The eudicots, Eudicotidae, or eudicotyledons are a clade of flowering plants (angiosperms) which are mainly characterized by having two seed leaves (cotyledons) upon germination.[1] The term derives from dicotyledon (etymologically, eu = true; di = two; cotyledon = seed leaf). Historically, authors have used the terms tricolpates or non-magnoliid dicots. The current botanical terms were introduced in 1991, by evolutionary botanist James A. Doyle and paleobotanist Carol L. Hotton, to emphasize the later evolutionary divergence of tricolpate dicots from earlier, less specialized, dicots.[2]

Eudicots
Temporal range: Early Cretaceous - recent
Two seed leaves during germination (Brassica sp.)
Scientific classification Edit this classification
Kingdom: Plantae
Clade: Streptophyta
Clade: Embryophytes
Clade: Polysporangiophytes
Clade: Tracheophytes
Clade: Spermatophytes
Clade: Angiosperms
Clade: Eudicots
Clades (APG IV)
Arabis pollen has three colpi.

Scores of familiar plants are eudicots, including many commonly cultivated and edible plants, numerous trees, tropicals and ornamentals. Among the most well-known eudicot genera are those of the sunflower (Helianthus), dandelion (Taraxacum), forget-me-not (Myosotis), cabbage (Brassica), apple (Malus), buttercup (Ranunculus), maple (Acer) and macadamia (Macadamia). Most leafy, mid-latitude trees are also classified as eudicots, with notable exceptions being the magnolias and American tulip tree (Liriodendron)—which belong to the magnoliids—and Ginkgo biloba, which is not an angiosperm.

Description

edit

The close relationships among flowering plants with tricolpate pollen grains was initially seen in morphological studies of shared derived characters. These plants have a distinct trait in their pollen grains of exhibiting three colpi or grooves paralleling the polar axis.[3]

Later molecular evidence confirmed the genetic basis for the evolutionary relationships among flowering plants with tricolpate pollen grains and dicotyledonous traits. The term means "true dicotyledons", as it contains the majority of plants that have been considered dicots and have characteristics of the dicots. One of the genetic traits which defines the eudicots is the duplication of DELLA protein-encoding genes in their most recent common ancestor.[4] The term "eudicots" has subsequently been widely adopted in botany to refer to one of the two largest clades of angiosperms (constituting over 70% of the angiosperm species), monocots being the other. The remaining angiosperms include magnoliids and what are sometimes referred to as basal angiosperms or paleodicots, but these terms have not been widely or consistently adopted, as they do not refer to a monophyletic group.[citation needed]

According to molecular clock calculations, the lineage that led to eudicots split from other plants about 134 million years ago[5] or 155-160 million years ago.[6]

Taxonomy

edit

The earlier name for the eudicots is tricolpates, a name which refers to the grooved structure of the pollen. Members of the group have tricolpate pollen, or forms derived from it. These pollens have three or more pores set in furrows called colpi. In contrast, most of the other seed plants (that is the gymnosperms, the monocots and the paleodicots) produce monosulcate pollen, with a single pore set in a differently oriented groove called the sulcus. The name "tricolpates" is preferred by some botanists to avoid confusion with the dicots, a nonmonophyletic group.[7]

The name "eudicots" (plural) is used in the APG systems (from APG system, of 1998, to APG IV system, of 2016) for classification of angiosperms. It is applied to a clade, a monophyletic group, which includes most of the (former) dicots.[citation needed]

"Tricolpate" is a synonym for the "Eudicot" monophyletic group, the "true dicotyledons" (which are distinguished from all other flowering plants by their tricolpate pollen structure). The number of pollen grain furrows or pores helps classify the flowering plants, with eudicots having three colpi (tricolpate), and other groups having one sulcus.[8][7]

Pollen apertures are any modification of the wall of the pollen grain. These modifications include thinning, ridges and pores, they serve as an exit for the pollen contents and allow shrinking and swelling of the grain caused by changes in moisture content. The elongated apertures/ furrows in the pollen grain are called colpi (singular colpus), which, along with pores, are a chief criterion for identifying the pollen classes.[9]

Subdivisions

edit

The eudicots can be divided into two groups: the basal eudicots and the core eudicots.[10] Basal eudicot is an informal name for a paraphyletic group. The core eudicots are a monophyletic group.[11] A 2010 study suggested the core eudicots can be divided into two clades, Gunnerales and a clade called Pentapetalae, comprising all the remaining core eudicots.[12]

The Pentapetalae can be then divided into three clades:[citation needed]

This division of the eudicots is shown in the following cladogram:[13]

eudicots

The following is a more detailed breakdown according to APG IV, showing within each clade and orders:[14]

References

edit
  1. ^ "EUDICOTS". Basic Biology. Basic Biology 2020. Retrieved 6 July 2020.
  2. ^ Endress, Peter K. (2002). "Morphology and Angiosperm Systematics in the Molecular Era" (PDF). Botanical Review. Structural Botany in Systematics: A Symposium in Memory of William C. Dickison. 68 (4): 545–570. doi:10.1663/0006-8101(2002)068[0545:maasit]2.0.co;2. JSTOR 4354438. S2CID 39486751.
  3. ^ Furness, Carol A.; Rudall, Paula J. (March 2004). "Pollen aperture evolution – a crucial factor for eudicot success?". Trends in Plant Science. 9 (3): 154–158. doi:10.1016/j.tplants.2004.01.001. PMID 15003239.
  4. ^ Phokas, A.; Coates, J. C. (2021). "Evolution of DELLA function and signaling in land plants". Evolution & Development. 23 (3): 137–154. doi:10.1111/ede.12365. PMC 9285615. PMID 33428269.
  5. ^ Magallon, S; Gomez-Acevedo, S; Sanchez-Reyes, LL; Tania Hernandez-Hernandez, T (2015). "A metacalibrated time-tree documents the early rise of flowering plant phylogenetic diversity". New Phytologist. 207: 437–453. doi:10.1111/nph.13264.
  6. ^ Zeng, Liping; Zhang, Qiang; Sun, Renran; Kong, Hongzhi; Zhang, Ning; Ma, Hong (24 September 2014). "Resolution of deep angiosperm phylogeny using conserved nuclear genes and estimates of early divergence times". Nature Communications. 5 (4956): 4956. Bibcode:2014NatCo...5.4956Z. doi:10.1038/ncomms5956. PMC 4200517. PMID 25249442.
  7. ^ a b Judd & Olmstead 2004
  8. ^ Sporne, Kenneth R. (1972). "Some Observations on the Evolution of Pollen Types in Dicotyledons". New Phytologist. 71 (1): 181–5. doi:10.1111/j.1469-8137.1972.tb04826.x.
  9. ^ Davis, Owen (1999). "Pollen Aperture Definitions". University of Arizona - Geosciences. Archived from the original on 2009-02-03. Retrieved 2009-02-16.
  10. ^ Worberg, A; Quandt, D; Barniske, A-M; Löhne, C; Hilu, KW; Borsch, T (2007). "Phylogeny of basal eudicots: insights from non-coding and rapidly evolving DNA". Organisms Diversity & Evolution. 7 (1): 55–77. doi:10.1016/j.ode.2006.08.001.
  11. ^ Soltis, Douglas E.; Soltis, Pamela S.; Endress, Peter K.; Chase, Mark W. (2005). Phylogeny and Evolution of Angiosperms. Sunderland, MA: Sinauer Associates. ISBN 9780878938179.
  12. ^ Moore, Michael J.; Soltis, Pamela S.; Bell, Charles D.; Burleigh, J. Gordon & Soltis, Douglas E. (2010). "Phylogenetic analysis of 83 plastid genes further resolves the early diversification of eudicots". Proceedings of the National Academy of Sciences. 107 (10): 4623–8. Bibcode:2010PNAS..107.4623M. doi:10.1073/pnas.0907801107. PMC 2842043. PMID 20176954.
  13. ^ Based on:
    Stevens, P.F. (2001–2014). "Trees". Angiosperm Phylogeny Website. Retrieved 2014-11-17.
    Stevens, P.F. (2001–2016). "Eudicots". Angiosperm Phylogeny Website. Retrieved 2014-11-17.
  14. ^ Angiosperm Phylogeny Group (2016). "An update of the Angiosperm Phylogeny Group classification for the orders and families of flowering plants: APG IV". Botanical Journal of the Linnean Society. 181 (1): 1–20. doi:10.1111/boj.12385.

Bibliography

edit
edit