Die Homologie des Perigons der Zingiberaceen Ein Beitrag zur Morphologie und Phylogenie des Monokotylen-Perigons

Nicolaia elatior is used as an example to demonstrate that the mucronate tepals ofZingiberaceae correspond to hypsophylls (bracts) consisting of a leaf sheath and a rudimentary Oberblatt (= leaf petiole + lamina) represented by the mucro. Evidence for this interpretation is furnished by all available criteria: leaf sequence (exhibiting a complete continuum of forms from foliage leaves over cata- and hypsophylls to the tepals), nervature, and ontogeny.The present conception is compared with the well-founded thesis ofLeinfellner that the perigone ofLiliaceae is derived from the androecium. The different morphological status of the perigone in both families is not regarded as the result of different phylogenetic origin, but as a manifestation of morphogenetic transgressions from one phyllome category to an adjacent one: In theLiliaceae the perigone is under a strong morphogenetic influence of the androecium, and therefore displays staminal characters, in theZingiberaceae it is under the dominating influence of the extrafloral region, and thus appears as a hypsophyllous structure. If this assumption of a morphologically oscillating perigone is correct, it will be fundamentally impossible to demonstrate unequivocally the phylogenetic origin of the monocotyledonous perigone.

Im wissenschaftlichen Werk Prof. Dr.Walter Leinfellners steht an erster Stelle die Morphologie der Blütenorgane. Als sein dankbarer Schüler möchte ich ihm aus Anlaß seines 70. Geburtstages die folgende Studie zu einem Thema zueignen, das ihn wie mich gleichermaßen angesprochen hat und schon Gegenstand der Forschungsarbeit des Jubilars war: die Homologie des Monokotylen-Perigons.     

小花草玉梅正常和自然变异植株的AP3-3基因研究

野生小花草玉梅(Anemone rivularis var.flore-minore)正常植株和花被片自然变异植株的外观形态差异很大,该研究以二者为材料,利用常规PCR和高效热不对称PCR(Hi-Tail PCR)技术从其正常和变异植株的基因组中各分离得到1个B类基因。序列分析证明,二者隶属于B类MADS-box基因AP3家族的旁系同源基因AP3-3分枝,分别命名为NArAP3-3(正常植株)和VArAP3-3(变异植株)。NArAP3-3基因全长3 795bp,VArAP3-3基因全长3 898bp,二者均含有1个666bp的开放阅读框(ORF),可编码221个氨基酸,具有典型的植物MADS-box基因结构,其编码肽链包含了MADS区、K区、Ⅰ区和C区。对比NArAP3-3和VArAP3-3基因的全长序列,发现VArAP3-3基因比NArAP3-3多了1段49bp的插入,且在ORF序列与NArAP3-3基因相比有4个碱基突变。对二者的全长序列、所编码的221个氨基酸及插入序列的生物信息学分析显示,二者在基因启动子、蛋白质基本性质、结构功能域、二级三级预测结构等方面均有差异,推测这些差异可能是花被片变异产生的原因之一。该研究结果为进一步探索其变异机制奠定了基础。     

诱导风信子再生花芽不断分化花被片的研究

通过外源激素及外植体年龄的控制,诱导风信子再生花芽不断分化花被片已经获得成功。在２５０ｄ的继代培养中平均每个花芽可分化７０多片花被片,最多的可分化１４０多片。对这种花芽不断分化花被片的形态发生过程以及生长发育特点的观察表明,花芽的第１轮器官与风信子野生型花基本相同,查花被,它由花被筒及其上部的裂片－花被片组成。     

蜡梅花被片表层形态观察及其意义

为探究蜡梅花被片表层蜡质的微形态结构特征和差异性,采用扫描电子显微镜对蜡梅和山蜡梅的花被片进行观察。结果表明:蜡梅花被片表层无明显蜡质覆盖物,细胞排列平滑,内表层有加厚透明状覆盖物; 山蜡梅花被片表层有厚蜡质覆盖物和表皮毛; 山蜡梅、蜡梅花被片均无气孔。以上独特的结构形态对于蜡梅花开放于寒冷季节,应对外界环境胁迫可能有一定的保护作用和生态意义。     

Floral development and floral phyllotaxis in Anaxagorea (Annonaceae)

Background and Aims Anaxagorea is the phylogenetically basalmost genus in the large tropical Annonaceae (custard apple family) of Magnoliales, but its floral structure is unknown in many respects. The aim of this study is to analyse evolutionarily interesting floral features in comparison with other genera of the Annonaceae and the sister family Eupomatiaceae. Methods Live flowers of Anaxagorea crassipetala were examined in the field with vital staining, liquid-fixed material was studied with scanning electron microscopy, and microtome section series were studied with light microscopy. In addition, herbarium material of two other Anaxagorea species was cursorily studied with the dissecting microscope. Key Results Floral phyllotaxis in Anaxagorea is regularly whorled (with complex whorls) as in all other Annonaceae with a low or medium number of floral organs studied so far (in those with numerous stamens and carpels, phyllotaxis becoming irregular in the androecium and gynoecium). The carpels are completely plicate as in almost all other Annonaceae. In these features Anaxagorea differs sharply from the sister family Eupomatiaceae, which has spiral floral phyllotaxis and ascidiate carpels. Flat stamens and the presence of inner staminodes differ from most other Annonaceae and may be plesiomorphic in Anaxagorea. However, the inner staminodes appear to be non-secretory in most Anaxagorea species, which differs from inner staminodes in other families of Magnoliales (Eupomatiaceae, Degeneriacae, Himantandraceae), which are secretory. Conclusions Floral phyllotaxis in Anaxagorea shows that there is no signature of a basal spiral pattern in Annonaceae and that complex whorls are an apomorphy not just for a part of the family but for the family in its entirety, and irregular phyllotaxis is derived. This and the presence of completely plicate carpels in Anaxagorea makes the family homogeneous and distinguishes it from the closest relatives in Magnoliales.     

云南卷叶小檗(小檗科)花与果实特征的变异式样

在云南省腾冲县通过野外居群取样,结合模式标本检查及统计分析方法,研究了小檗科卷叶小檗花和果实特征的变异式样。结果显示:(1)2013年5月,在12株卷叶小檗上取样的53朵花中,各花花被片数目为13~18个,平均为15.25±0.96个,其中,来自11株植物的34朵花都具有15个花被片,占个体总数的91.67%,占花总数的64.15%;此外,各花内部与雄蕊对生的6个花被片先端缺裂。(2)2013年12月,在12株卷叶小檗上分别取样的20个成熟果实中,单个果实内种子数目为1~4个,平均为1.79±0.48个,其中74.17%的果实都含有2粒种子;2013年5月,自6株卷叶小檗上采集的2012年宿存的150个果实中,单个果实内种子数目为1~3个,平均为2.11±0.43个,其中80.67%的果实都含有2粒种子;而已有文献皆记载卷叶小檗子房具胚珠2个。(3)在卷叶小檗个体内花和果实特征的变异系数中,花被片数目(0.05±0.03)果实长度(0.07±0.02)果实宽度(0.11±0.02)果柄长度(0.16±0.05)果实内种子数目(0.25±0.08)花被片长度(0.36±0.04)花被片宽度(0.38±0.04)。(4)对《中国植物志》小檗属中卷叶小檗花和果实等重要分类学性状特征进行了订正,同时为该种一直空缺的绘图补充了图片资料。     

云南近光滑小檗(小檗科)主要分类学性状特征的变异式样

通过野外居群取样,结合实验室观察、标本检查及统计分析方法,研究了云南省腾冲县近光滑小檗主要分类学性状特征的变异式样。结果显示:(1)近光滑小檗叶片长度为1.95~12.91(5.54±2.15)cm,宽度为0.45~1.94(0.97±0.32)cm;单个簇生花序中花数目为2~14(5.1±2.2)个,花黄色,花被片数目为13~20(15.36±1.34)个;具蜜腺花被片为狭倒卵形至宽倒卵形,先端常缺裂,偶全缘,长3.18~5.94(4.82±0.52)mm,宽1.45~4.41(2.65±0.54)mm。(2)子房内胚珠数目及果实内种子数目都是1个;浆果椭圆形至卵状椭圆形,紫黑色,长3.37~8.36(6.91±0.82)mm,宽2.85~5.13(4.02±0.46)mm;果柄长0.47~2.20(1.10±0.32)cm。(3)在变异系数方面,簇生花序中花数目(0.37)叶长(0.21)叶宽(0.18)果柄长度(0.17)具蜜腺花被片宽度(0.14)具蜜腺花被片长度(0.08)=花被片数目(0.08)果长(0.07)=果宽(0.07)。(4)对《中国植物志》中近光滑小檗空缺的绘图补充了叶、花和果实等图片资料;并讨论了生境条件对近光滑小檗居群间变异的影响,及其与同域种卷叶小檗的种间关系。     

Solute leakage, lipid peroxidation, and protein degradation during the senecence of Iris tepals

A colour change and inrolling of the tepal edges are the first symptoms of senescence of Iris flowers ( Iris x hollandica Tub., cv. Blue Magic). Tepals showed an increase in leakage of both ions and anthocyanins, prior to the visible senescence symptoms. Increased leakage occurred irrespective of the time at which the tepals were severed and placed in water, indicating that the senescence process is inherent in the tepal cells. Net loss of proteins in the tepal edges started after flower opening, and after two more days, when the first symptoms of senescence were observed, the protein level was only 20% of that at harvest. Cycloheximide delayed senescence and resulted in a lower rate of protein loss. Phenylmethylsulfony fluoride (PMSF), a protease inhibitor, had a similar effect on protein levels but did not affect the time to visible senescence, and also several other protease inhibitors did not affect the time to senescence.
During senescence the rate of respiration of the tepals remained unchanged and their rate of ethylene production decreaased. The rate of ethane production, an indicator of lipid peroxidation, was very low and remained unaltered. Antioxidants ( l ascorbic acid, benzoic acid, butylated hydroxytoluene, diphenylamine, propyl gallate, propyl- p -hydroxybenzoate and sodium benzoate) had no effect on the time to tepal senescence. It is concluded that tepal wilting is due to transfer of solutes from the symplast to the apoplast. Although net protein degradation occurs early during the senescence process, its inhibition is not correlated with a delay in the time to senescence. Furthermore, the results do not support the hypothesis that the increase in solute leakage is due to (free radical-mediated) peroxidation of membrane lipids. The present results are in contrast with the ethylene-regulated petal senescence of carnation, which is accompanied by lipid peroxidation.     

Induction of Continuous Tepal Differentiation from in Vitro Regenerated Flower Buds of Hyacinthus orientalis

Continuous differentiation of tepals was successively induced from regenerated flower buds in Hyacinthus orientalis L. cv. White Pearl by controlling the exogenous hormones and explant ages. In 250 days of subculture, each flower bud differentiated an average of more than 70 tepals, with a maximum of over 140 tepals. Studies on the morphogenesis and characteristics of growth and development of the flower buds indicate that the first whorled organ of the flower bud was perianth which consisted of perianth tube and tepals grown at the top of the perianth tube, which is the same as the flower bud of the wild type in H. orentalis. The second and third whorls of the flower bud, which should be stamen and pistil in the wild type, but remained as the tepals in the regenerated flower bud. Growth of the regenerated flower bud was faster in the first several months of culture, then slowed down gradually with time. After 150 days in culture the flower bud growth and organ differentiation became very slow. Other than the tepal differentiation the regenerated flower buds also differentiated at random positions some small flower buds that also differentiated the tepals only. Histological observation revealed that the origin of the regenerated flower buds was jointly participated by some cells in the epidermal and subepidermal layers at the inner surface of the perianth explant, and the inner small flower buds were originated from the meristem which was formed by the transformation of the parenchyma at the base of the very young tepal. The authors also compared and discussed the similarities and differences of the phenotypes between the regenerated flower bud in Hyacinthus and agamous flower in Arabidopsis, from which, they have hypothesized on the role of the hormones in the promotion and termination of the gene expressions by an order of development in plant.