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1.
小花糖芥(Erysimum cheiranthoides L.)花蜜腺位于雄蕊部花托上,仅有2枚侧蜜腺,属十字花科侧蜜腺类型中的侧半环亚型,其2枚密腺均由分泌表皮,产蜜组织和维管束组成。分泌表皮上有变态气孔器,产蜜组织中有维管束分布,属较进化的十字花科花蜜腺亚型类型。蜜腺原基是在花的各部分原基基本分化完成后,由花托表面及雄蕊基部区域的1-2层细胞,经反分化形成,在蜜腺发育过程中,蜜腺组织中的液泡和多糖物质都发生了有规律的变化,其原蜜汁在产蜜组织中加工合成,最后由表皮细胞和变态气孔泌出。  相似文献   

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龙眼花蜜腺的发育解剖学研究   总被引:4,自引:0,他引:4  
对龙眼(Dimocarpus longan Lour.)花蜜腺的形态结构、发育过程以及蜜腺的组织化学变化进行了较为系统的研究;对花蜜腺结构与泌蜜的关系、泌蜜方式、起源和系统演化等作了初步的探讨。结果表明:龙眼的花盘蜜腺位于花托上,呈环状环绕在雌雄蕊基部外围,花芽分化约30d,在雄蕊和花被之间的花托表面,蜜腺原基也开始形成,由花托表面2~3层细胞脱分化形成居间分生组织发育而来;龙眼花蜜腺由分泌表皮和产蜜组织构成,属结构蜜腺;分泌表皮角质层极薄,密布单细胞绒毛,未发现有气孔;产蜜组织由亚腺细胞、产蜜细胞、油细胞和维管束组成;在蜜腺发育过程中,产蜜细胞的液泡和多糖物质发生有规律的变化;蜜腺的原蜜汁来源于韧皮部,蜜汁经表皮角质层渗出。  相似文献   

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革苞菊花蜜腺的发育解剖学研究   总被引:2,自引:0,他引:2  
革苞菊(Tugarinovia mongolica)花蜜腺为筒状,围绕花柱基部着生,属于花柱蜜腺类型。蜜腺中无维管束分布,只具分泌表皮和泌蜜组织。分泌表皮细胞排列整齐,表皮细胞之间分散分布着许多气孔,气孔的孔下室发达。蜜腺基部细胞与花柱维管束想念相邻。随着蜜腺的发育,泌蜜组织的细胞结构和储藏物质呈规律性变化。原蜜汁的来源主要是由花柱基部维管束提供多糖,经过泌蜜组织加工成蜜汁后,由分泌表皮上的气孔将蜜汁排出体外。同时讨论了革苞菊花蜜腺结构与进化的相关性问题。  相似文献   

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鹅掌柴花蜜腺的发育解剖学研究   总被引:1,自引:0,他引:1  
对鹅掌柴(Scheffler octophylla Harms.)花蜜腺的发育进行解剖结构观察。鹅掌柴花盘蜜腺位于下位子房上方环绕花柱基部。蜜腺由分泌表皮、产蜜组织组成,心皮维管束与其相邻并发出一些伸入蜜腺基部的短分枝。蜜腺起源于心皮原基基部外侧的几层细胞。鹅掌柴花蜜腺为淀粉型蜜腺,淀粉粒为许多微小颗粒聚集成的复粒。原蜜汁由蜜腺基部维管束的筛管提供,达产蜜组织细胞和表皮细胞后以淀粉粒的形式贮藏。泌出的蜜汁一部分来自淀粉粒的降解,一部分来自泌蜜期输入的原蜜汁。表皮和产蜜组织细胞均具泌蜜功能。泌出的蜜汁大部分通过气孔排出,还有部分由角质层渗出。  相似文献   

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紫苏花蜜腺的发育解剖学研究   总被引:1,自引:0,他引:1  
紫苏花蜜腺位于不均等分裂的花盘裂片上,属于子房基部的盘状蜜腺。3枚小裂片上的蜜腺由分泌表皮和产蜜组织组成,而另一枚大裂片上的指状蜜腺则由分泌表皮、产蜜组织和维管束组成。4枚蜜腺的表皮细胞外均具薄的角质层,仅在指状蜜腺的顶部分布着密集的气孔器。蜜腺来源于花盘表面的2~3层细胞。在蜜腺发育过程中,液泡和淀粉粒呈现有规律的消长变化,这与蜜汁的合成与分泌有关。3枚小裂片蜜腺的原蜜汁来源和泌蜜途径与指状蜜腺不同。  相似文献   

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密花香薷花蜜腺的解剖学研究   总被引:6,自引:0,他引:6  
密花香薷花密腺分布于子房基部和子房表面,属于一朵花中具二种花蜜腺类型,子房基部的盘状蜜腺由分泌表皮、产蜜组织及维管束三部分组成,分泌表皮上角质层局部有小孔。子房蜜腺由分泌表皮和产蜜组织组成。  相似文献   

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短果大蒜芥(Sisymbrium loeselii L.var.brevicarpum Z.X.An)花蜜腺位于雄蕊基部花托上,属十字花科环状花蜜腺类型中的侧棱环四圆环亚型。蜜腺由分泌表皮,产蜜组织和维管束组成。分泌表皮上有变态气孔器,蜜腺中部的气孔器呈舟状分布。产蜜组织中的维管束来自于花托中的维管束分支,属较进化的十字花科花蜜腺的亚型类型。蜜腺原基是在花的各部分原基分化后,由雄蕊基部花托表面区域的2-3层细胞,经反分化形成,环状蜜腺发生发育同步,在蜜腺的发育过程中,蜜腺组织中的液泡和淀粉粒都发生了有规律的变化,其原蜜汁由维管束提供,运转至产蜜组织,最后由变态气孔泌出。  相似文献   

8.
油菜花蜜腺的发育过程及组织化学变化   总被引:7,自引:3,他引:4  
油菜花蜜腺4枚,2故侧蜜腺和2枚中蜜腺。蜜腺由分泌表皮、产蜜组织和维管束组成。蜜腺原基是在花的各部分原基发生后,由花托局部区域的表面数层细胞经反分化形成。但它在短期内,完成了形态建成,与花的成熟同步。在蜜腺的发育过程中,产蜜组织细胞的液泡发生有规律的变化。同时,淀粉粒、蛋白质的动态也较为明显,以上变化与蜜汁的合成和分泌密切相关。其蜜腺的原蜜汁是由韧皮部提供,运转至产蜜组织内加工,最后由变态气孔和泌蜜通道泌出。  相似文献   

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新疆鼠尾草(Salvia deserta Schang)花蜜腺位于子房基部的花托上,为盘状的花托蜜腺,其顶部裂成4片,其裂片大小不等,比例悬殊。蜜腺由产蜜组织和分泌表皮构成,又为结构蜜腺。组织化学染色显示淀粉粒动态明显,因此又属淀粉蜜腺。在发育的过程中细胞液泡化动态明显,且淀粉粒和蛋白质具有明显的消长变化,但PAS反应和苏木精脂类染色无明显变化。其泌蜜过程可能为:原蜜汁由邻近的韧皮部提供,经薄壁细胞运送至产蜜组织,在产蜜组织中进一步积聚、合成后,最终蜜汁通过变态气孔和分泌表皮细胞的角质层泌出。  相似文献   

10.
异株百里香(Thymus marschallianus Willd)花蜜腺分布于子房基部的花托上,结构蜜腺盘状,成熟时膨大,环绕在花托外。蜜腺组织由分泌表皮、产蜜组织和维管束三部分组成;组织化学染色显示淀粉粒的积累是在蜜腺细胞发育的最初和最后,因此将其归为非淀粉型蜜腺。在发育的过程中细胞液泡化动态明显,而淀粉粒和多糖均不具有明显的消长变化;蜜汁是由韧皮部运转到泌蜜组织中的,再由表皮细胞的角质层渗到细胞外。  相似文献   

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It has now been over twenty years since a novel herpesviral genome was identified in Kaposi's sarcoma biopsies. Since then, the cumulative research effort by molecular biologists, virologists, clinicians, and epidemiologists alike has led to the extensive characterization of this tumor virus, Kaposi's sarcoma-associated herpesvirus(KSHV; also known as human herpesvirus 8(HHV-8)), and its associated diseases. Here we review the current knowledge of KSHV biology and pathogenesis, with a particular emphasis on new and exciting advances in the field of epigenetics. We also discuss the development and practicality of various cell culture and animal model systems to study KSHV replication and pathogenesis.  相似文献   

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正Dear Editor,In December 2019, a novel human coronavirus caused an epidemic of severe pneumonia(Coronavirus Disease 2019,COVID-19) in Wuhan, Hubei, China(Wu et al. 2020; Zhu et al. 2020). So far, this virus has spread to all areas of China and even to other countries. The epidemic has caused 67,102 confirmed infections with 1526 fatal cases  相似文献   

16.
Curcumin is the yellow pigment of turmeric that interacts irreversibly forming an adduct with thioredoxin reductase (TrxR), an enzyme responsible for redox control of cell and defence against oxidative stress. Docking at both the active sites of TrxR was performed to compare the potency of three naturally occurring curcuminoids, namely curcumin, demethoxy curcumin and bis-demethoxy curcumin. Results show that active sites of TrxR occur at the junction of E and F chains. Volume and area of both cavities is predicted. It has been concluded by distance mapping of the most active conformations that Se atom of catalytic residue SeCYS498, is at a distance of 3.56 from C13 of demethoxy curcumin at the E chain active site, whereas C13 carbon atom forms adduct with Se atom of SeCys 498. We report that at least one methoxy group in curcuminoids is necessary for interation with catalytic residues of thioredoxin. Pharmacophore of both active sites of the TrxR receptor for curcumin and demethoxy curcumin molecules has been drawn and proposed for design and synthesis of most probable potent antiproliferative synthetic drugs.  相似文献   

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Comprises species occurring mostly in subtidal habitats in tropical, subtropical and warm-temperate areas of the world. An analysis of the type species, V. spiralis (Sonder) Lamouroux ex J. Agardh, a species from Australia, establishes basic characters for distinguishing species in the genus. These characters are (1) branching patterns of thalli, (2) flat blades that may be spiralled on their axis, (3) width of the blade, (4) primary or secondary derivation of sterile and fertile branchlets and (5) position of sterile and fertile branchlets on the thalli. Application of the latter two characters provides an important basic method for separation of species into three major groups. Osmundaria , a genus known only in southern Australia, was studied in relation to Vidalia , and its separation from the Vidalia assemblage is not accepted. Species of Vidalia therefore are transferred to the older genus name, Osmundaria. Two new species, Osmundaria papenfussii and Osmundaria oliveae are described from Natal. Confusion in the usage of the epithet, Vidalia fimbriala Brown ex Turner has been clarified, and Vidalia gregaria Falkenberg, described as an epiphyte on Osmundaria pro/ifera Lamouroux, is revealed to be young branches of the host, Osmundaria prolifera.  相似文献   

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Fifteen chromosome counts of six Artemisia taxa and one species of each of the genera Brachanthemum, Hippolytia, Kaschgaria, Lepidolopsis and Turaniphytum are reported from Kazakhstan. Three of them are new reports, two are not consistent with previous counts and the remainder are confirmations of very scarce (one to four) earlier records. All the populations studied have the same basic chromosome number, x = 9, with ploidy levels ranging from 2x to 6x. Some correlations between ploidy level, morphological characters and distribution are noted.  相似文献   

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