Floral ontogeny and anatomy of the shrub Gaiadendron punctatum and a comparison of floral characters in the tribes Gaiadendrinae and Nuytsiae (Loranthaceae)

Introducction: Gaiadendron punctatum is a hemiparasitic species of Loranthaceae (Tribe Gaiadendreae) that is widely distributed in mountainous regions of Central and South America. Embryological and phylogenetic studies in the family indicate a trend towards reduction of the gynoecium and ovules, the morphology of which supports the current circumscription of Tribe Gaiadendreae (Gaiadendron and Atkinsonia). Molecular phylogenetic studies suggest that Nuytsia, Atkinsonia and Gaiadendron diverged successively, forming a grade at the base of the Loranthaceae, but support values are low. Objetive: In the present study, the floral anatomy of Gaiadendron punctatum was investigated in order to provide additional data to permit comparisons among the three basal-most genera in the Loranthaceae and reevaluate their relationships. Methods: Flowers of G. punctatum were collected at different developmental stages and serial sections were prepared and analyzed by light microscopy. Results: Inflorescence development is acropetal; the flowers are bisexual with an inferior ovary surmounted by a calyculus, a ring-shaped structure lacking vascular tissue; the ovary is comprised of seven basal locules, each with an ategmic, tenuinucellate ovule. Above the locules is a mamelon that is fused with the adjacent tissues. The androecium is comprised of seven epipetalous stamens, the anthers with fibrous endothecium dehiscence through a single longitudinal slit, releasing tricolpated pollen. Conclusions: The results of this study show that Gaiadendron and Atkinsonia share versatile, dorsifixed anthers, while Gaiadendron and Nuytsia share the same mode of anther dehiscence. On the other hand, Gaiadendron shares with members of Tribe Elytrantheae an amyliferous mamelon and an unvascularized calyculus. Combined phylogenetic analyses of morphological and molecular data are desirable to determine whether Tribe Gaiadendreae comprises a clade, a grade or if the two genera are more distantly related.

Pitfall Flower Development and Organ Identity of Ceropegia sandersonii (Apocynaceae-Asclepiadoideae)

Deceptive Ceropegia pitfall flowers are an outstanding example of synorganized morphological complexity. Floral organs functionally synergise to trap fly-pollinators inside the fused corolla. Successful pollination requires precise positioning of flies headfirst into cavities at the gynostegium. These cavities are formed by the corona, a specialized organ of corolline and/or staminal origin. The interplay of floral organs to achieve pollination is well studied but their evolutionary origin is still unclear. We aimed to obtain more insight in the homology of the corona and therefore investigated floral anatomy, ontogeny, vascularization, and differential MADS-box gene expression in Ceropegia sandersonii using X-ray microtomography, Light and Scanning Electronic Microscopy, and RT-PCR. During 10 defined developmental phases, the corona appears in phase 7 at the base of the stamens and was not found to be vascularized. A floral reference transcriptome was generated and 14 MADS-box gene homologs, representing all major MADS-box gene classes, were identified. B- and C-class gene expression was found in mature coronas. Our results indicate staminal origin of the corona, and we propose a first ABCDE-model for floral organ identity in Ceropegia to lay the foundation for a better understanding of the molecular background of pitfall flower evolution in Apocynaceae.

Floral development and anatomy of two species of Aechmea (Bromeliaceae, Bromelioideae)

Aechmea (Bromeliaceae) is a large genus with controversial systematics and distinct flower shapes and pollinators. We explored floral anatomy and development in two Aechmea spp. belonging to different subgenera to contribute useful information on reproductive biology and taxonomy. We examined floral buds using scanning electron and light microscopy to characterize the development of septal nectaries, petal appendages, ovules, stamens and carpels. In A. gamosepala, we confirmed that the petal appendages develop late, whereas in A. correia-araujoi they develop earlier during floral development. Petal appendage formation included positional changes, possibly affecting floral attributes and visitation by insects, rather than vertebrates. Nectar is released through three basal orifices distally on the ovary, and here we document the link between the nectary region, through discrete canals, upward to the conduplicate lobes of the wet stigma. Improved understanding of the floral development and morphology of Aechmea may help to explain the existence of polymorphic flowers in this genus and may have implications for studies on interactions with pollinators and systematics.

Floral anatomy of Tristerix longebracteatus (Loranthaceae)

Introduction: Most of the New World members of the Loranthaceae comprise a clade that corresponds to the tribe Psittacantheae. Previous studies on floral anatomy and development in this tribe have concentrated on the highly diversified subtribe Psittacanthinae, while the smaller subtribe Ligarineae has received less attention. A detailed anatomical description of Tristerix longebracteatus helps to fill this information gap. Objetive: The present research analyzes the anatomy of Tristerix longebracteatus flowers, detailing the structure of androecium and gynoecium, including megasporogenesis and microsporogenesis. Methodology: Anatomical serial sections of flowers at different stages of development were prepared, following processing with fixation techniques, incorporation in paraffin, microtome sectioning and staining with Astra-blue and basic fuchsin. Results: The large-sized flowers of Tristerix longebracteatus present a complex pattern of vascularization with 18-20 vascular bundles at the base of the inferior ovary. A group of three vascular bundles irrigate the 4-5 petals and associated stamens, and ten bundles continue through the gynoecium. The androecium is composed of four or five anthers with simultaneous microsporogenesis. The gynoecium as a single ovarian cavity with a central mamelon in which the archesporial tissue is oriented towards the style. The base of the style forms a nectary similar to that found in the sister genus Ligaria. Conclusions: The gynoecium with a single ovarian cavity and central mamelon is a condition shared by Tristerix (subtribe Ligarinae) and all the genera of the subtribe Psittacanthinae, except Tripodanthus. The base of the style forms a nectary similar to that found in the sister genus Ligaria. This type of stylar nectary is of taxonomic value for grouping species of the subtribe Ligarinae and difers from the annular nectary of subtribe Psittacanthinae.

Floral anatomy of the plant Psittacanthus schiedeanus (Loranthaceae)

Anatomía floral de la planta Psittacanthus schiedeanus (Loranthaceae). Loranthaceae hemiparasitic family comprises 76 genera and about 1 050 species distributed in temperate and tropical regions. The subtribe Psittacanthinae contains 14 genera of neotropical mistletoe including Psittacanthus with over 120 species, characterized by large, brightly colored (red, orange, yellow) flowers that are mostly pollinated by hummingbirds. During the 20th century, a number of morphological and embryological studies were conducted mainly on Old World Loranthaceae genera. More recently, attention has been focused on neotropical Psittacanthinae where among the 14 genera, floral anatomy has been examined in only seven. The aim of this study is to describe the floral anatomy of Psittacanthus schiedeanus and compares the results with those derived from related mistletoe, interpreting the variation of the floral characters of the calyculus, nectary, gynoecium and from floral dissections and serial histological sections, detailing the structure of androecium and gynoecium and anthers in the context of the new phylogenetic information. Flowers of P. schiedeanus at different developmental stages were examined using stained serial sections visualized with light microscopy. These flowers have a vascularized, cupular pedicel fused to a bracteole, a non-vascularized calyculus, an annular nectary, a unilocular gynoecium with a single central mamelon and an androecium formed by epipetalous septate stamens. The morphological comparison of pedicel, bracteole and calyculus provides support for the interpretation of the calyculus as a reduced calyx. The annular nectary seems to be a character shared by the entire subtribe Psittacanthinae, which distinguishes it from Ligarinae which has stylar nectary. The unilocular gynoecium formed by a single central structure is a character shared with other genera in Psittacanthinae except Tripodanthus. The androecium is composed of dithecal, tetrasporangiate stamens with septate locules that are here considered an adaptation for pollen releasing over an extended time period rather than previous suggestions that they result from evolutionary pressure to reduce anther size or to facilitate the nutrition of microspores in large anthers.

Floral development and anatomy of Macarthuria australis (Macarthuriaceae): key to understanding the unusual initiation sequence of Caryophyllales

We investigated the floral anatomy and development of Macarthuria australis Hügel ex Endl., an unusual genus endemic to Australia, in the context of floral evolution of core Caryophyllales. Flower initiation is spiral, with sepals developing quincuncially. The first two petals continue the sequence of sepal initiation, but the remaining petals arise from common stamen–petal primordia. The androecium develops sequentially as three inner antesepalous and five outer antepetalous stamens. The globular ovary is trimerous with a short symplicate zone and two arillate ovules per locule. The rapid emergence of the androecium leads to a partial absorption of the petal primordia within the androecial tissue. The two first-formed petals have more room for development and precede the androecium, supporting the fact that petals are not staminodial in origin. This heterochronic shift correlates with an inversed developmental sequence of the antesepalous stamens. The constraint caused by the spatial occupation of sepals and carpels leads to the loss of two stamens, and the re-arrangement of stamens and petals along the flanks of the carpels. The floral development of Macarthuria anticipates a syndrome of stamen and petal development in other core Caryophyllales and culminating in the Caryophyllaceae.