The stigma plays several roles such as pollen hydration and selection, and pollen tube nutrition. In the Ficus-fig wasp mutualism, stigmata have an additional, almost unknown, function by representing a physical interface for both plant and wasp reproduction. We used light and electron microscopy to compare the detailed morphology of the stigmata of nine Ficus species of different sections and with different pollination modes and sexual expressions. Figs were collected at the stage when the stigmata were receptive for pollination. Stigmata in actively pollinated monoecious species have well developed papillae concentrated on the adaxial surface exposed towards the fig cavity. Conversely, the passively pollinated monoecious species have the whole surface of the stigmata covered by somewhat smaller papillae. In both actively and passively pollinated monoecious species these features are consistent, irrespective of style length. In all actively pollinated gynodioecious species, the stigmata of pistillate flowers were tubular or infundibuliform whereas in almost all actively pollinated monoecious species (except F. racemosa) the stigmata were filiform, with one branch or two asymmetric branches. In gynodioecious species the short-styled flowers in "male" figs show a limited receptive surface with small papillae, while the stigmata of long-styled flowers in "female" figs are covered by papillae that extend down the sides of the style, increasing the stigmatic surface. In actively pollinated species, stigmata are cohesive, forming a common surface for pollen tube germination (= synstigma). The synstigma arrangement was quite variable: lax, cohesive or very cohesive, with entanglement by stigmatic papillae and stylar trichomes. Entanglement by stylar trichomes is common in gynodioecious species. The synstigma arrangement did not correlate with phylogeny or breeding system. This study is the first to report a very loose synstigma in actively pollinated monoecious Ficus species. Our analyses revealed that, in Ficus, the synstigma is functionally analogous to an extra-gynoecial compitum. Comparative studies will be required to test further hypotheses about the evolutionary determinants of such variation.

Pollen transport to a receptive stigma can be facilitated through different pollinators, which submits the pollen to different selection pressures. This study aimed to associate pollen and stigma morphology with zoophily in species of the tribe Phaseoleae. Species of the genera Erythrina, Macroptilium and Mucuna with different pollinators were chosen. Pollen grains and stigmas were examined under light microscopy (anatomy), scanning electronic microscopy (surface analyses) and transmission electronic microscopy (ultrastructure). The three genera differ in terms of pollen wall ornamentation, pollen size, pollen aperture, thickness of the pollen wall, amount of pollenkitt, pollen hydration status and dominant reserves within the pollen grain, while species within each genus are very similar in most studied characteristics. Most of these features lack relationships to pollinator type, especially in Erythrina and Mucuna. Pollen reserves are discussed on a broad scale, according to the occurrence of protein in the pollen of invertebrate- or vertebrate-pollinated species. Some pollen characteristics are more associated to semi-dry stigma requirements. This apical, compact, cuticularised and secretory stigma occurs in all species investigated. We conclude that data on pollen and stigma structure should be included together with those on floral morphology and pollinator behaviour for the establishment of functional pollination classes.

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The synstigma is a structure formed by clusters of two to several stigmas, whether in the same or between different flowers. Although rare in angiosperms, synstigmas are found in c. 500 out of the c. 750 Ficus spp. (Moraceae). This floral structure is associated with fig-fig wasp pollinating mutualism. The synstigma structure and pollen tube pathways were studied in six Ficus spp. from Ficus section Americanae to test the hypothesis that the synstigma allows pollen grains deposited on a stigma to emit pollen tubes that can grow laterally and fertilize surrounding flowers. Syconia containing recently pollinated stigmas were collected and dissected, and the stigmas were processed for analyses with light and scanning and transmission electron microscopy. The arrangement of the synstigmas across species can be spaced or congested, with the number of stigmas per synstigma ranging from two to 20. Contact between the stigmas in a synstigma occurs by the intertwining of the stigmatic branches and papillae; their union is firm or loose. The pollen tube grows through live cells of the transmitting tissue until reaching the ovule micropyle. Curved pollen tubes growing from one stigma to another were observed in five out of the six species studied. The curvilinear morphology of pollen tubes probably results from competition by pollen between the stigmas composing a synstigma via chemotropic signals. The synstigma appears to be a key adaptation that ensures seed production by flowers not exploited by the fig wasps in actively pollinated Ficus spp.

Changes in ovary position of Melastomataceae are due to intercalary meristematic activity, which is one of the main mechanisms for the origin of morphological innovations among plants. Our data illustrate the importance of the intercalary meristems in floral development, and we discuss the implications of this ontogenetic model for understanding the evolution of ovary position in Melastomataceae.

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