JSTOR is a not-for-profit service that helps scholars, researchers, and students discover, use, and build upon a wide range of content in a trusted digital archive. We use information technology and tools to increase productivity and facilitate new forms of scholarship. For more information about JSTOR, please contact support@jstor.org. ABSTRACT Transmitting tissue in Ornithogalum is divided into three regions corresponding to classical divisions of the gynoecium: stigma, style, and ovary. The stigma differentiates from epidermal cells of the stylar apex. These cells form the stigmal papillae and have dense cytoplasm with abundant ER and lipid bodies. Papillae have walls with small transfer-ingrowths. At floral receptivity, papillae secrete a small amount of surface exudate. Epidermal cells of the style contain numerous spherosomes and have thin filaments of cytoplasm traversing the central vacuole. The stylar cortex is composed of 3-6 layers of parenchyma cells which contain numerous spherosomes and often have secondary vacuoles. Vascular tissue in the style consists of one collateral bundle in each lobe. Cells of the epidermal layer lining the stylar canal are secretory.They are initially vacuolate but fill progressively with dense cytoplasm as their secretory activity increases. Secretory activity occurs in three phases, each characterized by a particular organelle population and secretory product. At anthesis, the canal is filled with an exudate consisting of carbohydrate, protein, and lipid. In the ovary, the obturator differentiates from cells at the base of the funiculus and the tip of the carpel margins. It forms a pad of tissue which covers most of the former placenta. The obturator is secretory and produces a surface exudate. We believe our observations on Ornithogalum support the hypothesis that all transmitting tissue is of the same morphological origin and that it provides nutritive and chemotropic factors for pollen tube growth.

Seven types of chalazal modifications have been reported to occur as normal developmental changes in angiosperm ovules. Among them is the hypostase, a group of usually lignified cells. In Ornithogalum, hypostase differentiation becomes evident during the meiotic–mitotic interphase. Differentiation proceeds toward the micropylar end of the ovule at first but later becomes bidirectional. Differentiation is usually completed after the third mitotic division of the megagametophyte has occurred. One to three hypostase cells per ovule have what appears to be a nonstarch carbohydrate storage product. The greatest proportion of starch reserves in the mature ovule occurs in the chalazal end of the nucellus and, although the hypostase does not seem to be an important storage tissue, it probably has an integral function in the translocation of nutrients into the megagametophyte and, after fertilization, into the embryo sac.

The nucellar epidermis of Ornithogalum caudatum is modified in its micropylar region to form a nucellar cap. The cells become palisadelike with lignified walls and dense, RNA-rich cytoplasm and a large distal vacuole. High vesicular activity is associated with the greatly thickened proximal walls. The micropyle is formed by the inner integument and at anthesis, it is filled with an exudate secreted by the nucellar cap and inner integument. The exostomium is sealed by a hymen. The exudate and hymen probably function as surfaces for localized deposition of synergid-synthesized chemotropic agents. After fertilization the micropyle is occluded by a plug of flocculent material which appears to be more dense than the prefertilization material. This plug probably serves to preclude pathogen invasion and prevent desiccation of embryo and endosperm.

SUMMARYThe chalazal end of the egg projects beyond the synergids while the micropylar end is in contact with the nucellar epidermis. The egg nucleus and nucleolus are large and, along with most of the cytoplasm, are located chalazally while a large vacuole occupies the micropylar end. The egg cell wall is attenuated chalazally but, based on preliminary light microscope observations, it does appear to surround the entire cell in some cases. The synergids each have a large chalazal vacuole with the majority of their cytoplasm in the micropylar half of the cell. Nuclei and nucleoli are large and other organelles are numerous. Plastids and endoplasmic reticulum (ER) are more numerous chalazally while mitochondria appear to be evenly distributed. Filiform apparatus (FA) formation occurs late in synergid maturation. The FA is large, well developed, and is surrounded by a vacuolate zone. Various sized vesicles with fibrillar or flocculent contents occur within the FA. The FA stains for both protein and RNA in addition to carbohydrate which is the dominant component. The synergid walls have a knobbed ingrowth around the periphery of their micropylar end. Neither egg nor synergids store any metabolites.This information, coupled with overwhelming evidence from the literature reviewed, has led me to conclude all angiosperm synergids are active in synthesizing and, \ ia the FA, in secreting a substance(s) which influences the final phases of pollen tube growth. Movement of materials into a megagametophyte via the FA seems unlikely, but if it does occur, it is probably an inconsistent feature and only of trivial consequence.

Transmitting tissue in Ornithogalum is divided into three regions corresponding to classical divisions of the gynoecium: stigma, style, and ovary. The stigma differentiates from epidermal cells of the stylar apex. These cells form the stigmal papillae and have dense cytoplasm with abundant ER and lipid bodies. Papillae have walls with small transfer‐ingrowths. At floral receptivity, papillae secrete a small amount of surface exudate. Epidermal cells of the style contain numerous spherosomes and have thin filaments of cytoplasm traversing the central vacuole. The stylar cortex is composed of 3‐6 layers of parenchyma cells which contain numerous spherosomes and often have secondary vacuoles. Vascular tissue in the style consists of one collateral bundle in each lobe. Cells of the epidermal layer lining the stylar canal are secretory. They are initially vacuolate but fill progressively with dense cytoplasm as their secretory activity increases. Secretory activity occurs in three phases, each characterized by a particular organelle population and secretory product. At anthesis, the canal is filled with an exudate consisting of carbohydrate, protein, and lipid. In the ovary, the obturator differentiates from cells at the base of the funiculus and the tip of the carpel margins. It forms a pad of tissue which covers most of the former placenta. The obturator is secretory and produces a surface exudate. We believe our observations on Ornithogalum support the hypothesis that all transmitting tissue is of the same morphological origin and that it provides nutritive and chemotropic factors for pollen tube growth.