骆马湖泥-水界面磷铁硫原位同步变化特征

利用薄膜梯度扩散（DGT）原位采样装置获取了骆马湖全湖8个典型湖区泥-水界面（SWI）活性磷（P）、铁（Fe）、硫（S）垂向分布信息，据此定量估算三者交换通量.结果表明，骆马湖沉积物剖面P、Fe、S浓度范围分别为0~2.05，0~11.10和0.01~0.63mg/L，并在微小尺度呈高度空间异质性.在水平方向上活性P、Fe主要表现为西北湖区高于东南湖区，而活性S则未表现出明显的分布规律；就垂直剖面而言，活性P、Fe、S自界面向下呈升高趋势，并在60mm深度内出现峰值，且活性P和Fe剖面呈明显的同步变化特征；活性P、Fe在多数点位具有显著的正相关性（r>0.65，P<0.01），且各采样点沉积物中的总铁与总磷比值[w（∑Fe）/w（∑P）]均高于15，这表明Fe的地球化学循环过程对于骆马湖内源磷释放起重要控制作用；8个采样点样品中活性P、Fe、S交换通量分别为0.066~0.698，1.671~5.592和0.007~0.071mg/（m²·d），表明P、Fe、S由沉积物向水体释放.西北湖区表现出较高的P通量和活性P浓度，这可能会增加南水北调过程中水质污染的风险，应予以重视.以上结果支持了P、Fe耦合释放机制，明确了骆马湖SWI的活性P、Fe、S迁移特征.     

Identification and mapping of submerged plants in a shallow lake using Quickbird satellite data

Turkey is a country rich in lakes and wetlands--monitoring of all these will require advances in technology such as remote sensing. In this study, the aquatic plants of the large and shallow Lake Mogan, located in Central Anatolia were identified and mapped using high spatial resolution Quickbird imagery. As Lake Mogan is an important bird area the assessment of submerged plant species is of great value for ecosystem conservation and management. Quickbird multispectral image acquired on August 6, 2005 was geometrically corrected and a water mask was used based on strong absorption of Near Infrared (NIR) wavelengths by calm, clear and deep water. The water mask was applied using band reflectance values for a specific pixel satisfying the conditions of band decreasing property (Green>Red>NIR) and NIR相似文献   

Modelling Seasonal Dynamics from Temporal Variation in Agricultural Practices in the UK Ammonia Emission Inventory

Most ammonia (NH₃) emission inventories have been calculated on an annual basis and do not take into account the seasonal variability of emissions that occur as a consequence of climate and agricultural practices that change throughout the year. When used as input to atmospheric transport models to simulate concentration fields, these models therefore fail to capture seasonal variations in ammonia concentration and dry and wet deposition. In this study, seasonal NH₃ emissions from agriculture were modelled on a monthly basis for the year 2000, by incorporating temporal aspects of farming practice. These monthly emissions were then spatially distributed using the AENEID model (Atmospheric Emissions for National Environmental Impacts Determination). The monthly model took the temporal variation in the magnitude of the ammonia emissions, as well as the fine scale (1-km) spatial variation of those temporal changes into account to provide improved outputs at 5-km resolution. The resulting NH₃ emission maps showed a strong seasonal emission pattern, with the highest emissions during springtime (March and April) and the lowest emissions during summer (May to July). This emission pattern was mainly influenced by whether cattle were outside grazing or housed and by the application of manures and fertilizers to the land. When the modelled emissions were compared with measured NH₃ concentrations, the comparison suggested that the modelled emission trend corresponds fairly well with the seasonal trend in the measurements. The remaining discrepancies point to the need to develop functional parametrisations of the interactions with climatic seasonal variation.     

网络域名与商标的法律纠纷

随着新技术的发展和计算机的广泛应用,知识产权领域出现了许多前所未有的新课题,域名的知识产权保护问题即是其中之一。对域名的含义、域名与商标的法律关系以及如何认定注册、使用域名等行为构成侵权或者不正当竞争等问题进行了分析。     

关于环境纠纷解决方式的探讨

在当前的环境执法与环境管理中，因污染受害者提出权利主张，而导致的环境纠纷相当普遍。选择合适的解决方式、对当事人十分重要。目前我国解决环境纠纷主要有当事人自行解决、行政解决、司法解决和促裁解决等方式。对上述4种主要解决方式，从法律依据、解决程序、解决效力等方面作了分析和评述，并对建立和完善我国环境纠纷解决体系提出建议。     

含泥沙水样总磷测定方法的研究

对含泥沙水样消解后不用滤膜过滤而改为直接定容于 5 0mL比色管中 ,经钼酸盐、抗坏血酸试剂显色后离心 ,取清液测定。经对比实验表明 ,该法灵敏度、精确度、准确度均满足环境监测技术规范要求 ,有效消除了泥沙对TP测定的影响     

用国务院《决定》指导环境宣传教育工作--学习国务院《关于落实科学发展观加强环境保护的决定》的体会

笔者结合环境保护宣传教育工作的实际，就如何贯彻落实国务院《关于落实科学发展观加强环境保护的决定》做好环保宣传教育工作进行了思考，提出了做好有关工作的建议。     

State-By-State Carbon Dioxide Emissions from Fossil Fuel Use in the United States 1960–2000

Time series of fossil fuel carbon emissions from 1960–2000 for each of the U.S. states and the District of Columbia are presented and discussed. Comparison of the nationally summarized results with other national datasets shows generally good agreement, usually within 2%, and gives insight into the quality of all the data series. Our extension of the state-by-state emissions estimates back to 1960 reveals patterns of change that are coherent across states and can be related to historic events such as energy crises and federal legislation. Most notable is the changing pattern of coal usage, as coal-producing states produce increasingly more energy (mostly for electricity) for other states so that per capita CO₂ emissions diverge for states that import as opposed to those that export electricity. The decline in carbon emissions from petroleum products following the 1970s is also evident. Per capita emissions range over an order of magnitude for the different states. The data suggest that differences in per capita emissions arise from differences in many technological, physical, resource, social, and economic factors. The data presented here and the few correlations briefly noted pose a challenge for trying to use per capita emissions as a measure of equity or to provide mitigation targets.     

Retention time profiling of all 136 tetra- through octa- chlorinated dibenzo-p-dioxins and dibenzofurans on a variety of Si-Arylene gas chromatographic stationary phases

The applicability of three different Silphenylene Silicone co-polymer (Si-Arylene) GC stationary phases (J&W Scientific DB-5ms, Varian VF-5ms, and VF-Xms) has been evaluated for the separation of all 136 tetra- through the octa- chlorinated dibenzo-p-dioxins (PCDD) and chlorinated dibenzofurans (PCDF) from closely eluting isomers using gas chromatography/high resolution mass spectrometry (GC/HRMS). Their relative performance data are compared to the “conventional” 5% diphenyl 95% dimethylpolysiloxane GC column (Supelco Equity-5) and to each other based on absolute retention times, visualized mass chromatograms, and the separation of 2,3,7,8-substituted isomers. VF-Xms GC column was able to demonstrate a better performance towards separation of 2,3,7,8-substituted PCDD/PCDF compared to other Si-Arylene GC columns tested, where only 2,3,4,7,8-PnCDF can not be resolved from 1,2,3,6,9-PnCDF and 2,3,4,6,7,8-/1,2,3,6,8,9-HxCDF and 1,2,3,7,8,9-/1,2,3,4,8,9-HxCDF can be at least partially resolved. These data suggest that the development of a single GC column for the separation of all 17 2,3,7,8-substituted dioxins and furans is feasible, which therefore could be used as a standard tool for the PCDD/PCDF methods globally including USEPA methods 1613b, 8290A, 8280B, European Standard Method EN 1948, Canadian methods DFPCB-E3418, EPS 1/RM/19, Japanese methods JIS K0311 and JIS K0312. Having one specific GC column to separate all 2,3,7,8-substituted PCDD/PCDF will significantly improve the data quality, comparability by the various methods and assessment techniques while simultaneously leading to a more cost and time efficient operation.