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Racemose inflorescences of monocots: structural and morphogenetic interaction at the flower/inflorescence level
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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/j.1537-2197.1965.tb06754.xopenalex-snapshot
PERIANTH DEVELOPMENT OF POTAMOGETON RICHARDSONII
inferredcites →https://doi.org/10.1002/j.1537-2197.1967.tb10669.xopenalex-snapshot
A SURVEY OF FLORAL ANATOMY IN ARACEAE
inferredcites →https://doi.org/10.1002/j.1537-2197.1974.tb06048.xopenalex-snapshot
FLORAL DEVELOPMENT OF POTAMOGETON RICHARDSONII
inferredcites →https://doi.org/10.1002/j.1537-2197.1975.tb11774.xopenalex-snapshot
DEVELOPMENT AND ORGANIZATION OF THE PRIMARY VASCULAR SYSTEM IN POPULUS DELTOIDES ACCORDING TO PHYLLOTAXY
inferredcites →https://doi.org/10.1002/j.1537-2197.1983.tb06432.xopenalex-snapshot
RE‐EVALUATION OF CERTAIN KEY RELATIONSHIPS IN THE ALISMATIDAE: FLORAL ORGANOGENESIS OF SCHEUCHZERIA PALUSTRIS (SCHEUCHZERIACEAE)
inferredcites →https://doi.org/10.1002/j.1537-2197.1988.tb11234.xopenalex-snapshot
HOMEOSIS IN PLANTS
inferredcites →https://doi.org/10.1002/j.1537-2197.1992.tb13710.xopenalex-snapshot
IRREGULAR FLORAL DEVELOPMENT IN CALLA PALUSTRIS (ARACEAE) AND THE CONCEPT OF HOMEOSIS
inferredcites →https://doi.org/10.1002/tax.604011openalex-snapshot
Harperocallis is congeneric with Isidrogalvia (Tofieldiaceae, Alismatales): Evidence from comparative floral morphology
inferredcites →https://doi.org/10.1006/anbo.2001.1498openalex-snapshot
Developmental Genetics and Morphological Evolution of Flowering Plants, Especially Bladderworts (Utricularia): Fuzzy Arberian Morphology Complements Classical Morphology, , , , , , , , ,
inferredcites →https://doi.org/10.1006/bojl.2001.0460openalex-snapshot
Flower structure and development of Araceae compared with alismatids and Acoraceae
inferredcites →https://doi.org/10.1007/978-3-642-61663-1openalex-snapshot
The Families of the Monocotyledons
inferredcites →https://doi.org/10.1007/bf02814485openalex-snapshot
Evo-devo and the search for homology (“sameness”) in biological systems
inferredcites →https://doi.org/10.1007/s00425-005-0088-9openalex-snapshot
Role of auxin in regulating Arabidopsis flower development
inferredcites →https://doi.org/10.1007/s00606-005-0397-3openalex-snapshot
Evolution of the monocot gynoecium: evidence from comparative morphology and development in Tofieldia, Japonolirion, Petrosavia and Narthecium
inferredcites →https://doi.org/10.1007/s00606-011-0475-6openalex-snapshot
Floral development of Urospatha: merosity and phylogeny in the Lasioideae (Araceae)
inferredcites →https://doi.org/10.1007/s006060200023openalex-snapshot
The correlation between development of atypical bisexual flowers and phylogeny in the Aroideae (Araceae)
inferredcites →https://doi.org/10.1007/s10265-010-0387-5openalex-snapshot
Molecular phylogenetic analyses of Tofieldiaceae (Alismatales): family circumscription and intergeneric relationships
inferredcites →https://doi.org/10.1007/s11174-005-0012-zopenalex-snapshot
Basic principles of terminal flower formation
inferredcites →https://doi.org/10.1016/0304-3770(93)90074-7openalex-snapshot
Evolution of the helobial flower
inferredcites →https://doi.org/10.1016/b978-0-08-057430-1.50009-3openalex-snapshot
HOMOLOGY AND SYSTEMATICS
inferredcites →https://doi.org/10.1016/j.pbi.2009.09.019openalex-snapshot
All in a spin: centrifugal organ formation and floral patterning
inferredcites →https://doi.org/10.1016/j.tplants.2004.02.003openalex-snapshot
Towards a comprehensive integration of morphological and genetic studies of floral development
inferredcites →https://doi.org/10.1016/j.tplants.2007.03.005openalex-snapshot
Towards the systems biology of auxin-transport-mediated patterning
inferredcites →https://doi.org/10.1016/j.tplants.2009.03.004openalex-snapshot
The key role of morphology in modelling inflorescence architecture
inferredcites →https://doi.org/10.1016/s0169-5347(00)89041-2openalex-snapshot
Diversity and evolutionary biology of tropical flowers
inferredcites →https://doi.org/10.1016/s0367-1615(17)31756-1openalex-snapshot
Über Vorblattbildung bei Monokotylen
inferredcites →https://doi.org/10.1016/s1369-5266(00)00135-7openalex-snapshot
Vascular patterning and leaf shape
inferredcites →https://doi.org/10.1017/cbo9781139002950.002openalex-snapshot
A well-supported phylogenetic framework for the monocot order Alismatales reveals multiple losses of the plastid NADH dehydrogenase complex and a strong long-branch effect
inferredcites →https://doi.org/10.1017/cbo9781139002950.009openalex-snapshot
Patterns of bract reduction in racemose inflorescences of early-divergent monocots
inferredcites →https://doi.org/10.1023/b:rudo.0000036712.64312.e8openalex-snapshot
Structure of Flower in Arabidopsis thaliana: Spatial Pattern Formation
inferredcites →https://doi.org/10.1038/1781386a0openalex-snapshot
The Floral Meristem as a Reaction System
inferredcites →https://doi.org/10.1046/j.1469-8137.2003.00769.xopenalex-snapshot
Primary vascular pattern and expression of ATHB‐8 in shoots of Arabidopsis
inferredcites →https://doi.org/10.1086/297178openalex-snapshot
Developmental Morphology of Reproductive Structures of Phyllospadix (Zosteraceae)
inferredcites →https://doi.org/10.1086/297236openalex-snapshot
Developmental Morphology of Reproductive Structures of Zostera and a Reconsideration of Heterozostera (Zosteraceae)
inferredcites →https://doi.org/10.1086/297504openalex-snapshot
Floral Developmental Studies: Some Old and New Questions
inferredcites →https://doi.org/10.1086/314241openalex-snapshot
Floral Structure and Development of Acoraceae and Its Systematic Relationships with Basal Angiosperms
inferredcites →https://doi.org/10.1086/336309openalex-snapshot
Morphological and Anatomical Studies in Helobiae II. Vascular Anatomy of the Flower of Potamogetonaceae
inferredcites →https://doi.org/10.1086/375421openalex-snapshot
Shape Matters: Hofmeister’s Rule, Primordium Shape, and Flower Orientation
inferredcites →https://doi.org/10.1086/376879openalex-snapshot
Monocot Pseudanthia Revisited: Floral Structure of the Mycoheterotrophic Family Triuridaceae
inferredcites →https://doi.org/10.1086/590476openalex-snapshot
Fascicles and Filamentous Structures: Comparative Ontogeny of Morphological Novelties in Triuridaceae
inferredcites →https://doi.org/10.1086/658922openalex-snapshot
Ontogenetic Course and Spatial Constraints in the Appearance and Disappearance of the Terminal Flower in Inflorescences
inferredcites →https://doi.org/10.1093/aob/mcq010openalex-snapshot
Spikelet structure and development in Cyperoideae (Cyperaceae): a monopodial general model based on ontogenetic evidence
inferredcites →https://doi.org/10.1093/aob/mcr213openalex-snapshot
Diversity, phylogeny, and evolution in the monocotyledons
inferredcites →https://doi.org/10.1093/jxb/erj042openalex-snapshot
Flower primordium formation at the Arabidopsis shoot apex: quantitative analysis of surface geometry and growth
inferredcites →https://doi.org/10.1093/jxb/erl126openalex-snapshot
Flower-like terminal structures in racemose inflorescences: a tool in morphogenetic and evolutionary research
inferredcites →https://doi.org/10.1093/jxb/erm060openalex-snapshot
Computer models of auxin transport: a review and commentary
inferredcites →https://doi.org/10.1093/jxb/erm290openalex-snapshot
Flowering and apical meristem growth dynamics
inferredcites →https://doi.org/10.1093/jxb/erq262openalex-snapshot
Open and closed inflorescences: more than simple opposites
inferredcites →https://doi.org/10.1093/nq/cxlix.oct10.269aopenalex-snapshot
Monocotyledons: A morphological study
inferredcites →https://doi.org/10.1093/oxfordjournals.aob.a084135openalex-snapshot
Initiation of Procambial Strands in Leaf Primordia of Bread Wheat, Triticum aestivum L
inferredcites →https://doi.org/10.1093/oxfordjournals.aob.a084189openalex-snapshot
Initiation of Procambial Strands in Leaf Primordia of Dactylis glomerata L. as an Example of a Temperate Herbage Grass
inferredcites →https://doi.org/10.1105/tpc.108.060871openalex-snapshot
Patterning of Inflorescences and Flowers by the F-Box Protein DOUBLE TOP and the LEAFY Homolog ABERRANT LEAF AND FLOWER of Petunia
inferredcites →https://doi.org/10.1111/j.1095-8312.1990.tb00509.xopenalex-snapshot
Patterns of floral construction in ontogeny and phylogeny
inferredcites →https://doi.org/10.1111/j.1095-8339.2008.00850.xopenalex-snapshot
Floral evolution in the monocot family Nartheciaceae (Dioscoreales): evidence from anatomy and development in Metanarthecium luteo-viride Maxim.
inferredcites →https://doi.org/10.1111/j.1095-8339.2008.00905.xopenalex-snapshot
Floral development inNymphaea tetragona(Nymphaeaceae)
inferredcites →https://doi.org/10.1111/j.1095-8339.2012.01267.xopenalex-snapshot
Flower development and vasculature in Xyris grandis (Xyridaceae, Poales); a case study for examining petal diversity in monocot flowers with a double perianth
inferredcites →https://doi.org/10.1111/j.1469-8137.1952.tb06144.xopenalex-snapshot
ON THE SHOOT APEX AND PHYLLOTAXIS OF COSTUS
inferredcites →https://doi.org/10.1111/j.1759-6831.2010.00087.xopenalex-snapshot
Disentangling confusions in inflorescence morphology: Patterns and diversity of reproductive shoot ramification in angiosperms
inferredcites →https://doi.org/10.1111/j.1759-6831.2011.00172.xopenalex-snapshot
Delimitation and phylogeny of Aletris (Nartheciaceae) with implications for perianth evolution
inferredcites →https://doi.org/10.1126/science.1213100openalex-snapshot
Elastic Domains Regulate Growth and Organogenesis in the Plant Shoot Apical Meristem
inferredcites →https://doi.org/10.1127/0006-8152/2003/0124-0255openalex-snapshot
Inflorescence and floral morphology in Tofieldia (Tofieldiaceae) compared with Araceae, Acoraceae and Alismatales s.str.
inferredcites →https://doi.org/10.1134/s1021443712040048openalex-snapshot
Flower and shoot fasciation: From phenomenology to the construction of models of apical meristem transformations
inferredcites →https://doi.org/10.1134/s106235900606001xopenalex-snapshot
Type specification and spatial pattern formation of floral organs: A dynamic development model
inferredcites →https://doi.org/10.1134/s1062360411040084openalex-snapshot
Morphogenetic lability of the Ruppia maritima (Ruppiaceae, Alismatales) reproductive organs: From two lateral flowers to a terminal flower
inferredcites →https://doi.org/10.1139/b06-126openalex-snapshot
The shoot apical meristem and development of vascular architectureThis review is one of a selection of papers published on the Special Theme of Shoot Apical Meristems.
inferredcites →https://doi.org/10.1139/b06-133openalex-snapshot
Inhibition fields for phyllotactic pattern formation: a simulation studyThis article is one of a selection of papers published on the Special Theme of Shoot Apical Meristems.
inferredcites →https://doi.org/10.1139/b73-079openalex-snapshot
Floral development of Potamogeton densus
inferredcites →https://doi.org/10.1139/b77-128openalex-snapshot
Floral development of Aponogeton natans and A. undulatus
inferredcites →https://doi.org/10.1139/b81-069openalex-snapshot
Unicarpellate floral development in Potamogeton zosteriformis
inferredcites →https://doi.org/10.1139/b81-274openalex-snapshot
Features of the inflorescence of Triglochin maritima
inferredcites →https://doi.org/10.1242/dev.129.10.2519openalex-snapshot
Interaction of LEAFY , AGAMOUS and TERMINAL FLOWER1 in maintaining floral meristem identity in Arabidopsis
inferredcites →https://doi.org/10.1371/journal.pone.0028762openalex-snapshot
Simulation of Organ Patterning on the Floral Meristem Using a Polar Auxin Transport Model
inferredcites →https://doi.org/10.15740/has/ijpsopenalex-snapshot
INTERNATIONAL JOURNAL OF PLANT SCIENCES
inferredcites →https://doi.org/10.1600/036364406777585766openalex-snapshot
Morphological Phylogenetic Analysis of Pandanales: Testing Contrasting Hypotheses of Floral Evolution
inferredcites →https://doi.org/10.2307/2807789openalex-snapshot
Monocotyledons: Systematics and Evolution.
inferredcites →https://doi.org/10.3417/2009142openalex-snapshot
Evolutionary History of the Monocot Flower 1
inferredcites →https://doi.org/10.3732/ajb.0800047openalex-snapshot
Reconstructing the ancestral angiosperm flower and its initial specializations
inferredcites →https://doi.org/10.3732/ajb.1200227openalex-snapshot
Flowers and inflorescences of the seagrass Posidonia (Posidoniaceae, Alismatales)
inferredcites →https://doi.org/10.5642/aliso.20062201.02openalex-snapshot
Robust Inference of Monocot Deep Phylogeny Using an Expanded Multigene Plastid Data Set
inferredcites →https://doi.org/10.5642/aliso.20062201.06openalex-snapshot
Multigene Analyses of Monocot Relationships
inferredcites →https://doi.org/10.5642/aliso.20062201.09openalex-snapshot
Perianth Development in the Basal Monocot Triglochin Maritima (Juncaginaceae)
inferredcites →https://doi.org/10.5642/aliso.20062201.13openalex-snapshot
Patterns of Floral Structure and Orientation in Japonolirion , Narthecium, and Tofieldia
inferredcites →https://doi.org/10.5860/choice.27-6338openalex-snapshot
Morphology of flowers and inflorescences
inferredcites →https://doi.org/10.5860/choice.38-1564openalex-snapshot
Monocots: systematics and evolution
inferredcites →https://doi.org/10.5860/choice.38-2737openalex-snapshot
Grasses: systematics and evolution
inferredcites →https://doi.org/10.5962/p.330488openalex-snapshot
Floral vascular anatomy of Japonolirion osense Nakai (Liliaceae) and its tribal relationship
inferredcites →https://doi.org/10.5962/p.330817openalex-snapshot
Floral vascular anatomy of the monotypic Japanese Metanarthecium luteoviride Maxim. (Liliaceae-Melanthioideae)
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Incoming claims: where this work appears in other papers’ reference lists and arguments.
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inferred← citeshttps://doi.org/10.11646/phytotaxa.268.4.1zenodo-depositor-declared
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inferred← citeshttps://doi.org/10.3897/phytokeys.249.127632zenodo-depositor-declared
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inferred← citeshttps://doi.org/10.1007/s12229-026-09339-wopenalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.flora.2021.151934openalex-snapshot
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inferred← citeshttps://doi.org/10.1093/aob/mcaf167openalex-snapshot
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inferred← citeshttps://doi.org/10.7287/peerj.10205v0.1/reviews/1openalex-snapshot
Peer Review #1 of "Flower structure and development in Vietnamese Sciaphila (Triuridaceae: Pandanales): refined knowledge of the morphological misfit family and implications for taxonomy (v0.1)"
inferred← citeshttps://doi.org/10.7287/peerj.10205v0.1/reviews/2openalex-snapshot
Peer Review #2 of "Flower structure and development in Vietnamese Sciaphila (Triuridaceae: Pandanales): refined knowledge of the morphological misfit family and implications for taxonomy (v0.1)"
inferred← citeshttps://doi.org/10.7717/peerj.10205openalex-snapshot
Flower structure and development in Vietnamese Sciaphila (Triuridaceae: Pandanales): refined knowledge of the morphological misfit family and implications for taxonomy
Editorial review for independent work. ICSAC — the Institute for Complexity
Science and Advanced Computing — runs a structured editorial panel for researchers
publishing outside journals, and publishes on CiteStamp rails. Submission is free
and goes through ORCID: icsacinstitute.org/submit.