Flower and inflorescence development of Moraceae species.

Author(s)

Viviane Gonçalves Leite

• Document type: Doctoral Thesis
• Press: Ribeirão Preto.
• Institution: Universidade de São Paulo (USP). Faculdade de Filosofia, Ciências e Letras de Ribeirão Preto (PCARP/BC)
• Defense date: 2016-11-04

Examining board members

Simone de Pádua Teixeira; Silvia Rodrigues Machado; Vidal de Freitas Mansano; Juliana Villela Paulino; Léo Correia da Rocha Filho

• Advisor: Simone de Pádua Teixeira

Abstract

The flowers of the species of Moraceae are diclinous (= unisexual), achlamydeous or monochlamydeous, small, drawing attention the gynoecium for being unilocular and uniovular but with tubular shape in the course of development, a result of pseudomonomery. These flowers are inserted in structurally diverse inflorescences, and show different pollination syndromes. The objectives of this study were to clarify the pathways that cause the different forms of inflorescences, and to elucidate enigmatic floral conditions as the absence of perianth and pseudomonomerous gynoecium in Moraceae, by using seven species of different lineages of the family as study models: Brosimum gaudichaudii, Castilla elastica, Clarisia ilicifolia, Ficus citrifolia, F. pertusa, Maclura tinctoria and Morus nigra. Infllorescences, buds and flowers in several developmental stages were prepared for examination under scanning electron and light microscopies. The meristem of the inflorescence is similar in shape among the species only in the early stages of development. In Ficus pertusa the inflorescence closes along the margins due to the presence of orobracts. The inflorescence of the Castilla elastica forms a central depression (pistillate inflorescence) and may become bivalvar (staminate inflorescence), being surrounded by involucral bracts. In Brosimum gaudichaudii the meristem becomes flat, and the staminate and pistillate flowers are immersed in the receptacle and covered by interfloral bracts; in Clarisia ilicifolia and Maclura tinctoria the meristem of the staminate and pistillate inflorescences becomes flat and lengthens, however, the pistillate inflorescence acquires a globose shape; in Morus nigra the meristem is elongated. Interfloral bracts are absent only in Morus nigra. The floral morphology and development differ among the species studied especially in terms of number of floral organs. The perianth consists of robust green sepals, present in the majority of the species studied, with the exception of Brosimum gaudichaudii, whose staminate flower exhibits a bract involving the floral organs and the pistillate flower is achlamydeous, as well as the staminate flower of Castilla elastica. In all species the sepals vary in number (two to five), and show asynchronous initiation. There is no initiation of petal primordia, individualized or originated from division of stamen primordia. The stamen primordia initiated in the staminate flower (1-5, depending on the species) become functional; so there is no stamen abortion in the staminate flower. The pistillate flower of Castilla elastica rarely initiates staminodes. The anatomical structure of the sepals and stamens varies among species, representing possible adaptations to the entomophily or anemophily described for the family. The epidermis may have glandular and/or non glandular trichomes, depending on the species. The mesophyll varies in number of layers in the species, and this variation is reflected in the union of the organs. Laticifers and crystal and phenolic idioblasts occur in the mesophyll of the sepals and connective of the stamens in all species, probably acting on flower protection against herbivores and UV radiation. The stamens vary in terms of filament and connective shape. In the staminate flowers of Morus nigra and Maclura tinctoria the cells of the mesophyll are larger with intercellular spaces; and in the final structure of the flower, the four sepals are accompanied by inflexed stamens and a pistillode, which compose a complex structure that acts in the pollen grain dispersal. The pseudomonomerous gynoecium is transformed into pistillodes in the staminate flowers of Maclura tinctoria and Morus nigra. The carpel initiates as a single central primordium which divides and originates two others, which elongate asymmetrically. The next stages differ among species and have been summarized in two ontogenetic pathways: (1) the total contribution of the two carpels in the formation of the ovary, style and stigma, however, in only one of the carpels an ovule arises at the single locule - found in most species. (2) Partial contribution of the two carpels, wherein the carpel with greater length participates in the formation of the ovary, style, stigma and ovule, while the carpel with shortest length is only involved in the formation of ovary - found in Maclura tinctoria. The species of Moraceae share early stages of development of the inflorescence, the perianth, androecium and pseudomonomerous gynoecium, and the main differences occur in the intermediate stages, which alters the structure of the flower and inflorescence. These developmental pathways seem to be stable within the urticalean rosids and contribute to the reduction of the floral structure in this group. (AU)

• FAPESP's process: 12/15644-8 - Flower and inflorescence development in species of Moraceae
• Grantee: Viviane Gonçalves Leite
• Support Opportunities: Scholarships in Brazil - Doctorate