Plant reproductive morphology
Among all living organisms, flowers, which are the reproductive structures of 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. The breeding system, or how the sperm from one plant fertilizes the ovum of another, depends on the reproductive morphology, and is the single most important determinant of the genetic structure of nonclonal plant populations. Christian Konrad Sprengel (1793) studied the reproduction of flowering plants and for the first time it was understood that the pollination process involved both biotic and abiotic interactions. Charles Darwin's theories of natural selection utilized this work to build his theory of evolution, which includes analysis of the coevolution of flowers and their insect pollinators.
Use of sexual terminologyEdit
This section relies largely or entirely upon a single source. (June 2021)
Plants have complex lifecycles involving alternation of generations. One generation, the sporophyte, gives rise to the next generation, the gametophyte asexually via spores. Spores may be identical (isospores) or come in different sizes (microspores and megaspores), but strictly speaking, spores and sporophytes are neither male nor female because they do not produce gametes. The alternate generation, the gametophyte, produces gametes, eggs and/or sperm. In bryophytes and isosporous vascular plants such as ferns, a gametophyte can be monoicous (bisexual), producing both eggs and sperm or dioicous (unisexual), either female (producing eggs) or male (producing sperm). In seed plants and other heterosporous species such as the Selaginellales the gametophytes are dioicous.
In the bryophytes (liverworts, mosses and hornworts), the sexual gametophyte is the dominant generation. In clubmosses, ferns and seed plants (including cycads, conifers, flowering plants, etc.) the sporophyte is the dominant generation. The obvious visible plant, whether a small herb or a large tree, is the sporophyte, and the gametophyte is very small. In bryophytes and ferns the gametophytes are independent, free-living plants. In seed plants, each female megagametophyte, and the megaspore that gives rise to it, is hidden within the sporophyte and is entirely dependent on it for nutrition. Each male gametophyte typically consists of from two to four cells enclosed within the protective wall of a pollen grain.
The sporophyte of a flowering plant is often described using sexual terms (e.g. "female" or "male") based on the sex of the gametophyte it gives rise to. For example, a sporophyte that produces spores that give rise only to male gametophytes may be described as "male", even though the sporophyte itself is asexual, producing only spores. Similarly, flowers produced by the sporophyte may be described as "unisexual" or "bisexual", meaning that they give rise to either one sex of gametophyte or both sexes of gametophyte.
Basic flower morphologyEdit
The flower is the characteristic structure concerned with sexual reproduction in flowering plants (angiosperms). Flowers vary enormously in their construction (morphology). A "complete" flower, like that of Ranunculus glaberrimus shown in the figure, has a calyx of outer sepals and a corolla of inner petals. The sepals and petals together form the perianth. Next inwards there are numerous stamens, which produce pollen grains, each containing a microscopic male gametophyte. Stamens may be called the "male" parts of a flower and collectively form the androecium. Finally in the middle there are carpels, which at maturity contain one or more ovules, and within each ovule is a tiny female gametophyte. Carpels may be called the "female" parts of a flower and collectively form the gynoecium.
Each carpel in Ranunculus species is an achene that produces one ovule, which when fertilized becomes a seed. If the carpel contains more than one seed, as in Eranthis hyemalis, it is called a follicle. Two or more carpels may be fused together to varying degrees and the entire structure, including the fused styles and stigmas may be called a pistil. The lower part of the pistil, where the ovules are produced, is called the ovary. It may be divided into chambers (locules) corresponding to the separate carpels.
A "perfect" flower has both stamens and carpels, and may be described as "bisexual" or "hermaphroditic". A "unisexual" flower is one in which either the stamens or the carpels are missing, vestigial or otherwise non-functional. Each flower is either "staminate" (having only functional stamens) and thus "male", or "carpellate" (or "pistillate") (having only functional carpels) and thus "female". If separate staminate and carpellate flowers are always found on the same plant, the species is called monoecious. If separate staminate and carpellate flowers are always found on different plants, the species is called dioecious. A 1995 study found that about 6% of angiosperm species are dioecious, and that 7% of genera contain some dioecious species.
Members of the birch family (Betulaceae) are examples of monoecious plants with unisexual flowers. A mature alder tree (Alnus species) produces long catkins containing only male flowers, each with four stamens and a minute perianth, and separate stalked groups of female flowers, each without a perianth. (See the illustration of Alnus serrulata.)
Most hollies (members of the genus Ilex) are dioecious. Each plant produces either functionally male flowers or functionally female flowers. In Ilex aquifolium (see the illustration), the common European holly, both kinds of flower have four sepals and four white petals; male flowers have four stamens, female flowers usually have four non-functional reduced stamens and a four-celled ovary. Since only female plants are able to set fruit and produce berries, this has consequences for gardeners. Amborella represents the first known group of flowering plants to separate from their common ancestor. It too is dioecious; at any one time, each plant produces either flowers with functional stamens but no carpels, or flowers with a few non-functional stamens and a number of fully functional carpels. However, Amborella plants may change their "sex" over time. In one study, five cuttings from a male plant produced only male flowers when they first flowered, but at their second flowering three switched to producing female flowers.
In extreme cases, all of the parts present in a complete flower may be missing, so long as at least one carpel or one stamen is present. This situation is reached in the female flowers of duckweeds (Lemna), which comprise a single carpel, and in the male flowers of spurges (Euphorbia) which comprise a single stamen.
A species such as Fraxinus excelsior, the common ash of Europe, demonstrates one possible kind of variation. Ash flowers are wind-pollinated and lack petals and sepals. Structurally, the flowers may be bisexual, consisting of two stamens and an ovary, or may be male (staminate), lacking a functional ovary, or female (carpellate), lacking functional stamens. Different forms may occur on the same tree, or on different trees. The Asteraceae (sunflower family), with close to 22,000 species worldwide, have highly modified inflorescences made up of flowers (florets) collected together into tightly packed heads. Heads may have florets of one sexual morphology – all bisexual, all carpellate or all staminate (when they are called homogamous), or may have mixtures of two or more sexual forms (heterogamous). Thus goatsbeards (Tragopogon species) have heads of bisexual florets, like other members of the tribe Cichorieae, whereas marigolds (Calendula species) generally have heads with the outer florets bisexual and the inner florets staminate (male).
Like Amborella, some plants undergo sex-switching. For example, Arisaema triphyllum (Jack-in-the-pulpit) expresses sexual differences at different stages of growth: smaller plants produce all or mostly male flowers; as plants grow larger over the years the male flowers are replaced by more female flowers on the same plant. Arisaema triphyllum thus covers a multitude of sexual conditions in its lifetime: nonsexual juvenile plants, young plants that are all male, larger plants with a mix of both male and female flowers, and large plants that have mostly female flowers. Other plant populations have plants that produce more male flowers early in the year and as plants bloom later in the growing season they produce more female flowers.
The complexity of the morphology of flowers and its variation within populations has led to a rich terminology.
- Androdioecious: having male flowers on some plants, bisexual ones on others.
- Androecious: having only male flowers (the male of a dioecious population); producing pollen but no seed.
- Androgynous: see bisexual.
- Androgynomonoecious: having male, female, and bisexual flowers on the same plant, also called trimonoecious.
- Andromonoecious: having both bisexual and male flowers on the same plant.
- Bisexual: each flower of each individual has both male and female structures, i.e. it combines both sexes in one structure. Flowers of this kind are called perfect, having both stamens and carpels. Other terms used for this condition are androgynous, hermaphroditic, monoclinous and synoecious.
- Dichogamous: having sexes developing at different times; producing pollen when the stigmas are not receptive, either protandrous or protogynous. This promotes outcrossing by limiting self-pollination. Some dichogamous plants have bisexual flowers, others have unisexual flowers.
- Diclinous: see Unisexual.
- Dioecious: having either only male or only female flowers. No individual plant of the population produces both pollen and ovules. (From the Greek for "two households". See also the Wiktionary entry for dioecious.)
- Gynodioecious: having hermaphrodite flowers and female flowers on separate plants.
- Gynoecious: having only female flowers (the female of a dioecious population); producing seed but not pollen.
- Gynomonoecious: having both bisexual and female flowers on the same plant.
- Hermaphroditic: see bisexual.
- Imperfect: (of flowers) having some parts that are normally present not developed, e.g. lacking stamens. See also Unisexual.
- Monoclinous: see bisexual.
- Monoecious: In the commoner narrow sense of the term, it refers to plants with unisexual flowers which occur on the same individual. In the broad sense of the term, it also includes plants with bisexual flowers. Individuals bearing separate flowers of both sexes at the same time are called simultaneously or synchronously monoecious and individuals that bear flowers of one sex at one time are called consecutively monoecious. (From the Greek monos "single" + oikia "house". See also the Wiktionary entry for monoecious.)
- Perfect: (of flowers) see bisexual.
- Polygamodioecious: mostly dioecious, but with either a few flowers of the opposite sex or a few bisexual flowers on the same plant.
- Polygamomonoecious: see polygamous. Or, mostly monoecious, but also partly polygamous.
- Polygamous: having male, female, and bisexual flowers on the same plant. Also called polygamomonoecious or trimonoecious. Or, with bisexual and at least one of male and female flowers on the same plant.
- Protandrous: (of dichogamous plants) having male parts of flowers developed before female parts, e.g. having flowers that function first as male and then change to female or producing pollen before the stigmas of the same plant are receptive. (Protoandrous is also used.)
- Protogynous: (of dichogamous plants) having female parts of flowers developed before male parts, e.g. having flowers that function first as female and then change to male or producing pollen after the stigmas of the same plant are receptive.
- Subandroecious: having mostly male flowers, with a few female or bisexual flowers.
- Subdioecious: having some individuals in otherwise dioecious populations with flowers that are not clearly male or female. The population produces normally male or female plants with unisexual flowers, but some plants may have bisexual flowers, some both male and female flowers, and others some combination thereof, such as female and bisexual flowers. The condition is thought to represent a transition between bisexuality and dioecy.
- Subgynoecious: having mostly female flowers, with a few male or bisexual flowers.
- Synoecious: see bisexual.
- Trimonoecious: see polygamous and androgynomonoecious.
- Trioecious: see polygamous.
- Unisexual: having either functionally male or functionally female flowers. This condition is also called diclinous, incomplete or imperfect.
This section needs additional citations for verification. (June 2021)
Outcrossing, cross-fertilization or allogamy, in which offspring are formed by the fusion of the gametes of two different plants, is the most common mode of reproduction among higher plants. About 55% of higher plant species reproduce in this way. An additional 7% are partially cross-fertilizing and partially self-fertilizing (autogamy). About 15% produce gametes but are principally self-fertilizing with significant out-crossing lacking. Only about 8% of higher plant species reproduce exclusively by non-sexual means. These include plants that reproduce vegetatively by runners or bulbils, or which produce seeds without embryo fertilization (apomixis). The selective advantage of outcrossing appears to be the masking of deleterious recessive mutations.
The primary mechanism used by flowering plants to ensure outcrossing involves a genetic mechanism known as self-incompatibility. Various aspects of floral morphology promote allogamy. In plants with bisexual flowers, the anthers and carpels may mature at different times, plants being protandrous (with the anthers maturing first) or protogynous (with the carpels maturing first). Monoecious species, with unisexual flowers on the same plant, may produce male and female flowers at different times.
Dioecy, the condition of having unisexual flowers on different plants, necessarily results in outcrossing, and might thus be thought to have evolved for this purpose. However, "dioecy has proven difficult to explain simply as an outbreeding mechanism in plants that lack self-incompatibility". Resource-allocation constraints may be important in the evolution of dioecy, for example, with wind-pollination, separate male flowers arranged in a catkin that vibrates in the wind may provide better pollen dispersal. In climbing plants, rapid upward growth may be essential, and resource allocation to fruit production may be incompatible with rapid growth, thus giving an advantage to delayed production of female flowers. Dioecy has evolved separately in many different lineages, and monoecy in the plant lineage correlates with the evolution of dioecy, suggesting that dioecy can evolve more readily from plants that already produce separate male and female flowers.
- Barrett, S.C.H. (2002). "The evolution of plant sexual diversity" (PDF). Nature Reviews Genetics. 3 (4): 274–284. doi:10.1038/nrg776. PMID 11967552. S2CID 7424193.
- Hickey, M. & King, C. (2001). The Cambridge Illustrated Glossary of Botanical Terms. Cambridge University Press.
- Sporne 1974, pp. 14–15.
- Whittemore, Alan T. "Ranunculus". Flora of North America. Retrieved 2013-03-04 – via www.eFloras.org.
- Sporne 1974, pp. 125–127.
- Beentje, Henk (2010). The Kew Plant Glossary. Richmond, Surrey: Royal Botanic Gardens, Kew. ISBN 978-1-84246-422-9.
- Renner, S.S. & Ricklefs, R.E. (1995). "Dioecy and its correlates in the flowering plants". American Journal of Botany. 82 (5): 596–606. doi:10.2307/2445418. JSTOR 2445418.
- Stace 2010, pp. 292–296.
- Stace 2010, p. 669.
- Buzgo, Matyas; Soltis, Pamela S. & Soltis, Douglas E. (2004). "Floral Developmental Morphology of Amborella trichopoda (Amborellaceae)". International Journal of Plant Sciences. 165 (6): 925–947. doi:10.1086/424024. S2CID 84793812.
- Sporne 1974, pp. 15–16.
- Barkley, Theodore M.; Brouillet, Luc & Strother, John L. "Asteraceae". Flora of North America. Retrieved 2013-03-04 – via www.eFloras.org.
- Barkley, Theodore M.; Brouillet, Luc & Strother, John L. "Chichorieae". Flora of North America. Retrieved 2013-03-04 – via www.eFloras.org.
- Strother, John L. "Calendula". Flora of North America. Retrieved 2013-03-04 – via www.eFloras.org.
- Ewing, J.W. & Klein, R.M. (1982). "Sex Expression in Jack-in-the-Pulpit". Bulletin of the Torrey Botanical Club. 109 (1): 47–50. doi:10.2307/2484467. JSTOR 2484467.
- Janick, J. (2010). Plant Breeding Reviews. Wiley. ISBN 9780470650028.
- Stace, H.M. (1995). "Protogyny, Self-Incompatibility and Pollination in Anthocercis gracilis (Solanaceae)". Australian Journal of Botany. 43 (5): 451–459. doi:10.1071/BT9950451.
- Baskauf, Steve (2002). "Sexual systems in angiosperms". Archived from the original on 2018-07-03. Retrieved 2013-02-27.
- "Gynodioecious". Dictionary of Botany. Retrieved 2013-04-10.
- G. J. H. Grubben (2004). Vegetables. PROTA. pp. 255–. ISBN 978-90-5782-147-9.
- Cook 1968, p. 131.
- Dinesh Kumar (20 August 2008). Definitional Glossary of Agricultural Terms. I. K. International Pvt Ltd. pp. 115–. ISBN 978-81-906757-4-1.
- Geber, Monica A. (1999). Gender and sexual dimorphism in flowering plants. Berlin: Springer. ISBN 3-540-64597-7. p. 4
- Testolin, R; Cipriani, G; Costa, G (May 1995). "Sex segregation ratio and gender expression in the genus Actinidia". Sexual Plant Reproduction. 8. doi:10.1007/BF00242255. Retrieved 30 December 2020.
- Olson, Matthew S. & Antonovics, Janis (2000). "Correlation between male and female reproduction in the subdioecious herb Astilbe biternata (Saxifragaceae)". American Journal of Botany. 87 (6): 837–44. doi:10.2307/2656891. JSTOR 2656891. PMID 10860914.
- Strittmatter, L.I.; Negrón-Ortiz, V. & Hickey, R.J. (2002). "Subdioecy in Consolea spinosissima (Cactaceae): breeding system and embryological studies". American Journal of Botany. 89 (9): 1373–1387. doi:10.3732/ajb.89.9.1373. PMID 21665739.
- Bernstein, C. & Bernstein, H. (1991). Aging, Sex, and DNA Repair. San Diego: Academic Press. ISBN 978-0-12-092860-6.
- Cook, J. Gordon (1968). ABC of plant terms. Watford, UK: Merrow. OCLC 474319451.
- Sporne, K.R. (1974). The Morphology of Angiosperms. London: Hutchinson. ISBN 978-0-09-120611-6.
- Stace, Clive (2010). New Flora of the British Isles (3rd ed.). Cambridge, UK: Cambridge University Press. ISBN 978-0-521-70772-5.
- Media related to Plant reproductive morphology at Wikimedia Commons
- Images of sexual systems in flowering plants at bioimages.vanderbilt.edu