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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估EDU在黄瓜UV-B保护中的作用

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Abstract: 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. !32
机译:摘要:荧光成像系统和叶绿素荧光发射用于评估EDU,N- $ LB @ 2-(2-oxo-1-咪唑啉基)乙基$ RB @ -N'-苯基脲是否对紫外线B(在黄瓜(Cucumis sativus L.)叶中进行UV-B)照射(290-320 nm)。植物在生长室中生长,每天用400 W高压钠灯和金属卤化物灯照明14小时。在每个周期的开始和结束时提供1小时的光合有效辐射(PAR)为270 $ mu @ mol m $ + $ MIN @ 2 $ / s $ + $ MIN @ 1 $ / PAR;在光周期的其他12小时内,植物接受了840美元/摩尔m $ + $ MIN @ 2 $ / s $ + $ MIN @ 1 $ / PAR。从第十二天开始,将植物暴露于UV-B辐射(0.2和18.0 kJ m $ + $ MIN @ 2 $ / d $ + $ MIN @ 1 $ /)下,每天放置2天,每天8 h。光周期。使用荧光成像系统,可以快速获取(少于1 s),完整的近轴叶片表面的高空间分辨率(少于1 mm $ + 2 $ /)图像。在四个光谱区域中获取了稳态荧光图像:蓝色(F450 nm),绿色(F550 nm),红色(F680 nm)和远红色(F740 nm)。通过在280和380 nm(280EX 300-530 nm; 380EX 400-800 nm)激发获得二甲基亚砜(DMSO)中提取的叶色素的荧光发射光谱。 UV-B和EDU均可诱导黄瓜叶片的胁迫反应,从而改变了从提取物中获得的荧光发射。在荧光图像中,仅观察到UV-B诱导的应激反应,但是在视觉上看不到这种损害之前就已经检测到了。没有证据表明EDU可以抵抗UV-B辐射。荧光成像的使用可以提供早期的胁迫检测能力,以帮助评估对植物的光合装置的损害。 !32

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