Detection of Rice Yellow Mottle at the Asymptomatic Stage by Hyperspectral Fluorescence and Reflectance Spectroscopies

Rice yellow mottle is considered the most destructive disease threatening rice production in Africa. Early detection of this infection in rice is essential to limit its expansion and proliferation. However, there is no research devoted to the spectral detection of rice yellow mottle virus (RYMV) infection, especially in the asymptomatic or early stages. This work proposes the use of hyperspectral fluorescence and reflectance data at leaf level for the detection of this disease in asymptomatic stages. A greenhouse experiment was therefore conducted to collect hyperspectral fluorescence and reflectance data at different stages of infection. These data allowed to calculate nine vegetation indices: one from fluorescence spectra and eight from reflectance spectra. A t-test made it possible to identify, from the second day after infection, four relevant reflectance vegetation indices to discriminate healthy leaves from those infected: these are Photochemical Reflectance Index (PRI), Transformed Chlorophyll Absorption in Reflectance Index (TCARI), Structure Intensive Pigment Index (SIPI) and Simple Ratio Pigment Index (SRPI). The fluorescence index was less sensitive in detecting infection. The four significant vegetation indices for the detection of RYMV were then used to build and evaluate models for discriminating plants according to their health status by the supervised classification of support vector machine (SVM) at different stages of infection. The maximum overall accuracy is 92.5% six days after inoculation (6 DAI). The sixth day after inoculation would be the adequate day to detect RYMV. This plants discrimination was validated by the mean reflectance spectra and by the histograms showing the differences between the average reflectance vegetation indices values of the two types of plants. Our results demonstrate the feasibility of differentiating RYMV-infected samples. They suggest that support vector machine learning models could be developed to diagnose RYMV-infected plants based on vegetation indices derived from spectral profiles at early stages of disease development.

Research of Three-Dimensional Fluorescence Spectra of RE^(3+)(RE=Eu,Tb) and Na_2WO_4 Co-doped Silica Luminescence Materials

In the preparation of this precursor tetraethlortho silicate (TEOS), sodium tungstate, ethyl alcohol, HCl and RECl3(RE=Eu,Tb) were mixed and then heated at 800 ℃ for 2 h, leading to a luminescent compound. The structure of the materials was characterized by TG-DTA and IR analysis, and the results indicate that the materials were in SiO2 network structure. Three-dimensional fluorescence spectra was used to characterize the luminescent properties of the materials. The luminescence property of doped and un-doped Eu3+or Tb3+ and Na2WO4 in silica materials were prepared and measured. The results show that good energy transfer from WO2-4 to Eu3+ ion, sensitized the luminescence intensity of Eu3+ remarkably. Tb3+ ion incorporated silica materials expressed the inverse energy transition from Tb3+ to WO2-4, however, we got the materials with homogeneous green blue fluorescent light. Finally, the energy transfer of WO2-4 and Eu3+, WO2-4 and Tb3+ were explained by energy levels diagram.

TEMPERATURE DEPENDENCE OF THE FLUORESCENCE SPECTRA OF LADDERLIKE POLYPHENYLSILSESQUIOXANE AND LADDERLIKE 1,4-PHENYLENE-BRIDGED POLYVINYLSILOXANE

Fluorescence spectra of ladderlike polyphenylsilsesquioxane (LPPS) and ladderlike 1,4-phenylene-bridged polyvinylsiloxane (LPPVS) have been measured as a function of temperature (4-55 degreesC), in dilute tetrahydrofuran solution. The excimer (IF) to monomer (I-M) intensity ratio (I-E/I-M) of LPPS dilute solution shows a double linear Arrhenius plot with a break point ascribable to a transition temperature Tt. This behavior has not been found for single chain polyorganosiloxanes. When In/(E) of LPPS was plotted against 1/T, it also gave a double linear plot with one break point, which was found in single chain polyorganosiloxanes. The different behaviors between LPPS and single chain polyorganosiloxanes may be mainly attributed to the relatively rigid double-chain macromolecular backbone of LPPS. However, the 1n(I-E/I-M) of dilute LPPVS solution versus 1/T shows a simple linear variation with a positive slope which confirms our proposition. The difference between the fluorescence results of LPPS and those of LPPVS may possibly derive from their structure differences and cooperative motion in backbone chain bonds.

Fluorescence Spectra of the Poly (N-vinylcarbazole)Obtained with Asymmetric Polymerization

The fluorescence spectra of the poly (N-vinylcarbazole) in solution obtained with chirally organic salts or acid as catalyst or initiator [ (-)Sp: (-)-Sparteine, (+)CSA: D- (+)Camphor-10-sulfonic acid)], respectively, have been investigated. It is found that the two emission peaks at the longer wavelength (lambda max, ca, 415nm) and the shorter wavelength (lambda max, ca, 370nm) are assigned to the sandwich excimer and second excimer (partial overlap) fluorescence, respectively. The sandwich excimer and partially overlapped excimer are attributed to a fully overlapped structure of neighbouring carbazole chromophores in a totally elipsed conformation of the isotactic sequence, and partially overlapped structure of the syndiotactic sequence. The estimated values of I-415/I-370 and isotactic sequence content by using the fluorescence spectra are in the order: (-)Sp(+) (+)CSA(-)> (+)CSA(-)> (-)Sp(+)ClO(4)(-) (no peak at 415nm for AIBN).

Characteristics of the ThreeDimensional Fluorescence Spectra of Fossil Fuels

We have found some fluorescence characteristics of fossil fuels based on the contour maps of the three dimensional fluorescence spectra of their non quenching samples. The common fluorescence characteristic is that the main peaks of various fossil fuels are located in the vicinity of excitation/emission wavelength pair 228nm/340nm.The diversity of fluorescence characteristics can be represented with several indexes α,K,F and R ,and these indexes provide measurable parameters for division of fluorescence fingerprints of fossil fuels. The fluorescence fingerprints of fossil fuels can be divided into five models named O,B,Q,P and G that are corresponding to condensate oil, light oil, heavy oil, coal and natural gas, respectively. The technique has a potential application in study of environment pollution on crude oil and geochemical exploration of fossil fuels.

X-RAY FLUORESCENCE SPECTRA ANALYSIS ON THE STRUCTURE AROUND Ti^(4+) OF BaO-SiO_2-B_2O_3-TiO_2 SYSTEM GLASSES

The structure around Ti^(4+) in Bao-SiO_2 -B_2O_3-TiO_2 had been studied by X-ray fluorescence spectra. The results show that the Ti^(4+) mainly exists in the [TiO_4] and enters the network of [SiO_4]. [TiO_4] has the tendency to change to [TiO_6] with the increase of TiO_2 con-tent. When the TiO_2 content increases to about 20mol% the tendency reaches its maximum.

STUDIES ON FLUORESCENCE SPECTRA OF SAMARIUM EUROPIUM TERBIUM AND DYSPROSIUM WITH BENZOYL UREA DERIVATIVES AND PHENANTHROLINE

Rare earth chelates of benzoyl urea derivatives were prepared in ethanol and fluorescence spectra of these chelates were studied in detail. A composition of [RE(BU)_3Phen] (NO_3)_3 was obtained. Correlation between chemical properties of ligands, chelates and spectroscopy was discussed. Intramolecular energy transfer in rare earth chelates was explained.

Molecular fluorescence significantly enhanced by gold nanoparticles@zeolitic imidazolate framework-8

Noble metal nanoparticles exhibit unique surface plasmon resonance dependent optical properties.On this basis,gold nanoparticles(AuNPs)encapsulated in metal–organic frameworks(MOFs)can form AuNPs@MOFs composites to modulate the optical properties of fluorescent molecules,which is less reported.In this paper,based on the fluorescence enhancement effect of AuNPs on 2-(2-hydroxyphenyl)-1H-benzimidazole(HPBI)molecules,zeolitic imidazolate framework-8(ZIF-8)crystals with structural stability were introduced.AuNPs@ZIF-8 exhibited a significantly pronounced fluorescence enhancement of the HPBI molecules.In addition,by comparing the fluorescence characteristics of the HPBI molecules adsorbed on AuNPs@ZIF-8 and those captured in AuNPs@ZIF-8,we found that the ZIF-8 can act as a spacer layer with highly effective near-field enhancement.All our preliminary results shed light on future research on the composite structures of noble metal particles and MOFs for fluorescent probes and sensing applications.

Elemental composition x-ray fluorescence analysis with a TES-based high-resolution x-ray spectrometer

The accurate analysis of the elemental composition plays a crucial role in the research of functional materials.The emitting characteristic x-ray fluorescence(XRF)photons can be used for precisely discriminating the specified element.The detection accuracy of conventional XRF methodology using semiconductor detector is limited by the energy resolution,thus posing a challenge in accurately scaling the actual energy of each XRF photon.We adopt a novel high-resolution x-ray spectrometer based on the superconducting transition-edge sensor(TES)for the XRF spectroscopy measurement of different elements.Properties including high energy resolution,high detection efficiency and precise linearity of the new spectrometer will bring significant benefits in analyzing elemental composition via XRF.In this paper,we study the Ledge emission line profiles of three adjacent rare earth elements with the evenly mixed sample of their oxide components:terbium,dysprosium and holmium.Two orders of magnitude better energy resolution are obtained compared to a commercial silicon drift detector.With this TES-based spectrometer,the spectral lines overlapped or interfered by background can be clearly distinguished,thus making the chemical component analysis more accurate and quantitative.A database of coefficient values for the line strength of the spectrum can then be constructed thereafter.Equipped with the novel XRF spectrometer and an established coefficient database,a direct analysis of the composition proportion of a certain element in an unknown sample can be achieved with high accuracy.

Fluorescence characteristic changes of dissolved organic matter during municipal solid waste composting

Dissolved organic matter（DOM） of municipal solid waste（MSW） consists of minerals, water, ash and humic substances, and is known to enhance plant growth. In this study, inoculating microbes（Z J, MS） were used in municipal solid wastes composting, and composting implemented a industrialized technology. During composting, dissolved organic matter was extracted from the compost and purified. The spectral characteristics of dissolved organic matter was determined by fluorescence emission, excitation, and synchronous spectroscopy. Fluorescence emission, excitation, and synchronous spectra characterized by different relative fluorescent intensities and peaks over time. Fluorescence spectra were similar to that of fulvic acid in sewage sludge, indicating the presence of dissolved organic matter with aromatic structures and a high degree of molecular polymerization. Compared with the controls with no microbial inoculation, the microbe-inoculated treatments exhibited the increase of aromatic polycondensation, in the following order： MS ＋ ZJ 〉 ZJ 〉 MS 〉 CK.

Synthesis, Characterization and Fluorescence of Terbium(Ⅲ) Complexes with Phenylglyoxylic Acid and 2,2-Dipyridine, 1,10-Phenanthroline, Triphenyl Phosphine Oxide

Three new complexes TbL3dipy （H2O）2, TbL3phen （H2O） 2 and TbL2 （TPPO） 2NO3 were synthesized （L = phenylglyoxylate ion, dipy = 2, 2-dipyridine, phen = 1,10-phenanthmline, TPPO = Triphenyl phosphine oxide）. Elemental analysis, conductivity, IR spectra, and ^1HNMR spectra studies were performed. IR spectra indicate that the carboxylate ion of phenylglyoxylate is coordinated to the Tb（Ⅲ） ion as an unidentate ligand. In ^1HNMR, the signals of different hydrogens in phenylglyoxylate ion shift upfield. The excitation and emission spectra of the three solid complexes were recorded at morn temperature, in which the optimum excitation wavelengths are, 361.0, 359.0 and 367.0 nm for these three complexes, respectively. Four emission bands due to the ^5D4-^7Fj（j = 6, 5, 4, 3） transitions were observed for TbL3dipy（H2O）2（489.0, 545.0, 584.0, 620.0 nm） and TbL3phen（H2O）2（490.0, 544.0, 583.0, 620.0 nm）. Under the same conditions, only one emission band due to the ^5D4-^7F5 transition was observed for the complex TbL2（TPPO）2NO3. The emission intensity of TbL3dipy（H2O）2 is the strongest among the three complexes.

Fluorescence of complexes of EuⅢwith aromatic carboxylic acid-1,10-phenanthroline

The 1,10 phenan throline aromatic carboxylic acid(benzoic acid and o phthalic acid) binary and ternary complexes of europium were synthesized.The fluorescence and FT IR spectroscopy,elemental analysis,UV spectroscopic studies on these complexes were also performed.These complexes can emit strong red fluorescence of Eu? excited by UV light.At the same excited wavelength,the fluorescence spectra of the complexes were also studied.The results indicated that the fluorescence intensities of ternary complexes are stronger than that of binary complexes.The reason is that phenanthroline has higher electron density and higher orbit scope in the conjugated system and consequently an easier energy transfer to the europium ion,which makes the fluorescence intensity of ternary complexes be stronger than that of binary complexes.

The LB Films of Dansyl Chloride Labeled Octadecylamine and Its Fluorescence Lifetime

Octadecylamine was derivatized with dansyl chloride (5-dimethylaminonaphthalene-1-sulfonyl chloride) In order to simplify and understand the LB films of fluorescent probe labeling proteins. its monolayer and multilayers in the absence and presence of stearic acid were deposited by LB technique. Fluorescence spectra and lifetimes of the fluorescent products were studied to elucidate the microenvironment of molecules in the LB films.

Crystal growth and spectral properties of Tb：Lu2O3

The crystal growth,x-ray diffraction pattern,absorption spectrum,emission spectrum,and fluorescence lifetime of a Tb：Lu2O3 single crystal were studied.Excited at 483 nm,the peak absorption cross-section was calculated to be 3.5×10（-22）cm2,and the full width at half maximum was found to be 2.85 nm.The Judd-Ofelt（J-O）intensity parameters 2,4,and 6 were computed to be 3.79×10（-20）cm2,1.30×10（-20）cm2,and 1.08×10（-20）cm2,with a spectroscopic quality factor 4/6 being 1.20.The emission cross-sections of green emission around 543 nm and yellow emission around 584 nm were calculated to be 9.43×10（-22）cm2 and 1.32×10（-22）cm2,respectively.The fluorescence lifetimeτexp of -5D4 was fitted to be 1.13 ms.The data suggest that the Tb：Lu2O3 crystal could be a potential candidate for green and yellow laser operation.

Synthesis, Characterization and Fluorescence Studies on Complexes of Terbium with Phenylglyoxylic Acid, 2,2-Dipyridine, 1,10-Phenanthroline, Triphenyl Phosphine Oxide

Three new complexes TbL3dipy （H2O）2, TbL3phen （ H2O ）2 and TbL2 （ TPPO ）2NO3 have been synthesized （L = phenylglyoxylate ion, dipy = 2, 2- dipyfidine, phen = 1,10-phenanthroline, TPPO = Triphenyl phosphine oxide ）. Elemental analysis, conductivity, IR spectra and ^1HNMR spectra studies were performed on them. IR spectra indicate that carboxylate ions in the phenylglyoxylate are coordinated to Tb （Ⅲ） ions as unidentate ligands. In ^1HNMR, the signals of hydrogens in phenylglyoxylate shift upfield. The excitation and emission spectra of the three comolexes were recorded at room temoerature, the excitation spectra show that the optimum excitation wavelengths are 361.0, 359.0 and 367.0 nm, respectively. Four emission bands due to ^5D4-^7Fj （j = 6, 5, 4, 3 ） transitions were observed for TbLadipy （ H2O ）2 （489.0, 545. 0, 584.0,620.0 nm） and TbL3phen （H2O）2 （490. , 544.0, 583.0, 620.0 nm）. And under the same conditions, only one emission band due to ^5Da-^7F5 transition was observed for TbL2 （TPPO）ENO3. The emission intensity of TbLadipy （H2O）2 is the strongest among the three complexes.

Dual-parameter Correlation Analysis of the Fluorescence Data of 1-Methyl-2-formyl-5-substituted Pyrrole(4-nitrophenyl)hydrazones

By using 1-methyl-2-formyl-5 -Y-substituted pyrrole (4-nitrophenyl)hydrazones as a model for nitrogen-containing heterocyclic aromatic compounds, the emission wavelength [lambda(max(em))] values df their fluorescence spectra have been measured. Correlation results show that the Delta E-em values are mainly affected by polar effects, but spin-delocalizatin effects also exist.

Fabrication and Fluorescence Study of Sensitizing Dye/TiO_2 Films

Fluorescence spectra of the sensitizing dye/ TiO2 bilayer films were studied. Charge-transfer complexes were formed in the above bilayer.

Fluorescence Properties of Eu^(3+) :Y_2SiO_5 Single Crystal

Fluorescence properties of Eu 3+ :Y 2SiO 5 have been investigated. Transitions between 5D and 7Fwere were studied with transmission spectra, fluorescence spectra, photoluminescence excitation ( or absorption ) spectra and site selective fluorescence spectra. The X ray powder diffraction pattern of Eu 3+ :Y 2SiO 5 shows that the crystal belong to monoclinic, and lattice's constants a, b, c and β are obtained by a simulation with the measured diffraction angles.

Synthesis, Structure and Spectra Properties of a Novel BOIMPY Compound

A bis-2-iminopyrrole compound（1） and its difluoroboron complex（2） were synthesized and characterized. The crystal of 2 is in the monoclinic system, P2_1/n space group with a = 21.5113（15）, b = 6.3036（3）, c = 21.5064（15） A, V = 2826.3（7） A^3, Z = 4, C_（26.5） H_（25） B_2 ClF_4 N_4 O, M_r = 548.57, D_c = 1.390 g/cm, F（000） = 1132 and μ（MoKα） = 1.787 mm^-1. The final R = 0.0647 and wR = 0.1817 for 10346 observed reflections with I 〉 2σ（I）, and R = 0.0889 and wR = 0.1993 for all data. The molecules of complex 2 self-assemble through C–H×××F hydrogen bonds and form tubular structures which are filled by CH_2 Cl_2 molecules stabilized by C–H×××π interaction. The UV-Vis spectra of complex 2 show great bathochromic shift compared to that of compound 1 due to the difluoroboron complexing. Complex 2 shows fluorescence emission both in solid state and in solution, whereas compound 1 only exhibits fluorescence emission in solid state.

Three-dimensional fluorescence spectral characterization of soil dissolved organic matters in the fluctuating water-level zone of Kai County,Three Gorges Reservoir

Three-dimensional fluorescence spectroscopy was used to investigate the fluorescent properties of soil dissolved organic matter(DOM)in the water-levelfluctuation zone(WLFZ)of Kai County,Three Gorges Reservoir(TGR).Most of the soil DOM analyzed in this study was found to contain four fluorescence peaks.Peaks A and C represent humic-like fluorescence,whereas peaks B and D represent tryptophan-like fluorescence.Peaks E and F,which represent tyrosine-like fluorescence,only appeared in certain soils.Soil humus was the main source of DOM in soil,and higher concentration of soil DOM was found in the exposed soil than submerged soil.Compared to the peaks A and B,the fluorescence intensities of peaks C and D were strongly influenced by the fluctuating water level.Analysis of fluorescence intensities of different peaks in soil DOM showed that WLFZ soil was not contaminated significantly.Soil DOM contained at least two types of humic-like fluorescence groups and two types of protein-like fluorescence groups.The proportion of the content of peak A in soil organic matter was quite stable.The soil DOM in exposed soil had relatively high humification and aromaticity,and periodic submerging and exposure of soil had an impact on the humification of soil DOM.