高光谱遥感及其在青藏高原的应用潜力分析

高光谱遥感以其波段数目多、光谱分辨率高、带宽窄等特点受到了国内外研究者的广泛关注,它的发展可以说是遥感技术领域的巨大进步。本文主要介绍高光谱遥感的发展,以及针对高光谱影像独有的特点所要进行的数据处理方法。在此基础上,结合青藏高原独特的地理地质环境,探讨高光谱遥感在青藏高原的应用潜力。     

电感耦合等离子体发射光谱法测定钛铁矿中主、微量元素

采用氢氟酸-盐酸-硝酸-硫酸四酸溶矿,建立了电感耦合等离子体发射光谱仪法(ICP-AES)同时测定钒钛磁铁矿、钛铁矿中铝、钙、镁、钾、钠、锰、钛、铬、锶、锌和钒11种元素的方法。对最佳仪器条件及分析谱线进行了优化筛选,并探讨了4种消解方法及酸度对测定的影响。实验结果表明:ICP-AES法测定钒钛磁铁矿、钛铁矿中铝、钙、镁、钾、钠等元素,与原子吸收光谱法、分光光度法、滴定法、重量法等单一元素测定方法相比较,具有检出限低、灵敏度高、测量范围宽、操作简便,适合大批量样品测定等突出优点。方法准确度(RE)小于10%,元素精密度(RSD,n=12)为0.68%~5%。采用国家一级标准物质进行了方法验证,取得了令人满意的结果。     

南极绿藻中类菌胞素氨基酸对UV-B胁迫的响应

南极上空臭氧层的破坏导致了紫外辐射日益增强,高强度的UV-B辐射会造成细胞中DNA的损伤,影响蛋白质、脂类和色素的代谢过程。生长在南极的绿藻具有一系列防御机制以应对增强的UV-B辐射,其中类菌胞素氨基酸(Mycosporine-like amino acids, MAAs)是一类重要的紫外防御物质。为探究类菌胞素氨基酸对UV-B辐射的响应,本文以南极冰藻(Chlamydomonassp.ICE-L)、针丝藻(Raphidonema nivale Lagerheim, NIES-2290)和胶球藻(Coccomyxa subellipsoidea E.Acton, NIES-2166)三种生活在南极的绿藻为材料,采用UV-B辐射胁迫(强度0.35 W/m~2,短时处理3 h),并通过液相色谱-质谱联用法检测类菌胞素氨基酸的种类和含量的变化。Mycosporine-glycine为三种南极绿藻中共有的MAAs,在UV-B辐射胁迫下三种南极绿藻中Mycosporine-glycine含量变化不尽相同,表明不同的南极绿藻中MAAs对UV-B辐射的响应各有其特性。首次在绿藻(南极冰藻和胶球藻)中检测到Gadusol。Gadusol作为MAAs的合成前体,它的合成积累使得生活在海冰环境的南极冰藻和胶球藻具有良好的抗UV-B辐射能力。其中南极冰藻抗紫外能力最强,这可能得益于不同MAAs间的动态转化,含量升高的Palythine及Usujirene/Palythene可能对南极冰藻的紫外屏蔽起着至关重要的作用。     

星载雷达波谱仪反演海浪谱的精度研究

介绍了星载雷达波谱仪的观测原理及误差分析模型,并在Hauser等提出的SWI M(sea wave investigation and monitoring by satellite)的基础上分析了波谱仪反演海浪谱的波长分辨率和角度分辨率。为了减小反演调制谱的波动,在数据处理过程中时域和波数域相邻单元的平均个数分别为10和8个。系统在不同的模式下工作,为了获取20°的角度分辨率,对调制谱平均次数分别取3次(模式1)、7次(模式2)、10次(模式3)。使用解析法和仿真法分析了SWI M工作在模式2时海浪谱观测的能量误差,两种方法的结果一致。对于给定的海浪条件,能量误差小于20%。     

SZ36-1油田污水悬浮物无机组分研究

综合利用扫描电镜能谱分析、X-射线衍射仪等先进仪器对SZ36-1油田滤膜组分燃烧前后进行综合分析研究。通过分析无机组分中Fe、Ca等元素的变化规律,并结合现场水质监测数据,研究发现SZ36-1油田回注污水由CEP向AJ、平台输送过程中水质逐级恶化;同时污水由CEP到A平台再到J平台过程中,Fe原子百分比平均值依次为4.45%、13.03%、19.45%,Ca原子百分比平均值依次为4.33%、5.43%、5.66%。腐蚀、结垢现象逐渐加剧,是导致注水水质恶化的主要原因。     

时空混合调制型偏振干涉成像光谱仪数据处理研究

研究了基于Savart偏光镜的偏振干涉成像光谱仪在时空混合调制模式下图像形成、数据分布的特点,论证了视场补偿型偏振干涉成像光谱仪更适用于单色光条件下的时空混合调制工作模式,并提出了时空混合调制模式下数据采集与处理的基本原理及其需要注意的问题与解决方法.最后,应用这种方法对实验获取的干涉图进行了数据处理,并成功复原出了光谱.     

Size dependent partitioning of organic material: evidence for the formation of organic coatings on aqueous aerosols

Organic aerosol formation resulting from the ozonolysis of α-pinene, myrcene and sabinene was investigated in a large aerosol chamber in the presence of aqueous seed aerosols. The chemical composition of the particles was monitored by an aerosol mass spectrometer (Aerodyne Research Inc.) as a function of time and the particle size. Smaller particles were found to contain more organics relative to sulfate than the larger ones. In contrast, the water to sulfate mass ratio was not dependent on the particle size. These experimental findings indicate the formation of organic layers on the particles. With the aid of an aerosol dynamic model we demonstrate that the observations are consistent with the formation of multilayered organic films having thicknesses of approximately 10 nm. The results also suggest that the films were formed through condensation of low-volatile oxidation products that did not take up water considerably. Even though dissolution of oxidation products into the particle aqueous phase cannot be conclusively ruled out, the most plausible interpretation of the results is that the monoterpene ozonolysis lead to the formation of organic coatings on aqueous aerosols. Such films are likely to form in regions with monoterpene emissions.     

A novel high-resolution small ion spectrometer to study ion nucleation of aerosols in ambient indoor and outdoor air

An electrically based ion spectrometer is described, capable of measuring particle sizes and mobilities from molecular ions (small ions) to aerosol particles across a size range of 0.4 to 30 nm in diameter. It consists of a single cylindrical capacitor divided into three electrically insulated sections. The current arriving at the central section is measured by an electrometer and represents the ion flux over a known range of mobilities determined by the applied voltage. The applied voltage is scanned in steps to measure the ion fluxes over a large number of overlapping mobility ranges. The recorded signal and the response function of the instrument are unfolded using a maximum entropy procedure to give a high-resolution measured mobility spectrum. The maximum entropy approach offers a considerable improvement over traditional aspiration collectors and can approach the resolution of a drift tube system. In this way, the spectrometer successfully overcomes the diffusion limit to small ion resolution. Illustrative spectra are shown, demonstrating for the first time the presence of some resolved structure within the small ion spectrum at the highest mobilities. It is demonstrated that the actual mobility spectrum of small ions falls in the range 0.8–2.0 × 10⁻⁴ m² V⁻¹ s⁻¹. This represents a narrower range than that previously measured which is attributed to improved spectral resolution in the present work.     

地下水中NO-3的15N和18O同位素测试新技术--密封石英管燃烧法

近40年来,硝酸盐(NO-3)已成为最普遍的地下水污染源之一。在本文中,介绍了在野外用阴离子交换树脂收集地下水中的NO-3的新技术;用AgNO3和氧化铜丝及铜颗粒燃烧反应测定氮同位素比值;用AgNO3 C(石墨)测定NO-3中氧同位素比值的密封石英管燃烧法,它们是1995年以后发展起来的最新测试技术。