ANGIOSPERM FLOWERS AND TRICOLPATE POLLEN OF BUXACEOUS AFFINITY FROM THE POTOMAC GROUP (MID-CRETACEOUS) OF EASTERN NORTH AMERICA

A new genus of fossil angiosperms (Spanomera gen. nov.) is established for flowers from two localities in the mid-Cretaceous Potomac Group of Maryland, eastern North America. The type species, Spanomera mauldinensis sp. nov., from the early Cenomanian Elk Neck beds, has inflorescence units with terminal pistillate, and lateral staminate flowers. The organization of inflorescences and flowers is opposite and decussate. Staminate flowers typically have five tepals: two lateral, one posterior, and two in the anterior position. Each tepal is opposed to a stamen with a short filament, dorsifixed anther, and two pairs of pollen sacs. Stamens contain pollen comparable to the dispersed pollen species Striatopollis paraneus (Norris) Singh. Pistillate flowers have two lateral tepals and two anterior-posterior tepals that are opposed to two carpels. Carpels are slightly fused basally along their ventral margins and are semicircular in outline with a long, decurrent, papillate ventral stigma. Frequently this stigmatic surface has abundant attached pollen of the Striatopollis paraneus type. Spanomera marylandensis sp. nov., from the late Albian Patapsco Formation, is similar to S. mauldinensis but is known only from isolated flowers and floral parts. Staminate flowers have four stamens with dorsifixed anthers and each is opposed to a tepal. Stamens contain pollen comparable to the dispersed pollen species Striatopollis vermimurus (Brenner) Srivastava. Carpels have pollen of S. vermimurus on the stigma. Spanomera provides further evidence of unisexual but probably insect-pollinated flowers among mid-Cretaceous, early nonmagnoliid (“higher”) dicotyledons, and is interpreted as closely related to extant Buxaceae. Characters that Spanomera shares with other taxa suggest that the Buxaceae themselves may be closely related to Myrothamnaceae and other “lower” Hamamelididae.     

Pollination function transferred: modified tepals of Albuca (Hyacinthaceae) serve as secondary stigmas

Background and Aims

The stigma, a structure which serves as a site for pollen receipt and germination, has been assumed to have evolved once, as a modification of carpels, in early angiosperms. Here it is shown that a functional stigma has evolved secondarily from modified tepals in some Albuca species (Hyacinthaceae).

Methods

Deposition of pollen on Albuca floral organs by bees was recorded. Pollen germination and fruit set was measured in flowers that had pollen deposited solely on their tepals or had their tepal tips experimentally isolated or removed after pollination.

Key Results

Leafcutter bees deposit pollen onto the papillate apices of the inner tepals of Albuca flowers. Pollen germinates in tepal-derived fluid secreted 2 or 3 d after anthesis and pollen tubes subsequently penetrate the style during flower wilting. Application of cross-pollen to the inner tepal apices of A. setosa flowers led to high fruit set. No fruits were produced in pollinated flowers in which the inner tepals were mechanically isolated or removed.

Conclusions

Pollen capture by tepals in the Albuca clade probably evolved in response to selection for floral morphology that maximizes the accuracy of pollen transfer. These findings show how pollination function can be transferred among floral organs, and shed light on how the original angiosperm stigma developed from sporophylls.     

Hormonal changes during flower development in floral tissues of Lilium

Much effort has been focussed on better understanding the key signals that modulate floral senescence. Although ethylene is one of the most important regulators of floral senescence in several species, Lilium flowers show low sensitivity to ethylene; thus their senescence may be regulated by other hormones. In this study we have examined how (1) endogenous levels of hormones in various floral tissues (outer and inner tepals, androecium and gynoecium) vary throughout flower development, (2) endogenous levels of hormones in such tissues change in cut versus intact flowers at anthesis, and (3) spray applications of abscisic acid and pyrabactin alter flower longevity. Results show that floral tissues behave differently in their hormonal changes during flower development. Cytokinin and auxin levels mostly increased in tepals prior to anthesis and decreased later during senescence. In contrast, levels of abscisic acid increased during senescence, but only in outer tepals and the gynoecium, and during the latest stages. In addition, cut flowers at anthesis differed from intact flowers in the levels of abscisic acid and auxins in outer tepals, salicylic acid in inner tepals, cytokinins, gibberellins and jasmonic acid in the androecium, and abscisic acid and salicylic acid in the gynoecium, thus showing a clear differential response between floral tissues. Furthermore, spray applications of abscisic acid and pyrabactin in combination accelerated the latest stages of tepal senescence, yet only when flower senescence was delayed with Promalin. It is concluded that (1) floral tissues differentially respond in their endogenous variations of hormones during flower development, (2) cut flowers have drastic changes in the hormonal balance not only of outer and inner tepals but also of androecium and gynoecium, and (3) abscisic acid may accelerate the progression of tepal senescence in Lilium.     

Comparative floral ontogenies among Persoonioideae including Bellendena (Proteaceae)

Floral ontogeny is described and compared in five species and four genera of the hypothetically basal proteaceous subfamily Persoonioideae sensu Johnson and Briggs. The hypotheses surrounding the origin of the peculiar proteaceous flower and homologous structures within the flowers are examined using ontogenetic morphological techniques. Ontogenetic evidence reveals that the proteaceous flower is simple, composed of four tepals, each tepal initiated successively with the lateral tepals being initiated first and second followed by the successive initiation of the sagittal tepals. Each of four stamens is initiated opposite a tepal in a similar sequence to tepal initiation. A single carpel develops terminally from the remaining floral meristem. In taxa of Persoonieae, nectaries are initiated from a broadened receptacle in alternistamenous sites after zonal growth beneath and between the tepals and stamens has begun. The nectaries are interpreted as secondary organs, not reduced homologues of a “lost” petal or stamen series. Developmental variation is present among the examined taxa in several forms including the development of a Vorlaüferspitze (spine) on the upper portion of the tepals, adnation between the anthers and tepals, and formation of the carpel. In Placospermum the early formation of the carpel cleft extends to the floral receptacle and in the other taxa, the carpel cleft is distinctly above the receptacle. Different developmental pathways result in similar mature morphologies of the carpel in Persoonia falcata and Placospermum coriaceum. Bellendena montana is unique relative to the other taxa in having free stamens, a punctate stigma, reduced (not lost) floral bracts, and the floral and bract primordia are initiated from a common meristem. This study provides a foundation for future studies of the developmental basis of floral diversity within Proteaceae.     

Leaf and tepal anatomy, plastid ultrastructure and chlorophyll content in Galanthus nivalis L. and Leucojum aestivum L.

The leaf structure of Galanthus nivalis L. (snowdrop) and Leucojum aestivum L. (snowflake) is characterized by a homogeneous mesophyll tissue. The dominant characters of the leaves are cavities with mucose substance. There is a striking difference between these plants tepal anatomy. A central cavity occurs only in snowdrop tepals. Plastids from white parts of the tepals have a poorly developed membrane system. Leaves and green parts of tepals of both species possess amoeboid chloroplasts and contain chlorophyll a and b. The chlorophyll content in tepals is lower than in leaves, but the chlorophyll a:b ratio is always 2:1. Both, snowdrop and snowflake are from the family Amaryllidaceae, but their ecology is different. This paper presents common features related to systematic relatedness and differences induced by ecological factors.     

Biosystematic studies onDisporum (Liliaceae-Polygonatae)

Both the floral biology and morphometrics of two Japanese species of AsianDisporum (sectionEudisporum) are presented. These two species,D. sessile andD. smilacinum, represent extremes in both floral morphology and divergence in pollination within the section. The inverted flowers ofD. sessile have an elongate floral tube formed by the imbrication of the oblanceolate tepals. The tepal bases are modified into well developed, saccate nectaries. The stamens have rigid, vertical filaments which tightly encircle the ovary-style axis, and extrorse anthers located within a floral cavity which can accommodate a large pollinator (cross-pollination). The stigma is exserted and the depth of its cleft formation constant.D. smilacinum, in contrast, has an open, nodding campanulate flower with lanceolate tepals which have only shallow nectaries at their bases. The stamens have widely divergent filaments with versatile anthers that have laterally introrse dehiscence (wind and/or self-pollination). The depth of the stigma cleft is variable. For both species, the pattern of differential UV absorption and reflectance is similar. It is suggested on morphological grounds and by pollinator observation, thatD. sessile with a high energy flower requiring specialized visitors represents a more advanced condition than that observed inD. smilacinum, which is more generalized and primitive. Seasonal herbivore pressure on the tepal nectaries ofD. sessile is discussed in relation to its pollination.     

Expression of AODEF,a B-functional MADS-box gene,in stamens and inner tepals of the dioecious species Asparagus officinalis L.

Garden asparagus (Asparagus officinalis L.) is a dioecious species with male and female flowers on separate unisexual individuals. Since B- and C-functional MADS-box genes specify male and female reproductive organs, it is important to characterize these genes to clarify the mechanism of sex determination in monoecious and dioecious species. In this study, we isolated and characterized AODEF gene, a B-functional gene in the development of male and female flowers of A. officinalis. Southern hybridization identified a single copy of AODEF gene in asparagus genome. Northern blot analysis showed that this gene was specifically expressed in flower buds and not in vegetative tissues. In situ hybridization showed that during early hermaphrodite stages, AODEFgene was expressed in the inner tepal and stamen whorls (whorls 2 and 3, respectively), but not in the outer tepals (whorl 1), in both male and female flowers. In late unisexual developmental stages, the expression of AODEF gene was still detected in the inner tepals and stamens of male flowers, but the expression was reduced in whorls 2 and 3 of female flowers. Our results suggest that AODEF gene is probably not involved in tepal development in asparagus and that the expression of AODEF gene is probably controlled directly or indirectly by sex determination gene in the late developmental stages.     

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.     

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 ANATOMY OF IDIOSPERMUM AUSTRALIENSE (IDIOSPERMACEAE)

The floral anatomy of Idiospermum australiense (Diels) S. T. Blake is described from studies on relatively mature but unopened flower buds. The vascular system and general morphology of the flower is compared with that of Calycanthus and Chimonanthus (Calycanthaceae), especially with Calycanthus, the genus in which Diels originally placed Idiospermum. Inverted cortical bundles are present in both taxa but occur in different patterns. The tepals of Calycanthus are all 3-trace, whereas in Idiospermum only the upper tepals have three traces, the lower tepals having five to seven. All tepals of Calycanthus are spirally arranged; the lower tepals of Idiospermum are opposite or decussate in 1–3 pairs. The axial and recurrent bundle systems in Calycanthus are discrete except where the axial system turns downward, but in Idiospermum these systems, together with cortical bundles, are largely intermixed. The vascular supply to the carpel of Idiospermum, while possibly a modification of that of the carpels of Calycanthus, could also be interpreted as having an independent origin. Other differences and resemblances are described.     

IRREGULAR FLORAL DEVELOPMENT IN CALLA PALUSTRIS (ARACEAE) AND THE CONCEPT OF HOMEOSIS

About two-thirds of the more than 100 genera in the Araceae lack tepals and their absence is considered derived. Unlike most of these atepalate genera, Calla palustris has about twice as many stamens per flower. Using epi-illumination microscopy, we studied floral development in Calla to see if the supernumerary stamens form in positions corresponding to tepal positions in perigonate Araceae. If so, this would be an example of homeosis—in this case, the replacement of tepals with stamens—in the evolution of this genus. We found the positions of stamen primordia in many floral buds too irregular to conclude that they replace tepals positionally. However, in more regular floral buds the first formed stamens do form in what correspond to tepal sites in related genera. If the immediate ancestor to Calla had tepals, as is generally assumed, stamen positions in the more regular flowers, at least, support a homeotic interpretation. There is no evidence that the supernumerary stamens arise by dédoublement, but since morphogenesis in Calla is only partly comparable to other aroids, and the phylogeny in the family is not well understood, further studies are needed to resolve the interpretation of the flower in Calla. With regard to systematics and evolution, the absence of tepals in Calla may not be homologous with atepaly in other members of the family, as has been assumed for the past century.     

八角目(Illiciales)植物花被片表皮比较形态

在光学显微镜和扫描电镜下,观察了八角科(Illiciaceae)八角属(Illicium Linn.)2组11种20个材料、五味子科(Schisandraceae)南五味子属(Kadsura Ksempf. ex Juss.)2亚属2组8种15个材料和五味子属(Schisandra Michx.)2亚属4组6种17个材料的花被片表皮形态特征。首次报道了八角目2个科（八角科和五味子科）3个属（八角属、南五味子属和五味子属）植物花被片表皮细胞的形状、分泌细胞的形状及分布、气孔器的形状及分布、花被片表面的纹饰。通过与八角目2个科3个属植物的叶表皮形态比较,发现花被片表皮气孔器外拱盖均为单层,与叶表皮气孔器外拱盖层数（常绿种类为双层和落叶种类为单层）之间没有相关性,还在五味子科中发现2个新的性状（气孔对和环列型气孔）。通过对两性花、雌花和雄花花被片表皮观察,发现花被片表皮形态与花的性别之间没有相关性。通过对八角属、南五味子属和五味子属花被片表皮比较,发现五味子属与南五味子属相比,其花被片表皮表现出更多的衍生性状;南五味子属与八角属相比,前者花被片表皮具有更多的衍生性状;而南五味子属花被片表皮形态与五味子属的相似性程度较大,支持五味子科包含南五味子属和五味子属、八角科包含八角属的观点。     

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.     

Carpellodes or staminodes? Problems in the genus Pandanus (Pandanaceae), and their taxonomic significance

Carpellodes or staminodes? Problems in the genus Pandanus (Pandanaceae), and their taxonomic significance. The staminodes of the male flower of Pandanus palustris (section Megakeura) and the carpellodes of that of P. barklyi (section Barklya) were studied by both light microscopy and SEM. Comparison of these staminodes and carpellodes with those of the male flowers of P. androcephalanthos, P. hermaphroditus, and P. kariangensis (section Martellidendron), and with the staminodes of the male flower of P. brosimos (section Karuka) revealed that the staminodes are devoid of fibres, each having a single vascular bundle, whereas the carpellodes contain several strands of fibres, each associated with a vascular bundle. These distinctive characters are identical to those differentiating the stamens from the carpels in the genus. These staminodes and carpellodes are of taxonomic value, since they vary markedly between the species, though their main structure is similar within each section. In P. barklyi the male flower had no genuine column, and the filaments were fused to form a staminal tube.     

Nectary morphology in South West Asian Fritillaria (Liliaceae)

Nectaries of 3 1 taxa belonging to 4 subgenera of the genus Fritillaria are investigated by scanning electron and light microscopy. In most of the material investigated nectary cells were smaller and narrower, and less irregular in shape than those of the neighbouring tissue of the tepals. Species belonging to subgenus Rhinopetalum clearly differ from all other species. Their nectaries are deeply impressed, and the slit-like nectary orifice is bordered by two lobes, at least in the lower part densely hairy. In F. gibbosa, E karelinii and F. ariana, the flowers are ± zygomorphic as the nectary on the upper tepal is more deeply depressed than the others, and the nectary lobes are rather broad and fringed. In E stenanthera and E bucharica, nectaries are equally impressed in all tepals and the nectary orifice is bordered by narrow, unfringed ridges. The unique structure of nectaries in all species of this subgenus supports its separation from Fritillaria into a separate genus (Rhinopetalum Fisch. ex Alexand.). In the other subgenera, the nectaries are less impressed, often ± flattish, and usually linear to lanceolate or ovate, except in subgenus Petzlium where they are ± circular. One complex in subgenus Fritillaria is markedly distinguished from the rest of the subgenus: in the F. crassifolia group, the nectaries consist of a long and linear raised ridge with a median furrow. F. crassifolia ssp. poluninii is raised to specific level, E poluninii (fix) Bakhshi Khaniki & K. Persson, stat. nov. It is concluded that data on nectary morphology support the latest classification of the genus Fritillaria into subgenera and informal groups.     

Two GLOBOSA-like genes are expressed in second and third whorls of homochlamydeous flowers in Asparagus officinalis L

Garden asparagus (Asparagus officinalis L.) has homochlamydeous flowers. Like Liliaceae plants such as lily and tulip, the perianths of asparagus have two whorls of almost identical petaloid organs, called tepals. Floral structures of these homochlamydeous flowers could be explained by a modified ABC model, in which the expression of the class B genes has expanded to whorl 1, so that the organs of whorls 1 and 2 have the same petaloid structure. In this study, we isolated and characterized two GLOBOSA-like genes (AOGLOA and AOGLOB), one of class B gene, from asparagus. Southern blot showed that AOGLOA and AOGLOB genes are single copy genes. Northern blot analysis indicated that these genes were specifically expressed in male and female flowers. In situ hybridization showed that the expression of AOGLOA and AOGLOB genes is confined to whorls 2 and 3 (inner tepal and stamen) and not detected in whorl 1 (outer tepal). The other asparagus class B gene, AODEF, was also not expressed in outer tepal [Park et al. (2003) Plant Mol Biol. 51: 867]. These results indicate that the class B genes are not involved in the outer tepal development in asparagus, not supporting the modified ABC model in asparagus.     

RE-EVALUATION OF CERTAIN KEY RELATIONSHIPS IN THE ALISMATIDAE: FLORAL ORGANOGENESIS OF SCHEUCHZERIA PALUSTRIS (SCHEUCHZERIACEAE)

Transition to flowering in the North-temperate bog plant Scheuchzeria palustris occurs in early May and results in the formation of a simple raceme with six flowers. Five of the flowers are subtended by large foliar bracts, while the sixth and last-formed flower on the inflorescence remains ebracteate. The individual flowers develop along a clearly trimerous pattern. The three outer tepals develop first, arising almost simultaneously at the periphery of the triangular floral apex. They are followed closely by the development of the three anti-tepalous outer stamens. The three inner tepals are next in the developmental sequence, alternating with the outer whorl of tepal-stamen pairs but arising at a slightly higher level on the floral meristem. Three inner stamens are initiated opposite the inner tepal primordia. Finally, three gynoecial primordia are initiated on the remaining central portion of the floral apex and alternating with the inner whorl of tepal-stamen pairs. Each carpel develops at first as a horseshoe-shaped structure. Two ovules form in each carpel, initiating on the adaxial margin of the carpel wall. Histogenesis of all floral appendages involves initially periclinal divisions in the second tunica layer followed by corresponding anticlinal divisions in the first tunica layer and concurrent activity in the underlying corpus. Separate procambial strands differentiate acropetally from the inflorescence axis to each tepal-stamen pair and then bifurcate. The vascular connection to the gynoecium develops directly from the strands in the tepal-stamen pairs. The results of this developmental study of the flower of S. palustris have a significant bearing on the positioning of this and related taxa within the Alismatidae and on the speculation of the phylogeny of the monocotyledon flower.     

荨麻科三新种

该文描述了荨麻科三新种:(1)自中国重庆市发现的荨麻科荨麻属一新种,城口荨麻。此种与异株荨麻有亲缘关系,区别特征为此种的茎被少数刺毛,叶片多为心形,雄、雌花序均不分枝,瘦果在中央稍凹陷。(2)自中国广西发现的荨麻科赤车属一新种,来宾赤车。此种与特产云南东南部的富宁赤车相近缘,与后者的区别在于本种茎的毛开展或向上弯曲,叶片长椭圆形,基部斜楔形,雌花具3~4枚花被片,其中1~2枚较大花被片在背面顶端具一长筒状突起。(3)自缅甸北部发现的荨麻科楼梯草属一新种,克钦楼梯草。此种在体态上与骤尖楼梯草甚为相似,与后者的区别在于本种的每一茎节具正常叶和一退化叶,托叶狭披针状条形和无脉,雌总苞苞片无角状突起,雌小苞片较大,呈楔状长圆形,雌花具一小花被片,以及雌蕊具一宽倒卵球形柱头。