语义因子支持的多源POI分类信息一致化处理

为了解决网络POI分类异构导致多源POI数据匹配与整合困难的问题,该文利用分类特征词提取、特征词去重与优化等关键技术,构建POI分类的语义概念格,然后通过概念格之间的语义关联关系,实现多源异构POI分类体系的映射与转换。最后通过实验验证了该文方法的有效性,并将其成功应用于省级地理信息公共服务平台(政务版)数据更新。     

平阴县土壤中重金属元素异常成因研究

通过对平阴县周边及其西部农田区采样调查,平阴县周边元素异常具有异常衬度较高,富集系数大等特征,西部农田区异常具有各元素套合关系好,多数异常衬度不高,富集系数小的特点。结果表明,西部农田区异常是以As,Cd为主要成分的异常,元素含量与SiO2,Al2O3,Fe2O3等常量组分间具有显著的相关性,随SiO2含量的增加而降低,随Al2O3,Fe2O3含量的增加而增加,说明土壤常量组分及其所决定的土壤质地是导致异常形成的主要因素;而平阴城区异常是以S,Hg,As,Zn,Mn等元素为主的异常,是典型的人为综合因素（化工烟尘、工厂污水、生活垃圾）产生的异常。     

Diagnosis of trace metal contamination in sediments: the example of Ensenada and El Sauzal, two harbors in Baja California, Mexico

Total metal concentrations in sediments from within Ensenada and El Sauzal Harbors are generally higher than at the mouths. Grain-size analyses suggested that this enrichment could be due to the presence of fine-grained sediments in the inner part of the harbors rather than to anthropogenic perturbations. The (Me/Al)(sample) ratios for Pb, Co, Ni and Fe were significantly higher for Ensenada Harbor relative to El Sauzal Harbor, whereas the ratios for Cd, Mn, Zn and Cu were statistically equivalent for both harbors. Calculated enrichment factors [EF(Me)=(Me/Al)(sample)/(Me/Al)(shale)] indicated that the metals showing slight enrichment were those associated with anthropogenic contamination (Pb, Zn), or probably related to primary productivity in the water column (Cd, Co). The levels of most of the metals were not greatly enriched, a consideration that is of the utmost importance when contamination issues are at stake.     

Isotopic,trace element and nutrient characterization of coastal waters from Ubatuba inner shelf area,south-eastern Brazil

Stable isotopes, tritium, radium isotopes, radon, trace elements and nutrients data were collected during two sampling campaigns in the Ubatuba coastal area (south-eastern Brazil) with the aim of investigating submarine groundwater discharge (SGD) in the region. The isotopic composition (δD, δ¹⁸O, ³H) of submarine waters was characterised by significant variability and heavy isotope enrichment. The stable isotopes and tritium data showed good separation of groundwater and seawater groups. The contribution of groundwater in submarine waters varied from a few % to 17%. Spatial distribution of ²²²Rn activity concentration in surface seawater revealed changes between 50 and 200 Bq m⁻³ which were in opposite relationship with observed salinities. Time series measurements of ²²²Rn activity concentration in Flamengo Bay (from 1 to 5 kBq m⁻³), obtained by in situ underwater gamma-spectrometry showed a negative correlation between the ²²²Rn activity concentration and tide/salinity. This may be caused by sea level changes as tide effects induce variations of hydraulic gradients, which increase ²²²Rn concentration during lower sea level, and opposite, during high tides where the ²²²Rn activity concentration is smaller. The estimated SGD fluxes varied during 22–26 November between 8 and 40 cm d⁻¹, with an average value of 21 cm d⁻¹ (the unit is cm³/cm² per day). The radium isotopes and nutrient data showed scattered distributions with offshore distance and salinity, which implies that in a complex coast with many small bays and islands, the area has been influenced by local currents and groundwater–seawater mixing. SGD in the Ubatuba area is fed by coastal contaminated groundwater and re-circulated seawater (with small admixtures of groundwater), which claims for potential environmental concern with implications on the management of freshwater resources in the region.     

Otolith chemical signature and growth of Chaetodon speculum in coastal areas of New Caledonia

Coral reefs are one of the most diverse ecosystems on Earth. They are currently exposed to increasing levels of anthropogenic perturbations. Several recent reviews point to the lack of good indicators for these perturbations especially to monitor their effects on fish populations or fish assemblages. The SW lagoon of New Caledonia is an ideal location to test indicator species in this context as contrasting sites are present within a small geographical range. This study analysed fish from four sites, one with heavy industrial pollution, another dominated by domestic waste, a third with historic mining activities, and the fourth as a control. The butterfly fish, Chaetodon speculum, was chosen to determine C. speculum's potential as an indicator species due to its link to coral, its sedentary behaviour and its wide geographical distribution. The size distribution, growth rate, age distribution and whole otolith composition were analysed at each site. Age and mean growth rate were analysed from daily increments of the otoliths. The concentrations of eight elements (Li, Mg, Co, Ni, Cu, Rb, Sr, and Ba) were measured by ICP-MS in the otoliths of a subset of individuals. The sites under anthropogenic impact were distinct from the control site by fish size frequencies, age distributions, and the chemical content of their otoliths. The chemical elements Mg, Co, Ni, Cu, and Rb showed differences amongst sites. Fish belonging to the sites furthest from Nouméa could be discriminated in nearly 80% of samples or 60% of the cases when otolith weight or fish age respectively were taken into account. Ni concentrations of the otoliths were also higher in the bays where water concentrations of this element were known to be higher, but these differences were no longer significant once corrected for otolith weight. These results should be mitigated by the fact that: (1) despite significant differences between sites in age distribution and size frequencies there were no differences in growth rates or body condition; (2) differences in age or size were not correlated to perturbation levels; and (3) discrimination between sites based on chemical levels in the otoliths, even though significant, was not sufficient to identify the origin of the fish at a level useful for screening tests. The hypothesis that environmental differences between sites would be reflected in the otolith chemical composition is therefore not fully supported by our results.     

Trace elements and polycyclic aromatic hydrocarbons (PAHs) concentrations in deep Gulf of Mexico sediments

The concentrations of polycyclic aromatic hydrocarbons (PAHs) and trace elements were determined for surface (top 2 cm) sediment samples collected during the deep Gulf of Mexico benthos (DGoMB) study .These elements and compounds are known to be toxic to organisms at high concentrations and may affect biological communities. There is no indication of major anthropogenic input of the elements Be, Co, Cr, Fe, Si, Tl, V, K, Mg, Ca, Sr and Zn, based on normalization to Al. The concentrations of these metals in the sediment are a function of the relative amounts of trace-metal-rich Mississippi River-derived silicate material and trace-metal-poor plankton-derived carbonate. This is not true for the elements Ba, Ni, Pb, Cd, As, Cu and Mn, whose concentrations show considerable scatter when normalized to Al and a general enrichment. On a normalized basis, Mn is enriched 5–10 fold, Cu and Ni 2–3 fold and Pb 2 fold over Mississippi River-derived material. These enrichments are likely the result of remobilization of metals from depths in the sediment column where reducing conditions exist. The Ba concentrations at selected sites are higher than those of average clay-rich sediments, but are typical of sediments from near oil well platforms in the northern Gulf of Mexico. In the case of Ba, it seems likely that the enrichments, as high as a factor of 10, are due to disposal of oil well drilling mud. The Ba-enriched samples are from the three shallowest water sites in the Mississippi Trough (sites MT1, 2 and 3) and from site C1 and WC5. All are in an area of intense petroleum exploration and development. PAH concentrations are also elevated at MT1, MT3 and C1. The total PAH concentration ranged from not detected (ND) to 1033 ng/g with a mean of 140 ng/g. Even at the sites most enriched in PAHs and trace elements, the concentrations are not at the levels expected to adversely affect the biota. However, these predicted non-effects are based on research using mostly near-shore estuarine species, not on the indigenous species at the sampling sites.     

SELFE: A semi-implicit Eulerian–Lagrangian finite-element model for cross-scale ocean circulation

Unstructured-grid models grounded on semi-implicit, finite-volume, Eulerian–Lagrangian algorithms, such as UnTRIM and ELCIRC, have enjoyed considerable success recently in simulating 3D estuarine and coastal circulation. However, opportunities for improving the accuracy of this type of models were identified during extensive simulations of a tightly coupled estuary–plume–shelf system in the Columbia River system. Efforts to improve numerical accuracy resulted in SELFE, a new finite-element model for cross-scale ocean modeling. SELFE retains key benefits, including computational efficiency of existing semi-implicit Eulerian–Lagrangian finite-volume models, but relaxes restrictions on grids, uses higher-order shape functions for elevation, and enables superior flexibility in representing the bathymetry. Better representation of the bathymetry is enabled by a novel, “localized” vertical grid that resembles unstructured grids. At a particular horizontal location, SELFE uses either S coordinates or SZ coordinates, but the equations are consistently solved in Z space. SELFE also performs well relative to volume conservation and spurious oscillations, two problems that plague some finite-element models. This paper introduces SELFE as an open-source code available for community use and enhancement. The main focus here is on describing the formulation of the model and on showing results for a range of progressively demanding benchmark tests. While leaving details to separate publications, we also briefly illustrate the superior performance of SELFE over ELCIRC in a field application to the Columbia River estuary and plume.     

长江口外缺氧区沉积物中元素分布的氧化还原环境效应

对取自长江口外缺氧区及其邻近海域表层沉积物样品进行了粒度组成和元素(主要包括氧化还原敏感性元素和亲碎屑元素)丰度的分析与测试,对长江口外缺氧区缺氧环境对元素分布的影响进行了探讨,提出了长江口外缺氧区沉积物中氧化还原敏感性元素(Redox sensitive elements,简称RSE)分布的氧化还原环境效应。亲碎屑元素丰度的分布显示出明显的粒控效应,而氧化还原敏感元素的分布受粒度效应的制约很弱,主要受离岸缺氧区还原环境的制约,具有在缺氧区富集的特点。缺氧环境对RSE分布的影响超过了元素的粒控效应,从而使研究区RSE的分布呈现出典型的氧化还原环境效应。     

顺序提取法探讨沉积物中主量元素在不同相态的分配特征

在Tessier以及欧共体标准局BCR等前人顺序提取方法的基础上,采用一套改进的顺序提取法对海洋沉积物以及一些水系沉积物标准物质的主量元素进行逐步提取。利用ICP—AES、ICP—MS方法分析了各提取液中Ti、A1、Na、Mg、K、Ca、P、Fe、Mn的含量以及它们在不同相态的分配特征,同时,进一步探讨了酸去除沉积物中非陆源组分的效果,结果显示,最后经盐酸淋滤后的样品,沉积物中的生物、自生组分已经被溶解,而残留下来的剩余物质基本上可代表海洋沉积物的陆源碎屑组分。     

长江和黄河入海沉积物不同粒级组分中稀土元素的比较

为探索区分黄、东海陆架沉积物中来自长江和黄河源的有效替代性指标,从长江和黄河河口区各取3个沉积物样品作为长江和黄河入海沉积物的端元样品。研究结果表明:长江和黄河沉积物不同粒级组分中REE的变化范围分别为145.49~256.77μg/g和121.22~135.56μg/g,随粒度由细变粗分别呈下倾的"双峰"型分布和倒"S"型分布;长江沉积物中REE约为黄河的1.5倍,最低值比黄河的最高值高出20%;8~16μm和2~4μm是凸显长江和黄河沉积物稀土元素差异的敏感粒级,REE、LREE/HREE和(La/Yb)n等稀土元素特征参数在这两个粒级组分中差异明显。本次实验结果大幅度地提高了两条河流REE差异的灵敏度和可信度,为建立区分长江与黄河入海沉积物物源实用的有效指标提供了可能。