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Mechanisms for the evolution of complex and diversely elaborated sepals in Iris identified by comparative analysis of developmental sequences
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What this work says
Outgoing claims: the papers this work cites, builds on, or argues with.
inferredcites →https://doi.org/10.1002/dvg.20622openalex-snapshot
The maize milkweed pod1 mutant reveals a mechanism to modify organ morphology
inferredcites →https://doi.org/10.1002/j.1537-2197.1990.tb13562.xopenalex-snapshot
DEVELOPMENT OF DIFFERENCES IN LEAF SHAPE IN BEGONIA DREGEI (BEGONIACEAE)
inferredcites →https://doi.org/10.1002/j.1537-2197.1992.tb13695.xopenalex-snapshot
PETAL APPENDAGES IN BROMELIACEAE
inferredcites →https://doi.org/10.1002/jmor.10014openalex-snapshot
Sequence Heterochrony and the Evolution of Development
inferredcites →https://doi.org/10.1002/tax.601004openalex-snapshot
Subgeneric classification in Iris re‐examined using chloroplast sequence data
inferredcites →https://doi.org/10.1007/s10265-010-0336-3openalex-snapshot
Perspectives on leaf dorsoventral polarity
inferredcites →https://doi.org/10.1016/j.ode.2005.09.005openalex-snapshot
Elaborate petals and staminodes in eudicots: Diversity, function, and evolution
inferredcites →https://doi.org/10.1016/j.pbi.2003.11.002openalex-snapshot
Shaping up: the genetic control of leaf shape
inferredcites →https://doi.org/10.1016/j.pbi.2006.11.013openalex-snapshot
Mixing and matching pathways in leaf polarity
inferredcites →https://doi.org/10.1016/j.pbi.2007.07.012openalex-snapshot
From genes to shape: regulatory interactions in leaf development
inferredcites →https://doi.org/10.1016/j.ydbio.2009.05.542openalex-snapshot
Old dogs, new tricks: Regulatory evolution in conserved genetic modules leads to novel morphologies in plants
inferredcites →https://doi.org/10.1016/s0168-9525(01)02601-4openalex-snapshot
Establishment of polarity in angiosperm lateral organs
inferredcites →https://doi.org/10.1016/s0960-9822(02)00721-2openalex-snapshot
Spontaneous Mutations in KNOX Genes Give Rise to a Novel Floral Structure in Antirrhinum
inferredcites →https://doi.org/10.1017/s0094837300006588openalex-snapshot
Size and shape in ontogeny and phylogeny
inferredcites →https://doi.org/10.1017/s0094837300016195openalex-snapshot
Heterochrony and heterotopy: stability and innovation in the evolution of form
inferredcites →https://doi.org/10.1086/509079openalex-snapshot
The Ancestral Developmental Tool Kit of Land Plants
inferredcites →https://doi.org/10.1093/aob/mcl204openalex-snapshot
Labellar Micromorphology of Bifrenariinae Dressler (Orchidaceae)
inferredcites →https://doi.org/10.1093/aob/mcl209openalex-snapshot
Elaborate Petals in Australian Spermacoce (Rubiaceae) Species: Morphology, Ontogeny and Function
inferredcites →https://doi.org/10.1093/aob/mcp067openalex-snapshot
Floral convergence in Oncidiinae (Cymbidieae; Orchidaceae): an expanded concept of Gomesa and a new genus Nohawilliamsia
inferredcites →https://doi.org/10.1093/aob/mcp119openalex-snapshot
Comparative histology of floral elaiophores in the orchids Rudolfiella picta (Schltr.) Hoehne (Maxillariinae sensu lato) and Oncidium ornithorhynchum H.B.K. (Oncidiinae sensu lato)
inferredcites →https://doi.org/10.1093/aob/mcp199openalex-snapshot
Elaiophores in Gomesa bifolia (Sims) M.W. Chase & N.H. Williams (Oncidiinae: Cymbidieae: Orchidaceae): structure and oil secretion
inferredcites →https://doi.org/10.1101/gad.1819909openalex-snapshot
Signals and prepatterns: new insights into organ polarity in plants
inferredcites →https://doi.org/10.1105/tpc.8.8.1277openalex-snapshot
KNAT1 Induces Lobed Leaves with Ectopic Meristems When Overexpressed in Arabidopsis
inferredcites →https://doi.org/10.1111/j.0014-3820.2000.tb00568.xopenalex-snapshot
SPATIOTEMPORAL REORGANIZATION OF GROWTH RATES IN THE EVOLUTION OF ONTOGENY
inferredcites →https://doi.org/10.1111/j.1095-8339.2010.01033.xopenalex-snapshot
Comparative labellum micromorphology of the sexually deceptive temperate orchid genusOphrys: diverse epidermal cell types and multiple origins of structural colour
inferredcites →https://doi.org/10.1139/b02-021openalex-snapshot
Floral development and anatomy ofPentadiplandra(Pentadiplandraceae): a key genus in the identification of floral morphological trends in the core Brassicales
inferredcites →https://doi.org/10.1139/b05-158openalex-snapshot
Functional differentiation in pollination processes between the outer and inner perianths in Iris gracilipes (Iridaceae)
inferredcites →https://doi.org/10.1139/b09-109openalex-snapshot
Floral nectary structure, nectar production, and carbohydrate composition in theLiliumAsiatic hybrid ‘Trésor’
inferredcites →https://doi.org/10.1146/annurev.cellbio.18.020402.140619openalex-snapshot
Gene Co-Option in Physiological and Morphological Evolution
inferredcites →https://doi.org/10.1146/annurev.cellbio.20.031803.093824openalex-snapshot
THE ROLE OF KNOX GENES IN PLANT DEVELOPMENT
inferredcites →https://doi.org/10.1387/ijdb.14756337openalex-snapshot
Time's arrow: heterochrony and the evolution of development
inferredcites →https://doi.org/10.1600/036364410790862489openalex-snapshot
Species Delimitations and Phylogenetic Relationships within the Fully Myco-heterotrophic Hexalectris (Orchidaceae)
inferredcites →https://doi.org/10.1600/036364413x674724openalex-snapshot
Molecular Phylogeny of Crested Iris Based on Five Plastid Markers (Iridaceae)
inferredcites →https://doi.org/10.2307/2425304openalex-snapshot
The Influence of Pollinators on the Breeding System of Iris douglasiana
inferredcites →https://doi.org/10.3732/ajb.0900194openalex-snapshot
Flower and fruit characters in the early‐divergent lamiid family Metteniusaceae, with particular reference to the evolution of pseudomonomery
inferredcites →https://doi.org/10.3732/ajb.89.12.1867openalex-snapshot
Floral anatomy and systematics of Alliaceae with particular reference to Gilliesia, a presumed insect mimic with strongly zygomorphic flowers
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
inferred← citeshttps://doi.org/10.11646/phytotaxa.232.1.1zenodo-depositor-declared
Can a rainbow consist of a single colour? A new comprehensive generic arrangement of the ‘Iris sensu latissimo’ clade (Iridaceae), congruent with morphology and molecular data
inferred← citeshttps://doi.org/10.3897/phytokeys.271.176663zenodo-depositor-declared
Descriptions of a new species, validation of a name, and elevation of a variety in Iris (Iridaceae) from China
inferred← citeshttps://doi.org/10.1002/njb.04860openalex-snapshot
Iris anvarbekii (Iridaceae), a new species of I. subg. Scorpiris from the southern Pamir‐Alay in Uzbekistan
inferred← citeshttps://doi.org/10.1016/j.flora.2018.10.001openalex-snapshot
Organization, available space and organ morphology within floral buds of Iris (Iridaceae)
inferred← citeshttps://doi.org/10.1016/j.flora.2025.152744openalex-snapshot
Comparative anatomy of the gynoecia of Iris species (Iridaceae) with different degrees of longitudinal fusion of the carpels
inferred← citeshttps://doi.org/10.1093/aob/mcaf275openalex-snapshot
Developmental timing in the female reproductive cycle of Araucaria araucana : seasonality and evolutionary perspectives
inferred← citeshttps://doi.org/10.1111/njb.04389openalex-snapshot
Iris luojiensis (Iridaceae), a new species from southwest China
inferred← citeshttps://doi.org/10.23902/trkjnat.558252openalex-snapshot
COMPARATIVE MORPHOLOGICAL AND ANATOMICAL STUDIES ON Iris peshmeniana Güner & T. Hall. AND Iris aucheri (Baker) Sealy (IRIDACEAE)
inferred← citeshttps://doi.org/10.3389/fpls.2018.01349openalex-snapshot
The Times They Are A-Changin’: Heterochrony in Plant Development and Evolution
inferred← citeshttps://doi.org/10.3390/biology14121767openalex-snapshot
Watching the South China Sea—Portiodora (Iridaceae), a New Genus for Iris speculatrix Based on Comprehensive Evidence: The Contribution of Taxonomic Resolution to Biodiversity Conservation
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