The stigma (pl.: stigmas or stigmata) [1] is the receptive tip of a carpel, or of several fused carpels, in the gynoecium of a flower.
The stigma (pl.: stigmas or stigmata) [1] is the receptive tip of a carpel, or of several fused carpels, in the gynoecium of a flower.
The stigma, together with the style and ovary (typically called the stigma-style-ovary system) comprises the pistil, which is part of the gynoecium or female reproductive organ of a plant. The stigma itself forms the distal portion of the style, or stylodia, and is composed of stigmatic papillae, the cells of which are receptive to pollen. These may be restricted to the apex of the style or, especially in wind pollinated species, cover a wide surface. [2]
The stigma receives pollen and it is on the stigma that the pollen grain germinates. Often sticky, the stigma is adapted in various ways to catch and trap pollen with various hairs, flaps, or sculpturings. [3] The pollen may be captured from the air (wind-borne pollen, anemophily), from visiting insects or other animals (biotic pollination), or in rare cases from surrounding water (hydrophily). Stigma can vary from long and slender to globe shaped to feathery. [4]
Pollen is typically highly desiccated when it leaves an anther. Stigma have been shown to assist in the rehydration of pollen and in promoting germination of the pollen tube. [5] Stigma also ensure proper adhesion of the correct species of pollen. Stigma can play an active role in pollen discrimination and some self-incompatibility reactions, that reject pollen from the same or genetically similar plants, involve interaction between the stigma and the surface of the pollen grain.
The stigma is often split into lobes, e.g. trifid (three lobed), and may resemble the head of a pin (capitate), or come to a point (punctiform). The shape of the stigma may vary considerably: [2]
The style is a narrow upward extension of the ovary, connecting it to the stigmatic papillae. Occasionally, it may be absent, in which case the stigma is described as sessile. Styles are generally tube-like—either long or short. [6] The style can be open (containing few or no cells in the central portion) with a central canal which may be filled with mucilage. Alternatively the style may be closed (densely packed with cells throughout). Most syncarpous monocots and some eudicots have open styles, while many syncarpous eudicots and grasses have closed (solid) styles containing specialised secretory transmitting tissue, linking the stigma to the centre of the ovary. This forms a nutrient rich tract for pollen tube growth. [4]
Where there are more than one carpel to the pistil, each may have a separate style-like stylodium, or share a common style. In irises and others in the family Iridaceae, the style divides into three petal-like (petaloid) style branches (sometimes also referred to as 'stylodia' [7] ), almost to the base of the style and is called a tribrachiate. [8] These are flaps of tissue, running from the perianth tube above the sepal. The stigma is a rim or edge on the underside of the branch, near the end lobes. [9] Style branches also appear on Dietes , Pardanthopsis and most species of Moraea . [10]
In Crocus , there are three divided style branches, creating a tube. [11] Hesperantha has a spreading style branch. Alternatively, the style may be lobed rather than branched. Gladiolus has a bi-lobed style branch (bilobate). Freesia , Lapeirousia , Romulea , Savannosiphon and Watsonia have bifurcated (two branched) and recurved style branches. [10] [2]
Asparagales is an order of plants in modern classification systems such as the Angiosperm Phylogeny Group (APG) and the Angiosperm Phylogeny Web. The order takes its name from the type family Asparagaceae and is placed in the monocots amongst the lilioid monocots. The order has only recently been recognized in classification systems. It was first put forward by Huber in 1977 and later taken up in the Dahlgren system of 1985 and then the APG in 1998, 2003 and 2009. Before this, many of its families were assigned to the old order Liliales, a very large order containing almost all monocots with colorful tepals and lacking starch in their endosperm. DNA sequence analysis indicated that many of the taxa previously included in Liliales should actually be redistributed over three orders, Liliales, Asparagales, and Dioscoreales. The boundaries of the Asparagales and of its families have undergone a series of changes in recent years; future research may lead to further changes and ultimately greater stability. In the APG circumscription, Asparagales is the largest order of monocots with 14 families, 1,122 genera, and about 36,000 species.
In botany, a fruit is the seed-bearing structure in flowering plants that is formed from the ovary after flowering.
Pollen is a powdery substance produced by most types of flowers of seed plants for the purpose of sexual reproduction. It consists of pollen grains, which produce male gametes. Pollen grains have a hard coat made of sporopollenin that protects the gametophytes during the process of their movement from the stamens to the pistil of flowering plants, or from the male cone to the female cone of gymnosperms. If pollen lands on a compatible pistil or female cone, it germinates, producing a pollen tube that transfers the sperm to the ovule containing the female gametophyte. Individual pollen grains are small enough to require magnification to see detail. The study of pollen is called palynology and is highly useful in paleoecology, paleontology, archaeology, and forensics. Pollen in plants is used for transferring haploid male genetic material from the anther of a single flower to the stigma of another in cross-pollination. In a case of self-pollination, this process takes place from the anther of a flower to the stigma of the same flower.
The stamen is the pollen-producing reproductive organ of a flower. Collectively, the stamens form the androecium.
Malvaceae, or the mallows, is a family of flowering plants estimated to contain 244 genera with 4225 known species. Well-known members of economic importance include okra, cotton, cacao, roselle and durian. There are also some genera containing familiar ornamentals, such as Alcea (hollyhock), Malva (mallow), and Tilia. The genera with the largest numbers of species include Hibiscus, Pavonia, Sida, Ayenia, Dombeya, and Sterculia.
In seed plants, the ovule is the structure that gives rise to and contains the female reproductive cells. It consists of three parts: the integument, forming its outer layer, the nucellus, and the female gametophyte in its center. The female gametophyte — specifically termed a megagametophyte — is also called the embryo sac in angiosperms. The megagametophyte produces an egg cell for the purpose of fertilization. The ovule is a small structure present in the ovary. It is attached to the placenta by a stalk called a funicle. The funicle provides nourishment to the ovule. On the basis of the relative position of micropyle, body of the ovule, chalaza and funicle, there are six types of ovules. (a) Orthotropous ovule - the micropyle, chalaza and funicle all lie in the same straight line, this is the most primitive type of ovule. Eg: Piper, Polygonum and Cycas.
Gynoecium is most commonly used as a collective term for the parts of a flower that produce ovules and ultimately develop into the fruit and seeds. The gynoecium is the innermost whorl of a flower; it consists of pistils and is typically surrounded by the pollen-producing reproductive organs, the stamens, collectively called the androecium. The gynoecium is often referred to as the "female" portion of the flower, although rather than directly producing female gametes, the gynoecium produces megaspores, each of which develops into a female gametophyte which then produces egg cells.
In botany, the style of an angiosperm flower is an organ of variable length that connects the ovary to the stigma. The style does not contain ovules; these are limited to the region of the gynoecium called the "ovary."
Parnassiaceae Gray were a family of flowering plants in the eudicot order Celastrales. The family is not recognized in the APG III system of plant classification. When that system was published in 2009, Parnassiaceae were treated as subfamily Parnassioideae of an expanded family Celastraceae.
In the flowering plants, an ovary is a part of the female reproductive organ of the flower or gynoecium. Specifically, it is the part of the pistil which holds the ovule(s) and is located above or below or at the point of connection with the base of the petals and sepals. The pistil may be made up of one carpel or of several fused carpels, and therefore the ovary can contain part of one carpel or parts of several fused carpels. Above the ovary is the style and the stigma, which is where the pollen lands and germinates to grow down through the style to the ovary, and, for each individual pollen grain, to fertilize one individual ovule. Some wind pollinated flowers have much reduced and modified ovaries.
Trochodendraceae is the only family of flowering plants in the order Trochodendrales. It comprises two extant genera, each with a single species along with up to five additional extinct genera and a number of extinct species. The living species are native to south east Asia. The two living species both have secondary xylem without vessel elements, which is quite rare in angiosperms. As the vessel-free wood suggests primitiveness, these two species have attracted much taxonomic attention.
Nectar is a viscous, sugar-rich liquid produced by plants in glands called nectaries or nectarines, either within the flowers with which it attracts pollinating animals, or by extrafloral nectaries, which provide a nutrient source to animal mutualists, which in turn provide herbivore protection. Common nectar-consuming pollinators include mosquitoes, hoverflies, wasps, bees, butterflies and moths, hummingbirds, honeyeaters and bats. Nectar plays a crucial role in the foraging economics and evolution of nectar-eating species; for example, nectar foraging behavior is largely responsible for the divergent evolution of the African honey bee, A. m. scutellata and the western honey bee.
Ruppia, also known as the widgeonweeds, ditch grasses or widgeon grass, is the only extant genus in the family Ruppiaceae, with eight known species. These are aquatic plants widespread over much of the world. The genus name honours Heinrich Bernhard Rupp, a German botanist (1688-1719). They are widespread outside of frigid zones and the tropics.
This page provides a glossary of plant morphology. Botanists and other biologists who study plant morphology use a number of different terms to classify and identify plant organs and parts that can be observed using no more than a handheld magnifying lens. This page provides help in understanding the numerous other pages describing plants by their various taxa. The accompanying page—Plant morphology—provides an overview of the science of the external form of plants. There is also an alphabetical list: Glossary of botanical terms. In contrast, this page deals with botanical terms in a systematic manner, with some illustrations, and organized by plant anatomy and function in plant physiology.
Tetrachondra is a plant genus and a member of the family Tetrachondraceae. It comprises two species of creeping succulent, perennial, aquatic or semi-aquatic herbaceous plants. Its distribution range is disjunct: one species is endemic to New Zealand while the other one is endemic to southern Patagonia and Tierra del Fuego. These plants bear essential oils.
This glossary of botanical terms is a list of definitions of terms and concepts relevant to botany and plants in general. Terms of plant morphology are included here as well as at the more specific Glossary of plant morphology and Glossary of leaf morphology. For other related terms, see Glossary of phytopathology, Glossary of lichen terms, and List of Latin and Greek words commonly used in systematic names.
In phylogenetic nomenclature, the Pentapetalae are a large group of eudicots that were informally referred to as the "core eudicots" in some papers on angiosperm phylogenetics. They comprise an extremely large and diverse group accounting for about 65% of the species richness of the angiosperms, with wide variability in habit, morphology, chemistry, geographic distribution, and other attributes. Classical systematics, based solely on morphological information, was not able to recognize this group. In fact, the circumscription of the Pentapetalae as a clade is based on strong evidence obtained from DNA molecular analysis data.
The monocots are one of the two major groups of flowering plants, the other being the dicots. In order to reproduce they utilize various strategies such as employing forms of asexual reproduction, restricting which individuals they are sexually compatible with, or influencing how they are pollinated. Nearly all reproductive strategies that evolved in the dicots have independently evolved in monocots as well. Despite these similarities and their close relatedness, monocots and dicots have distinct traits in their reproductive biologies.
Sexual selection is described as natural selection arising through preference by one sex for certain characteristics in individuals of the other sex. Sexual selection is a common concept in animal evolution but, with plants, it is oftentimes overlooked because many plants are hermaphrodites. Flowering plants show many characteristics that are often sexually selected for. For example, flower symmetry, nectar production, floral structure, and inflorescences are just a few of the many secondary sex characteristics acted upon by sexual selection. Sexual dimorphisms and reproductive organs can also be affected by sexual selection in flowering plants.
In botany, floral morphology is the study of the diversity of forms and structures presented by the flower, which, by definition, is a branch of limited growth that bears the modified leaves responsible for reproduction and protection of the gametes, called floral pieces.
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