科学大数据开放共享机制研究及其对环境信息共享的启示

科学大数据得以充分利用和增值的前提是开放共享,而影响数据开放共享的关键问题是共享机制.本文首先分析了科学大数据的产生方式、数据类型、投资方式、管理主体和服务定位及其与共享程度的关系.进一步在分析国内外自上而下和自下而上科学数据共享通用机制与原则的基础上,结合国家地球系统科学数据共享平台、全球变化科学数据出版等实践,提出了数据汇交、数据出版、数据联盟和服务激励四种数据共享机制,并分析了每种机制中的关键问题及具体做法.最后,结合云计算、"互联网+"等新一代信息技术和思维,对环境保护大数据共享机制提出四点建议,即:国家统一投资建设的环境保护核心业务数据强制汇交机制,其他部委、机构环境保护相关数据联盟交换机制,企业、科学家个人数据出版等激励机制,以及社会公众数据的"众创机制".     

淋滤水量对多环芳烃在土壤剖面中纵向迁移的影响研究

为了揭示淋滤作用对多环芳烃(PAHs)在土壤剖面中纵向迁移的影响,选取北京市昌平区一条具有代表性的土壤剖面作为实验样品,进行了PAHs土柱淋滤模拟研究。结果表明:经过淋滤作用后,淋滤水量不同的三个土柱(A1,A2,A3,淋滤水量依次增大)表层土中残留PAHs总量逐渐降低,但不同环数PAHs含量降低幅度存在较大的差别,低环数PAHs受影响程度更大;在淋滤水量相同的情况下,不同环数PAHs的含量均存在随土柱深度的增大而逐渐降低的趋势,但降低程度存在一定差别。由此推测,通过长期淋滤作用,表层土中的PAHs可以向深层土壤迁移,这些认识可以为深层土壤及浅层地下水的多环芳烃污染评价及保护提供合理的理论依据。     

Representation of critical natural capital in China

Traditional means of assessing representativeness of conservation value in protected areas depend on measures of structural biodiversity. The effectiveness of priority conservation areas at representing critical natural capital (CNC) (i.e., an essential and renewable subset of natural capital) remains largely unknown. We analyzed the representativeness of CNC‐conservation priority areas in national nature reserves (i.e., nature reserves under jurisdiction of the central government with large spatial distribution across the provinces) in China with a new biophysical‐based composite indicator approach. With this approach, we integrated the net primary production of vegetation, topography, soil, and climate variables to map and rank terrestrial ecosystems capacities to generate CNC. National nature reserves accounted for 6.7% of CNC‐conservation priority areas across China. Considerable gaps (35.2%) existed between overall (or potential) CNC representativeness nationally and CNC representation in national reserves, and there was significant spatial heterogeneity of representativeness in CNC‐conservation priority areas at the regional and provincial levels. For example, the best and worst representations were, respectively, 13.0% and 1.6% regionally and 28.9% and 0.0% provincially. Policy in China is transitioning toward the goal of an ecologically sustainable civilization. We identified CNC‐conservation priority areas and conservation gaps and thus contribute to the policy goals of optimization of the national nature reserve network and the demarcation of areas critical to improving the representativeness and conservation of highly functioning areas of natural capital. Moreover, our method for assessing representation of CNC can be easily adapted to other large‐scale networks of conservation areas because few data are needed, and our model is relatively simple.     

Polycyclic aromatic hydrocarbons in river sediments from the western and southern catchments of the Bohai Sea, China: toxicity assessment and source identification

The concentration, distribution, and origin of 16 USEPA priority polycyclic aromatic hydrocarbons (PAHs) were investigated in river sediments from the western and southern catchments of the Bohai Sea, China. A toxicity assessment of 28 sediment samples collected from 15 main rivers was conducted by utilizing threshold and probable effect concentrations (TEC and PEC, respectively) derived from consensus-based sediment quality guidelines. The concentrations of total PAHs (∑PAH₁₆) ranged from 0.14 to 10,757 μg/kg dry weight (mean?=?1,368.6 μg/kg). The high concentrations of PAHs found in Binhai New Area of Tianjin and Binzhou City are likely the result of rapid population and heavy industry growth, resulting in elevated point and nonpoint source inputs of PAHs. Of the samples collected, samples 1 and 10 (7.1 % of the total) were categorized as toxic since some of the PAH concentrations exceeded the corresponding PECs. Twenty samples were classified as nontoxic, with both the individual PAH and the∑PAH₁₆ concentrations falling below the corresponding TECs. Analyses of selected PAH isomer ratios aided in the identification of PAH origins, allowing for a discrimination between pyrogenic and petrogenic sources. Spatial variability confirmed source heterogeneity within the study area. The most significant PAH-associated contamination was found in the Beitang River and Ji Canal, which are located in Binhai New Area. The magnitude of contamination and the likelihood of an ongoing influx of PAHs support the need for a better understanding of pollution sources and methods for both control and sediment restoration.     

5种不同晶型的纳米二氧化钛对金属铜生物积累的影响

纳米二氧化钛(nTiO_2)作为一种具有独特物理化学性质的纳米材料被广泛应用。然而,在生产、使用的过程中,nTiO_2会不可避免地进入于水环境中。重金属是水体中常见的污染物之一,nTiO_2进入水体后是否会与水体中的重金属发生相互作用,进而影响重金属的生物积累,目前相关报道还很少。本论文以大型溞为模式生物,考察了5种不同晶型nTiO_2对常见的重金属铜生物积累影响。结果表明,nTiO_2对Cu2+的吸附降低了试验液中Cu2+浓度。但5种不同晶型nTiO_2的吸附能力并不一样,其中锐钛矿晶型(A-S)的吸附能力最高,这可能是由于结构缺陷和表面羟基的存在,为Cu2+提供了更多的结合位点,从而提高了A-S的吸附能力。nTiO_2的存在降低了金属铜在大型溞体内的积累,这可能是由于nTiO_2对金属铜的吸附,降低了自由Cu2+的生物可利用性。由于nTiO_2样品之间比表面积的差异,不同晶型之间单位nTiO_2引起的铜积累有显著性差异性(P0.05),其中锐钛矿和金红石之比为4:1混合晶型(M1)最高,A-S最低。     

通榆河南段控制单元最大日负荷估算及分配研究

以通榆河南段控制单元为研究区,利用现有的平原感潮河网区水量模型、面源污染负荷统计模型和水环境容量模型,估算研究区2010年污染物最大日负荷总量（TMDL）,并进行负荷削减和分配研究。结果表明：研究区COD、氨氮（NH3-N）90％保证率（2004年）下的水环境容量分别为7．76万t,0．37万t;xCN2010年污染物入河量,COD、NH3-N的最大年负荷分别为1．99万t,0．28万t。在研究区涉及的各县市中,海安、姜堰、东台是负荷削减的重点区域;对于不同的污染源,城镇生活点源和农业面源是研究区污染物总量控制的关键。     

柳州地区建筑材料放射性水平及其致居民剂量

本文采用全国统一方法,检测了广西柳州地区常用建材中~(226)Ra、~(232)Th、~(40)K的比活度.以煤灰砖最高,石灰石最低。比活度依次为煤灰砖>粘土砖≈土壤>水泥>灰砂砖>混凝土制品>石灰石.经估算,煤灰砖致居民的有效剂量当量较大,为3.98mSv·a~(-1);其它各种建材致居民的有效剂量当量在0.23—1.01mSv·a~(-1)之间,低于、等于或略高于本底.     

应用陆地卫星TM图象编制闽北土壤图(1:10万)的方法研究

以TM原图象合成的标准假彩色和似自然色图象作目视解译为主,根据土壤及其相关地物的野外光谱测定数据,分析其影象色调特征;用TM 7个波段原始黑白图象作对比解译,以预测不同地物的彩色合或效果并选择最佳合成方案;用TM6热红外图象作假彩色等密度分割处理,以提取随海而异的地面温度场和土壤类型垂直分带信息;用TM比值图象及其假彩色合成处理,以逐步增强并提取土壤信息;最后参照同比例尺地质图和地形图等相关资料,完成土壤图的编制。     

重金属螯合剂处理焚烧飞灰的稳定化技术研究

进行了垃圾焚烧飞灰的新型稳定化药剂－－重金属螯合剂的实验室研究,探讨了本螯合剂处理焚烧飞灰的稳定化工艺流程及处理效果。结果表明,本螯合剂夺悄灰中重金属的总捕集效率高达９７％以上,其效果显著优于无机稳定化药剂Ｎａ２Ｓ和石灰,且处理后的飞灰能达到重金属废物的填埋控制标准,同时,其处理后的飞灰的最大浸出量远低于无机稳定化药剂处理后的飞灰,且能在较宽的ｐＨ范围内都具有好的稳定化效果,减少了稳定化产物在环境     

Ozonation of azo dye Acid Red 14 in a microporous tube-in-tube microchannel reactor: decolorization and mechanism

Despite the great success of time-weighted average passive sampling of hydrophobic contaminants, such as PCBs and PAHs, the sampling of polar organic compounds still presents a challenge because the equilibrium between water and most sampling phases is attained in a relatively short time. In this study, we proposed a new time-integrative sampler using in situ solvent extraction (TISIS) for polar organic chemicals. The sampler was composed of a 15 cm poly(dimethylsiloxane) (PDMS) tubing, with an internal diameter of 0.5 mm and wall thickness of 0.5 mm, through which an extraction solvent (acetonitrile) was passed. Four polar organic contaminants, caffeine, atrazine, diuron and 17α-ethynylestradiol, were chosen for the evaluation of the performance of the sampler. Without the use of in situ solvent extraction, the PDMS tubing when exposed to a constant aqueous concentration of the four model compounds was able to linearly accumulate those compounds for less than 12 h and equilibrium between the PDMS tubing and water was attained in 2 d under our laboratory conditions. However, TISIS when exposed to a constant aqueous concentration was able to linearly accumulate all the model compounds without any exposure time limitation. The measured sampling rates at three different extraction flow rates (0.2, 0.5, 1.5 mL min⁻¹) were similar, regardless of the chemicals, indicating that the overall mass transfer from aqueous solution to the extraction solvent was most likely dominated by partitioning to the PDMS tubing and the internal diffusion within PDMS. In addition, a pulsed exposure experiment confirmed that TISIS operated in a time-integrative mode when the environmental concentration was highly fluctuated.