Entomofauna visitante de Stenolobium stans (Juss.) Seem (Bignoniaceae), durante seu período de floração

Realizaram-se estudos sobre as formas de reprodução de Stenolobium stans (Juss.) Seem e determinou-se a diversidade, freqüência e constância dos insetos visitantes nas flores em diferentes horas, durante quatro anos. As flores de S. stans começam a se abrir nas primeiras horas do dia entre 5 e 6h, com duração de 3 a 8h. Quando o estigma está receptivo, o pólen tem 90% de viabilidade. Além do pólen, a flor possui outros atrativos para os insetos visitantes, ou seja, os osmóforos responsáveis pelo odor adocicado, luz ultravioleta refletida e néctar com 25% de açúcar. A planta é autocompatível, reproduzindo-se por autogamia, geitonogamia ou xenogamia o que determina a necessidade de polinizadores externos e justifica ser a espécie vegetal em estudo uma séria invasora de campos e pastagens. Grande diversidade de insetos foi verificada visitando as flores, com predominância das abelhas. Os polinizadores foram Centris collaris Lepeletier, Bombus morio (Swederus), Eulaema nigrita Lepeletier e Epicharis sp. No meio rural houve menor incidência das espécies nativas do que no ambiente urbano, com predominância da abelha introduzida Apis mellifera L. Fatores ambientais, principalmente a temperatura, luminosidade, umidade relativa do ar e velocidade do vento, influenciaram a atividade forrageadora dos insetos.

Saranthe klotzschiana (Koer.) Eichl. (Marantaceae) e seu mecanismo explosivo de polinização

A biologia da polinização de Saranthe klotzschiana (Koer.) Eichl. foi estudada em uma Mata Serrana (brejo de altitude) no Parque Ecológico João Vasconcelos Sobrinho, Caruaru-PE (8º18'36"S e 36º00'00"W). Saranthe klotzschiana apresenta inflorescências com 2,5-5,5 cm de comprimento, com ca. 10-30 flores, as quais medem 6-10 mm de comprimento. A antese é diurna, as flores abrem à partir das 4:00 h e fecham por volta das 14:30 h, abrindo cerca de 4-12 flores por inflorescência/dia. É produzido 1-3 µL de néctar por flor, com concentração de açúcares entre 27% e 32%. Ao amanhecer, foram observadas visitas freqüentes de mariposas e de abelhas, das famílias Anthophoridae (Centris aenea, Epicharis (Epicharoides) sp., Mesoplia similis, Rhathymus acutiventris e R. bicolor nigripes), Apidae (Euglossa truncata, E. carinilabris, Eulaema bombiformis, E. cingulata, E. nigrita e Melipona scutellaris) e Colletidae (Ptiloglossa sp.). As abelhas visitaram as flores ao longo de todo o período de antese, sendo o pico de visitas das 6:00 h às 11:00 h. A partir das 8:00 h iniciavam as visitas dos beija-flores Amazilia fimbriata, Chlorostilbon aureoventris e Phaethornis ruber. Antes das visitas o estilete encontra-se em posição vertical em relação ao ovário, preso por tensão pelo estaminódio. Ao toque do visitante floral, o estilete se enrola, havendo deposição de pólen na probóscide (mariposa), língua (abelhas) ou no bico (beija-flores). As abelhas grandes e os beija-flores foram considerados os principais polinizadores devido à eficiência no desencadeamento do mecanismo de polinização.

Esfingofilia e sistema de reprodução de Bauhinia curvula Benth. (Leguminosae: Caesalpinioideae) em cerrado no Centro-Oeste brasileiro

A biologia reprodutiva de Bauhinia curvula foi estudada em remanescente de cerrado em Mato Grosso do Sul. Bauhinia curvula é um subarbusto que floresce por seis a sete meses (junho a novembro/dezembro) e possui caule subterrâneo, espessado e gemífero, com função regenerativa. As flores são hermafroditas, zigomorfas, brancas, de antese noturna, exalam odor desagradável e duram 11 horas. O estigma é amplo e fica situado acima e/ou à frente das anteras que apresentam pólen com viabilidade de 98,5%. Néctar é produzido no interior do hipanto, com volume médio de 26 µL e concentração de solutos em torno de 15%. Embora flores de B. curvula apresentem diversas características associadas às síndromes de quiropterofilia e esfingofilia, o pequeno volume de néctar e a estreita entrada da câmara nectarífera parecem não estimular visitas de morcegos. Bauhinia curvula é auto-incompatível e depende de polinizadores, pois não frutificou após autopolinização espontânea. A população estudada apresentou eficácia reprodutiva reduzida (0,07), provavelmente devido à limitação de pólen. Agrius cingulatus (Sphingidae) foi o único visitante floral que apresentou comportamento de visita e comprimentos do corpo e da probóscide adequados para polinizar efetivamente as flores. Esse fato pode favorecer, a médio e longo prazo, a seleção de genótipos autogâmicos.

Biossistemática do complexo Cryptanthus zonatus (Vis.) Beer

The taxonomic delimitation at the species level in plants is not an easy task due to the large polymorphism of plants. In this project we aimed to evaluate three morphotypes (forms) of Cryptanthus zonatus (Vis.) Beer ( Bromeliaceae, Bromelioideae ) described in the literature using fl oral biology and phenology, as well as flo ral morphology and leaf anatomy . These studies were conducted in the Parque Estadual das Dunas de Natal, Rio Grande Norte (RN) and Private Reserve of Natural Patrimony Mata Estrela , in the municipality of Ba í a Form osa. The survey of the phenology of the morphotypes involved monthly specimen observation in the field, during one year. In each visit, we observed the status of flowering and fruiting phenophases of the population of the three forms of C. zonatus . For flo ral biology we sought to evaluate data like: observed floral visitors, nectar volume and concentration, time of anthesis and closing of flowers . Flowers of the three fo rms were collected in the field , analyzed by stereomicroscope, and measurements of the f loral pieces were made with the help of a caliper . Transversal and paradermal sections of the leaves of the three forms were stained and then examined under an optical microscope. Observations of the epidermis under scanning electron microscopy were also conducted. The three m orphotypes could not be sepated based on all evidence investigated. Thus, we conclude that there is not evidences to support the recognition of C. zonatus morphotypes as taxonomic entities, and also that the tools of phenology, anatomy, biology and floral morphology were not useful to delimit these three forms . Yet to characterize better the Flora of Bromeli aceae of RN, the leaf anatomy of Orthophytum disjunctum was also studied. Orthophytum is the sister genus to Cryptanthus and only recently documented in the semiarid of RN. The anatomical comparison between Cryptanthus and Orthophytum allowed the separatio n of both genera based on the arrangement of stomata and thickness of aquiferous parênquima . During the fieldwork, it was still possible to document the first occurrence of Aechmea muricata in RN, inside the Mata Estrela preserve, aiding the understanding of the distribution of the taxon that is currently threatened with extinction.

Biologia floral e reprodutiva de Casearia grandiflora Camb. (Flacourtiaceae)

A biologia de reprodução de Casearia grandiflora (Flacourtiaceae) foi estudada em um remanescente de mata mesófila do Parque do Sabiá, Uberlândia - MG. A espécie é importante no sub-bosque de matas da região, florescendo durante quase todo o ano, mas com maior abundância nos meses de março, abril e maio. As flores são branco-esverdeadas com cerca de 7 mm de diâmetro, dispostas em capítulos sésseis axilares. Não apresentam odor perceptível e duram apenas 1 dia. Possuem 10 estames férteis livres entre si e unidos à corola na base. Entre os estames existem estruturas pilosas originárias do receptáculo floral. Os estames e estas estruturas formam um cone em torno do pistilo, onde se acumula o néctar. A antese ocorre de forma irregular, principalmente no início da manhã. O néctar é relativamente abundante (4 miL) e com concentração média de 38% de equivalentes de sacarose. O pólen é liberado nas horas mais quentes do dia, com alta viabilidade (96,6%). Neste horário também ocorre a receptividade estigmática. O visitante mais freqüente foi a mosca Ornidia obesa (Syrphidae), que visita as flores durante quase todo o dia, embora tenham sido observados também outros visitantes casuais como abelhas Meliponinae, borboletas e outras moscas não identificadas. Polinizações controladas mostraram que a planta é auto-incompatível e não apomítica. No entanto, foram observados tubos polínicos crescendo até o ovário e penetrando os óvulos em flores autopolinizadas, sugerindo a ocorrência de fenômenos de auto-esterilidade de ação tardia (pós-fertilização) ou depressão de endogamia. A auto-esterilidade em C. grandiflora contrasta com a autogamia observada na maior parte das plantas miófilas e de flores generalistas ocorrendo nas florestas do Brasil central, mas é semelhante aos sistemas de reprodução de outras Flacourtiaceae lenhosas estudadas em florestas Neotropicais.

Entomofauna visitante de Belamcanda chinensis (L.) DC (Iridaceae) durante o período de floração

A study of the reproductive biology of B. chinensis (L.) DC. (Iridaceae) was realized comprising floral biology and breeding systems. The floral biology studies included analyses of nectar production, occurence of osmophores, corolla pigments, ultraviolet reflexion and absortion patterns, viability of pollen, pollinators and flower visitors. The breeding systems were studied taking into account the results of manual pollinators tests. B. chinensis is self-compatible bul cross-pollination is more frequent. The effective pollinators are Plebeia droryana (Friese, 1906) (45,7%), Trigona spinipes (Fabricius, 1793) (27,3%), Tetragonisca angustula (Latreille, 1811) (9,3%). Others insects visitors are considered nectar and pollen thieves. The flowering begins generally in January and February. The complete reproductive cicle, as here considered, begining with floral bud production ending with development of mature fruits, lasts January to June. Seed dispersion is ornitocoric.

Nectar Robbery By A Hermit Hummingbird: Association To Floral Phenotype And Its Influence On Flowers And Network Structure.

Interactions between flowers and their visitors span the spectrum from mutualism to antagonism. The literature is rich in studies focusing on mutualism, but nectar robbery has mostly been investigated using phytocentric approaches focused on only a few plant species. To fill this gap, we studied the interactions between a nectar-robbing hermit hummingbird, Phaethornis ruber, and the array of flowers it visits. First, based on a literature review of the interactions involving  P. ruber, we characterized the association of floral larceny to floral phenotype. We then experimentally examined the effects of nectar robbing on nectar standing crop and number of visits of the pollinators to the flowers of Canna paniculata. Finally, we asked whether the incorporation of illegitimate interactions into the analysis affects plant-hummingbird network structure. We identified 97 plant species visited by P. ruber and found that P. ruber engaged in floral larceny in almost 30 % of these species. Nectar robbery was especially common in flowers with longer corolla. In terms of the effect on C. paniculata, the depletion of nectar due to robbery by P. ruber was associated with decreased visitation rates of legitimate pollinators. At the community level, the inclusion of the illegitimate visits of P. ruber resulted in modifications of how modules within the network were organized, notably giving rise to a new module consisting of P. ruber and mostly robbed flowers. However, although illegitimate visits constituted approximately 9 % of all interactions in the network, changes in nestedness, modularity, and network-level specialization were minor. Our results indicate that although a flower robber may have a strong effect on the pollination of a particular plant species, the inclusion of its illegitimate interactions has limited capacity to change overall network structure.

EVOLUTION OF FLORAL MORPHOLOGY AND POLLINATION SYSTEM IN BIGNONIEAE (BIGNONIACEAE)

The radiation of angiosperms is associated with shifts among pollination modes that are thought to have driven the diversification of floral forms. However, the exact sequence of evolutionary events that led to such great diversity in floral traits is unknown for most plant groups. Here, we characterize the patterns of evolution of individual floral traits and overall floral morphologies in the tribe Bignonieae (Bignoniaceae). We identified 12 discrete traits that are associated with seven floral types previously described for the group and used a penalized likelihood tree of the tribe to reconstruct the ancestral states of those traits at all nodes of the phylogeny of Bignonieae. In addition, evolutionary correlations among traits were conducted using a maximum likelihood approach to test whether the evolution of individual floral traits followed the correlated patterns of evolution expected under the ""pollination syndrome"" concept. The ancestral Bignonieae flower presented an Anemopaegma-type morphology, which was followed by several parallel shifts in floral morphologies. Those shifts occurred through intermediate stages resulting in mixed floral morphologies as well as directly from the Anemopaegma-type morphology to other floral types. Positive and negative evolutionary correlations among traits fit patterns expected under the pollination syndrome perspective, suggesting that interactions between Bignonieae flowers and pollinators likely played important roles in the diversification of the group as a whole.

Intercellular transport of epidermis-expressed MADS domain transcription factors and their effect on plant morphology and floral transition

P>During the lifetime of an angiosperm plant various important processes such as floral transition, specification of floral organ identity and floral determinacy, are controlled by members of the MADS domain transcription factor family. To investigate the possible non-cell-autonomous function of MADS domain proteins, we expressed GFP-tagged clones of AGAMOUS (AG), APETALA3 (AP3), PISTILLATA (PI) and SEPALLATA3 (SEP3) under the control of the MERISTEMLAYER1 promoter in Arabidopsis thaliana plants. Morphological analyses revealed that epidermal overexpression was sufficient for homeotic changes in floral organs, but that it did not result in early flowering or terminal flower phenotypes that are associated with constitutive overexpression of these proteins. Localisations of the tagged proteins in these plants were analysed with confocal laser scanning microscopy in leaf tissue, inflorescence meristems and floral meristems. We demonstrated that only AG is able to move via secondary plasmodesmata from the epidermal cell layer to the subepidermal cell layer in the floral meristem and to a lesser extent in the inflorescence meristem. To study the homeotic effects in more detail, the capacity of trafficking AG to complement the ag mutant phenotype was compared with the capacity of the non-inwards-moving AP3 protein to complement the ap3 mutant phenotype. While epidermal expression of AG gave full complementation, AP3 appeared not to be able to drive all homeotic functions from the epidermis, perhaps reflecting the difference in mobility of these proteins.

Floral development in the tribe Cedreleae (Meliaceae, sub-family Swietenioideae): Cedrela and Toona

Background and Aims Floral development of Cedrela and Toona, the genera comprising the basal tribe Cedreleae of the sub-family Swietenioideae of Meliaceae, is described. The focus was on three endangered, ecologically and economically important species: Cedrela fissilis, Cedrela odorata and Toona ciliata. The aims of the study were to characterize the patterns of floral development in the tribe and to establish apomorphic and plesiomorphic floral characters in relation to other taxa within the family based on the current molecular phylogeny of Meliaceae. Methods A detailed floral structural and developmental study was completed using both scanning electron microscopy and visualization of microtome sections with a light microscope. Key Results Twelve floral developmental stages were identified. The initial development of the pentamerous flowers of both Toona and Cedrela is strikingly similar. The morphological differences observed between them are due to differential patterns of organ elongation and adnation/connation occurring late in development. Additionally, the formation of functionally male and female flowers was found to occur at specific positions within the inflorescence. Conclusions Due to the basal position of the tribe Cedreleae in the phylogeny of Meliaceae, functionally either male or female pentamerous flowers and the presence of (at least partially) free stamens may be considered plesiomorphic traits within the family. In contrast, sympetaly and the absence of nectaries in Cedrela species are synapomorphies.

Inflorescence and floral development of Dahlstedtia species (Leguminosae: Papilionoideae: Millettieae)

Inflorescence and floral development of two tropical legume trees, Dahlstedtia pinnata and Dahlstedlia pentaphylla, occurring in the Atlantic Forest of south-eastern and southern Brazil, were investigated and compared with other papilionoids. Few studies have been made of floral development in tribe Millettieae, and this paper is intended to fill that gap in our knowledge. Dahlstedtia species have an unusual inflorescence type among legumes, the pseudoraceme, which comprises axillary units of three or more flowers, each with a subtending bract. Each flower exhibits a pair of opposite bractcoles. The order of flower initiation is acropetal; inception of the floral organs is as follows: sepals (5), petals (5), carpel (1) plus outer stamens (5) and finally inner stamens (5). Organ initiation in sepal, petal and inner stamen whorls is unidirectional; the carpel cleft is adaxial. The vexillum originates from a tubular-shaped primordium in mid-development and is larger than other petals at maturity, covering the keels. The filament tube develops later after initiation of inner-stamen primordia. Floral development in Dahlstedtia is almost always similar to other papilionoids, especially species of Phaseoleae and Sophoreae. But one important difference is the precocious ovule initiation (open carpel with ovules) in Dahlstedtia, the third citation of this phenomenon for papilionoids. No suppression, organ loss or anomalies occur in the order of primordia initiation or structure. Infra-generic differences in the first stages of ontogeny are rare; however, different species of Dahlstedtia are distinguished by the differing distribution pattern of secretory cavities in the flower. (C) 2009 Elsevier GmbH. All rights reserved.

Floral anatomy of the Lecointea clade (Leguminosae, Papilionoideae, Swartzieae sensu lato)

Flower and inflorescence anatomy and morphology of Exostyles, Harleyodendron, Holocalyx, Lecointea, and Zollernia (Leguminosae, Lecointea clade) were studied. Features common to all genera but otherwise rare within the Leguminosae include: (1) the presence of phenolic compounds in the epidermal cells of the anthers and subepidermal cells of the bracteoles, sepals, petals, and ovaries (absent in Holocalyx balansae); (2) simple trichomes on the adaxial base of the bracteoles and on the surface of the calyx and ovaries; and (3) tapetum persisting until the androspores are formed. Other notable anatomical features are: (1) colleters on the adaxial bases of the bracts and bracteoles of Holocalyx balansae and Zollernia ilicifolia; (2) trichomes on the anthers of Harleyodendron unifoliolatum, Holocalyx balansae, Lecointea hatschbachii, Zollernia ilicifolia and Z. magnifica; (3) osmophores on the petals of Exostyles godoyensis; (4) asynchronous pollen development in the anthers of Holocalyx balansae and Zollernia magnifica; and (5) vascular bundles surrounded by lignified fibers in Harleyodendron unifoliolatum. These anatomical characters are discussed according to their possible phylogenetic implications.

ELUCIDATING ENIGMATIC FLORAL ISSUES IN COPAIFERA LANGSDORFFII DESF. (LEGUMINOSAE, CAESALPINIOIDEAE)

This study focuses on the floral development of Copaifera langsdorffii to elucidate uncertain features in its floral morphology, such as the tetramerous calyx, lack of petals, blackened anthers and their supposed sterility, as well as polyembryony. Buds and flowers were dissected and prepared for examination under scanning electron and light microscopes. The floral apex initiates two bracteoles, five sepals, five petals, five outer stamens, five inner stamens, and one carpel. Order is helical for sepals, reversed unidirectional for the petals, and unidirectional for two whorls of stamens. The tetramerous calyx results from the union of two adaxial sepal primordia, which forms one large sepal and three other smaller sepals. Although the flower lacks petals, the petal primordia are initiated but do not elongate like the other floral organs, remaining as petal rudiments. Ten stamens are formed in two distinct whorls. Formation within each whorl is almost simultaneous, and the inner whorl is formed shortly after the outer. During organ elongation, the inner stamen primordia bases are reoriented outward, resulting in a single whorl of stamens. The darkened anthers have viable pollen grains. Thus, there is no relation between sterility and the dark coloration of the anthers. No signs of extranumerary embryos are observed; therefore, polyembryony is not confirmed. Although studies on floral development of Detarieae have been reported, few Neotropical genera of the tribe (such as Copaifera) have been studied.

Floral developmental morphology of three Indigofera species (Leguminosae) and its systematic significance within Papilionoideae

Inflorescence and floral development of three species of Indigofera (Leguminosae-Papilionoideae), I. lespedezioides, I. spicata, and I. suffruticosa, were investigated and compared with that of other papilionoid groups, especially with members of the recently circumscribed Millettioid clade, which was merged as sister to Indigofereae in a recent cladistic analysis. Although Indigofera is a genus of special interest, because of its great richness in species and its economic importance, few studies have been made of floral development in the genus or in Indigofereae as a whole. Flower buds and inflorescences were analysed at several stages of development in the three species. Our results confirmed that Indigofera species bear a usual inflorescence type among legumes, the raceme, which comprises flowers initiated in acropetal succession, each with a subtending bract and no bracteoles initiated. The inception of the floral organs is as follows: sepals (5), petals (5), carpel (1), outer stamens (5), and, finally, inner stamens (5). Organ initiation in the sepal, petal, and both stamen whorls is unidirectional, from the abaxial side; the carpel cleft is adaxial. The vexillum is larger than other petals at maturity, covering the keels, which are fused edge-to-edge. Nine filaments are fused to form an adaxially open sheath, and the adaxial stamen of the inner whorl remains free (diadelphous androecium) in the mid-stage of development. Most of the infra-generic differences occurred in the later stages of development. Data on floral development in Indigofera obtained here were also compared with those from other members of Papilionoideae. This comparison showed that the early expression of zygomorphy is shared with other members of the Millettioid clade but is rarely found in other papilionoids, corresponding to a hypothetically morphological synapomorphy in the pair Indigoferae plus millettioids.