基于计算机视觉技术的番茄叶片叶绿素含量的检测

 研究利用计算机视觉技术快速测定叶绿素含量的方法,建立了根据番茄叶片颜色特征确定其叶绿素含量的一元二次拟合模型。在计算机视觉图像采集系统中采集番茄叶片图像,利用MATLAB图像处理工具提取图像的颜色特征参数,对颜色特征参数和番茄功能叶叶绿素含量做相关分析,建立回归模型。结果表明：RGB颜色系统的R/G、(G-R)/(G+R)、G-R、色度坐标r、r-g及HIS颜色系统的H值均与叶绿素含量呈极显著非线性相关性,可用于测定番茄叶片叶绿素含量。从建立的6组模型中筛选出拟合度较高的3组模型进行检验,预测误差在0～22.22%之间。用预测精度最高的G-R颜色特征预测叶绿素含量的模型为Chl.a = 0.0926 + 0.1208 (G-R) - 0.0009 (G-R)²,Chl b = - 0.0252 + 0.0397 (G-R) - 0.0003 (G-R)²和Chl.(a+b) = 0.1271 + 0.1600 (G-R) - 0.0011 (G-R)²。     

茶树新品种‘佛香3号’

 ‘佛香3号’是利用‘福鼎大白茶’ ( ♀) ב长叶白毫’ ( ♂) 人工授粉杂交, 从F1 中单株选育而成, 为高香、优质、高产、抗逆性强, 适制绿茶的新品种。绿茶外形满披银毫, 香气高长, 滋味鲜醇, 叶底黄绿明亮; 优质干茶产量2 371.2 kg·hm^-2, 适宜在云南大叶茶区推广种植。     

樱桃透光和郁闭树冠相对光照强度及其果实品质和产量的差异

 以13年生‘红灯’甜樱桃（Prunus avium L.）为试材,应用树冠分格方法,研究了树冠透光和郁闭两种冠型内相对光照强度及其果实品质和产量的差异,以及相对光照强度与果实产量品质的关系。结果表明,两种树冠内相对光照强度均自下而上逐渐增高,透光和郁闭树冠小于30%的相对光照区域分别占树冠总体积的25.23%和52.78%。透光树冠果实分布均匀,主要集中在树冠1.5～2.5 m的高度;而郁闭树冠果实分布差异较大,主要在树冠的外围和上部;产量分别是9.02t.hm-2和3.53t.hm-2。果实品质因素与相对光照强度的回归分析表明樱桃单果质量、果实硬度、果实可溶性固形物含量、可滴定酸含量、固酸比最佳的相对光照强度值分别为76.52%、46.84%、100.00%、41.63%和75.77%。     

茄子离体叶片光系统Ⅱ的冷激胁迫效应及热力学分析

 以耐冷性较强的短把黑圆茄和耐热性较强的黑帅圆茄为试材,经冷激胁迫后采用植物效率仪PEA,进行快速叶绿素荧光参数测定,并利用最大光化学效率Fv/F m和活性中心RC/CSo的标准状态变性自由能变△GD进行PSⅡ冷稳定性的热力学分析。随着冷激胁迫温度的降低和时间的延长,PSⅡ的Fv/Fm、实际光化学效率ΔF/Fm′、RC/CSo呈"S"型下降趋势;单位反应中心DIo/RC和非光化学猝灭qN呈"S"型上升趋势;综合分析反映出冷激胁迫下PSⅡ反应中心的可逆失活和依赖于叶黄素循环的热耗散的双重机制在保护PSⅡ防止光抑制中起到重要作用。另外,通过两品种间PSⅡ行为差异,引入了两组新的参数作为便于直观比较冷胁迫的评价指标。黑帅圆茄Fv/Fm、ΔF/Fm＇的半衰温度T1/2和t1/2值分别高于短把黑圆茄1.4 ℃和0.8 ℃。茄子叶片Fv/Fm和RC/CSo的△GD随着冷激胁迫温度的降低而减少呈瀑布型的下降趋势。黑帅圆茄的△GD值和变性中点温度Tm都低于短把黑圆茄。它们均反映出黑帅圆茄的耐冷性低于短把黑圆茄。     

IBA对芍药扦插生根的影响及生根过程中相关酶活性的变化

以芍药‘大富贵’品种为材料, 用1 000、2 000和3 000 mg·L^-1 3个浓度的IBA处理进行扦插对比试验, 研究其生根过程中过氧化物酶( POD) 、多酚氧化酶( PPO) 、吲哚乙酸氧化酶( IAAO) 活性的动态变化。结果表明: IBA处理极显著地提高了插穗的生根率、根数和总根长, 其中以2 000 mg·L ^-1为IBA最佳生根浓度, 将生根周期缩短18 d, 并明显提高了生根质量。在生根过程中, 插穗中POD、PPO活性分别呈现“缓慢上升→下降→急剧上升→下降”和“降→升→降”的变化趋势, 但与对照组相比, 处理组的变化更为剧烈, 峰值出现提前了18 d。IAAO活性在对照和处理中呈现不同的变化趋势: 前者为“升→降→升”, 而后者为“降→降→升”。此外, 高活性的POD、PPO有利于不定根的形成, 低活性的IAAO则促进生根。     

‘糯米糍’荔枝碳素营养储备动态与坐果的关系

 以10～12年生的‘糯米糍’荔枝(Litchi chinensis Sonn. ) 为材料, 研究了高产树(60～65 kg·株^{- 1} ) 和低产树(5～10 kg·株^{- 1} ) 不同部位(叶片、各级枝条和主干) 碳素营养储备(淀粉) 的差异及季节动态; 分析了不同果实发育阶段树体碳素营养水平与坐果率的关系。结果表明, 果实成熟时高产树各部位的淀粉含量均低于低产树, 而可溶性糖含量高于低产树。果实采收后, 低产树早于高产树抽发新梢。入冬季前(11月底前) , 低产树和高产树分别抽发了3次和2次秋梢。7～11月秋梢生长发育期间, 高产树和低产树均无显著淀粉积累, 11月中旬以后枝梢生长停滞期间, 各部位, 尤其是4 cm直径以内的枝条大量积累淀粉, 在花穗发育前达到高峰。之后, 随花穗发育、开花及坐果而持续降低。高产树和低产树各部位淀粉高峰并无明显差异, 表明坐果量对树体碳素营养储备的累积并无明显的长期影响。叶片、主枝和主干积累的淀粉含量较低, 总体相对稳定; 而4 cm直径以下的枝梢淀粉含量变化剧烈, 说明这些枝梢是更为活跃的碳素储备库。本研究还表明, 坐果早期(花后3周内) 枝条(2 cm直径) 的淀粉含量与该枝条上最终坐果率呈显著正相关, 而果实发育中期(花后8周) 枝条淀粉含量与坐果率无关, 说明早期果实发 育一定程度依赖树体碳素营养储备, 而中后期果实发育几乎不依赖树体储备。     

西葫芦银叶病发病叶片叶绿素代谢及其荧光特性

 研究了西葫芦银叶病发病叶片和叶柄叶绿素代谢特性和叶片叶绿素荧光参数的变化。与对照相比,发病叶片和叶柄叶绿素总量(Chl.a+b),叶绿素a (Chl.a),叶绿素b (Chl.b)含量均下降;轻度与重度发病叶片叶绿素a/b增加,中度发病叶片与对照差异不显著,而叶柄比对照降低。西葫芦银叶病对叶片Chl.b的影响比Chl.a大,而对叶柄Chl.a的影响比Chl.b大。发病叶片和叶柄叶绿素酶活性升高,从而使叶绿素降解加速,叶绿素合成中间产物Protoporphyrin IX (Proto IX),Magnesium protoporphyrin IX (Mg-Proto IX),Protochlorophyllide (Pchlide)含量降低,Uroporphyrinogen Ⅲ (Uro Ⅲ)含量增加,表明叶绿素合成在 Uro Ⅲ到 Proto Ⅸ受阻。发病叶片最大光化学量子产量(Fv/Fm),光系统Ⅱ(PSⅡ)的潜在活性(F_v/F_o),实际光化学效率(φPSⅡ),光化学淬灭系数(q_P)降低,非光化学淬灭系数(NPQ)增加。试验结果表明,西葫芦银叶病破坏了叶绿素合成和降解的动态平衡,叶绿素合成受阻和叶绿素降解加速是导致叶片叶绿素含量降低的原因;发病叶片叶绿体PSⅡ活性受到抑制。     

Effects of salvianolic acid B on neurons during oxygen/glucose deprivation and reintroduction

AIM: To observe the damage induced in the primary cultured rat cortical neurons by oxygen/glucose deprivation and reintroduction, and to investigate the neuroprotective mechanism of salvianolic acid B (SalB). METHODS: Primary cultured rat cortical neurons were randomly divided into the control group, the model group and the SalB group. The cell model was established by oxygen/glucose deprivation for 3 h followed oxygen/glucose reintroduction for 24 h. The cortical neurons viability was determined by MTT assay. The leakage rate of lactate dehydrogenase (LDH) was measured by chromatometry. The mitochondrial membrane potentials (MMP) and the apoptosis rate were quantitatively analyzed by flow cytometry. The cytosolic free calcium was assessed using LSCM. The morphologic changes of neuronal nuclei were observed by Hoechst 33342 fluorescence staining. RESULTS: Compared to the model group, the cortical neurons viability, the survival rate and the fluorescence value of MMP in the SalB group were obviously increased (P<0.05,P<0.01). In addition, in the SalB group, the leakage rate of LDH, the fluorescence intensity of cytosolic free calcium and the apoptosis rate were significantly lower than those in the model group (P<0.01). CONCLUSION: The neuroprotective mechanism of SalB in the oxygen/glucose deprivation and reintroduction neurons would be due to the fact that SalB maintains the MMP and the calcium homeostasis.     

Jagged1 knocking down in endothelial cells accelerates PDGF induced proliferation and migration of vascular smooth muscle cells in rats

AIM: To investigate the effect of Jagged1 expression in endothelial cells (EC) on platelet derived growth factor (PDGF) induced proliferation and migration of vascular smooth muscle cells (VSMC) in rat.METHODS: Rat aorta EC was inoculated in the lower chamber and VSMC were in the upper chamber of the cell coculture system. Three groups were divided: control, sicontrol and siJagged1. The EC Jagged1 protein expression was assayed by Western blotting to evaluate small RNA interfering (RNAi) efficiency. After the cells were cocultured with PDGF for 24 h, the proliferation and migration of VSMC were respectively evaluated by ［3H］-TdR incorporation and migrating cells counting. Protein expression of α-SM-actin in VSMC was assayed by Western blotting. RESULTS: The Jagged1 protein expression in EC was significantly lower in siJagged1 group than that in control group (0.26±0.02 vs 0.67±0.02, P<0.05), and no statistic significance was observed between control and sicontrol groups. The VSMC ［3H］-TdR incorporation and migration were higher in PDGF +siJagged1 group than those in PDGF group {［3H］-TdR incorporation (23 074±2 702) counts·min-1·well-1 vs (16 442±1 803)counts·min-1·well-1, n=5, P<0.05; migration (27±4) cells/field vs (15±3)cells/field, n=5, P<0.05}. The α-SM-actin protein in VSMC was lower in PDGF + siJagged1 group than that in PDGF group (0.25±0.06 vs 0.49±0.04, n=3, P<0.05).CONCLUSION: Jagged1 knock down in rat EC accelerates PDGF induced proliferation and migration of VSMC. These results suggest that Jagged1 expression in EC plays an important role in maintaining VSMC contract phenotype and inhibiting VSMC overgrowth after arterial injury.