Coherent spectroscopy of a strongly driven triple quantum dot molecule

Based on a calculation model, we study the interference phenomena of serially coupled V-type and Λ-type triple quantum dots (CTQDs) driven simultaneously by a strong driving field and a weak probe field. Strongly depending on the configuration of the three-level CTQD, the probe absorption spectra, which are shown in the tunneling current, exhibit various quantum coherence properties. In the case where the two pairs of transitions of the CTQD have a small eigenfrequency difference Δω, the double-coupling effect of the driving field results in two Autler-Townes doublets and one weak Mollow triplet in one spectrum. With the value of Δω increasing, only one Autler-Townes splitting remains due to the single-coupling of the field. We also find that the effect of spontaneous emission of phonons may lead to an obvious background current, which can be used to distinguish which transition is driven by the driving field in experiment. The interesting quantum property of a CTQD revealed in our results suggests its potential applications in quantum modulators and quantum logic devices.     

基于遥感光谱反射率反演黄河口海域Ⅱ类水体悬浮泥沙浓度模型

依据黄河口海域含沙水体野外实测光谱反射率为参考实验数据,结合水体表面光谱观测数据建立了经验回归模型,从而定量估测黄河口海域水体表层悬浮泥沙质量浓度,最终得出黄河口海域不同年份水体的悬浮泥沙质量浓度图,这对分析河口海岸带冲淤变化过程具有重要的意义。     

Multivariate analysis of fluorescence and source identification of dissolved organic matter in Jiaozhou Bay, China

Hierarchical clustering analysis and principal component analysis (PCA) methods were used to assess the similarities and dissimilarities of the entire Excitation-emission matrix spectroscopy (EEMs) data sets of samples collected from Jiaozhou Bay, China. The results demonstrate that multivariate analysis facilitates the complex data treatment and spectral sorting processes, and also enhances the probability to reveal otherwise hidden information concerning the chemical characteristics of the dissolved organic matter (DOM). The distribution of different water samples as revealed by multivariate results has been used to track the movement of DOM material in the study area, and the interpretation is supported by the results obtained from the numerical simulation model of substance tracing technique, which show that the substance discharged by Haibo River can be distributed in Jiaozhou Bay.     

兴凯湖沉积物磁化率和色度反映的28kaBP以来区域古气候环境演化

对兴凯湖长269 cm的沉积岩心的研究结果显示:沉积物的色度和磁化率特征可以较好地反映区域气候环境变化。沉积物明度分别与红度、磁化率、黏土和有机质含量之间及磁化率与黏土之间有很好的相关性;红度高值与明度低值对应暖湿气候环境,磁化率低值反映沉积物较粗的较低湖面,对应冷干气候。28480~26160 cal.aBP,湖区处于温湿气候时期;22880~18170 cal.aBP,岩心孢粉浓度很低,流域处于末次盛冰期疏桦林草原环境;18170~12650 cal.aBP处于Bφlling/Older Dryas/Allerφd暖期。岩心深度90~78 cm段,对应于新仙女木期;11500~4570 cal.aBP,进入全新世暖期,其中8000~5000 cal.aBP,本区处于全新世大暖期(气候适宜期);4570~1470 cal.aBP气候变为凉干;1470 cal.aBP以来,流域又变为暖湿气候环境,同时,人类活动逐渐增强造成水土流失加剧。     

镜质组反射率测试及其所反映的构造应力场

为了利用煤镜质组反射率推断豫北构造应力场,基于构造应力是造成镜质组反射率各向异性（VRA）的主要控制因素,对在豫北焦作、安阳、鹤壁三个矿区井下取的定向煤样品进行了室内显微镜下反射率测试,对测试数据按有关公式进行计算后就得出了由最大反射率值、中间反射率值、最小反射率值为轴组成的镜质组反射率椭球体（VRI）.结果表明,研究区煤样显示二轴晶正光性,它们经过了强烈的构造变形,研究区煤样镜质组反射率各向异性是由构造应力所引起;由镜质组反射率椭球体（VRI）得出的豫北构造应力场与钻探、节理统计、河南省区域构造应力场分析等方法得出的应力场基本上是吻合的,但也有一定的区别,主要体现在应力场到安阳、鹤壁矿区后发生了向左的偏转.总之,利用煤镜质组反射率各向异性推断构造应力场的方法是可行的、是有效的.     

Hyperspectral feature analysis of chlorophyll a and suspended solids using field measurements from Taihu Lake,eastern China

Abstract

We report results of three field campaigns conducted at 39 stations. At each station, we measured reflectance spectra in situ and collected water samples for measuring chlorophyll a (CHL) and suspended solids (SS) concentrations in the laboratory. To identify the indicative bands and develop suitable estimation models for CHL (C _CHL) and SS (C _SS) concentrations in Taihu Lake, a spectral-feature method and a derivative method were applied. The following conclusions were drawn: (a) the critical C _CHL and C _SS probably causing their spectral variation are, respectively: 0, 10, 50 and 75 μg L^?1, and 0, 10, 50 and 100 mg L^?1; (b) the derivative method is better than the spectral-feature method for estimating C _CHL and C _SS; (c) the optimal variable for CHL is a reflectance second-order derivative at 501 nm or a reflectance first-order derivative at 698 nm; the optimal variable for SS can change when its concentration is low and the range is narrow; otherwise, the optimal variable is a reflectance first-order derivative at 878 nm; and (d) the CHL and SS have an effect on one another's retrieval. The C _CHL estimation accuracy would benefit from narrowing the C _SS range. With C _CHL increasing and its range broadening, the corresponding C _SS estimation accuracy decreases gradually.     

徐湾—石头岗花岗闪长岩体对围岩的热影响

对徐海—石头岗花岗闪长岩体围岩中黑云母及有机质变质程度的研究发现:距岩体580m范围内的接触带岩石皆具有角岩化现象。黑云母含量受原岩成分影响,其鳞片粒径与岩体距离密切有关。围岩中镜质组反射率,(R_(mas))值与岩体距离之间有十分明显的规律。     

Fabry-Perot spectroscopy in space science

The paper describes use of Fabry-Perot (fp) systems in spectroscopic studies of astronomy and earth’s upper atmosphere. Factors influencing the resolution, luminosity and instrumental line shape offp spectrometer are discussed and the need for their optimization is emphasised, if desired luminosity gain is to be realised in practice. Use offp as imaging spectrometer, scanning spectrometer and as a narrow band filter are illustrated. Tandemfp systems are briefly dealt with.     

Measurements of tropospheric OH concentrations: A comparison of field data with model predictions

Using long path UV absorption spectroscopy we have measured OH concentrations close to the earth's surface. The OH values observed at two locations in Germany during 1980 through 1983 range from 0.7×10⁶ to 3.2×10⁶ cm^-3. Simultaneously we measured the concentrations of O₃, H₂O, NO, NO₂, CH₄, CO, and the light non methane hydrocarbons. We also determined the photolysis rates of O₃ and NO₂. This allows calculations of OH using a zero dimensional time depdendent model. The modelled OH concentrations significantly exceed the measured values for low NO _x concentrations. It is argued that additional, so far unidentified. HO _x loss reactions must be responsible for that discrepancy.     

Infrared estimates of aliphatic kerogen carbon in sedimentary rocks

An infrared routine has been developed to estimate the aliphatic portion of kerogen carbon in sedimentary rocks. The procedure does not require isolation of the organic matter and is based on a computer-assisted determination of global band areas in the region of the aliphatic carbon-hydrogen stretching vibrations around 2900cm⁻¹. From these integrated absorptions the amount of aliphatic carbon C_al (mg of aliphatic carbon per gram of solvent-extracted rock) is calculated by means of a calibration with model rocks. Carbonate overtones which interfere in the case of limestones are eliminated by comparison to a CaCO₃ standard.The method has been applied to rocks containing kerogens of different types and maturities at TOC levels of 0.5 to 12%. The aliphatic carbon concentrations range from 0.5 to 60mg·g⁻¹ and correlate reasonably well with the residual genetic potentials of the rocks as measured by S₂ values from Rock-Eval pyrolysis. The ratio S₂/C_al is found to decrease with burial depth reflecting a maturity enhanced conversion of aliphatic carbon to fixed aromatic carbon under Rock-Eval conditions.