Integral field spectroscopy with the GEMINI multiobject spectrographs

We describe the integral field unit (IFU) which converts the Gemini Multiobject Spectrograph (GMOS) installed on the Gemini-North telescope to an integral field spectrograph,which produces spectra over a contiguous field of view of 7 × 5 arcsec with spatial sampling of 0.2 arcsecover the wavelength range 0.4-1.0 μm.GMOS is converted to this mode by the remote insertion of the IFU into thebeam in place of the masks used for the multiobject mode. A separate fieldof half the area of the main field, but otherwise identical, is alsoprovided to improve background subtraction. The IFU contains 1500lenslet-coupled fibres and was the first facility of any type for integralfield spectroscopy employed on an 8/10 m telescope.We describe the design, construction and testing of the GMOS IFU and present measurements of the throughput both in the laboratory and at the telescope. We compare these with a theoretical prediction made before construction started. All are in good agreement with each other, with the on-telescope throughput exceeding 60% (averaged over wavelength). Finallywe show an example of data obtained during commissioning to illustrate the power of the device.     

Influence of the total atmospheric optical depth and cloud cover on solar irradiance components

Broadband solar irradiance data obtained in the spectral range 400–940 nm at Kwangju, South Korea from 1999–2000 have been analyzed to investigate the effects of cloud cover and atmospheric optical depth on solar radiation components. Results from measurements indicate that the percentage of direct and diffuse horizontal components of solar irradiance depend largely on total optical depth (TOD) and cloud cover. During summer and spring, the percentages of diffuse solar irradiance relative to the global irradiance were 5.0% and 4.9% as compared to 2.2% and 3.0% during winter and autumn. The diffuse solar irradiance is higher than the direct in spring and summer by 24.2%, and 40.6%, respectively, which may largely be attributed to the attenuation (scattering) of radiation by heavy dust pollution and large cloud amount. In cloud-free conditions with cloud cover ≤2/10, the fraction of the direct and diffuse components were 66.0% and 34.0%, respectively, with a mean daily global irradiance value of 7.92±2.91 MJ m⁻² day⁻¹. However, under cloudy conditions (with cloud cover ≥8/10), the diffuse and direct fractions were 97.9% and 2.2% of the global component, respectively. The annual mean TOD under cloudless conditions (cloud cover≤2/10) yields 0.74±0.33 and increased to as much as 3.15±0.67 under cloudy conditions with cloud amount ≥8/10. An empirical formula is derived for estimating the diffuse and direct components of horizontal solar irradiance by considering the total atmospheric optical depth (TOD). Results from statistical models are shown for the estimation of solar irradiance components as a function of TOD with sufficient accuracy as indicated by low standard error for each solar zenith angle (SZA).     

含钒石煤的穆斯堡尔谱研究

本文收集了我国湘鄂淅地区含钒石煤样品,使用化学分析和穆斯堡尔谱方法,测定和研究了石煤中钒铁的赋存方式和价态,以及不同焙烧温度下钒铁价态变化等。初步研究表明,石煤中钒铁价态及价态变化的测定,对含钒石煤中钒铁矿物和成因研究,钒的提取和石煤的综合利用有重要意义。     

Spectral identification of materials by reflectance spectral library search

Spectral library search is emerging as a viable approach for material identification and mapping by reusing spectral knowledge gained from hyperspectral remote sensing across space and time. The potential of retrieving meaningful spectral material identifications in the presence of reflectance of spectra of various material types and with various similarity metrics has been assessed in this study. Test reflectance spectra of various vegetation, minerals, soils and urban material types are identified by searching through the composite reflectance spectral library obtained by combining various institutional reflectance spectral libraries. The accuracy of material identifications under various conditions: (i) in the presence of identical, similar and dissimilar spectra; (ii) in the presence of only identical and dissimilar spectra; and (iii) in the presence of only dissimilar spectra has been assessed with several similarity metrics. Results indicate the possibility of obtaining 100% accurate material identifications by library search if the spectral library contains identical spectra. However, the presence of a large number of similar spectra, despite the presence of identical spectra, is found to increase false positives, thereby reducing the accuracy of retrievals to 82% at best. Further, the accuracy of material identifications in the presence of similar spectra is similarity metric-dependent and varied from about 52% (obtained from Binary Encoding) to 82% (obtained from Normalized Spectral Similarity Score). Overall, results support the possibility of using independent reflectance spectral libraries for material identification while calling for robust spectral similarity metrics.     

Assessment of the effects of hydrocarbon contamination on the sedimentary bacterial communities and determination of the polar lipid fraction purity: Relevance of intact phospholipid analysis

This in situ study reports on the relevance of intact phospholipids as new biomarkers and highlights the limits of the classical fatty acid analysis after the hydrolysis of the polar lipid fraction. The analysis of polar lipid fractions revealed significant contributions of marine macrophytes with either non-phospholipid compounds (sulfoquinovosyl diacylglycerol) or with both non-bacterial phospholipid classes (phosphatidylcholine) and non-bacterial phospholipid molecular species (some molecular species of phosphatidylglycerol). The analysis of intact phospholipids showed also the predominance of gram-negative bacteria in sediments whereas the analysis of fatty acids alone cannot confirm such information. Lastly, as regard to the effects of petroleum hydrocarbons on the sedimentary bacterial communities, we observed a higher degree of saturation of the fatty acyl chains of the phospholipids extracted from sediment exposed to a massive and chronic crude oil contamination. Such a result was interpreted as an adaptive response resulting in higher membrane rigidity of the bacterial communities.     

CT图像存档与管理解决方案

本文针对数字影像设备（如CT、MRI等）日益突出的图像存储和管理问题，进行深入的分析和研究。鉴于不同厂家和时期设备配置不同，提出了4种切实可行的解决方案：胶片扫描，视频采集，光盘或MOD输入，DICOM接口连接，完全解决了图像长期大量存储的问题。同时具有网络联机查询，图文报告，电子病历管理，激光相机接口等丰富的增值功能，是数字化医院的理想选择。     

Sorption Characteristics of Rare Earth Element Eu^3＋ onto Silica-Water Interfaces Studied by Fluorescence Spectroscopy

The sorption of Eu species onto nano-size silica-water interfaces was investigated using fluorescence spectroscopy for Ph ranges of 1-8.5 and an initial Eu concentration (Ceu) of 2×10-4 M. The sorption rate of Eu was initially low, but significantly increased at Ph>4. The sorption density of Eu species on a silica surface was ～1.58×10-7 mol/m2 when the dissolved Eu species were completely sorbed onto silica-water interfaces at Ph=～5.8. The sorbed Eu species at Ph<6 is aquo Eu3 , which is sorbed onto silica-water interfaces as an outer-sphere complex at Ph<5, but may be sorbed as an inner-sphere bidentate complex at 5相似文献   

Identification of Uranyl Minerals Using Oxygen K‐Edge X‐Ray Absorption Spectroscopy

Although most of the world's uranium exists as pitchblende or uraninite, this mineral can be weathered to a great variety of secondary uranium minerals, most containing the uranyl cation. Anthropogenic uranium compounds can also react in the environment, leading to spatial–chemical alterations that could be useful for nuclear forensics analyses. Soft X‐ray absorption spectroscopy (XAS) has the advantages of being non‐destructive, element‐specific and sensitive to electronic and physical structure. The soft X‐ray probe can also be focused to a spot size on the order of tens of nanometres, providing chemical information with high spatial resolution. However, before XAS can be applied at high spatial resolution, it is necessary to find spectroscopic signatures for a variety of uranium compounds in the soft X‐ray spectral region. To that end, we collected the near edge X‐ray absorption fine structure (NEXAFS) spectra of a variety of common uranyl‐bearing minerals, including uranyl carbonates, oxyhydroxides, phosphates and silicates. We find that uranyl compounds can be distinguished by class (carbonate, oxyhydroxide, phosphate or silicate) based on their oxygen K‐edge absorption spectra. This work establishes a database of reference spectra for future spatially resolved analyses. We proceed to show scanning X‐ray transmission microscopy (STXM) data from a schoepite particle in the presence of an unknown contaminant.     

An atlas of the optical spectrum of supernova 1987A in the large magellanic cloud

Photographic spectra of SN1987A in the LMC have been obtained from 1987 February 25 to 1988 June 30. Microdensitometer tracings of these have been reduced to intensity and corrections for instrumental response have been applied to the spectra. This paper presents these data in an atlas format, discusses the reduction procedures in detail, and presents radial velocity measurements of selected lines in the spectra     

大气气溶胶光学厚度的宽带消光遥感方法及其应用

该文发展了遥感气溶胶光学厚度的一个宽带消光遥感方法 ,它应用地面上太阳直射表探测的宽波段太阳直射信息反演 0 75 μm大气柱光学厚度。这方法的主要误差因子是气溶胶谱的不确定性。数值试验表明 ,气溶胶谱分布的误差所引起光学厚度解的误差一般小于 5 %。 1995年 1— 10月进行的 12 6 7组对比实验表明 ,由本方法探测的气溶胶光学厚度与光度计探测的气溶胶光学厚度的标准差为 10 5 % ,两者平均结果的偏差只有 0 7%。该文还应用这个方法 ,从气象台站辐射观测资料反演得到北京、沈阳等 10个地方 1980— 1994年间晴天气溶胶光学厚度资料 ,并分析其变化规律