Study of homeosis in the flower of Philodendron (araceae): a qualitative and quantitative approach

This study deals specifically with floral organogenesis and the development of the inflorescence of Philodendron squamiferum and P. pedatum. Pistillate flowers are initiated on the lower portion of the inflorescence and staminate flowers are initiated on the distal portion. An intermediate zone consisting of sterile male flowers and atypical bisexual flowers with fused or free carpels and staminodes is also present. This zone is located between the sterile male and female floral zones. In general, the portion of bisexual flowers facing the male zone forms staminodes, and the portion facing the female zone develops an incomplete gynoecium with few carpels. The incomplete separation of some staminodes from the gynoecial portion of the whorl shows that they belong to the same whorl as the carpels. There are two levels of aberrant floral structures in Philodendron: The first one is represented by the presence of atypical bisexual flowers, which are intermediates between typical female flowers and typical sterile male flowers. The second one is the presence of intermediate structures between typical carpels and typical staminodes on a single atypical bisexual flower. The atypical bisexual flowers of P. squamiferum and P. pedatum are believed to be a case of homeosis where carpels have been replaced by sterile stamens on the same whorl. A quantitative analysis indicates that in both species, on average, one staminode replaces one carpel.     

Homeosis, morphogenetic gradient and the determination of floral identity in the inflorescences ofPhilodendron solimoesense (Araceae)

A comparative developmental study of the inflorescence ofPhilodendron solimoesense was conducted using scanning electron microscopy. The spadix ofP. solimoesense is characterized by unisexual flowers. Staminate flowers are initiated on the upper portion of the spadix while pistillate flowers develop on the lower portion of the spadix. An intermediate zone located between the upper male and lower female portion of the inflorescence consists of sterile male flowers. Within this intermediate zone a row of flowers exhibit polarity with respect to the identity of sexual organs. Stamens are initiated on the flank of the floral meristem facing the upper male zone and carpels are initiated on the portion of the floral meristem facing the lower female zone. The resulting flowers therefore assume a bisexual identity. At the level of the inflorescence, all floral buds are initiated along a series of contact parastichies and the continuity of these parastichies is not disrupted at any level in the male, intermediate, and female zones on the spadix. Results from this study support the presence of a morphogenetic gradient acting at the level of the inflorescence and appears to be independent of the boundaries of floral primordia.     

花叶芋(天南星科)的花器官发生

利用扫描电镜首次观察了天南星科花叶芋(Colocasia bicolor) 的花器官发生过程。花叶芋的肉穗花序由无花被的单性花构成, 雌花发生于花序基部, 雄花发生于花序上部, 中性花位于花序中间部位。雄花: 3 或4 个初生雄蕊原基轮状发生, 随后每个初生原基一分为二, 形成6或8个次生原基; 一部分次生原基在其后的发育过程中融合, 形成5 或7 枚雄蕊; 雄花发育过程中未见雌性结构的分化; 花药的分化先于花丝; 雄蕊合生成雄蕊柱。雌花: 合生心皮, 3或4个心皮原基轮状发生, 未见雄性结构的分化。中性花来源于雌雄花序过渡带上, 属于雄蕊原基的滞后发育以及发育成熟过程中的退化; 与彩叶芋属(Caladium)不同, 此过渡区未见畸形两性花。初生雄蕊原基二裂产生次生原基的次生现象在目前天南星科花器官发生中显得比较特殊, 同时初步探讨了次生原基的融合方式。     

Resource partitioning to male and female flowers of Spinacia oleracea L. in relation to whole-plant monocarpic senescence

Male plants of spinach (Spinacea oleracea L.) senesce following flowering. It has been suggested that nutrient drain by male flowers is insufficient to trigger senescence. The partitioning of radiolabelled photosynthate between vegetative and reproductive tissue was compared in male (staminate) versus female (pistillate) plants. After the start of flowering staminate plants senesce 3 weeks earlier than pistillate plants. Soon after the start of flowering, staminate plants allocated several times as much photosynthate to flowering structures as did pistillate plants. The buds of staminate flowers with developing pollen had the greatest draw of photosynthate. When the staminate plants begin to show senescence 68% of fixed C was allocated to the staminate reproductive structures. In the pistillate plants, export to the developing fruits and young flowers remained near 10% until mid-reproductive development, when it increased to 40%, declining to 27% as the plants started to senesce. These differences were also present on a sink-mass corrected basis. Flowers on staminate spinach plants develop faster than pistillate flowers and have a greater draw of photosynthate than do pistillate flowers and fruits, although for a shorter period. Pistillate plants also produce more leaf area within the inflorescence to sustain the developing fruits. The (14)C in the staminate flowers declined due to respiration, especially during pollen maturation; no such loss occurred in pistillate reproductive structures. The partitioning to the reproductive structures correlates with the greater production of floral versus vegetative tissue in staminate plants and their more rapid senescence. As at senescence the leaves still had adequate carbohydrate, the resources are clearly phloem-transported compounds other than carbohydrates. The extent of the resource redistribution to reproductive structures and away from the development of new vegetative sinks, starting very early in the reproductive phase, is sufficient to account for the triggering of senescence in the rest of the plant.     

Homeosis in Araceae Flowers: The Case of Philodendron melinonii

The early stages of development of the inflorescence of Philodendronmelinonii were examined using scanning electron microscopy.Pistillate flowers are initiated on the lower portion of theinflorescence and staminate flowers are initiated on the distalportion. The male flowers have four to five stamens. The femaleflowers have a multilocular ovary consisting of four to sixlocules. A transition zone consisting of sterile male flowersand bisexual flowers with fused or free carpels and staminodesis also present on the inflorescences. This zone is locatedbetween the male and female flower zones. Generally, the portionof the bisexual flower facing the male zone forms stamens, andthe portion facing the female zone develops an incomplete gynoeciumwith few carpels. In P. melinonii, the incomplete separationof staminodes from the gynoecial portion of the whorl showsthat the staminodes and carpels belong to the same whorl. Thebisexual flowers of P. melinonii are believed to be a case ofhomeosis where carpels have been replaced by sterile stamenson the same whorl. At the level of the inflorescence, pistillateand staminate flowers are inserted on the same contact parastichiesalong the inflorescence; there is no discontinuity between thefemale zone, the bisexual zone, and the male zone. The presenceof bisexual flowers is believed to correspond to a morphogeneticgradient at the level of the inflorescence as a whole. Copyright2000 Annals of Botany Company Flower, development, gradient, inflorescence     

Flower structure and potential bisexuality in Freycinetia reineckei (Pandanaceae), a species of the Samoa Islands

In Freycinetia reineckei the staminate flower (on the staminate spikes) comprises 3 or 4 (sometimes 2) stamens and a pistillode with 2 (sometimes 4) carpellodes, and the pistillate flower (on the pistillate spikes) is formed of a pistil with 2 (sometimes 4) carpels and of 3 or 4 (sometimes 2) staminodes. This perfect floral homology, also observed in all the other species that were studied with both pistillate and staminate material, strongly suggests that the flower of Freycinetia is basically and potentially bisexual, and may explain the occasional sexual lability and bisexuality of that flower (occurrence of both pistillate and staminate inflorescences, and/or of bisexual inflorescences with bisexual flowers and/or unisexual flowers, on the same individuals) in some species, and also the frequent occurrence of bisexual spikes in this species. These may be partitioned into pistillate, staminate, mixed and sterile zones. In the pistillate zones the flowers have the same aspect and structure as the pistillate flowers. In the staminate zones the flowers generally comprise 3 or 4 (sometimes 2) stamens and a ‘semi-pistil’ some have both stamens and staminodes. The semi-pistils are intermediate between pistils and pistillodes in length, aspect and structure, but always have placentas and ovules. In the mixed zones the flowers are generally formed of a pistil and 3 or 4 (sometimes 2) stamens, and are therefore true hermaphrodite flowers; some have both stamens and staminodes. In the sterile zones the flowers comprise a semi-pistil and 3 or 4 (sometimes 2) staminodes. The staminodes are anatomically very similar to the stamens, especially in the staminate, mixed, and sterile zones, in which they exhibit a wide range of variation in length, aspect and structure. The perfect floral homology as generic character on one hand, and the occasional bisexuality both with and without bisexual flowers and other aspects of sex expression (e.g. occurrence of both pistillate and staminate shoots on the same individuals) in some species on the other hand, seem to indicate that Freycinetia is a basically monoecious, sex changing genus.     

Morphological variation in the flowers of Jacaratia mexicana A. DC. (Caricaceae), a subdioecious tree

The Caricaceae is a small family of tropical trees and herbs in which most species are dioecious. In the present study, we extend our previous work on dioecy in the Caricaceae, characterising the morphological variation in sexual expression in flowers of the dioecious tree Jacaratia mexicana . We found that, in J. mexicana , female plants produce only pistillate flowers, while male plants are sexually variable and can bear three different types of flowers: staminate, pistillate and perfect. To characterise the distinct types of flowers, we measured 26 morphological variables. Our results indicate that: (i) pistillate flowers from male trees carry healthy-looking ovules and are morphologically similar, although smaller than, pistillate flowers on female plants; (ii) staminate flowers have a rudimentary, non-functional pistil and are the only flowers capable of producing nectar; and (iii) perfect flowers produce healthy-looking ovules and pollen, but have smaller ovaries than pistillate flowers and fewer anthers than staminate flowers, and do not produce nectar. The restriction of sexual variation to male trees is consistent with the evolutionary path of dioecy from hermaphrodite ancestors through the initial invasion of male-sterile plants and a subsequent gradual reduction in female fertility in cosexual individuals (gynodioecy pathway), but further work is needed to confirm this hypothesis.     

SEX DIFFERENTIAL FLORAL LONGEVITY,NECTAR SECRETION,AND POLLINATOR FORAGING IN A PROTANDROUS SPECIES

Sex differential nectar production, floral longevity and pollinator foraging were examined in Lobelia cardinalis, a self-compatible, protandrous species that is hummingbird pollinated. The staminate phase of the flowers lasts significantly longer and produces significantly more nectar (total sugar) per day than the pistillate phase of the flowers. Additional pollen is presented throughout the staminate phase. Because inflorescences of L. cardinalis mature acropetally, the nectar reward on any given day is greatest at the top of the inflorescence (where staminate phase flowers are located). Hummingbirds appear to be sensitive to this pattern of nectar presentation as they most commonly began foraging in the middle of an inflorescence and proceeded upward. This foraging pattern tends to promote outcrossing and suggests that staminate phase flowers are visited more often than pistillate phase flowers. We conclude that L. cardinalis emphasizes the male function at anthesis. Others have hypothesized that the features of this species are a logical consequence of intrasexual selection, but further research is needed before we place great confidence in a sexual selection interpretation of our data.     

Pistillate and staminate flower development in dioecious Pistacia vera (Anacardiaceae)

The development of staminate and pistillate flowers in the dioecious tree species Pistacia vera L. (Anacardiaceae) was studied by scanning electron microscopy with the objective of determining organogenetic patterns and phenology of floral differentiation. Flower primordia are initiated similarly in trees of both sexes. Stamen and carpel primordia are initiated in both male and female flowers, and the phenology of organ initiation is essentially identical for flowers of both sexes. Vestigial stamen primordia arise at the flanks of pistillate flower apices at the same time functional stamens are initiated in the staminate flowers. Similarly, a vestigial carpel is initiated in staminate flowers at the same time the primary, functional carpel is initiated in pistillate flower primordia. Differences between the two sexes become apparent early in development as, in both cases, development of organs of the opposite sex becomes arrested at the primordial stage. Male flowers produce between four and six mature functional stamens and female flowers produce a gynoecium with one functional and two sterile carpels.     

MORPHOLOGY,VASCULAR ANATOMY AND EMBRYOLOGY OF PISTILLATE AND STAMINATE FLOWERS OF ASPARAGUS OFFICINALIS

Flowers of three pistillate (female), two heterogametic staminate (male) and two homogametic male genotypes of Asparagus officinalis L. were compared for morphology and vascular anatomy of the flower and for embryological development to the stage of mature ovules and pollen. Flowers are liliaceous, the staminate with rudimentary pistils and the pistillate with collapsed anthers. The uncomplicated vascular pattern differs between staminate and pistillate flowers only in the size and degree of maturation of bundles to stamens and carpels. Longer styles appear to be correlated with a greater extent of ovule development in ovaries of staminate flowers. Microsporogenesis in males is normal with wall development corresponding to the Monocotyledonous type. The tapetum is glandular and binucleate, cytokinesis successive, the tetrads isobilateral or occasionally decussate, and the mature pollen grain two-celled. A pair of heteromorphic, possibly sex, chromosomes was observed in heterogametic male plants. Anther development is initially the same in pistillate flowers, but the tapetum degenerates precociously followed by collapse of microspore mother cells. In pistillate flowers the ovules are hemitropous, bitegmic, and slightly crassinucellate. Megasporogenesis-megagametogenesis conforms to the Polygonum type. In staminate flowers ovule development is like that in pistillate flowers until degeneration starts in nucellar and integumentary cells at the chalazal end. Ovules in both homogametic male genotypes rarely complete meiosis, while in the heterogametic males it is normally completed with about one ovule in 20 flowers forming a mature megagametophyte. Since manipulation of sex expression in Asparagus could be important in developing inbred male and female lines for breeding purposes, those aspects of the morphological and embryological observations presented which might be useful in planning experiments to induce sex changes are discussed briefly.     

Observations of inflorescence patterns and flower sex in a population of Sagittaria papillosa Buch. (Alismataceae)

Sagittaria papillosa Buch. is monoecious with unisexual flowers, pistillate below, staminate above, typically with an unbranched scape. A large population with unusual numbers of staminate and bisexual flowers on the lowest whorl of the inflorescence and many particles was quantitatively evaluated. First-formed inflorescences had more staminate and bisexual flowers than those produced later. Branched scapes were predominantly found to be the second inflorescence produced by a given plant. Genetic crosses between flowers on recemes and panicles produced no branched inflorescences. When grown under greenhouse conditions all tested plants had racemes with pistillate flowers in the lower whorls and staminate ones above. Data from soil parameters, daylengths and air temperatures are compared to reported information on modification of flower sexuality by these factors.     

Anther structure and pollen development in Melicoccus lepidopetalus (Sapindaceae): An evolutionary approach to dioecy in the family

Anther and pollen development in staminate and pistillate flowers of dioecious Melicoccus lepidopetalus (Sapindaceae) were examined by light and electron microscopy. Young anthers are similar in both types of flowers; they consist of epidermis, endothecium, two to four middle layers and a secretory tapetum. The microspore tetrads are tetrahedral. The mature anther in staminate flowers presents compressed epidermal cells and endothecium cells with fibrillar thickenings. A single locule is formed in the theca by dissolution of the septum and pollen grains are shed at two-celled stage. The mature anthers of pistillate flowers differ anatomically from those of staminate flowers. The epidermis is not compressed, the endothecium does not develop fibrillar thickenings, middle layers and tapetum are generally persisting, and the stomium is nonfunctional. Microspore degeneration begins after meiosis of microspore mother cells. At anthesis, uninucleate microspores and pollen grains with vegetative and generative nuclei with no cytokinesis are observed. Some pollen walls display an abnormal exine deposition, whereas others show a well formed exine, although both are devoid of intine. These results suggest that in the evolution towards unisexuality, the developmental differences of anther wall tissues and pollen grains between pistillate and staminate flowers might become more pronounced in a derived condition, such as dioecy.     

Pollination ecology of Magnolia ovata may explain the overall large flower size of the genus

Flowering and fruiting biology of Magnolia ovata was studied in Atlantic forests in the interior of São Paulo State, Brazil. The large, bisexual flowers are protogynous, nocturnal, thermogenic and emit a strong scent in two consecutive evenings. In the first night of anthesis, the flowers are in the pistillate stage and thermogenesis starts at about sunset and lasts about 3 h. In the second night, the flowers enter the staminate stage and produce heat for 4 h. Heat is generated by the petals, gynoecium and anthers. Temperatures measured inside the petals reach 26.7 °C and 31.9 °C in the pistillate and staminate stages, 6.0 and 10.6 °C above ambient air, respectively. In the pistillate stage, the perianth opens after sunset and closes tightly a few hours later, and remains closed until the next evening. The initial opening and closing, however, is not synchronous for all flowers during the night. In the following evening, flowers in the staminate stage again open and remain so until the petals drop. Scent compounds, analyzed by GC–MS, contain C5-branched chain compounds, aliphatics, benzenoids and monoterpenoids. Emission of the most prominent compound, C5-branched methyl 2-methyl butyrate, commences before flower opening and continues throughout anthesis, but is accentuated in the thermogenic pistillate and staminate stages. Female and male individuals of only one beetle species, the dynastid scarab Cyclocephala literata, are attracted to the scented flowers in both pistillate and staminate stages. Once inside the flowers they feed on the petals and mate. Tests with synthetic methyl 2-methyl butyrate indicate that this compound is a strong attractant for the beetles. Because this scent compound is strongly emitted in both pistillate and staminate stages, the beetles fly indiscriminately between flowers of both stages. This behavior enhances pollen mixing and effective cross-pollination of the self-compatible species. The evolutionary history of Magnolia appears to be influenced by an ancestral condition of dynastid scarab beetle pollination. Large magnolia flowers are best explained as an archaic structure resulting from the initial association of tropical American species of section Talauma with large and voracious dynastid beetles.     

Subdioecy in Consolea spinosissima (Cactaceae): breeding system and embryological studies

The breeding system and the embryology of Consolea spinosissima, a tree-like opuntioid endemic to Jamaica, were investigated. Morphological and embryological studies revealed that the species is subdioecious, with three sexual morphs present in the 150 × 120 m plot studied at Hellshire Hills, Jamaica. The female morph has pistillate flowers with open stigma lobes, no pollen grains, and sets fruit. The male morph has cryptic staminate flowers with closed stigma lobes, viable pollen grains, and a nonfunctional gynoecium that does not set seed. The weak hermaphrodite morph has low fruit set and "perfect" flowers that superficially resemble the functionally staminate flowers of the male morph. These perfect flowers reach anthesis with viable pollen grains, with no or only a few functional ovules, and with the style supporting pollen tube growth. Embryological studies showed that the critical stage for sex determination occurs earlier in pistillate than in staminate and perfect flowers. Anthers of pistillate flowers abort prior to microspore tetrad formation, whereas ovules of the staminate and perfect flowers degenerate after the complete maturation of the embryo sac. Based on flower structure and embryological data, we hypothesize that the ancestor of C. spinosissima is/was hermaphroditic.     

THE INTRAFLORAL PHENOLOGY OF STREPTANTHUS TORTUOSUS (BRASSICACEAE)

The sequence of floral events during anthesis was examined in Streptanthus tortuosus to determine the relationship between the male and female floral phases. The flowers are strongly protandrous. In the staminate phase, the anthers mature sequentially over a 3–4-day period. Because pollinators quickly remove pollen from the anthers, sequential anther maturation prolongs the male phase relative to what it would be if anthers did not mature sequentially. Pollen applied to the stigma during the staminate phase does not adhere readily and does not germinate. The length of the pistillate phase depends on pollinator activity, as pollination accelerates the abscission of floral parts. Unpollinated flowers remain pistillate for 3–4 days, during which time stigmatic receptivity declines gradually. In the field, 72% to 80% of flowers are staminate at any time, indicating that the staminate phase is three times longer than the pistillate phase when pollinators have access to the flowers. The consequences of the relative length of the floral phases and the schedule of stigmatic receptivity are discussed in terms of outcrossing mechanism, floral longevity, and sexual selection models.     

The selective florivory of Erioscelis emarginata matches its role as a pollinator of Philodendron

Flowers commonly face the dilemma of needing to be attractive to pollinators but unattractive to nectar robbers or florivores. When the pollinator has chewing mouthparts, there is also a considerable risk of the pollinator consuming the flowers. Scant field records indicate that the florivorous beetle Erioscelis emarginata (Mannerheim) (Coleoptera: Scarabaeidae: Cyclocephalini), which pollinates Philodendron spp., feeds selectively on the sterile staminate flowers. Here, the hypothesis was tested that E. emarginata prefers sterile staminate flowers of Philodendron bipinnatifidum Schott and Philodendron melinonii Brongn. ex Regel (Araceae) over fertile flowers. This study also examined whether such a preference exists regardless of the proportion of fertile vs. sterile flowers in each Philodendron species. Analysis of nutritional and defensive compounds plus scanning electron microscopy on each flower type were performed. The feeding preference of florivores for either P. bipinnatifidum or P. melinonii was also examined. In both species, sterile flowers were significantly more consumed than fertile ones. The sterile zone of P. bipinnatifidum was significantly larger than that of P. melinonii, and sterile staminate flowers of both plants were consumed at similar rates. Calcium oxalate was markedly low in sterile flowers, which also presented smaller papillae than the other flowers. This study presents evidence that the balance between pollination and florivory has most likely evolved through a strong feeding preference for less‐defended sterile flowers regardless of the size of the sterile zone.     

Evidence of trimonoecy in Phyllanthaceae: Phyllanthus acidus

Pollen from staminate flowers and pistillate flowers with ??staminodes?? of Phyllanthus acidus Skeels were analyzed under scanning electron microscopy, and tests of pollen viability and in?vitro germination were carried out to verify possible similarities between the three types of flowers. The results show that pistillate flowers with ??staminodes?? are bisexual, indicating the occurrence of trimonoecy in this species.     

Reproductive Biology of the Monoecious Understory Palm Prestoea schultzeana in Amazonian Ecuador1

Prestoea schultzeana is a monoecious, protandrous palm in the forest understory of Amazonian Ecuador. We studied its leaf production, population density, sexual expression, phenology, pollination, and the specificity of the floral visitors. On average, 1.4 leaves and 0.9 inflorescences are produced per individual per year. The number of staminate flowers per inflorescence is relatively constant compared with the number of pistillate flowers which varies greatly. Flowering occurs in staminate and pistillate phases of approximately 19 and 0–7 days duration, respectively. Flowers open in the morning, and staminate flowers abscise in the afternoon of the same day whereas pistillate flowers last for two days. Flowers are whitish-yellow with a sweet odor and produce nectar. They were visited by Coleoptera (Chrysomelidae, Curculionidae, Nitidulidae, Ptiliidae, Staphylinidae), Hemiptera, Diptera (Drosophilidae, Syrphidae, Ceratopogonidae), Lepidoptera (Nymphalidae), and Hymenoptera (Formicidae, Halictidae). All examined individuals of the syrphid fly Copestylum sp. visiting pistillate flowers carried 100–500 grains of P. schultzeana pollen. Pollen occurred on all body parts, but especially on the legs, and this makes Copestylum sp. the most important pollinator. Most floral visitors were also frequent on the flowers of co-occurring plant species; notably the palm Hyospathe elegans shared most visitor species with P. schultzeana.     

麻疯树雌雄花中MADS-BOX基因的表达分析

麻疯树(Jatropha curcas)种子含油率高,种子中的油类物质可作为生物柴油被开发和利用,是极具潜力的生物质能源树种之一。麻疯树雌雄异花,在自然条件下雄花数量通常远远大于雌花,这大大限制了种子和油的产量,因此开展麻疯树性别分化与花发育分子机理的研究具有重要意义。该研究选取10个麻疯树的MADS-BOX基因(JcAGL1,JcAGL6,JcAGL9,JcAGL11,JcAGL15,JcAGL61-3,JcAGL62-1,JcAGL62-6,JcAGL62-7,JcAGL80-2),提取麻疯树早期发育各个阶段的雌雄花总RNA,并反转录成cDNA,采用实时荧光定量方法,探索早期发育不同阶段的麻疯树雌雄花目的基因的表达情况。结果表明:目的基因在发育起始的雌雄花中的表达具有差异,比如JcAGL6和JcAGL15在雄花中表达量要高于雌花,而JcAGL1,JcAGL9和JcAGL11在雌花中的表达量要高于雄花,这说明花原基中目的基因表达会直接或间接决定性别分化的方向;在之后的发育过程中,目的基因的表达情况在雌雄花中有所不同:随着花的发育,目的基因在雌雄花中的表达量变化存在差别,这反应出麻疯树雌雄花发育中目的基因表达模式上的差异;另外,也能看出在此过程中各个目的基因又发挥着不同的功能。该研究结果为进一步探究麻疯树雌雄花发育相关基因的表达提供了理论依据,为了解麻疯树性别分化和花发育的分子机理奠定了基础。     

Sex expression as affected by N6-benzylaminopurine in staminate inflorescence of Luffa cylindrica

The effect of N⁶-benzylaminopurine (BA) on the sex expressionof staminate inflorescences of Luffa cylindrica was investigated.Direct application of BA to the staminate inflorescence inducedbisexual and pistillate flowers and finally caused the inflorescenceto develop into a shoot that was similar to the main shoot.Such modification in a staminate inflorescence from the proximalto the distal nodes is usually in the order of staminate flowers,bisexual flowers, pistillate flowers and foliage leaves (shoot).Pinching of the main stem also caused the inflorescence to developinto a shoot in the absence of lateral shoots. BA-induced femalenesswas strengthened when the number of leaves remaining on theplant was increased. On the other hand, application of BA tothe shoot apex of the main stem starting at the 2-leaf stagesuppressed differentiation of the flower bud on the main stem. (Received December 22, 1979; )