Abstract is: The eudicots, Eudicotidae, or eudicotyledons are a clade of flowering plants mainly characterized by having two seed leaves upon germination. The term derives from Dicotyledons. Traditionally they were called tricolpates or non-magnoliid dicots by previous authors. The botanical terms were introduced in 1991 by evolutionary botanist and paleobotanist Carol L. Hotton to emphasize the later evolutionary divergence of tricolpate dicots from earlier, less specialized, dicots. Numerous familiar plants are eudicots, including many common food plants, trees, and ornamentals. Some common and familiar eudicots include sunflower, dandelion, forget-me-not, cabbage, apple, buttercup, maple, and macadamia. Most leafy trees of midlatitudes also belong to eudicots, with notable exceptions being magnolias and tulip trees which belong to magnoliids, and Ginkgo biloba, which is not an angiosperm.
| P7033 | Australian Educational Vocabulary ID | scot/16757 |
| P8072 | CAB ID | 28941 |
| P10565 | Encyclopedia of China (Third Edition) ID | 538680 |
| P830 | Encyclopedia of Life ID | 283 |
| P1417 | Encyclopædia Britannica Online ID | plant/eudicot |
| P646 | Freebase ID | /m/081yxz |
| P2671 | Google Knowledge Graph ID | /g/11bc5gcjpr |
| P6366 | Microsoft Academic ID | 2776143962 |
| 2778682995 | ||
| P8707 | NBIC taxon ID | 1295 |
| P685 | NCBI taxonomy ID | 71240 |
| P9157 | Open Tree of Life ID | 431495 |
| P10283 | OpenAlex ID | C2778682995 |
| P10376 | ScienceDirect topic ID | agricultural-and-biological-sciences/eudicot |
| biochemistry-genetics-and-molecular-biology/eudicot | ||
| immunology-and-microbiology/eudicot | ||
| pharmacology-toxicology-and-pharmaceutical-science/eudicot | ||
| P2892 | UMLS CUI | C1085203 |
| P12086 | WikiKids ID | 'Nieuwe'_tweezaadlobbigen |
| P171 | parent taxon | mesangiosperms | Q2710933 |
| P1843 | taxon common name | Eudicotiledònies | |
| P225 | taxon name | eudicots | |
| P910 | topic's main category | Category:Eudicots | Q7328661 |
| Q46544476 | 'Living stones' reveal alternative petal identity programs within the core eudicots |
| Q64266677 | (Ranunculaceae), a new species of C.sect.Meclatis from Xinjiang, China |
| Q104282765 | A Review of C4 Plants in Southwest Asia: An Ecological, Geographical and Taxonomical Analysis of a Region With High Diversity of C4 Eudicots |
| Q84972310 | A comparative study of ethylene growth response kinetics in eudicots and monocots reveals a role for gibberellin in growth inhibition and recovery |
| Q50676633 | A conserved network of transcriptional activators and repressors regulates anthocyanin pigmentation in eudicots. |
| Q34407972 | A fragment of chloroplast DNA was transferred horizontally, probably from non-eudicots, to mitochondrial genome of Phaseolus. |
| Q28730462 | A genome triplication associated with early diversification of the core eudicots |
| Q33575688 | A modern circadian clock in the common angiosperm ancestor of monocots and eudicots |
| Q28651189 | A precise chloroplast genome of Nelumbo nucifera (Nelumbonaceae) evaluated with Sanger, Illumina MiSeq, and PacBio RS II sequencing platforms: insight into the plastid evolution of basal eudicots |
| Q36094498 | AP2/ERF Transcription Factor in Rice: Genome-Wide Canvas and Syntenic Relationships between Monocots and Eudicots |
| Q59418318 | Activation of anthocyanin biosynthesis in Gerbera hybrida (Asteraceae) suggests conserved protein-protein and protein-promoter interactions between the anciently diverged monocots and eudicots |
| Q105625550 | An Analysis of CHS Gene Family for Some Basal Eudicots |
| Q46256591 | An S-RNase-based gametophytic self-incompatibility system evolved only once in eudicots |
| Q28757180 | Are petals sterile stamens or bracts? The origin and evolution of petals in the core eudicots |
| Q28708894 | Bees diversified in the age of eudicots |
| Q47254760 | C(4) eudicots are not younger than C(4) monocots |
| Q91863308 | Characterization of Cellulose Synthase A (CESA) Gene Family in Eudicots |
| Q28681243 | Combining phylogenetic and syntenic analyses for understanding the evolution of TCP ECE genes in eudicots |
| Q42474049 | Comparison of gene order of GIGANTEA loci in yellow-poplar, monocots, and eudicots |
| Q36964162 | Conserved microsynteny of NPR1 with genes encoding a signal calmodulin-binding protein and a CK1-class protein kinase in Beta vulgaris and two other eudicots |
| Q60697040 | Convergent Vessel Diameter–Stem Diameter Scaling across Five Clades of New and Old World Eudicots from Desert to Rain Forest |
| Q43781829 | Dating phylogenetically basal eudicots using rbcL sequences and multiple fossil reference points |
| Q47308591 | Dating the monocot-dicot divergence and the origin of core eudicots using whole chloroplast genomes |
| Q89889252 | Diel patterns of stem CO2 efflux vary among cycads, arborescent monocots, and woody eudicots and gymnosperms |
| Q36845280 | Differential freezing resistance and photoprotection in C3 and C4 eudicots and grasses |
| Q37054466 | Divergent Evolutionary Pattern of Sugar Transporter Genes is Associated with the Difference in Sugar Accumulation between Grasses and Eudicots |
| Q34189317 | Diversity of Kranz anatomy and biochemistry in C4 eudicots |
| Q48184491 | Does Early Embryogenesis in Eudicots and Monocots Involve the Same Mechanism and Molecular Players? |
| Q79508194 | Duplication and paralog sorting of RPB2 and RPB1 genes in core eudicots |
| Q56950304 | Early Cretaceous floral structures andin situtricolpate‐striate pollen: New early eudicots from Portugal |
| Q60060944 | Enigmatic morphology of Djinga felicis (Podostemaceae - Podostemoideae), a badly known endemic from northwestern Cameroon |
| Q49984950 | Eudicots from severely phosphorus-impoverished environments preferentially allocate phosphorus to their mesophyll |
| Q64904079 | Evolution of Alternative Splicing in Eudicots. |
| Q92199090 | Evolution of RADIALIS and DIVARICATA gene lineages in flowering plants with an expanded sampling in non-core eudicots |
| Q63380008 | Evolution of endoapertures in early-divergent eudicots, with particular reference to pollen morphology in Sabiaceae |
| Q59358034 | Evolutionary diversification of CYC/TB1-like TCP homologs and their recruitment for the control of branching and floral morphology in Papaveraceae (basal eudicots) |
| Q58542893 | Expansion and Functional Divergence of the SHORT VEGETATIVE PHASE (SVP) Genes in Eudicots |
| Q36244005 | Floral development of Berberidopsis beckleri - can an additional species of the Berberidopsidaceae add evidence to floral evolution in the core eudicots? |
| Q33207406 | Floral development of Berberidopsis corallina: a crucial link in the evolution of flowers in the core Eudicots |
| Q104785525 | Floristic diversity (Magnoliids and Eudicots) of Baraiyadhala National Park, Chittagong, Bangladesh |
| Q33920520 | Flower development of Meliosma (Sabiaceae): evidence for multiple origins of pentamery in the eudicots |
| Q60325584 | Flowering Plants. Eudicots |
| Q56655844 | Flowering Plants. Eudicots. Berberidopsidales, Buxales, Crossosomatales, Fabales p.p., Geraniales, Gunnerales, Myrtales p.p., Proteales, Saxifragales, Vitales, Zygophyllales, Clusiaceae Alliance... |
| Q60325576 | Flowering Plants. Eudicots. Malpighiales |
| Q57320004 | Flowering Plants. Eudicots. Santalales, Balanophorales |
| Q33353511 | Functional analyses of AGAMOUS family members in Nicotiana benthamiana clarify the evolution of early and late roles of C-function genes in eudicots |
| Q95460618 | Further Resolution of the Rapid Radiation of Saxifragales (Angiosperms, Eudicots) Supported by Mixed-Model Bayesian Analysis |
| Q42660080 | Gamma paleohexaploidy in the stem lineage of core eudicots: significance for MADS-box gene and species diversification |
| Q80469194 | Genomic isolation of genes encoding starch branching enzyme II (SBEII) in apple: toward characterization of evolutionary disparity in SbeII genes between monocots and eudicots |
| Q52108626 | Gunnerales are sister to other core eudicots: implications for the evolution of pentamery. |
| Q95465806 | Homology and Evolution of Petals in the Core Eudicots |
| Q51915377 | Interactions among proteins of floral MADS-box genes in basal eudicots: implications for evolution of the regulatory network for flower development. |
| Q56961480 | Investigating the evolutionary assembly of a Mediterranean biodiversity hotspot: deep phylogenetic signal in the distribution of eudicots across elevational belts |
| Q36022356 | Large-Scale Gene Relocations following an Ancient Genome Triplication Associated with the Diversification of Core Eudicots |
| Q56950350 | Late Cretaceous follicular fruits from southern Sweden with systematic affinities to early diverging eudicots |
| Q44733280 | MicroRNA superfamilies descended from miR390 and their roles in secondary small interfering RNA Biogenesis in Eudicots |
| Q41745278 | Molecular and genetic analyses of the silky1 gene reveal conservation in floral organ specification between eudicots and monocots |
| Q106887652 | Morphology of pollen in Apiales (Asterids, Eudicots) |
| Q89241097 | Multigenome analysis implicates miniature inverted-repeat transposable elements (MITEs) in metabolic diversification in eudicots |
| Q92785132 | Mutations in orthologous PETALOSA TOE-type genes cause dominant double-flower phenotype in phylogenetically distant eudicots |
| Q56210140 | Nectar secretion and nectaries in basal angiosperms, magnoliids and non-core eudicots and a comparison with core eudicots |
| Q21296862 | New Record Holders for Maximum Genome Size in Eudicots and Monocots |
| Q63380011 | Phylogenetic Pattern, Diversity, and Diversification of Eudicots |
| Q22066285 | Phylogenetic analysis of 83 plastid genes further resolves the early diversification of eudicots |
| Q34694839 | Phylogenetic analysis of the "ECE" (CYC/TB1) clade reveals duplications predating the core eudicots |
| Q47955314 | Phylogenetic relationships among early-diverging eudicots based on four genes: were the eudicots ancestrally woody? |
| Q44939550 | Phylogenetic signal in matK vs. trnK: a case study in early diverging eudicots (angiosperms). |
| Q38384236 | Phylogenomic and structural analyses of 18 complete plastomes across nearly all families of early-diverging eudicots, including an angiosperm-wide analysis of IR gene content evolution |
| Q56191453 | Phylogeny of Basal Eudicots Based on Three Molecular Data Sets: atpB, rbcL, and 18s Nuclear Ribosomal DNA Sequences |
| Q47436890 | Phylogeny of Saxifragales (angiosperms, eudicots): analysis of a rapid, ancient radiation |
| Q29393534 | Phylogeny of basal eudicots: Insights from non-coding and rapidly evolving DNA |
| Q55896013 | Phylogeny of the Eudicots: A Nearly Complete Familial Analysis Based on rbcL Gene Sequences |
| Q40581945 | Postmeiotic cytokinesis and pollen aperture number determination in eudicots: effect of the cleavage wall number |
| Q49087539 | Promoter analysis of MADS-box genes in eudicots through phylogenetic footprinting |
| Q119292768 | Root nodule bacteria and leguminous plants |
| Q34534931 | Rubisco evolution in C₄ eudicots: an analysis of Amaranthaceae sensu lato |
| Q31062794 | S-RNase-mediated gametophytic self-incompatibility is ancestral in eudicots |
| Q56016823 | Shoot and compound leaf comparisons in eudicots: dynamic morphology as an alternative approach |
| Q58046262 | Sierraphytoptines (Eriophyoidea: Phytoptidae) from relict eudicots: reassignment of Sierraphytoptus taiwanensus to a new genus Solenoplatilobus and refinement of generic diagnosis of Austracus |
| Q39213133 | Significant involvement of PEP-CK in carbon assimilation of C4 eudicots |
| Q38907029 | Testing the association of phenotypes with polyploidy: An example using herbaceous and woody eudicots |
| Q91518616 | The Aquilegia genome reveals a hybrid origin of core eudicots |
| Q42493715 | The NnCenH3 protein and centromeric DNA sequence profiles of Nelumbo nucifera Gaertn. (sacred lotus) reveal the DNA structures and dynamics of centromeres in basal eudicots |
| Q103834446 | The Tetracentron genome provides insight into the early evolution of eudicots and the formation of vessel elements |
| Q30919391 | The absence of Arabidopsis-type telomeres in Cestrum and closely related genera Vestia and Sessea (Solanaceae): first evidence from eudicots |
| Q28584511 | The emergence of core eudicots: new floral evidence from the earliest Late Cretaceous |
| Q42239824 | The essential role of NGATHA genes in style and stigma specification is widely conserved across eudicots. |
| Q52092958 | The four-celled female gametophyte of Illicium (Illiciaceae; Austrobaileyales): implications for understanding the origin and early evolution of monocots, eumagnoliids,and eudicots. |
| Q45352469 | The paleoAP3-type gene CpAP3, an ancestral B-class gene from the basal angiosperm Chimonanthus praecox, can affect stamen and petal development in higher eudicots |
| Q48117410 | Transcription factors in rice: a genome-wide comparative analysis between monocots and eudicots |
| Q46593574 | Transcriptome comparisons shed light on the pre-condition and potential barrier for C4 photosynthesis evolution in eudicots. |
| Q56196096 | Tropidogyne, a New Genus of Early Cretaceous Eudicots (Angiospermae) from Burmese Amber |
| Q33530790 | True yams (Dioscorea): a biological and evolutionary link between eudicots and grasses |
| Q28959012 | Vestured Pits: Their Occurrence and Systematic Importance in Eudicots |
| Q33352968 | Virus-induced gene silencing (VIGS) in Cysticapnos vesicaria, a zygomorphic-flowered Papaveraceae (Ranunculales, basal eudicots). |
| Q3059511 | Kerneudikotyledonen | different from | P1889 |
| Q869087 | core eudicots | subclass of | P279 |
| Q7328661 | Category:Eudicots | category's main topic | P301 |
| Q46986836 | /Eudicotyledoneae | said to be the same as | P460 |
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