结果高浓度的溶解CO2使得其溶解的碳酸盐岩比普通的岩溶泉溶解的碳酸盐岩高得多,同时也导致硅酸盐岩的溶解。黄龙沟中上游的泉水相对于方解石接近于平衡。溶解无机碳(DIC)的浓度和它们的δ13C值是大约由c=0.02mol·L1δ13C=-3‰的CO2(aq)与含有δ13C=+3‰的碳酸盐岩在封闭系统条件下反应的结果。估计这些CO2中约有70%来自上地幔。所有泉水的水化学数据均落在高岭石稳定域内,但对Na长石和Ca长石具有侵蚀性。由于这些长石矿物的溶解速率太慢,所以水中的化学成分远离长石稳定域。地表溪流的DIC种类之间达到同位素平衡,在不同观测点发现的δ13CDIC变化主要是由于从水中释放出的CO2的程度不同引起的。水样的δ18O值与其采集点的海拔高度之间存在线性关系;研究区的地表溪流的氧同位素组成受到蒸发的制约。在流经钙华沉积物的地表溪流中白天和夜晚的水化学及pH的日变化表明生物作用促进了碳酸盐的沉积,尽管作用不显著。据估计研究区碳酸钙的日沉积速率是4778kg·km2,即约1mm·a1。     

Estimation of heavy metal emission fluxes on the territory of the NIS

As the result of our research, the specific procedures to use emission factor methodology were developed and applied for trace metal emission evaluation into the atmosphere over the territory of the former Soviet Union. The existing data on heavy metal emissions were revised as background information from official sources and expert estimations. Source categories and different initial information as well as the concept of spatial emission distribution were defined and observed. The calculated atmospheric emissions of lead, cadmium and mercury were produced among the main source categories of 12 NIS countries for 1990, 1995 and 1997, using modified emission coefficients.Total cadmium emissions into the atmosphere from determined source categories were estimated as 388.4 tonnes in 1990 for the whole domain with reduction by up to 207.0 tonnes per year for 1997. Mercury emissions were estimated as equal to 303.2 tonnes in 1990 and 159.8 tonnes in 1997. Lead emission amounted to 24903.0 tonnes in 1990, and 9652.5 tonnes in 1997.The results of the evaluation demonstrated the general trends of atmospheric heavy metal emissions with a greater decrease during the first half of the 1990s followed later by the rather stable level to be explained by recession in industrial activity and fuel consumption in NIS in that period. The significant spatial variations of atmospheric emissions over vast territories are described based on the results of their distribution according to 1×1 degree grid with remarkably higher values in the location of industrial cities.     

S–O–C isotopic picture of sulphate–methane–carbonate system in freshwater lakes from Poland. A review

Microbial oxidation of organic compounds (including methane), in freshwater sediments, may result in precipitation of carbonates, which may become an important geochemical archive of paleoenvironmental variations. Most probably low δ¹³C value in calcite in eutrophic systems results from an advanced oxidation of organic compounds in turbulent or/and sulphate-rich conditions. Likewise, high δ¹³C value in calcite from organic-rich sediments may evidence low redox potential of the freshwater system. Oxidation of methane and organic matter results in significant isotope effects in sulphates dissolved in water. Therefore, to better understand the origin of carbon isotope signal in carbonates, concentration and stable isotope measurements in dissolved sulphate (water column), bubble methane and calcite (freshwater sediments) have been carried out in 24 lakes, 2 ponds and 4 rivers in Poland. The highest concentration of sulphate has been detected in rivers (85.47 SO₄ ²⁻ mg/l) and an artificial lake (70.30 SO₄ ²⁻ mg/l) located in the extremely SO₄ ²⁻-polluted region called the “Black Triangle”. The lowest concentration of sulphate is found in dystrophic and mountain lakes (from 0.5 SO₄ ²⁻ to about 3 mg/l). The lowest δ³⁴S(SO₄ ²⁻) and δ¹⁸O(SO₄ ²⁻) values occur in unpolluted lakes in eastern Poland (−0.94 and 1.38‰, respectively). The highest S and O isotopic ratios are found in a polluted lake in western Poland (δ¹⁴S(SO₄ ²)=12.95‰) and in a dystrophic lake in eastern Poland (δ¹⁸O(SO₄ ²) = 16.15‰) respectively. It is proposed that δ³⁴SO₄ ²⁻ and (¹⁸O(SO₄ ²⁻) values in lakes represent a good tool to assess and quantify anthropogenic impact by acid precipitation and to monitor variations in the trophic state and redox processes controlled by biodegradation of organic compounds in sediments and water column. In general, increasing depth (up to 12 m) of the water column is associated with decreasing trend the δ¹³C(CH₄) value from about –35 to about –78‰. However, δ¹³C value in sedimentary calcite (δ¹³C vary from –10 to 0.5‰) shows opposite trends as compared to the corresponding methane. This is probably due to redox processes and distribution of heavy isotopes between methane and calcite. Likewise, turbulent water (river) show high δ¹³C value in methane and low δ¹³C value in calcite—this is probably due to an enhanced oxidation of methane producing ¹³C-depleted CO₂. In contrast to clean lakes, it is observed that an increase of the δ¹³C(CH₄) value occurs with increasing depth of the water column in a strongly SO₄ ²⁻-contaminated lake. This is probably due to a loss of biological buffering potential of the lake accompanied by an active oxidation of methane precursors.     

Origins of black carbon from anthropogenic emissions and open biomass burning transported to Xishuangbanna, Southwest China

Black carbon (BC) has importance regarding aerosol composition, radiative balance, and human exposure. This study adopted a backward-trajectory approach to quantify the origins of BC from anthropogenic emissions ($\mathrm{B}{\mathrm{C}}_{\text{An}}$) and open biomass burning ($\mathrm{B}{\mathrm{C}}_{\text{BB}}$) transported to Xishuangbanna in 2017. Haze months, between haze and clean months, and clean months in Xishuangbanna were defined according to daily PM_2.5 concentrations of >75, 35–75, and <35 µg/m³, respectively. Results showed that the transport efficiency density (TED) of BC transported to Xishuangbanna was controlled by the prevailing winds in different seasons. The yearly contributions to the effective emission intensity of $\mathrm{B}{\mathrm{C}}_{\text{An}}$ and $\mathrm{B}{\mathrm{C}}_{\text{BB}}$ transported to Xishuangbanna were 52% and 48%, respectively. However, when haze occurred in Xishuangbanna, the average $\mathrm{B}{\mathrm{C}}_{\text{An}}$ and $\mathrm{B}{\mathrm{C}}_{\text{BB}}$ contributions were 23% and 77%, respectively. This suggests that open biomass burning (BB) becomes the dominant source in haze months. Myanmar, India, and Laos were the dominant source regions of BC transported to Xishuangbanna during haze months, accounting for 59%, 18%, and 13% of the total, respectively. Furthermore, India was identified as the most important source regions of $\mathrm{B}{\mathrm{C}}_{\text{An}}$ transported to Xishuangbanna in haze months, accounting for 14%. The two countries making the greatest contributions to $\mathrm{B}{\mathrm{C}}_{\text{BB}}$ transported to Xishuangbanna were Myanmar and Laos in haze months, accounting for 55% and 13%, respectively. BC emissions from Xishuangbanna had minimal effects on the results of the present study. It is suggested that open BB in Myanmar and Laos, and anthropogenic emissions in India were responsible for poor air quality in Xishuangbanna.     

Natural and anthropogenic sources of lead, zinc, and nickel in sediments of Lake Izabal, Guatemala

Sediments in Lake Izabal, Guatemala, contain substantial lead (Pb), zinc (Zn), and nickel (Ni). The lack of historical data for heavy metal concentrations in the sediments makes it difficult to determine the sources or evaluate whether inputs of metals to the lake have changed through time. We measured the relative abundances and concentrations of Pb, Zn, and Ni by X-Ray Fluorescence core scanning and by Inductively Coupled Plasma Optical Emission Spectrometry in three sediment cores to explore stratigraphic distributions of metals in the lake deposits. High amounts of Pb and Zn in the core taken near the Polochic Delta suggest that galena and sphalerite mining increased Pb and Zn delivery to Lake Izabal between ~1945 and 1965 CE. An up-core Ni increase in the core taken near a different mine on the north shore of Lake Izabal suggests that recent nickel mining operations led to an increase in Ni concentrations in the local sediments, but amounts in the other cores indicate that Ni is not widely distributed throughout the lake. Sediment cores from Lake Izabal are reliable recorders of heavy metal input to the lake, and were measured to establish background metal levels, which would otherwise be unavailable. Concentrations of Pb, Zn, and Ni in older, pre-20th-century Lake Izabal sediments reflect input from natural erosion of bedrock. Our results provide previously unavailable estimates of background metal concentrations in Lake Izabal before the onset of mining. These results are necessary for future monitoring related to mining contamination of the lake ecosystem.     

青藏高原中晚全新世人类活动的孢粉记录

利用孢粉记录追踪过去人类活动历史及其环境效应的研究较少。本文选取青藏高原28处地层化石孢粉序列,采用直接提取和集成方法获得568条具有年代的伴人孢粉（禾本科、石竹科、杨属、十字花科、委陵菜属、车前属、紫菀属、藜科、狼毒属）数据,经标准化处理后建立高原4个分区的人类活动指数。同时结合本区已有研究资料,探讨了中晚全新世以来的人类活动历史。研究表明：（1）Ⅰ区东北区,6.0~5.3 ka B.P.早期人类已开始活动,但低水平的生产方式对植被影响较弱;5.3~4.5 ka B.P.人类活动得到扩展,环境效应开始显现;4.5~3.5 ka B.P.人类活动强度明显增强,加剧了对植被的破坏;3.5~2.0 ka B.P.随着人类活动的进一步加强,导致过度放牧、森林面积减少及风沙活动增强。（2）Ⅱ区东南区,5.0 ka B.P.左右人类活动的环境效应开始显现;4.5~3.5 ka B.P.植被受人为干扰显著;3.5~2.0 ka B.P.人类活动扩张至高海拔地区,对植被影响范围随之扩大;（3）Ⅲ区西南区,5.7~4.5 ka B.P.农业生产活动开始且得到发展,环境效应逐渐凸出;4.5~2.0 ka B.P.人类活动进一步增强,对植被影响亦进一步加剧;（4）Ⅳ区西北无人区,受资料所限并未充分讨论,但已有研究表明,全新世早中期本区已有人类进行狩猎采集活动。     

人类活动对河流沉积物中反硝化厌氧甲烷氧化菌群落特征的影响

河流生态系统是陆地生态系统输出营养盐和有机质的主要接收器,是水-气界面CO2和CH4全球碳循环的重要环节.人类活动导致大量未经处理的硝酸盐和有机物质汇入河流,影响了N-DAMO(N-DAMO,Nitrate/nitrite-dependent anaerobic methane oxidation,反硝化厌氧甲烷氧化菌)细菌的群落特征.本文选取北运河作为研究区域,通过对比分析北运河中游和下游沉积物理化参数和N-DAMO细菌群落特征的差异性,探究由于人类活动的影响,河流沉积物中N-DAMO细菌的群落组成结构特征,及其与沉积物中NH+4-N、NO-3-N的响应关系.结果表明,北运河沉积物中NH+4-N为中游和下游氮素的主要形态,且下游NH+4-N浓度显著高于中游;人类活动对N-DAMO细菌16S rRNA和pmo A功能基因群落分布有影响,16S rRNA和pmo A功能基因均分别聚为中游和下游两类;系统发育树分析显示,人类活动影响北运河N-DAMO细菌高同源性菌群的来源,其高同源性菌群来源与北运河主要污染物氨氮的来源一致;RDA分析显示,人类活动影响N-DAMO细菌相关环境因子,沉积物中高浓度的NH+4-N、NO-3-N与16S rRNA和pmo A功能基因有显著的响应关系.沉积物N-DAMO细菌16S rRNA和pmo A功能基因的共生关系分析显示,北运河下游沉积物中N-DAMO细菌彼此之间的共存关系更强,细菌群落形成的模块化程度较高,其对环境变化的敏感程度更高,受人类活动的影响更大.     

生态系统服务价值与人类活动的时空关联分析——以长江中游华阳河湖群地区为例

以1990、2002和2010年华阳河湖群地区LandSat TM影像为数据源,构建生态系统服务价值评估模型、生态系统服务价值流向损益模型和人类活动强度评估模型,应用双变量空间自相关分析生态系统服务价值和人类活动强度的时空关联特征.结果表明：1990~2010年生态系统服务价值持续减少,水域、湿地转为耕地和建设用地是价值损失的主要原因.生态系统服务价值高值区在中部和东北部水域,湖滨价值量减少最严重,北部地区价值量增加,南部减少.人类活动强度低影响区位于水域,中高影响区和中影响区交错分布于北部地区,高影响区集中在南部和西南部地区.3个时期生态系统服务价值和人类活动强度均呈空间负相关,高-低聚集分布于南部和西南部,低-高聚集主要分布于水域.     

Characterizing the antibiotic resistance genes in a river catchment: Influence of anthropogenic activities

Previous studies on environmental antibiotics resistance genes(ARGs) have focused on the pollution sources such as wastewater treatment plants, aquaculture and livestock farms,etc. Few of them had addressed this issue in a regional scale such as river catchment. Hence,the occurrence and abundances of 23 ARGs were investigated in surface water samples collected from 38 sites which located from the river source to estuary of the Beijiang River.Among them, 11 ARGs were frequently detected in this region and 5 ARGs(sul I, sul II, tet B,tet C, and tet W) were selected for their distribution pattern analysis. The abundances of the selected ARGs were higher in the upstream(8.70 × 10~6 copies/ng DNA) and downstream areas(3.17 × 10~6 copies/ng DNA) than those in the midstream areas(1.23 × 10~6 copies/ng DNA), which was positively correlated to the population density and number of pollution sources. Pollution sources of ARGs along the Beijiang River not only had a great impact on the abundances and diversity, but also on the distribution of specific ARGs in the water samples. Both sul I and sul II were likely originated from aquaculture farms and animal farms,tet W gene was possibly associated with the mining/metal melting industry and the electric waste disposal and tet C gene was commonly found in the area with multiple pollution sources.However, the abundance of tet B was not particularly related to anthropogenic impacts. These findings highlight the influence of pollution sources and density of population on the distribution and dissemination of ARGs at a regional scale.     

Spatial and temporal variation of haze in China from 1961 to 2012

The purpose of this study is to analyze the climatic characteristics and long-term spatial and temporal variations of haze occurrence in China. The impact factors of haze trends are also discussed. Meteorological data from 1961 to 2012 and daily PM₁₀ concentrations from 2003 to 2012 were employed in this study. The results indicate that the annual-average hazy days at all stations have been increasing rapidly from 4 days in 1961 to 18 days in 2012. The maximum number of haze days occur in winter (41.1%) while the minimum occur in summer (10.4%). During 1961-2012, the high occurrence areas of haze shifted from central to south and east regions of China. The Beijing-Tianjin-Hebei (Jing-Jin-Ji) region, Shanxi, Shaanxi, and Henan Province are the high occurrence areas for haze, while the Yangtze River Delta (YRD) and the Pearl River Delta (PRD) have become regions with high haze occurrences in the last 25 years. Temperature and pressure are positively correlated with the number of haze days. However, wind, relative humidity, precipitation, and sunshine duration are negatively correlated with the number of haze days. The key meteorological factors affecting the formation and dissipation of haze vary for high and low altitudes, and are closely related to anthropogenic activities. In recent years, anthropogenic activities have played a more important role in haze occurrences compared with meteorological factors.