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1.
Directional reflectance (R) spectra from 380 to 780 nm for nadir illuminated leaves of four different plants (croton, Codiaeum variegatum; spotted eleagnus, Eleagnus pungens Maculata; Japanese pittosporum, Pittosporum tobira and Benjamin fig, Ficus benjamina Starlight) were acquired at a viewing angle of 30 degrees from the nadir direction. Chlorophyll-a and -b content of leaves covered a range of 1-60 and 0.5-21 microg/cm(2), respectively. In contrast with previous results from hemispherical reflectance measurements, directional reflectance data does not correlate well with chlorophyll concentration. This is mainly due to the external reflectance (R(E)) at the leaf epidermis, caused by the mismatch of the refractive index at the air-epidermis and epidermis-inner layer boundary. The external reflectance can be identified with the blue flat reflectance between 380 and 480 nm. The inner reflectance (R(I)), obtained by subtracting the external reflectance from the measured spectra, was found to be linearly related to the logarithm of the chlorophyll content. Good fitting of the log (Chl) versus R(I)(lambda) curves were obtained for R(I) in the green band (around 550 nm) and close to the inflection point in the red edge (around 700 nm). The coefficient of determination, r(2), of curve fitting improved (up to 0.97) when the normalised inner reflectance NR(I)(lambda)=R(I)(lambda)/R(I)(lambda(0)), with lambda(0)>or=750 nm, was used instead of the absolute reflectance. The best indices for Chl, Chl-a and Chl-b determination were R(I)(542)/R(I)(750), R(I)(706)/R(I)(750) and R(I)(556)/R(I)(750), respectively. However, since the content of Chl-a relative to Chl-b was almost constant for the plants investigated, the two last indices must be further validated on leaves with a high variability in the Chl-a:Chl-b ratio. The error in the determination of chlorophyll content was found to be of the order of 10%. This value was lower than those obtained by applying the vegetation indices previously suggested. Therefore, the normalised inner reflectance in the green and in the red edge represents a more suitable index for the chlorophyll determination than those up to now used.  相似文献   

2.
Absorption and reflectance spectra of maple (Acer platanoides), cotoneaster (Cotoneaster alaunica), dogwood (Cornus alba) and pelargonium (Pelargonium zonale) leaves with a wide range of pigment content and composition were studied in visible and near-infrared spectra in order to reveal specific anthocyanin (Anth) spectral features in leaves. Comparing absorption spectra of Anth-containing and Anth-free leaves with the same chlorophyll (Chl) content, absorption spectra of Anth in leaves were derived. The main spectral feature of Anth absorption in vivo was a peak around 550 nm; the peak magnitude was closely related to Anth content. A quantitative nondestructive technique was developed to subtract Chl contribution to reflectance in this spectral region and retrieve Anth content from reflectance over a wide range of pigment content and composition. Anth reflectance index in the form ARI = (R550)-1 - (R700)-1, where (R550)-1 and (R700)-1 are inverse reflectances at 550 and 700 nm, respectively, allowed an accurate estimation of Anth accumulation, even in minute amounts, in intact senescing and stressed leaves.  相似文献   

3.
通过溶胶 凝胶法结合水热处理制备了掺杂铁或铬离子的纳米尺寸锐钛矿型TiO2光催化剂.用XRD、BET、TEM、EPR和UV VisDRS对样品进行了系列表征.在对活性偶氮染料XRG的降解中,可见光激发下适量掺杂的TiO2呈现出优于纯TiO2和P25的活性,同时掺杂并未降低其在紫外光激发下的活性.  相似文献   

4.
The photocatalytic activity of meso-tetraphenylporphyrins with different metal centers (Fe, Co, Mn and Cu) adsorbed on TiO(2) (Degussa P25) surface has been investigated by carrying out the photodegradation of methyl orange (MO) under visible and ultraviolet light irradiation. The photocatalysts were characterized by X-ray diffraction (XRD), scanning electron microscopy (SEM), diffuse reflectance UV (DRS-UV-vis) and infrared spectra. Copper porphyrin-sensitized TiO(2) photocatalyst (CuP-TiO(2)) showed excellent activity for the photodegradation of MO whether under visible or ultraviolet light irradiation. Natural Bond Orbital (NBO) charges analysis showed that methyl orange ion is adsorbed easier by CuP-TiO(2) catalyst due to the increase of induced interactions.  相似文献   

5.
Diffuse reflectance (visible) and attenuated total internal reflection Fourier-transform infrared (ATR-FTIR) spectroscopies were used to examine a colloidal nontronite clay in the presence of Fe2+(aq). pH-dependent changes are observed in both types of spectra. In the visible region, a broad feature at approximately 750 nm appears as the pH is raised to circumneutral values. This absorbance band overlaps with a portion of the spectrum of the chemically reduced clay which is dominated by an intervalence charge-transfer transition between Fe2+ and Fe3+ within the mineral structure. The similarities between these spectra suggest that Fe2+(aq) adsorbs to the clay in such a way that it can undergo charge transfer with structural Fe3+ within the clay. ATR-FTIR spectra at pH 5-8 reveal a transformation in the Si-O stretching region between pH 6 and pH 7 with a shift of the component peaks to lower frequency. Taken together, these spectroscopic studies indicate that Fe2+ forms an inner-sphere complex with the clay at higher pH values. The pH threshold for these observed changes in physical and electronic structure is in good agreement with the point of zero charge (pzc) of the hydroxyl groups on the edge surfaces of the clay, suggesting that complexation of Fe2+ to deprotonated edge sites leads to the observed spectroscopic features.  相似文献   

6.
Changes in the room-temperature emission spectrum of chlorophyll (Chl) were analyzed using fast diode-array recordings during the Kautsky effect in mature and in greening barley leaves. In mature leaves, the comparison of F(O) (basal level of fluorescence yield at transient O) and F(M) (maximum level of fluorescence yield at transient M) spectra showed that the relative amplitude of total variable fluorescence was maximal for the 684 nm Photosystem II (PSII) band and minimal for the 725 nm Photosystem I band. During the increase from F(O) to F(M), a progressive redshift of the spectrum of variable fluorescence occurred. This shift reflected the different fluorescence rise kinetics of different layers of chloroplasts inside the leaf. This was verified by simulating the effect of screening on the emission spectrum of isolated chloroplasts and by experiments on greening leaves with low Chl content. In addition, experiments performed at different greening stages showed that the presence of uncoupled Chl at early-greening stages and light-harvesting complex II (LHCII) at later stages have detectable but minor effects on the shape of room-temperature emission spectra. When strong actinic light was applied to mature green leaves, the slow fluorescence yield, which declined from F(M) to F(T) (steady-state level of fluorescence yield at transient T), was accompanied by a slight redshift of the 684 nm PSII band because of nonphotochemical quenching of short-wavelength-emitting Chl ascribed to LHCII.  相似文献   

7.
Chlorophyll (Chl) a', the C13(2)-epimer of Chl a, is one of the two Chl molecules constituting the primary electron donor (P700) of photosystem (PS) I of a thermophilic cyanobacterium Synechococcus elongatus. To examine whether PS I of other oxygenic photosynthetic organisms in general contain one Chl a' molecule in P700, the pigment composition of thylakoid membranes and PS I preparations isolated from red algae Porphyridium purpureum and Cyanidium caldarium was examined by reversed-phase HPLC with particular attention to Chl a' and phylloquinone (PhQ), the secondary electron acceptor of PS I. The two red algae contained one Chl a' molecule at the core part of PS I. In PS I of C. caldarium, two menaquinone-4 (MQ-4) molecules were detected in place of PhQ used by higher plants and cyanobacteria. The 1:2:1 stoichiometry among Chl a', PhQ (MQ-4) and P700 in PS I of the red algae indicates that one Chl a' molecule universally exists in PS I of oxygenic photosynthetic organisms, and two MQ-4 molecules are associated with PS I of C. caldarium.  相似文献   

8.
Ag@TiO2 core-shell-type nanophotocatalysts have been prepared using a simple and convenient method. The products were characterized by TEM, XRD, and UV-vis spectra. To make the catalysts achieve the highest photocatalytic activity under UV light illumination, the Ag content of Ag@TiO2 was optimized. The results showed that Ag@TiO2-doped Fe3+ extend their absorption into the visible region. Among the Fe3+-doped samples, Ag@Fe-TiO2 with low Ag content showed higher photocatalytic activity under visible light illumination. An excessive added amount of Ag would reduce Fe3+ to Fe2+ and make them difficult to be incorporated into the lattice of titania. From the experiments, we found that Fe3+ ions could stabilize the Ag@TiO2 colloid by holding back the aggregation of the core-shell nanoparticles.  相似文献   

9.
Abstract— The chlorophyll a fluorescence properties of Gonyaulax polyedra cells before and after transfer from a lightdark cycle (LD) to constant dim light (LL) were investigated. The latter display a faster fluorescence transient from the level ‘I’ (intermediary peak) to ‘D’ (dip) to ‘P’ (peak) than the former (3 s as compared to 10 s), and a different pattern of decline in fluorescence from ‘I’ to ‘D’ and from ‘P’ to the steady state level with no clearly separable second wave of slow fluorescence change, referred to as ‘s' (quasi steady state)→‘M’ (maximum) →‘T’ (terminal steady state). The above differences are constant features of cells in LD and LL, and are not dependent on the time of day. They are interpreted as evidence for a greater ratio of photosystem II/photosystem I activity in cells in LL. After an initial photoadaptive response following transfer from LD to LL, the cell absorbance at room temperature and fluorescence emission spectra at 77 K for cells in LL and LD are comparable. The major emission peak is at 685–688 nm (from an antenna Chl a 680, perhaps Chl a-c complex), but, unlike higher plants and other algae, the emission bands at 696–698 nm (from Chl aII complex, Chl a 685, close to reaction center II) and 710–720 nm (from Chl a1, complexes, Chl a 695, close to reaction center I) are very minor and could be observed only in the fluorescence emission difference spectra of LL minus LD cells and in the ratio spectra of DCMU-treated to non-treated cells. Comparison of emission spectra of cells in LL and LD suggested that, in LL, there is a slightly greater net excitation energy transfer from the light-harvesting peridinin-Chl a (Chl a 670) complex, fluorescing at 675 nm, to the other antenna chlorophyll a complex fluorescing at 685–688 nm, and from the Chl a., complex to the reaction center II. Comparison of excitation spectra of fluorescence of LL and LD cells, in the presence of DCMU, confirmed that cells in LL transfer energy more extensively from the peridinin-Chl a complex to other Chl a complexes than do cells in LD.  相似文献   

10.
We report on investigations of the photochromic effect of BiVO4 pigments. Emphasis is placed on an approach widely used in industrial color testing. By means of colorimetry ΔEab*-values, which measure the perceived color difference, can be calculated from reflectance spectra of non-illuminated and illuminated pigment coatings. Pigments were prepared by either wet-chemical precipitation or solid-state reactions. Depending on the choice of starting compounds, lightfastness was found to vary significantly. Small amounts of impurity phases do not seem to affect photochromism. In contrast, impurities like Fe and Pb cause intense photochromism. The role of Fe is suggested by trace analyses, which (in case of pigments synthesized by precipitation reactions) reveal a correlation between concentration and ΔEab*. Indications are found that other effects like pigment-lacquer interactions might also be of importance. Difference reflectance spectra turn out to vary in shape depending on the type and concentration of impurities or dopants. For BiVO4 at least three different mechanisms of photochromism can be assumed.  相似文献   

11.
Six different sensors were prepared using hydrolytic and non-hydrolytic sol–gel routes and three different pH indicators as receptor elements. These materials were employed as dual-target sensors for ammonia gas sensing and pH measurements in real samples. Ultraviolet–visible diffuse reflectance spectroscopy and a colorimetric analysis were used to evaluate the pH transitions and the color change that resulted from the ammonia that was employed as a probe for gas sensing. The colorimetric analysis was performed using the CIELAB color space model with the D65 standard illuminant. The resulting $ \Updelta {\text{E}}_{\text{ab}}^{*} $ values correlated with the response time for the observation of the first visible color change detected by the human eye (N = 50), and the average time values ranged from 48 to 117 s. In addition, the response times were evaluated as a function of sample characteristics, namely, the gender, age and eye color. Only groups of these characteristics exhibited relevance to the response time and could be associated with a specific range of time. The sensors were also employed for pH measurements of an aqueous solution, and a double-color scale could be established both with the sensors synthesized by the acid route and with the pH indicators alizarin red and brilliant yellow. From this color scale, it was possible to identify a shift in the turning point of the pH indicator from the free molecule to the encapsulated molecule. The double-color scale was applied to evaluate real samples from a galvanic industry using the synthesized encapsulated sensors.  相似文献   

12.
采用溶胶-凝胶法制备了Fe3+掺杂的Fe-K2La2Ti3O10光催化剂, 并通过X射线衍射(XRD)、紫外-可见漫反射(DRS)、X射线光电子能谱(XPS)等技术对其进行了表征和分析, 考察了不同掺杂量对K2La2Ti3O10的性质及光催化分解水制氢活性的影响. 结果表明, Fe-K2La2Ti3O10在400-650 nm范围内显示强吸收, 光谱响应扩展到可见光区(λ>400 nm), 掺杂Fe3+后, K2La2Ti3O10的可见光区的光催化制氢活性显著提高, 掺杂量为nFe/nTi=0.04时活性最佳, 当催化剂用量为0.1 g, 反应液为CH3OH(30 mL)+H2O(90 mL)时, 产氢量达到1.92 μmol·h-1, 为未掺杂时的4倍.  相似文献   

13.
Spectroradiometric measurements of reflectance and CIELAB hue-angle, were tested for K(I) determination using disposable optical sensors based on ion exchange mechanism. The linearisation of the sigmoidal response function, using a logistic regression, increases the linear range noticeably to 7.65 × 10−8–1.5 M and 1.22 × 10−7–1.5 M for CIELAB hue-angle and reflectance, respectively. The trueness of both procedures was demonstrated comparing it with results obtained by a DAD spectrophotometer used as a reference measurement procedure. The usefulness of the procedure was checked by analysing K(I) in different types of waters and beverages. Additionally, we studied the possible visual discrimination for the whole potassium range tested, obtaining the possibility of discriminating twelve groups of concentrations.  相似文献   

14.
Assessing carotenoid content in plant leaves with reflectance spectroscopy   总被引:7,自引:0,他引:7  
Spectral reflectance of maple, chestnut and beech leaves in a wide range of pigment content and composition was investigated to devise a nondestructive technique for total carotenoid (Car) content estimation in higher plant leaves. Reciprocal reflectance in the range 510 to 550 nm was found to be closely related to the total pigment content in leaves. The sensitivity of reciprocal reflectance to Car content was maximal in a spectral range around 510 nm; however, chlorophylls (Chl) also affect reflectance in this spectral range. To remove the Chl effect on the reciprocal reflectance at 510 nm, a reciprocal reflectance at either 550 or 700 nm was used, which was linearly proportional to the Chl content. Indices for nondestructive estimation of Car content in leaves were devised and validated. Reflectances in three spectral bands, 510+/-5 nm, either 550+/-15 nm or 700+/-7.5 nm and the near infrared range above 750 nm are sufficient to estimate total Car content in plant leaves nondestructively with a root mean square error of less than 1.75 nmol/cm2.  相似文献   

15.
二氧化钛包裹碘单质(I2/TiO2)制备及其光催化降解苯酚   总被引:1,自引:0,他引:1  
采用水热法,以Ti(SO4)2为钛源,KIO3为掺碘剂制备了具有高可见光活性,高稳定性的二氧化钛包裹碘单质(I2/TiO2)光催化剂.利用X射线光电子能谱(XPS)、X射线晶体粉末衍射(XRD)、透射电子显微镜(TEM)和紫外可见漫反射光谱(DRS)等表征手段对样品进行表征.结果表明,I2/TiO2中除含有锐钛矿相二氧化钛外、还含有碘单质和碘酸;I2/TiO2粒径大小为45 nm左右;在波长384 nm至700 nm范围内,该催化剂有强烈的吸收.探讨了该催化剂的形成过程和可见光催化机理.以苯酚降解反应为探针,测定了I2/TiO2光催化活性.结果显示:在全谱光源照射下I2/TiO2活性略高于P25,在可见光范围内其活性是P25的3倍多.确定了降解苯酚的最佳条件:全谱光源照射,投加量为0.5 g/L,苯酚浓度大于10 mg/L,溶液pH为3.2.I2/TiO2重复使用4次后,催化活性没有明显下降.  相似文献   

16.
The impact of UV-B radiation on photosynthetic related parameters was studied in Oryza sativa L. cv. Safari plants, after an UV-B irradiation performed 1h per day for 7days (between 8 and 14days after germination) with a ten narrow-band (λ 311nm) that resulted in a total biological effective UV-B (UVB(BE)) of 2.975kJm(-2)day(-1) and a total of 20.825kJm(-2). Gas exchange measurements were severely affected, showing reductions higher than 80% in net photosynthesis (P(n)), stomatal conductance and photosynthetic capacity (A(max)), 1day after the end of the 7-days UV-B treatment. Similarly, several fluorescence parameters (F(o), F(v)/F(m), Fv'/Fm', ?(e), q(P) and q(E)) and thylakoid electron transport (involving both photosystems) were also severely reduced. Concomitantly, a decline of xanthophylls, carotenes, Chl a, Chl (a+b) and Chl (a/b) values was accompanied by the increase of the lipoperoxidation level in chloroplast membranes, altogether reflecting a loss of protection against oxidative stress. Seven days after of the end of UV-B treatment, most fluorescence parameters recovered, but in P(n), A(max), thylakoid electron transport rates, Chl a and lipid classes, as well as the level of lipoperoxidation, the impacts were even stronger than immediately after the end of stress, denoting a clear loss of performance of photosynthetic structures. However, only a moderate impact on total lipids was observed, accompanied by some changes in the relative weight of the major chloroplast membrane lipid classes, with emphasis on the decrease of MGDG and the increase of phospholipids. That suggested an ability to de novo lipid synthesis allowing qualitative changes in the lipid matrix. Notably, the leaves developed after the end of UV-B irradiation showed a much lower impact, with significantly decreased values only in P(n) and g(s), rises in several fluorescence parameters, thylakoid electron transport, photosynthetic pigments (xanthophylls and chls) and DEPS, while lipid classes presented values close to control. The results showed a global impact of UV-B in the photosynthetic structures and performance in irradiated leaves, but revealed also a low impairment extent in the leaves entirely developed after the end of the irradiation, reflecting a remarkable recovery of the plant after the end of stress, what could constitute an advantage under occasional UV-B exposure events in this vital worldwide staple food crop.  相似文献   

17.
任意取广州市越秀区1个月至满3周岁前男女婴幼儿218例,取其枕部头发测定Zn、Fe、Ca、Pb、Cu、Mn的含量,分性别统计其非正常值发生率。结果发现,本区婴幼儿微量元素失衡情况较明显,尤以缺锌、高铅为严重。另缺锌、缺铁、高铁、缺钙及高钙与性别有关。  相似文献   

18.
An aggregate of chlorophyll a' (Chi a' , C132-epimer of ChI a ) formed in a methanovwater (40160, vol/vol) mixed solvent was examined by visible absorption, circular dichro-ism (CD), fluorescence and resonance Raman spectrosco-pies in relation to its possible involvement in the core of photosystem I reaction center. The Chl a' aggregate exhibited a sharp, double-peaked absorption spectrum (690 and 715 nm) accompanied by an intense, conservative CD signal. The fluorescence excitation polarization spectrum showed that the doublet results from the exciton splitting in a single aggregate species. Time-dependent changes in the spectroscopic properties clearly point to a simple transformation process from one molecular species to another, though a minor component appears to coexist. This conclusion was supported also by the principal multicom-ponent spectral estimation analysis of the transients of absorption spectra. The species formed at the initial stage is most probably a T-shaped dimer or oligomer, which is then gradually converted into the final major product, presumably a stacked dimer. In both of these states, the Chl molecules are linked together via direct coordination of the C13'keto carbonyl oxygen onto the Mg atom of neighboring molecules, as suggested by almost identical resonance Raman spectra in ordinary and deuterated methanovwater mixed solvents. The stacked dimers probably further associate to form a colloidal state in this solvent system. Based on these results, a model for the Chl a' aggregation is proposed.  相似文献   

19.
Multivalency iodine (I(7)+/I(-)) doped TiO(2) were prepared via a combination of deposition-precipitation process and hydrothermal treatment. The as-prepared samples were characterized by X-ray diffraction, transmission electron microscopy, Brunauer-Emmett-Teller surface area, UV-vis diffuse reflectance spectra, X-ray photoelectron spectroscopy, surface photovoltage spectroscopy, and electric-field-induced surface photovoltage spectroscopy. The electronic structure calculations based on the density functional theory revealed that upon doping, new states that originated from the I atom of the IO(4) group are observed near the conduction-band bottom region of TiO(2), and the excitation from the valence band of TiO(2) to the surface IO(4-) is responsible for the visible-light response of the I-doped TiO(2). The as-prepared I-doped TiO(2) showed high efficiency for the photocatalytic decomposition of gaseous acetone under visible light irradiation (lambda > 420 nm). A possible mechanism for the photocatalysis on this multivalency iodine (I(7)+/I(-)) doped TiO(2) under visible light was also proposed.  相似文献   

20.
When the primary electron-donation pathway from the water-oxidation complex in photosystem II (PS II) is inhibited, chlorophyll (Chl(Z) and Chl(D)), beta-carotene (Car) and cytochrome b(559) are alternate electron donors that are believed to function in a photoprotection mechanism. Previous studies have demonstrated that high-frequency EPR spectroscopy (at 130 GHz), together with deuteration of PS II, yields resolved Car(+) and Chl(+) EPR signals (Lakshmi et al. J. Phys. Chem. B 2000, 104, 10 445-10 448). The present study describes the use of pulsed high-frequency EPR spectroscopy to measure the location of the carotenoid and chlorophyll radicals relative to other paramagnetic cofactors in Synechococcus lividus PS II. The spin-lattice relaxation rates of the Car(+) and Chl(+) radicals are measured in manganese-depleted and manganese-depleted, cyanide-treated PS II; in these samples, the non-heme Fe(II) is high-spin (S = 2) and low-spin (S = 0), respectively. The Car(+) and Chl(+) radicals exhibit dipolar-enhanced relaxation rates in the presence of high-spin (S = 2) Fe(II) that are eliminated when the Fe(II) is low-spin (S = 0). The relaxation enhancements of the Car(+) and Chl(+) by the non-heme Fe(II) are smaller than the relaxation enhancement of Tyr(D)(*) and P(865)(+) by the non-heme Fe(II) in PS II and in the reaction center from Rhodobactersphaeroides, respectively, indicating that the Car(+)-Fe(II) and Chl(+)-Fe(II) distances are greater than the known Tyr(D)(*)-Fe(II) and P(865)(+)-Fe(II) distances. The Car(+) radical exhibits a greater relaxation enhancement by Fe(II) than the Chl(+) radical, consistent with Car being an earlier electron donor to P(680)(+) than Chl. On the basis of the distance estimates obtained in the present study and by analogy to carotenoid-binding sites in other pigment-protein complexes, possible binding sites are discussed for the Car cofactors in PS II. The relative location of Car(+) and Chl(+) radicals determined in this study provides valuable insight into the sequence of electron transfers in the alternate electron-donation pathways of PS II.  相似文献   

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