FLORAL DEVELOPMENT IN GYMNOTHECA CHINENSIS (SAURURACEAE)

The development of the inflorescence and flowers are described for Gymnotheca chinensis Decaisne (Saururaceae), which is native only to southeast China. The inflorescence is a short terminal spike of about 50–70 flowers, each subtended by a small bract. There are no showy involucral bracts. The bracts are initiated before the flowers, in acropetal order. Flowers tend to be initiated in whorls of three which alternate with the previous whorl members. No perianth is present. The flower contains six stamens, and four carpels fused in an inferior ovary containing 40–60 ovules on four parietal placentae. Floral symmetry is dorsiventral from inception and throughout organ initiation. Floral organs are initiated in the following order: 1) median adaxial stamen, 2) a pair of lateral common primordia which bifurcate radially to produce two stamen primordia each, 3) median abaxial stamen, 4) a pair of lateral carpel primordia, 5) median adaxial carpel, 6) median abaxial carpel. This order of initiation differs from that of any other Saururaceae previously investigated. The inferior ovary results from intercalary growth below the level of stamen attachment; the style elongates by intercalary growth, and the four stigmas remain free. The floral structure of Gymnotheca is relatively advanced compared to Saururus, but its assemblage of specializations differs from that of either Anemopsis or Houttuynia, the other derived genera in the Saururaceae.     

INITIATION AND DEVELOPMENT OF INFLORESCENCE AND FLOWER IN ANEMOPSIS CALIFORNICA (SAURURACEAE)

All flowers of Anemopsis californica, the most specialized taxon of the family Saururaceae, are initiated as individual primordia subtended by previously initiated bracts, in contrast to the common-primordium initiation of all flowers of Saururus cernuus and of most flowers of Houttuynia cordata. Floral symmetry is bilateral and zygomorphic, and the sequence of initiation among floral parts is paired or whorled. In A. californica, the six stamens arise as three common primordia, each of which later bifurcates to form a pair. The three common primordia occupy sites corresponding to the positions of the three stamens in H. cordata flowers. In Anemopsis, the filaments of each pair are connate. Each stamen pair is vascularized by a single bifurcating vascular bundle. The three carpels per flower are usually initiated simultaneously although there may be some variation. Adnation between stamens and carpels results from zonal growth. Downward extension of the locule, and proliferation and expansion of receptacular tissue and inflorescence cortical tissue around the locule below the bases of the carpels produce the inferior ovary. The inflorescence terminates its activity as a flattened apical residuum, surrounded by bracts subtending reduced flowers most of which have stamens only.     

FLORAL DEVELOPMENT AND VASCULATURE IN HYDROCLEIS NYMPHOIDES (BUTOMACEAE)

The flower of Hydrocleis nymphoides consists of three sepals which arise in spiral succession, three simultaneously arising petals, numerous stamens and staminodia which arise in centrifugal order, and six carpels. A residual apex remains at maturity. The first-formed members of the androecium are stamens and the later-formed members are staminodia which develop below the stamens and which become outwardly displaced during expansion of the receptacle. The androecium is supplied by branching vascular trunk bundles. The carpels are completely open but the ventral margins are slightly conduplicately appressed basally. A single dorsal bundle provides the stigmatic area with vascular tissue, and a network of small placental bundles supplies the numerous laminar ovules. There are no clearly defined ventral bundles. It is suggested that Hydrocleis nymphoides is neither the most primitive nor the most advanced member of the family. A pattern of phylogenetic reduction in the androecium and receptacle is suggested for the entire family.     

黔产野生鱼腥草挥发油成分分析

对黔产野生鱼腥草（Ｈｏｕｔｔｕｙｎｉａ ｃｏｒｄａｔａ Ｔｈｕｎｂ）采取水蒸汽蒸馏和石油醚萃取的两种方法提取精油和净油。用ＧＣ／ＭＳ进行定性、定量分析,鉴定了其中４８种成分。比较两种提取方法的分析结果,发现净油中抗菌有效成分鱼腥草素（ｈｏｕｔｔｕｙｎｉｎｕｍ）的含量明显高于精油中的含量。除高沸点的脂肪酸酯外,两者其它化学成分无明显差异。     

FLORAL DEVELOPMENT IN MYRISTICA (MYRISTICACEAE)

Myristica fragrans and M. malabarica are dioecious. Both staminate and pistillate plants produce axillary flowering structures. Each pistillate flower is solitary, borne terminally on a short, second-order shoot that bears a pair of ephemeral bracts. Each staminate inflorescence similarly produces a terminal flower and, usually, a third-order, racemose axis in the axil of each pair of bracts. Each flower on these indeterminate axes is in the axil of a bract. On the abaxial side immediately below the perianth, each flower has a bracteole, which is produced by the floral apex. Three tepal primordia are initiated on the margins of the floral apex in an acyclic pattern. Subsequent intercalary growth produces a perianth tube. Alternate with the tepals, three anther primordia arise on the margins of a broadened floral apex in an acyclic or helical pattern. Usually two more anther primordia arise adjacent to each of the first three primordia, producing a total of nine primordia. At this stage the floral apex begins to lose its meristematic appearance, but the residuum persists. Intercalary growth below the floral apex produces a columnar receptacle. The anther primordia remain adnate to the receptacle and grow longitudinally as the receptacle elongates. Each primordium develops into an anther with two pairs of septate, elongate microsporangia. In pistillate flowers, a carpel primordium encircles the floral apex eventually producing an ascidiate carpel with a cleft on the oblique apex and upper adaxial wall. The floral ontogeny supports the morphological interpretation of myristicaceous flowers as trimerous with either four-sporangiate anthers or monocarpellate pistils.     

FLORAL INITIATION AND EARLY DEVELOPMENT IN ERIGERON PHILADELPHICUS (ASTERACEAE)

The order of floral initiation and subsequent organogeny of Erigeron philadelphicus L. (Asteraceae: Astereae) was found to deviate from the acropetal pattern generally reported for the Asteraceae. Light micrographs show periclinal divisions in the first, second, and deeper subsurface layers of cells on the flanks of the inflorescence apex as the earliest evidence of floral initiation. Scanning electron microscope micrographs indicate that the disk flowers appear first and arise as small protuberances approximately one-third of the way up the previously and undifferentiated highly convex inflorescence apex. A succession of disk flowers arises acropetally in a complex anthotaxy characterized by about 21 dextrorse and 12–15 sinistrorse parastichies (although this pattern is obscured at the apex). After one to three disk flowers have been initiated in each parastichy, the first ray flower initials can be seen to initiate in sites proximal to the oldest and largest disk flowers. Additional ray flowers then initiate basipetally following the dextrorse parastichies established by the disk flowers. Overall floral initiation on the inflorescence apex proceeds acropetally for the disk flowers and basipetally for the ray flowers until the available space is filled. Floral development adheres to the same plan—proceeding bidirectionally on the inflorescence meristem with the oldest and most complete flowers of both types located on the equator established at initiation.     

INFLORESCENCE AND FLOWER DEVELOPMENT IN THE PIPERACEAE. II. INFLORESCENCE DEVELOPMENT OF PIPER

The inflorescence development of three species of Piper (P. aduncum, P. amalago, and P. marginatum), representing Sections Artanthe and Ottonia, was studied. The spicate inflorescences contain hundreds or even thousands of flowers, depending on the species. Each flower has a tricarpellate syncarpous gynoecium and 4 to 6 free stamens, in the species studied. No sepals or petals are present. In P. marginatum the apical meristem of the inflorescence is zonate in configuration and is unusually elongate: up to 1,170 μm high and up to 480 μm wide during the most active period of organogenesis. Toward the time of apical cessation both height and diameter gradually diminish, leaving an apical residuum which may become an attenuate spine or may be cut off by an abscission zone just below the meristem. The active apex produces bract primordia; when each is 40–55 μm high, a floral apex is initiated in its axil. Both bract and floral apex are initiated by periclinal divisions in cells of the subsurface layer. The bracts undergo differentiation rather early, while the floral apices are still developing. The last-produced bracts near the tip of the inflorescence tend to be sterile.     

三白草科花部发育及其系统学意义

本研究从比较三白草科属间小花个体发育及分析花器官数量变异入手,探寻花器官在发生顺序、数目变化及排列方式等方面的演化趋势,揭示系统发育在个体发育中一定程度重现的事实及属间的进化关系。结果简述如下:首先,雄蕊和心皮发生顺序由中部优先演化到两侧优先。其次,由于远中雄蕊和心皮经历了从发育延迟、生长减缓到最终消失的历程,中部雄蕊和心皮由成对演化为单生。此外,两侧生雄蕊对由各自独立的原基发生演化到共同原基发生或减化为1枚,假银莲花属近中1枚雄蕊原基二裂成1对,蕺菜属3枚心皮发生于一环状共同原基等,都是该科花器官演化的重要事实并可归结为融合、减化和复化的结果。文章根据花器官的演化趋势及过渡类型的剖析,论述了三白草科属间的系统进化关系。     

PATTERNS OF FLORAL DEVELOPMENT IN AGALINIS AND ALLIES (SCROPHULARIACEAE). II. FLORAL DEVELOPMENT OF AGALINIS DENSIFLORA

Initiation of floral primordia begins in Agalinis densiflora with production of two lateral adaxial calyx lobe primordia followed by a midadaxial primordium, and then primordia of two abaxial calyx lobes. Initiation of three abaxial corolla lobe primordia is succeeded by that of two stamen pairs and then by primordia of two adaxial corolla lobes. The primordium of the abaxial carpel appears before the adaxial one. Except for the calyx, initiation of primordia proceeds unidirectionally from the abaxial to the adaxial side of the floral apex. Zygomorphy in the calyx, corolla, and androecium is evident during initiation of primordia and is accentuated during organogenesis. The calyx undergoes comparatively rapid organogenesis, but the inner three floral series undergo a protracted period of organogenesis. The perianth series reach maturation prior to meiosis in the anthers. Maturation of the androecium and gynoecium are postmeiotic events.     

PHYLOGENETIC IMPLICATIONS OF INFLORESCENCE AND FLORAL ONTOGENY OF MIMOSA STRIGILLOSA

Ontogeny of the inflorescence and flower of Mimosa strigillosa has been studied in order to explore the developmental basis for variation in number of parts, patterns of organ arrangement, and inflorescence architecture. Each racemose inflorescence of M. strigillosa has an acropetal order of initiation of bracts and flowers. Although flowers are initiated in acropetal order, they develop synchronously except for the basal flowers, which are retarded. The ring meristem in the calyx may be considered an expression of precocious fusion, a specialized condition within the genus. Two patterns of organ arrangement (nonsagittal and median sagittal) are distributed among 4- and 5-merous flowers along the inflorescences. Variability in number of parts probably has evolved through reduction of a basic, pentamerous structure, through fusion or suppression. It is proposed that the number of parts and pattern of organ arrangement are correlated features.     

FLORAL DEVELOPMENT AND STAMEN FILAMENT ELONGATION IN CLEOME HASSLERIANA

Floral development in Cleome hassleriana is briefly described. Experimental evidence is presented supporting the hypothesis that the anthers control stamen filament elongation by supplying IAA rather than kinetin or gibberellic acid. This control depends upon the developmental stage of the bud and does not exclude the effect of other floral organs on stamen filament elongation at early developmental stages. Evidence that the anthers also partially control stamen filament and floral abscission by supplying IAA is given.     

FLORAL STRUCTURE AND EVOLUTION IN LOPEZIEAE (ONAGRACEAE)

The Lopezieae present an interesting mixture of ancestral and derived characters: some members of the tribe retain the basic onagraceous chromosome number (n = 11), but the flowers are advanced in that they are mostly zygomorphic and always have a two-merous androecium. Species differ in the position of the nectaries, also in the way in which floral parts are united above the inferior ovary. These differences, when analyzed with information from a new monograph of the Lopezieae, provide the basis for a phylogenetic tree. It is inferred that ancestral Lopezieae were bird-pollinated woody perennials with regular flowers, two fertile stamens, and no floral tube distal to the ovary. Evolutionary events accompanying the emergence of modern taxa included abortion of the abaxial stamen (all surviving Lopezieae except Lopezia lopezioides), development of an epigynous floral tube (L. riesenbachia, L. semeiandra), decrease in floral symmetry without conversion to insect pollination (in two independent lines), and decrease in floral symmetry with conversion to insect pollination (in at least two independent lines). The prominent tubercles on upper petals of certain insect-pollinated species apparently evolved from the less prominent swollen areas still present in some of the bird-pollinated species. The tubercles and an associated snapping mechanism arose in response to increasing selection for fly pollination. Densely staining areas in some specimens may be osmophores; if so, scent plays a supplementary role in the orienting of insects to the upper petals. Interstaminal nectaries and the absence of a floral tube link the Lopezieae to Ludwigia; the relationship of these two taxa to Epilobium is presently unclear. Fossil records indicate that the Onagraceae had evolved by the beginning of the Tertiary Period and that the Ludwigia line is very old. The family's ancestral features are retained to a greater degree in Fuchsia, however, than in Ludwigia.     

INFLORESCENCE DEVELOPMENT IN BRASSICA CAMPESTRIS L.

Vegetative seedlings of the Ceres strain Brassica campestris L., a quantitative, long-day plant, were induced to flower by exposure to a 16-hr, long-day cycle. Cytohistological and cytohistochemical changes associated with inflorescence development were examined. Developing shoot apices were classified in vegetative, transitional, and reproductive stages. The vegetative apex possessed a biseriate tunica, central zone, peripheral zone and pith-rib meristem. The transitional stage at 48 hr was marked by an increase in size and by a stratification of the upper cell layers of the shoot apex with a concurrent decrease of apical cytohistochemical zonation. The reproductive stage was initiated at 58 hr by periclinal cell divisions in the 3rd and 4th cell layers of the flank region. Cytohistochemical zonation in the vegetative apical meristem was restored in the floral apex. An “intermediate developmental” phase was not observed between the vegetative and reproductive stage.     

HEAT INJURY DURING FLORAL DEVELOPMENT IN COWPEA (VIGNA UNGUICULATA,FABACEAE)

High night temperatures during floral development induce male sterility in cowpea (Vigna unguiculata [L.] Walp.). The objectives of this study were to determine: the possible causes of the male sterility; the stage of floral development when damage due to heat stress occurs; and whether specific tissues are damaged during the period of sensitivity to heat. Plants were grown under controlled temperatures in both greenhouses and growth chambers in separate experiments. Floral development was normal under a night temperature of 20 C, whereas flowers developed under high night temperature (30 C) set no pods due to low pollen viability and anther indehiscence. Anthers developed under 33/30 C day/night temperatures did not exhibit endothecial formation, whereas anthers developed under 33/20 C day/night temperatures exhibited normal development of the endothecial layer. Reciprocal transfers of plants between chambers with high or optimum night temperature demonstrated that the stage of floral development most sensitive to heat stress occurs 9 to 7 d before anthesis. Anthers developed under either optimal or high night temperatures were compared cytologically. Development was similar through meiosis, but after tetrad release, which occurred 8 d before anthesis, the tapetal layer degenerated prematurely under high night temperature. Premature degeneration of the tapetal layer and lack of endothecial development may be responsible for the low pollen viability, low anther dehiscence, and low pod set under high night temperatures.     

FLORAL FLAVONOIDS AND ULTRAVIOLET PATTERNS IN VIGUIERA (COMPOSITAE)

Variation occurs among species of Viguiera series Viguiera for ultraviolet (uv) absorption/reflection patterns of ligules. Floral flavonoids that cause uv absorption occur in epidermal papillae. Flavonoids are further localized to the proximal portion of the ligule in the seven taxa that have only proximal uv absorption. Floral flavonoids involved in uv absorption consist of flavone, flavonol, and anthochlor (chalcone/aurone) glycosides. Quercetin 3-methyl ether glycosides characterize the ligules of 10 taxa occurring in Baja California, Mexico, and nearby areas, and these taxa appear to form one taxonomic group. The anthochlor pair, marein/maritimein, characterizes V. dentata, and the lack of ligule flavonoids distinguishes V. potosina from the remaining taxa. The presence of the anthochlor pair, marein/maritimein, only in V. dentata and the lack of ligule flavonoids in V. potosina concur with other data to indicate that these species are not correctly placed with each other or with the other species currently included in series Viguiera.     

FLORAL VARIATION AND DISTYLY IN GUETTARDA SCABRA (RUBIACEAE)

Controversy exists as to whether the tropical shrub Guettarda scabra (Rubiaceae) is distylous. Variations in stigma and anther position and floral morphology of G. scabra were studied in a population in south Florida. Stigma and anther height have unimodal distributions, but stigma-anther separation is bimodally distributed and can be used to identify a long-styled and a short-styled morph. Stigma width varies between morphs, but anther length, pollen diameter, and stigma papillae length do not. The morphs occur in a 1:1 ratio in the two populations studied. G. scabra is self-compatible and can pollinate itself. Styles of the two morphs have similar relative growth rates in early development. Stylar growth is inhibited in the short-styled morph when buds are approximately 12 mm long. Anther height differs between morphs because of different relative growth rates and because the long-styled morph corolla tube, where the anthers are attached, stops growth before the tube of the short-styled morph. Reciprocity between morphs for average stigma and anther height falls within the range of reciprocity found in other distylous Rubiaceae. Thus G. scabra is morphologically distylous but unusual among distylous species in the variation within morphs and overlap between morphs in stigma and anther heights.     

FLORAL MORPHOLOGY AND CROSS-POLLINATION IN ERYTHRONIUM GRANDIFLORUM (LILIACEAE)

In bumblebee visits to flowers of Erythronium grandiflorum (Liliaceae), the ratio of self- to nonself- (“outcross”) pollen grains deposited on the stigma is positively correlated with the degree of stylar exsertion beyond the anthers. Natural populations show substantial, continuous variation in stylar exsertion.     

ANTHESIS AND FLORAL SENESCENCE IN CHLOROGALUM POMERIDIANUM (LILIACEAE)

Flowers of the soap-plant, Chlorogalum pomeridianum (DC.) Kunth., open for a few hours on only one day. The flowers open rapidly in the late afternoon, produce nectar, and close some 6-8 hr later. As the time of anthesis nears, the tepals become contorted, and progressively larger cavities appear in the tepal mesophyll. Multicellular trichomes at the tips of the tepals increase in length, untangle, and allow the flowers to spring open. Senescence is accompanied by the breakdown of mesophyll cells and by increased ethylene production as the perianth segments twist together and become deliquescent. Anthesis has a weak but discernible rhythmic component and is strongly influenced by alternating light and dark periods. Experiments showed that the length of the uninterrupted light period is of primary importance in the control of anthesis.