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Fluorescence imaging and chlorophyll fluorescence to evaluate the role of EDU in UV-B protection in cucumber

机译:荧光成像和叶绿素荧光,评价EDU在黄瓜UV-B保护中的作用

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A fluorescence imaging system and chlorophyll fluorescence emissions were used to evaluate whether EDU, N-$LB@2-(2-oxo-1- imidazolidinyl) ethyl$RB@-N'-phenylurea, provided protection against ultraviolet-B (UV-B) irradiation (290 - 320 nm) in cucumber (Cucumis sativus L.) leaves. Plants were grown in growth chambers illuminated for 14 h per day with 400 W high pressure sodium and metal halide lamps. Photosynthetically active radiation (PAR) for 1 hr at the beginning and end of each cycle was provided at 270 $mu@mol m$+$MIN@2$/ s$+$MIN@1$/ PAR; during the other 12 hr of the photoperiod, the plants received 840 $mu@mol m$+$MIN@2$/ s$+$MIN@1$/ PAR. Beginning on the twelfth day, the plants were exposed to UV-B radiation (0.2 & 18.0 kJ m$+$MIN@2$/d$+$MIN@1$/) for 2 days at 8 h per day centered in the photoperiod. Rapidly acquired (less than 1 s), high spatial resolution (less than 1 mm$+2$/) images were obtained for whole adaxial leaf surfaces using a fluorescence imaging system. The steady-state fluorescence images were acquired in four spectral regions: blue (F450 nm), green (F550 nm), red (F680 nm), and far-red (F740 nm). Fluorescence emission spectra for leaf pigments extracted in dimethyl sulfoxide (DMSO) were obtained by excitation at 280 and 380 nm (280EX 300 - 530 nm; 380EX 400 - 800 nm). Both UV-B and EDU induced stress responses in cucumber leaves that altered the fluorescence emissions obtained from extracts. In the fluorescence images only UV-B induced stress responses were observed but this damage was detected before it was visually apparent. There was no evidence that EDU afforded protection against UV-B irradiation. Use of fluorescence imaging may provide an early stress detection capability for helping to assess damage to the photosynthetic apparatus of plants.
机译:使用荧光成像系统和叶绿素荧光发射来评估EDU,N-$ LB @ 2-(2-氧代-1-咪唑烷基)乙基RB @ -N'-苯基脲,提供针对紫外线-B的保护(UV- b)黄瓜(Cucumis Sativus L.)叶中的辐照(290-320nm)。用400W高压钠和金属卤化物灯每天在14小时照射植物,植物生长。每循环开始和结束的光合作用辐射(PAR)为1小时,以270 $ MU @ Mol M $ + $ Min @ 2 $ / s $ + $ min @ 1 $ / par;在其他12小时的光周期,植物收到840美元@ mol m $ + $ min @ 2 $ / s $ + $ min @ 1 $ / par。从第十二天开始,植物暴露于UV-B辐射(0.2&18.0 KJ M $ + $ @ 2 $ / D $ + $ + $ + $ / 5美元@ 1 $ /),每天为8小时,以每天为中心photoperiod。使用荧光成像系统,为整个关于整个关于叶片表面获得的高空间分辨率(小于1秒),高空间分辨率(小于1mm $ + 2 $ /)图像。在四个光谱区域中获得稳态荧光图像:蓝色(F450nm),绿色(F550nm),红色(F680nm)和远红色(F740nm)。通过在280和380nm(280ex 300-530nm; 380ex 400-800nm)中激发,得到在二甲基亚砜(DMSO)中提取的叶片颜料的荧光发射光谱。 UV-B和EDU诱导黄瓜叶中的应力响应,从而改变从提取物中获得的荧光发射。在荧光图像中,仅观察到UV-B诱导的应力响应,但在视觉上的明显之前检测到这种损伤。没有证据表明EDU对UV-B照射提供了保护。荧光成像的使用可以提供早期应力检测能力,以帮助评估对植物光合仪的损坏。

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