Search for LIMS content across all our Wiki Knowledge Bases.
Type a search term to find related articles by LIMS subject matter experts gathered from the most trusted and dynamic collaboration tools in the laboratory informatics industry.
Flowering plants are plants that bear flowers and fruits, and form the cladeAngiospermae (/ˌændʒiəˈspərmiː/).[5][6] The term 'angiosperm' is derived from the Greek words ἀγγεῖον / angeion ('container, vessel') and σπέρμα / sperma ('seed'), meaning that the seeds are enclosed within a fruit. The group was formerly called Magnoliophyta.[7]
Angiosperms are terrestrial vascular plants; like the gymnosperms, they have roots, stems, leaves, and seeds. They differ from other seed plants in several ways.
Reduced gametophytes, three cells in male, seven cells with eight nuclei in female (except for basal angiosperms)[10]
The gametophytes are smaller than those of gymnosperms.[11] The smaller size of the pollen reduces the time between pollination and fertilization, which in gymnosperms is up to a year.[12]
Endosperm forms after fertilization but before the zygote divides. It provides food for the developing embryo, the cotyledons, and sometimes the seedling.[13]
Open vessel elements are stacked end to end to form continuous tubes, whereas gymnosperm xylem is made of tapered tracheids connected by small pits.[15]
Wolffia arrhiza, a rootless floating freshwater plant under 2 mm across
The largest angiosperms are Eucalyptus gum trees of Australia, and Shorea faguetiana, dipterocarp rainforest trees of Southeast Asia, both of which can reach almost 100 metres (330 ft) in height.[16] The smallest are Wolffia duckweeds which float on freshwater, each plant less than 2 millimetres (0.08 in) across.[17]
Photosynthetic and parasitic
Gunnera captures sunlight for photosynthesis over the large surfaces of its leaves, which are supported by strong veins.
Considering their method of obtaining energy, some 99% of flowering plants are photosyntheticautotrophs, deriving their energy from sunlight and using it to create molecules such as sugars. The remainder are parasitic, whether on fungi like the orchids for part or all of their life-cycle,[18] or on other plants, either wholly like the broomrapes, Orobanche, or partially like the witchweeds, Striga.[19]
Hot, cold, wet, dry, fresh, salt
Carnegiea gigantea, the saguaro cactus, grows in hot dry deserts in Mexico and the southern United States.
Dryas octopetala, the mountain avens, lives in cold arctic and montane habitats in the far north of America and Eurasia.
Nelumbo nucifera, the sacred lotus, grows in warm freshwater across tropical and subtropical Asia.
Zostera seagrass grows on the seabed in sheltered coastal waters.
In terms of their environment, flowering plants are cosmopolitan, occupying a wide range of habitats on land, in fresh water and in the sea. On land, they are the dominant plant group in every habitat except for frigid moss-lichen tundra and coniferous forest.[20] The seagrasses in the Alismatales grow in marine environments, spreading with rhizomes that grow through the mud in sheltered coastal waters.[21]
Gentiana verna, the spring gentian, flourishes in dry limestone habitats.[23]
Some specialised angiosperms are able to flourish in extremely acid or alkaline habitats. The sundews, many of which live in nutrient-poor acid bogs, are carnivorous plants, able to derive nutrients such as nitrate from the bodies of trapped insects.[22] Other flowers such as Gentiana verna, the spring gentian, are adapted to the alkaline conditions found on calcium-rich chalk and limestone, which give rise to often dry topographies such as limestone pavement.[23]
As for their growth habit, the flowering plants range from small, soft herbaceous plants, often living as annuals or biennials that set seed and die after one growing season,[24] to large perennial woody trees that may live for many centuries and grow to many metres in height. Some species grow tall without being self-supporting like trees by climbing on other plants in the manner of vines or lianas.[25]
Taxonomic diversity
The number of species of flowering plants is estimated to be in the range of 250,000 to 400,000.[26][27][28] This compares to around 12,000 species of moss[29] and 11,000 species of pteridophytes.[30] The APG system seeks to determine the number of families, mostly by molecular phylogenetics. In the 2009 APG III there were 415 families.[31] The 2016 APG IV added five new orders (Boraginales, Dilleniales, Icacinales, Metteniusales and Vahliales), along with some new families, for a total of 64 angiosperm orders and 416 families.[1]
The diversity of flowering plants is not evenly distributed. Nearly all species belong to the eudicot (75%), monocot (23%), and magnoliid (2%) clades. The remaining five clades contain a little over 250 species in total; i.e. less than 0.1% of flowering plant diversity, divided among nine families. The 25 most species-rich of 443 families,[32] containing over 166,000 species between them in their APG circumscriptions, are:
The botanical term "angiosperm", from Greek words angeíon (ἀγγεῖον 'bottle, vessel') and spérma (σπέρμα 'seed'), was coined in the form "Angiospermae" by Paul Hermann in 1690, including only flowering plants whose seeds were enclosed in capsules.[34] The term angiosperm fundamentally changed in meaning in 1827 with Robert Brown, when angiosperm came to mean a seed plant with enclosed ovules.[35][36] In 1851, with Wilhelm Hofmeister's work on embryo-sacs, Angiosperm came to have its modern meaning of all the flowering plants including Dicotyledons and Monocotyledons.[36][37] The APG system[31] treats the flowering plants as an unranked clade without a formal Latin name (angiosperms). A formal classification was published alongside the 2009 revision in which the flowering plants rank as the subclass Magnoliidae.[38] From 1998, the Angiosperm Phylogeny Group (APG) has reclassified the angiosperms, with updates in the APG II system in 2003,[39] the APG III system in 2009,[31][40] and the APG IV system in 2016.[1]
Dipsacales de Jussieu ex von Berchtold & Presl 1820
(euasterids II)
In 2024, Alexandre R. Zuntini and colleagues constructed a tree of some 6,000 flowering plant genera, representing some 60% of the existing genera, on the basis of analysis of 353 nuclear genes in each specimen. Much of the existing phylogeny is confirmed; the rosid phylogeny is revised.[46]
Fossilised spores suggest that land plants (embryophytes) have existed for at least 475 million years.[47] However, angiosperms appear suddenly and in great diversity in the fossil record in the Early Cretaceous (~130 mya).[48][49] Claimed records of flowering plants prior to this are not widely accepted.[50] Molecular evidence suggests that the ancestors of angiosperms diverged from the gymnosperms during the late Devonian, about 365 million years ago.[51] The origin time of the crown group of flowering plants remains contentious.[52] By the Late Cretaceous, angiosperms appear to have dominated environments formerly occupied by ferns and gymnosperms. Large canopy-forming trees replaced conifers as the dominant trees close to the end of the Cretaceous, 66 million years ago.[53] The radiation of herbaceous angiosperms occurred much later.[54]
The characteristic feature of angiosperms is the flower. Its function is to ensure fertilization of the ovule and development of fruit containing seeds.[55] It may arise terminally on a shoot or from the axil of a leaf.[56] The flower-bearing part of the plant is usually sharply distinguished from the leaf-bearing part, and forms a branch-system called an inflorescence.[37]
The flower may consist only of these parts, as in wind-pollinated plants like the willow, where each flower comprises only a few stamens or two carpels.[37] In insect- or bird-pollinated plants, other structures protect the sporophylls and attract pollinators. The individual members of these surrounding structures are known as sepals and petals (or tepals in flowers such as Magnolia where sepals and petals are not distinguishable from each other). The outer series (calyx of sepals) is usually green and leaf-like, and functions to protect the rest of the flower, especially the bud.[58][59] The inner series (corolla of petals) is, in general, white or brightly colored, is more delicate in structure, and attracts pollinators by colour, scent, and nectar.[60][61]
Most flowers are hermaphroditic, producing both pollen and ovules in the same flower, but some use other devices to reduce self-fertilization. Heteromorphic flowers have carpels and stamens of differing lengths, so animal pollinators cannot easily transfer pollen between them. Homomorphic flowers may use a biochemical self-incompatibility to discriminate between self and non-self pollen grains. Dioecious plants such as holly have male and female flowers on separate plants.[62]Monoecious plants have separate male and female flowers on the same plant; these are often wind-pollinated,[63] as in maize,[64] but include some insect-pollinated plants such as Cucurbita squashes.[65][66]
Double fertilization requires two sperm cells to fertilise cells in the ovule. A pollen grain sticks to the stigma at the top of the pistil, germinates, and grows a long pollen tube. A haploid generative cell travels down the tube behind the tube nucleus. The generative cell divides by mitosis to produce two haploid (n) sperm cells. The pollen tube grows from the stigma, down the style and into the ovary. When it reaches the micropyle of the ovule, it digests its way into one of the synergids, releasing its contents including the sperm cells. The synergid that the cells were released into degenerates; one sperm makes its way to fertilise the egg cell, producing a diploid (2n) zygote. The second sperm cell fuses with both central cell nuclei, producing a triploid (3n) cell. The zygote develops into an embryo; the triploid cell develops into the endosperm, the embryo's food supply. The ovary develops into a fruit. and each ovule into a seed.[67]
As the embryo and endosperm develop, the wall of the embryo sac enlarges and combines with the nucellus and integument to form the seed coat. The ovary wall develops to form the fruit or pericarp, whose form is closely associated with type of seed dispersal system.[68]
Other parts of the flower often contribute to forming the fruit. For example, in the apple, the hypanthium forms the edible flesh, surrounding the ovaries which form the tough cases around the seeds.[69]
Apomixis, setting seed without fertilization, is found naturally in about 2.2% of angiosperm genera.[70] Some angiosperms, including many citrus varieties, are able to produce fruits through a type of apomixis called nucellar embryony.[71]
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 often 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.[72]
Adaptive function of flowers
Charles Darwin in his 1878 book The Effects of Cross and Self-Fertilization in the Vegetable Kingdom[73] in the initial paragraph of chapter XII noted "The first and most important of the conclusions which may be drawn from the observations given in this volume, is that generally cross-fertilisation is beneficial and self-fertilisation often injurious, at least with the plants on which I experimented." Flowers emerged in plant evolution as an adaptation for the promotion of cross-fertilisation (outcrossing), a process that allows the masking of deleterious mutations in the genome of progeny. The masking effect is known as genetic complementation.[74] This beneficial effect of cross-fertilisation on progeny is also referred to as hybrid vigor or heterosis. Once flowers became established in a lineage as an evolutionary adaptation to promote cross-fertilization, subsequent switching to inbreeding usually becomes disadvantageous, in large part because it allows expression of the previously masked deleterious recessive mutations, i.e. inbreeding depression.[citation needed]
Also, Meiosis in flowering plants provides a direct mechanism for repairing DNA through genetic recombination in reproductive tissues.[75]Sexual reproduction appears to be required for maintaining long-term genomic integrity and only infrequent combinations of extrinsic and intrinsic factors permit shifts to asexuality.[75] Thus the two fundamental aspects of sexual reproduction in flowering plants, cross-fertilization (outcrossing) and meiosis appear to be maintained respectively by the advantages of genetic complementation and recombinational repair.[74]
Agriculture is almost entirely dependent on angiosperms, which provide virtually all plant-based food and livestock feed. Much of this food derives from a small number of flowering plant families.[76] For instance, half of the world's calorie intake is supplied by just three plants – wheat, rice and maize.[77]
Relatively few plant diversity assessments currently consider climate change,[87] yet it is starting to impact plants as well. About 3% of flowering plants are very likely to be driven extinct within a century at 2 °C (3.6 °F) of global warming, and 10% at 3.2 °C (5.8 °F).[91] In worst-case scenarios, half of all tree species may be driven extinct by climate change over that timeframe.[87]
Conservation in this context is the attempt to prevent extinction, whether in situ by protecting plants and their habitats in the wild, or ex situ in seed banks or as living plants.[88] Some 3000 botanic gardens around the world maintain living plants, including over 40% of the species known to be threatened, as an "insurance policy against extinction in the wild."[92] The United Nations' Global Strategy for Plant Conservation asserts that "without plants, there is no life".[93] It aims to "halt the continuing loss of plant diversity" throughout the world.[93]
^Cantino, Philip D.; Doyle, James A.; Graham, Sean W.; et al. (2007). "Towards a phylogenetic nomenclature of Tracheophyta". Taxon. 56 (3): E1–E44. doi:10.2307/25065865. JSTOR25065865.
^Friedman, William E.; Ryerson, Kirsten C. (2009). "Reconstructing the ancestral female gametophyte of angiosperms: Insights from Amborella and other ancient lineages of flowering plants". American Journal of Botany. 96 (1): 129–143. doi:10.3732/ajb.0800311. PMID21628180.
^Raven, Peter H.; Evert, Ray F.; Eichhorn, Susan E. (2005). Biology of Plants. W. H. Freeman. pp. 376–. ISBN 978-0-7167-1007-3.
^Baas, Pieter (1982). "Systematic, phylogenetic, and ecological wood anatomy — History and perspectives". New Perspectives in Wood Anatomy. Forestry Sciences. Vol. 1. Dordrecht: Springer Netherlands. pp. 23–58. doi:10.1007/978-94-017-2418-0_2. ISBN 978-90-481-8269-5. ISSN0924-5480.
^"Menara, yellow meranti, Shorea". Guinness World Records. 6 January 2019. Retrieved 8 May 2023. yellow meranti (Shorea faguetiana) ... 98.53 m (323 ft 3.1 in) tall ... swamp gum (Eucalyptus regnans) ... In 2014, it had a tape-drop height of 99.82 m (327 ft 5.9 in)
^"Angiosperms". University of Nevada, Las Vegas. Retrieved 6 May 2023.
^Kendrick, Gary A.; Orth, Robert J.; Sinclair, Elizabeth A.; Statton, John (2022). "Effect of climate change on regeneration of seagrasses from seeds". Plant Regeneration from Seeds. pp. 275–283. doi:10.1016/b978-0-12-823731-1.00011-1. ISBN 978-0-1282-3731-1.
^ abKarlsson, P. S.; Pate, J. S. (1992). "Contrasting effects of supplementary feeding of insects or mineral nutrients on the growth and nitrogen and phosphorous economy of pygmy species of Drosera". Oecologia. 92 (1): 8–13. Bibcode:1992Oecol..92....8K. doi:10.1007/BF00317256. PMID28311806. S2CID13038192.
^Goffinet, Bernard; Buck, William R. (2004). "Systematics of the Bryophyta (Mosses): From molecules to a revised classification". Monographs in Systematic Botany. 98: 205–239.
^Raven, Peter H.; Evert, Ray F.; Eichhorn, Susan E. (2005). Biology of Plants (7th ed.). New York: W. H. Freeman and Company. ISBN 0-7167-1007-2.
^Sadava, David; Heller, H. Craig; Orians, Gordon H.; et al. (December 2006). Life: the science of biology. Macmillan. pp. 477–. ISBN 978-0-7167-7674-1. Archived from the original on 23 December 2011. Retrieved 4 August 2010.
^Stewart, Wilson Nichols; Rothwell, Gar W. (1993). Paleobotany and the evolution of plants (2nd ed.). Cambridge University Press. p. 498. ISBN 978-0-521-23315-6.
^Bredmose, N. (2003). "Growth Regulation: Axillary Bud Growth". Encyclopedia of Rose Science. Elsevier. pp. 374–381. doi:10.1016/b0-12-227620-5/00017-3. ISBN 9780122276200.
^ abSalisbury, Frank B.; Parke, Robert V. (1970). "Sexual Reproduction". In Salisbury, Frank B.; Parke, Robert V. (eds.). Vascular Plants: Form and Function. Fundamentals of Botany Series. London: Macmillan Education. pp. 185–195. doi:10.1007/978-1-349-00364-8_13. ISBN 978-1-349-00364-8.
^Bortiri, E.; Hake, S. (13 January 2007). "Flowering and determinacy in maize". Journal of Experimental Botany. 58 (5). Oxford University Press (OUP): 909–916. doi:10.1093/jxb/erm015. ISSN0022-0957. PMID17337752.
^Mabberley, D. J. (2008). The Plant Book: A Portable Dictionary of the Vascular Plants. Cambridge: Cambridge University Press. p. 235. ISBN 978-0-521-82071-4.
^Eriksson, O. (2008). "Evolution of Seed Size and Biotic Seed Dispersal in Angiosperms: Paleoecological and Neoecological Evidence". International Journal of Plant Sciences. 169 (7): 863–870. doi:10.1086/589888. S2CID52905335.
^"Fruit Anatomy". Fruit & Nut Research & Information Center. University of California. Archived from the original on 2 May 2023.
^Gentile, Alessandra (18 March 2020). The Citrus Genome. Springer Nature. p. 171. ISBN 978-3-030-15308-3. Archived from the original on 14 April 2021. Retrieved 13 December 2020.
^ abcLughadha, Eimear Nic; Bachman, Steven P.; Leão, Tarciso C. C.; Forest, Félix; Halley, John M.; Moat, Justin; Acedo, Carmen; Bacon, Karen L.; Brewer, Ryan F. A.; Gâteblé, Gildas; Gonçalves, Susana C.; Govaerts, Rafaël; Hollingsworth, Peter M.; Krisai-Greilhuber, Irmgard; de Lirio, Elton J.; Moore, Paloma G. P.; Negrão, Raquel; Onana, Jean Michel; Rajaovelona, Landy R.; Razanajatovo, Henintsoa; Reich, Peter B.; Richards, Sophie L.; Rivers, Malin C.; Cooper, Amanda; Iganci, João; Lewis, Gwilym P.; Smidt, Eric C.; Antonelli, Alexandre; Mueller, Gregory M.; Walker, Barnaby E. (29 September 2020). "Extinction risk and threats to plants and fungi". Plants People Planet. 2 (5): 389–408. doi:10.1002/ppp3.10146. hdl:10316/101227. S2CID225274409.
^Shivanna, K. R. (2019). "The 'Sixth Mass Extinction Crisis' and Its Impact on Flowering Plants". Biodiversity and Chemotaxonomy. Sustainable Development and Biodiversity. Vol. 24. Cham: Springer International Publishing. pp. 15–42. doi:10.1007/978-3-030-30746-2_2. ISBN 978-3-030-30745-5.
Heywood, V. H.; Brummitt, R. K.; Culham, A.; Seberg, O. (2007). Flowering Plant Families of the World. Richmond Hill, Ontario, Canada: Firefly Books. ISBN 978-1-55407-206-4.
Hill, Christopher; Crane, Peter (January 1982). "Evolutionary Cladistics and the origin of Angiosperms". In Joysey, Kenneth Alan; Friday, A.E. (eds.). Problems of Phylogenetic Reconstruction. Special Volumes. Vol. 21. London: Systematics Association. pp. 269–361. ISBN 978-0-12-391250-3.