Plant reproductive morphology in the context of "Carpel"

⭐ In the context of Plant reproductive morphology, the gynoecium is primarily distinguished by its role in which process?

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⭐ Core Definition: Plant reproductive morphology

Plant reproductive morphology is the study of the physical form and structure (the morphology) of those parts of plants directly or indirectly concerned with sexual reproduction.

Among all living organisms, flowers, which are the reproductive structures of flowering plants (angiosperms), are the most varied physically and show a correspondingly great diversity in methods of reproduction. Plants that are not flowering plants (green algae, mosses, liverworts, hornworts, ferns and gymnosperms such as conifers) also have complex interplays between morphological adaptation and environmental factors in their sexual reproduction.

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👉 Plant reproductive morphology in the context of Carpel

Gynoecium (/ɡˈnsi.əm, ɪˈnʃi.əm/; from Ancient Greek γυνή (gunḗ) 'woman, female' and οἶκος (oîkos) 'house', pl. gynoecia) 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 (one or more) 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 (i.e. egg cells), the gynoecium produces megaspores, each of which develops into a female gametophyte which then produces egg cells.

The term gynoecium is also used by botanists to refer to a cluster of archegonia and any associated modified leaves or stems present on a gametophyte shoot in mosses, liverworts, and hornworts. The corresponding terms for the male parts of those plants are clusters of antheridia within the androecium. Flowers that bear a gynoecium but no stamens are called pistillate or carpellate. Flowers lacking a gynoecium are called staminate.

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Plant reproductive morphology in the context of Teak

Teak (Tectona grandis) is a tropical hardwood tree species in the family Lamiaceae. It is a large, deciduous tree that occurs in mixed hardwood forests. Tectona grandis has small, fragrant white flowers arranged in dense clusters (panicles) at the end of the branches. These flowers contain both types of reproductive organs (perfect flowers). The large, papery leaves of teak trees are often hairy on the lower surface. Teak wood has a leather-like smell when it is freshly milled and is particularly valued for its durability and water resistance. The wood is used for boat building, exterior construction, veneer, furniture, carving, turnings, and various small projects.

Tectona grandis is native to south and southeast Asia, mainly Bangladesh, India, Indonesia, Malaysia, Myanmar, Thailand, and Sri Lanka, but is naturalised and cultivated in many countries in Africa and the Caribbean. Myanmar's teak forests account for nearly half of the world's naturally occurring teak. Molecular studies show that there are two centres of the genetic origin of teak: one in India and the other in Myanmar and Laos.

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Plant reproductive morphology in the context of Sex cells

A germ cell is any cell that gives rise to the gametes of an organism that reproduces sexually. In many animals, the germ cells originate in the primitive streak and migrate via the gut of an embryo to the developing gonads. There, they undergo meiosis, followed by cellular differentiation into mature gametes, either eggs or sperm. Unlike animals, plants do not have germ cells designated in early development. Instead, germ cells can arise from somatic cells in the adult, such as the floral meristem of flowering plants.

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Plant reproductive morphology in the context of Zelkova

Zelkova (from the Georgian dzelkva, 'stone pillar') is a genus of six species of deciduous trees in the elm family Ulmaceae, native to southern Europe, and southwest and eastern Asia. They vary in size from shrubs (Z. sicula) to large trees up to 35 m (115 ft) tall (Z. carpinifolia). The bark is smooth, dark brown. Unlike elms, the branchlets are never corky or winged. The leaves are alternate, with serrated margins, and (unlike the related elms) a symmetrical base to the leaf blade. The leaves are in two distinct rows; they have pinnate venation and each vein extends to the leaf margin, where it terminates in a tooth. There are two stipules at each node, though these are caducous (shed early), leaving a pair of scars at the leaf base. Zelkova is polygamous. Staminate flowers are clustered in the lower leaf axils of young branchlets; the perianth is campanulate, with four to six (to seven) lobes, and the stamens are short. Pistillate and hermaphrodite flowers are solitary, or rarely in clusters of two to four, in the upper leaf axils of young branchlets. The fruit is a dry, nut-like drupe with a dorsal keel, produced singly in the leaf axils. The perianth and stigma are persistent.

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