Plant evolution

Plant evolution is the subset of evolutionary phenomena that concern plants. Evolutionary phenomena are characteristics of populations that are described by averages, medians, distributions, and other statistical methods. This distinguishes plant evolution from plant development, a branch of developmental biology which concerns the changes that individuals go through in their lives. The study of plant evolution attempts to explain how the present diversity of plants arose over geologic time. It includes the study of genetic change and the consequent variation that often results in speciation, one of the most important types of radiation into taxonomic groups called clades. A description of radiation is called a phylogeny and is often represented by type of diagram called a phylogenetic tree.

Plant Diversity (2)
Cladogram of plant evolution

Evolutionary trends

Differences between plant and animal physiology and reproduction cause minor differences in how they evolve.

One major difference is the totipotent nature of plant cells, allowing them to reproduce asexually much more easily than most animals. They are also capable of polyploidy – where more than two chromosome sets are inherited from the parents. This allows relatively fast bursts of evolution to occur, for example by the effect of gene duplication. The long periods of dormancy that seed plants can employ also makes them less vulnerable to extinction, as they can "sit out" the tough periods and wait until more clement times to leap back to life.

The effect of these differences is most profoundly seen during extinction events. These events, which wiped out between 6 and 62% of terrestrial animal families, had "negligible" effect on plant families.[1] However, the ecosystem structure is significantly rearranged, with the abundances and distributions of different groups of plants changing profoundly.[1] These effects are perhaps due to the higher diversity within families, as extinction – which was common at the species level – was very selective. For example, wind-pollinated species survived better than insect-pollinated taxa, and specialised species generally lost out.[1] In general, the surviving taxa were rare before the extinction, suggesting that they were generalists who were poor competitors when times were easy, but prospered when specialised groups became extinct and left ecological niches vacant.[1]


Speciation via polyploidy: A diploid cell undergoes failed meiosis, producing diploid gametes, which self-fertilize to produce a tetraploid zygote.

Polyploidy is pervasive in plants and some estimates suggest that 30–80% of living plant species are polyploid, and many lineages show evidence of ancient polyploidy (paleopolyploidy) in their genomes.[2][3][4] Huge explosions in angiosperm species diversity appear to have coincided with ancient genome duplications shared by many species.[5] 15% of angiosperm and 31% of fern speciation events are accompanied by ploidy increase.[6] Most polyploids display heterosis relative to their parental species, and may display novel variation or morphologies that may contribute to the processes of speciation and eco-niche exploitation.[3][7] The mechanisms leading to novel variation in newly formed allopolyploids may include gene dosage effects (resulting from more numerous copies of genome content), the reunion of divergent gene regulatory hierarchies, chromosomal rearrangements, and epigenetic remodeling, all of which affect gene content and/or expression levels.[8][9][10] Many of these rapid changes may contribute to reproductive isolation and speciation.

All eukaryotes probably have experienced a polyploidy event at some point in their evolutionary history. See paleopolyploidy. In many cases, these events can be inferred only through comparing sequenced genomes. Angiosperms have paleopolyploidy in their ancestry. Unexpected ancient genome duplications have recently been confirmed in mustard weed/thale cress (Arabidopsis thaliana) and rice (Oryza sativa).


Plagiomnium affine laminazellen.jpeg
Plant cells with visible chloroplasts (from a moss, Plagiomnium affine)

Cyanobacteria and the evolution of photosynthesis

Cyanobacteria remained principal primary producers throughout the Proterozoic Eon (2500–543 Ma), in part because the redox structure of the oceans favored photoautotrophs capable of nitrogen fixation. Green algae joined blue-greens as major primary producers on continental shelves near the end of the Proterozoic, but only with the Mesozoic (251–65 Ma) radiations of dinoflagellates, coccolithophorids, and diatoms did primary production in marine shelf waters take modern form. Cyanobacteria remain critical to marine ecosystems as primary producers in oceanic gyres, as agents of biological nitrogen fixation, and, in modified form, as the plastids of marine algae.[11]

Symbiosis and the origin of chloroplasts

Chloroplasts have many similarities with cyanobacteria, including a circular chromosome, prokaryotic-type ribosomes, and similar proteins in the photosynthetic reaction center.[12][13] The endosymbiotic theory suggests that photosynthetic bacteria were acquired (by endocytosis) by early eukaryotic cells to form the first plant cells. Therefore, chloroplasts may be photosynthetic bacteria that adapted to life inside plant cells. Like mitochondria, chloroplasts still possess their own DNA, separate from the nuclear DNA of their plant host cells and the genes in this chloroplast DNA resemble those in cyanobacteria.[14] DNA in chloroplasts codes for redox proteins such as photosynthetic reaction centers. The CoRR hypothesis proposes that this Co-location is required for Redox Regulation.

Evolution of plant transcriptional regulation

Transcription factors and transcriptional regulatory networks play key roles in plant development and stress responses, as well as their evolution. During plant landing, many novel transcription factor families emerged and are preferentially wired into the networks of multicellular development, reproduction, and organ development, contributing to more complex morphogenesis of land plants.[15]

See also


  1. ^ a b c d McElwain, J.C.; Punyasena, S.W. (2007). "Mass extinction events and the plant fossil record". Trends in Ecology & Evolution. 22 (10): 548–557. doi:10.1016/j.tree.2007.09.003. PMID 17919771.
  2. ^ Meyers LA, Levin DA (June 2006). "On the abundance of polyploids in flowering plants". Evolution. 60 (6): 1198–206. doi:10.1111/j.0014-3820.2006.tb01198.x. PMID 16892970.
  3. ^ a b Rieseberg LH, Willis JH (August 2007). "Plant speciation". Science. 317 (5840): 910–4. doi:10.1126/science.1137729. PMC 2442920. PMID 17702935.
  4. ^ Otto SP (November 2007). "The evolutionary consequences of polyploidy". Cell. 131 (3): 452–62. doi:10.1016/j.cell.2007.10.022. PMID 17981114.
  5. ^ de Bodt et al. 2005
  6. ^ Wood TE, Takebayashi N, Barker MS, Mayrose I, Greenspoon PB, Rieseberg LH (August 2009). "The frequency of polyploid speciation in vascular plants". Proc. Natl. Acad. Sci. U.S.A. 106 (33): 13875–9. doi:10.1073/pnas.0811575106. PMC 2728988. PMID 19667210.
  7. ^ Comai L (November 2005). "The advantages and disadvantages of being polyploid". Nat. Rev. Genet. 6 (11): 836–46. doi:10.1038/nrg1711. PMID 16304599.
  8. ^ Osborn TC, Pires JC, Birchler JA, Auger DL, Chen ZJ, Lee HS, Comai L, Madlung A, Doerge RW, Colot V, Martienssen RA (March 2003). "Understanding mechanisms of novel gene expression in polyploids". Trends Genet. 19 (3): 141–7. doi:10.1016/S0168-9525(03)00015-5. PMID 12615008.
  9. ^ Chen ZJ, Ni Z (March 2006). "Mechanisms of genomic rearrangements and gene expression changes in plant polyploids". BioEssays. 28 (3): 240–52. doi:10.1002/bies.20374. PMC 1986666. PMID 16479580.
  10. ^ Chen ZJ (2007). "Genetic and epigenetic mechanisms for gene expression and phenotypic variation in plant polyploids". Annu Rev Plant Biol. 58: 377–406. doi:10.1146/annurev.arplant.58.032806.103835. PMC 1949485. PMID 17280525.
  11. ^ Herrero A and Flores E (editor). (2008). The Cyanobacteria: Molecular Biology, Genomics and Evolution (1st ed.). Caister Academic Press. ISBN 978-1-904455-15-8.
  12. ^ Douglas SE (1998). "Plastid evolution: origins, diversity, trends". Curr. Opin. Genet. Dev. 8 (6): 655–61. doi:10.1016/S0959-437X(98)80033-6. PMID 9914199.
  13. ^ Reyes-Prieto A, Weber AP, Bhattacharya D (2007). "The origin and establishment of the plastid in algae and plants". Annu. Rev. Genet. 41: 147–68. doi:10.1146/annurev.genet.41.110306.130134. PMID 17600460.
  14. ^ Raven JA, Allen JF (2003). "Genomics and chloroplast evolution: what did cyanobacteria do for plants?". Genome Biol. 4 (3): 209. doi:10.1186/gb-2003-4-3-209. PMC 153454. PMID 12620099.
  15. ^ Jin JP; et al. (July 2015). "An Arabidopsis transcriptional regulatory map reveals distinct functional and evolutionary features of novel transcription factors". Molecular Biology and Evolution. 32 (7): 1767–1773. doi:10.1093/molbev/msv058. PMC 4476157. PMID 25750178.

An archegonium (pl: archegonia), from the ancient Greek ἀρχή ("beginning") and γόνος ("offspring"), is a multicellular structure or organ of the gametophyte phase of certain plants, producing and containing the ovum or female gamete. The corresponding male organ is called the antheridium. The archegonium has a long neck canal or venter and a swollen base. Archegonia are typically located on the surface of the plant thallus, although in the hornworts they are embedded.

Armen Takhtajan

Armen Leonovich Takhtajan or Takhtajian (Armenian: Արմեն Լևոնի Թախտաջյան; Russian: Армен Леонович Тахтаджян; surname also transliterated Takhtadjan, Takhtadzhi︠a︡n or Takhtadzhian, pronounced TAHK-tuh-jahn) (June 10, 1910 – November 13, 2009), was a Soviet-Armenian botanist, one of the most important figures in 20th century plant evolution and systematics and biogeography. His other interests included morphology of flowering plants, paleobotany, and the flora of the Caucasus. He was born in Shusha. He was one of the most influential taxonomists of the latter twentieth century.


Botany, also called plant science(s), plant biology or phytology, is the science of plant life and a branch of biology. A botanist, plant scientist or phytologist is a scientist who specialises in this field. The term "botany" comes from the Ancient Greek word βοτάνη (botanē) meaning "pasture", "grass", or "fodder"; βοτάνη is in turn derived from βόσκειν (boskein), "to feed" or "to graze". Traditionally, botany has also included the study of fungi and algae by mycologists and phycologists respectively, with the study of these three groups of organisms remaining within the sphere of interest of the International Botanical Congress. Nowadays, botanists (in the strict sense) study approximately 410,000 species of land plants of which some 391,000 species are vascular plants (including approximately 369,000 species of flowering plants), and approximately 20,000 are bryophytes.Botany originated in prehistory as herbalism with the efforts of early humans to identify – and later cultivate – edible, medicinal and poisonous plants, making it one of the oldest branches of science. Medieval physic gardens, often attached to monasteries, contained plants of medical importance. They were forerunners of the first botanical gardens attached to universities, founded from the 1540s onwards. One of the earliest was the Padua botanical garden. These gardens facilitated the academic study of plants. Efforts to catalogue and describe their collections were the beginnings of plant taxonomy, and led in 1753 to the binomial system of Carl Linnaeus that remains in use to this day.

In the 19th and 20th centuries, new techniques were developed for the study of plants, including methods of optical microscopy and live cell imaging, electron microscopy, analysis of chromosome number, plant chemistry and the structure and function of enzymes and other proteins. In the last two decades of the 20th century, botanists exploited the techniques of molecular genetic analysis, including genomics and proteomics and DNA sequences to classify plants more accurately.

Modern botany is a broad, multidisciplinary subject with inputs from most other areas of science and technology. Research topics include the study of plant structure, growth and differentiation, reproduction, biochemistry and primary metabolism, chemical products, development, diseases, evolutionary relationships, systematics, and plant taxonomy. Dominant themes in 21st century plant science are molecular genetics and epigenetics, which are the mechanisms and control of gene expression during differentiation of plant cells and tissues. Botanical research has diverse applications in providing staple foods, materials such as timber, oil, rubber, fibre and drugs, in modern horticulture, agriculture and forestry, plant propagation, breeding and genetic modification, in the synthesis of chemicals and raw materials for construction and energy production, in environmental management, and the maintenance of biodiversity.

Douglas E. Soltis

Douglas Soltis is a Distinguished Professor in the Laboratory of Molecular Systematics & Evolutionary Genetics, (Soltis lab.) Florida Museum of Natural History and Department of Biology at the University of Florida. His research interests are in plant evolution and phylogeny, an area in which he has published extensively together with his wife Pamela Soltis and together they were the joint awardees of the 2006 Asa Gray Award. They are the principal investigators in the Soltis laboratory, where they both hold the rank of Distinguished Professor and are contributing authors of the Angiosperm Phylogeny Group.

Professor Soltis holds a Ph.D. from the University of Indiana (1980).

E. B. Babcock

Ernest Brown Babcock (July 10, 1877 – December 8, 1954) was a United States plant geneticist who pioneered the understanding of plant evolution in terms of genetics. He is particularly known for seeking to understand by field investigations and extensive experiments, the entire polyploid apomictic genus Crepis, in which he recognize 196 species. In his career, he published more than 100 articles and books explaining plant genetics, including the seminal textbook (with Roy Elwood Clausen) Genetics in relation to agriculture.

Evolutionary history of plants

The evolution of plants has resulted in a wide range of complexity, from the earliest algal mats, through multicellular marine and freshwater green algae, terrestrial bryophytes, lycopods and ferns, to the complex gymnosperms and angiosperms of today. While many of the earliest groups continue to thrive, as exemplified by red and green algae in marine environments, more recently derived groups have displaced previously ecologically dominant ones, e.g. the ascendance of flowering plants over gymnosperms in terrestrial environments.There is evidence that cyanobacteria and multicellular photosynthetic eukaryotes lived in freshwater communities on land as early as 1 billion years ago, and that communities of complex, multicellular photosynthesizing organisms existed on land in the late Precambrian, around 850 million years ago.Evidence of the emergence of embryophyte land plants first occurs in the mid-Ordovician (~470 million years ago), and by the middle of the Devonian (~390 million years ago), many of the features recognised in land plants today were present, including roots and leaves. By Late Devonian (~370 million years ago) some free-sporing plants such as Archaeopteris had secondary vascular tissue that produced wood and had formed forests of tall trees. Also by late Devonian, Elkinsia, an early seed fern, had evolved seeds.

Evolutionary innovation continued into the Carboniferous and still continues today. Most plant groups were relatively unscathed by the Permo-Triassic extinction event, although the structures of communities changed. This may have set the scene for the appearance of the flowering plants in the Triassic (~200 million years ago), and their later diversification in the Cretaceous and Paleogene. The latest major group of plants to evolve were the grasses, which became important in the mid-Paleogene, from around 40 million years ago. The grasses, as well as many other groups, evolved new mechanisms of metabolism to survive the low CO2 and warm, dry conditions of the tropics over the last 10 million years.

G. Ledyard Stebbins

George Ledyard Stebbins Jr. (January 6, 1906 – January 19, 2000) was an American botanist and geneticist who is widely regarded as one of the leading evolutionary biologists of the 20th century. Stebbins received his Ph.D. in botany from Harvard University in 1931. He went on to the University of California, Berkeley, where his work with E. B. Babcock on the genetic evolution of plant species, and his association with a group of evolutionary biologists known as the Bay Area Biosystematists, led him to develop a comprehensive synthesis of plant evolution incorporating genetics.

His most important publication was Variation and Evolution in Plants, which combined genetics and Darwin's theory of natural selection to describe plant speciation. It is regarded as one of the main publications which formed the core of the modern synthesis and still provides the conceptual framework for research in plant evolutionary biology; according to Ernst Mayr, "Few later works dealing with the evolutionary systematics of plants have not been very deeply affected by Stebbins' work." He also researched and wrote widely on the role of hybridization and polyploidy in speciation and plant evolution; his work in this area has had a lasting influence on research in the field.

From 1960, Stebbins was instrumental in the establishment of the Department of Genetics at the University of California, Davis, and was active in numerous organizations involved in the promotion of evolution, and of science in general. He was elected to the National Academy of Science, was awarded the National Medal of Science, and was involved in the development of evolution-based science programs for California high schools, as well as the conservation of rare plants in that state.


Gnetophyta is a division of plants, grouped within the gymnosperms (which also includes conifers, cycads, and ginkgos), that consists of some 70 species across the three relict genera: Gnetum (family Gnetaceae), Welwitschia (family Welwitschiaceae), and Ephedra (family Ephedraceae). Fossilized pollen attributed to a close relative of Ephedra has been dated as far back as the Early Cretaceous. Though diverse and dominant in the Paleogene and the Neogene, only three families, each containing a single genus, are still alive today. The primary difference between gnetophytes and other gymnosperms is the presence of vessel elements, a system of conduits that transport water within the plant, similar to those found in flowering plants. Because of this, gnetophytes were once thought to be the closest gymnosperm relatives to flowering plants, but more recent molecular studies have brought this hypothesis into question.

Though it is clear they are all closely related, the exact evolutionary inter-relationships between gnetophytes are unclear. Some classifications hold that all three genera should be placed in a single order (Gnetales), while other classifications say they should be distributed among three separate orders, each containing a single family and genus. Most morphological and molecular studies confirm that the genera Gnetum and Welwitschia diverged from each other more recently than they did from Ephedra.

Green algae

The green algae (singular: green alga) are a large, informal grouping of algae consisting of the Chlorophyta and Charophyta/Streptophyta, which are now placed in separate divisions, as well as the potentially more basal Mesostigmatophyceae, Chlorokybophyceae and Spirotaenia.The land plants, or embryophytes, are thought to have emerged from the charophytes. Therefore, cladistically, embryophytes belong to green algae as well. However, because the embryophytes are traditionally classified as neither algae nor green algae, green algae are a paraphyletic group. Since the realization that the embryophytes emerged from within the green algae, some authors are starting to include them. The clade that includes both green algae and embryophytes is monophyletic and is referred to as the clade Viridiplantae and as the kingdom Plantae. The green algae include unicellular and colonial flagellates, most with two flagella per cell, as well as various colonial, coccoid and filamentous forms, and macroscopic, multicellular seaweeds. There are about 8,000 species of green algae. Many species live most of their lives as single cells, while other species form coenobia (colonies), long filaments, or highly differentiated macroscopic seaweeds.

A few other organisms rely on green algae to conduct photosynthesis for them. The chloroplasts in euglenids and chlorarachniophytes were acquired from ingested green algae, and in the latter retain a nucleomorph (vestigial nucleus). Green algae are also found symbiotically in the ciliate Paramecium, and in Hydra viridissima and in flatworms. Some species of green algae, particularly of genera Trebouxia of the class Trebouxiophyceae and Trentepohlia (class Ulvophyceae), can be found in symbiotic associations with fungi to form lichens. In general the fungal species that partner in lichens cannot live on their own, while the algal species is often found living in nature without the fungus. Trentepohlia is a filamentous green alga that can live independently on humid soil, rocks or tree bark or form the photosymbiont in lichens of the family Graphidaceae. Also the macroalga Prasiola calophylla (Trebouxiophyceae) is terrestrial, and

Prasiola crispa, which live in the supralittoral zone, is terrestrial and can in the Antarctic form large carpets on humid soil, especially near bird colonies.

Herbaceous plant

Herbaceous plants in Botany, frequently shortened to herbs, are vascular plants that have no persistent woody stem above ground. Herb has other meanings in cooking, medicine, and other fields. Herbaceous plants are those plants that do not have woody stems, they include many perennials,

and nearly all annuals and biennials, they include both forbs and graminoids.

Herbaceous plants most often are low growing plants, relative to woody plants like trees, and tend to have soft green stems that lack Lignification and their above ground growth is ephemeral and often seasonal in duration.

Index of evolutionary biology articles

This is a list of topics in evolutionary biology.

Late Devonian extinction

The Late Devonian extinction was one of five major extinction events in the history of life on Earth. A major extinction, the Kellwasser event, occurred at the boundary that marks the beginning of the last phase of the Devonian period, the Famennian faunal stage (the Frasnian–Famennian boundary), about 376–360 million years ago. Overall, 19% of all families and 50% of all genera became extinct. A second, distinct mass extinction, the Hangenberg event, closed the Devonian period.Although it is clear that there was a massive loss of biodiversity in the Late Devonian, the timespan of this event is uncertain, with estimates ranging from 500,000 to 25 million years, extending from the mid-Givetian to the end-Famennian. Nor is it clear whether there were two sharp mass extinctions or a series of smaller extinctions, though the latest research suggests multiple causes and a series of distinct extinction pulses during an interval of some three million years. Some consider the extinction to be as many as seven distinct events, spread over about 25 million years, with notable extinctions at the ends of the Givetian, Frasnian, and Famennian stages.By the Late Devonian, the land had been colonized by plants and insects. In the oceans were massive reefs built by corals and stromatoporoids. Euramerica and Gondwana were beginning to converge into what would become Pangaea. The extinction seems to have only affected marine life. Hard-hit groups include brachiopods, trilobites, and reef-building organisms; the reef-building organisms almost completely disappeared. The causes of these extinctions are unclear. Leading hypotheses include changes in sea level and ocean anoxia, possibly triggered by global cooling or oceanic volcanism. The impact of a comet or another extraterrestrial body has also been suggested, such as the Siljan Ring event in Sweden. Some statistical analysis suggests that the decrease in diversity was caused more by a decrease in speciation than by an increase in extinctions. This might have been caused by invasions of cosmopolitan species, rather than by any single event. Surprisingly, jawed vertebrates seem to have been unaffected by the loss of reefs or other aspects of the Kellwasser event, while agnathans were in decline long before the end of the Frasnian.

Mandla Plant Fossils National Park

Dindori Plant Fossils National Park is situated in Dindori district of Madhya Pradesh in India. This national park has plants in fossil form that existed in India anywhere between 40 million and 150 million years ago spread over seven villages of Dindori District (Ghuguwa, Umaria, Deorakhurd, Barbaspur, Chanti-hills, Chargaon and Deori Kohani). The Dindori Plant Fossils National Park is an area that spreads over 274,100 square metres. Such fossils are found in three other villages of the district also, but they lie outside the national park.

The Birbal Sahni Institute of Palaeobotany, Lucknow, has done some work on the plant fossils of Mandla, though the study is yet in a preliminary stage. In Ghuguwa and Umaria the standing, petrified trunks of trees have been identified as Gymnosperms and Angiosperms- Monocotyledons and palms. There are certain Bryophytes also. There is some question about whether the fossils are from the late Jurassic or the early and mid Cretaceous age. This is because when the breakup of the single land mass, Pangaea occurred, it was split by the continental drift into Laurasia and Gondwana somewhere between the Jurassic and Cretaceous ages. India formed a part of Gondwana. Depending on the age in which the split occurred, the fossils are either Jurassic or Cretaceous.

Interspersed with the plant fossils are to be found the fossils of molluscs. One theory is that the area in which the fossils are located, i.e., the Narmada Valley near Mandla, was actually a deep inundation of the sea into peninsular India until the Post- Cambrian Tertiary age, about 40 million years ago. This means that Narmada was a very short river which terminated in the inland sea above Mandla, and that the recession of the sea caused geological disturbances, which created the present rift valley through which the Narmada River and Tapti River flow in their present journey to the Arabian Sea. All this, however, is speculation and conjecture because it is only recently that an interest has developed in the fossils of Mandla and detailed scientific studies are still wanting.

A region as ancient as this tells a great deal about what Madhya Pradesh was like millions of years ago. The absence of dicotyledons suggests that plant evolution was still at an early stage. The whole matter requires much more detailed study. The national park is spread over agricultural fields in seven non-contiguous villages, which makes it difficult to protect the fossils. The fossils look like ordinary rocks and are either removed from the fields unwittingly by agriculturists or are damaged by tourists and those unscrupulous people who think they can make quick money out of their sale. In Chargaon and Deori Kohani villages there has been extensive damage, especially by excavation of embedded molluscs.

Some say that if the Fossil National Park is to be saved, a separate administrative unit for park management should be set up, the land on which fossils are located should be acquired and fenced and the nearest university, Jabalpur, should be asked to set up a special research unit on the fossils.

Mikhail Grigorevich Popov

Mikhail Grigorevich Popov (Russian: Михаил Григорьевич Попов) (April 5(17), 1893 – December 18, 1955) was a Soviet botanist. He is known for developing a theory on the role of hybridization in plant evolution, and studying the flora of the Soviet Union and Eastern Europe. The standard author abbreviation Popov is used to indicate this person as the author when citing a botanical name.

Physcomitrella patens

Physcomitrella patens, the spreading earthmoss, is a moss (bryophyte) used as a model organism for studies on plant evolution, development, and physiology.

Plant evolutionary developmental biology

Evolutionary developmental biology (evo-devo) is the study of developmental programs and patterns from an evolutionary perspective. It seeks to understand the various influences shaping the form and nature of life on the planet. Evo-devo arose as a separate branch of science rather recently. An early sign of this occurred in 1999.Most of the synthesis in evo-devo has been in the field of animal evolution, one reason being the presence of elegant model systems like Drosophila melanogaster, C. elegans, zebrafish and Xenopus laevis. However, since 1980, a wealth of information on plant morphology, coupled with modern molecular techniques has helped shed light on the conserved and unique developmental patterns in the plant kingdom also.

Plant morphology

Plant morphology or phytomorphology is the study of the physical form and external structure of plants. This is usually considered distinct from plant anatomy, which is the study of the internal structure of plants, especially at the microscopic level. Plant morphology is useful in the visual identification of plants.

Timeline of plant evolution

This article attempts to place key plant innovations in a geological context. It concerns itself only with novel adaptations and events that had a major ecological significance, not those that are of solely anthropological interest. The timeline displays a graphical representation of the adaptations; the text attempts to explain the nature and robustness of the evidence.

Plant evolution is an aspect of the study of biological evolution, predominantly involving evolution of plants suited to live on land, greening of various land masses by the filling of their niches with land plants, and diversification of groups of land plants.

Variation and Evolution in Plants

Variation and Evolution in Plants is a book written by G. Ledyard Stebbins, published in 1950. It is one of the key publications embodying the modern synthesis of evolution and genetics, as the first comprehensive publication to discuss the relationship between genetics and natural selection in plants. The book has been described by plant systematist Peter H. Raven as "the most important book on plant evolution of the 20th century" and it remains one of the most cited texts on plant evolution.[1]

This page is based on a Wikipedia article written by authors (here).
Text is available under the CC BY-SA 3.0 license; additional terms may apply.
Images, videos and audio are available under their respective licenses.