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Prophyll in Monocots: The Starting Point of Lateral Shoot Phyllotaxis

https://doi.org/10.3389/fpls.2022.855146
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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
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STUDIES IN THE MORPHOLOGY OF THE CYPERACEAE. II. THE PROPHYLL
inferredcites →https://doi.org/10.1002/j.1537-2197.1987.tb08751.xopenalex-snapshot
LEAF TYPES IN THE ARACEAE
inferredcites →https://doi.org/10.1002/j.1537-2197.1987.tb08752.xopenalex-snapshot
DIVERSITY OF SHOOT ORGANIZATION IN THE ARACEAE
inferredcites →https://doi.org/10.1006/dbio.1999.9572openalex-snapshot
Initiation of Axillary and Floral Meristems in Arabidopsis
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Generic relationships among the baccate-fruited Amaryllidaceae (tribe Haemantheae) inferred from plastid and nuclear non-coding DNA sequences
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Understanding the role of floral development in the evolution of angiosperm flowers: clarifications from a historical and physico-dynamic perspective
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Differential responses to defoliation frequency in little bluestem (Schizachyrium scoparium) in tallgrass prairie: implications for herbivory tolerance and avoidance
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Descriptive characters of growth form in Poaceae—An overview
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Florogenesis of the Mediterranean geophyte Narcissus tazetta and temperature requirements for flower initiation and differentiation
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Deep reticulation and incomplete lineage sorting obscure the diploid phylogeny of rain-lilies and allies (Amaryllidaceae tribe Hippeastreae)
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A critical revision of inflorescence structure in Crocus L. of the subgenus Nudiflori Maw (lridaceae)
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Patterns of bract reduction in racemose inflorescences of early-divergent monocots
inferredcites →https://doi.org/10.1038/058074a0openalex-snapshot
Organographie der Pflanzen
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Non-inductive conditions expose the cryptic bract of flower phytomeres in Arabidopsis thaliana.
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The ecology and significance of below-ground bud banks in plants
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Monocotyledons: A morphological study
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The Initiation and Growth of Narcissus Bulbs
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Sympodial Model of Bulb Growth in Amaryllidaceae: A Comparative Morphological Approach
inferredcites →https://doi.org/10.1159/000405172openalex-snapshot
Einleitung
inferredcites →https://doi.org/10.1242/dev.01517openalex-snapshot
INCOMPOSITA: a MADS-box gene controlling prophyll development and floral meristem identity inAntirrhinum
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Floral Evolution of Philodendron Subgenus Meconostigma (Araceae)
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JOURNAL AA
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Zur Morphologie der monokotylischen Knollen- und Zwiebelgewächse
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Periodicity of Inflorescence Initiation and Development in Nerine bowdenii W. Watson (Amaryllidaceae)
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Systematics of the Amazon Lilies, Eucharis and Caliphruria (Amaryllidaceae)
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Phylogenetic Relationships in the Commelinaceae: I. A. Cladistic Analysis of Morphological Data
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Phantom Leaves: A New Look to the Old Problem of Branching in Galanthus (Amaryllidaceae)
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Studies on the Growth and Flowering of Bulbous Plants of Amaryllidaceae
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Growth and Flowering of Leucojum aestivum L. and L. autumnale L. Grown Outdoors
inferredcites →https://doi.org/10.3372/wi.39.39116openalex-snapshot
Revision ofZephyranthes andina (Amaryllidaceae)including five new synonyms
inferredcites →https://doi.org/10.3389/fpls.2015.00955openalex-snapshot
Arabidopsis LEAFY COTYLEDON1 controls cell fate determination during post-embryonic development
inferredcites →https://doi.org/10.3732/ajb.1000158openalex-snapshot
Relationships within the Araceae: Comparison of morphological patterns with molecular phylogenies
inferredcites →https://doi.org/10.3732/ajb.1400434openalex-snapshot
Morphological diversity and evolution of Centrolepidaceae (Poales), a species‐poor clade with diverse body plans and developmental patterns
inferredcites →https://doi.org/10.4462/annbotrm-9067openalex-snapshot
PATTERNS OF FLOWER AND INFLORESCENCE ARCHITECTURE IN CROCUS L. (IRIDACEAE)
inferredcites →https://doi.org/10.5642/aliso.20062201.13openalex-snapshot
Patterns of Floral Structure and Orientation in Japonolirion , Narthecium, and Tofieldia
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The Never-ending Story: Multigene Approaches to the Phylogeny of Amaryllidaceae

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.647.1.4zenodo-depositor-declared
A preliminary study of the morphological variation of rhizomes in Zingiber Mill. and its role in taxonomy
inferred← citeshttps://doi.org/10.1002/9781394306350.refsopenalex-snapshot
References
inferred← citeshttps://doi.org/10.1007/s10265-024-01526-3openalex-snapshot
The interaction between heterochrony and mechanical forces as main driver of floral evolution
inferred← citeshttps://doi.org/10.1016/j.flora.2022.152138openalex-snapshot
Mathematical Modeling the Influence of Bracteoles on Sepal Arrangement
inferred← citeshttps://doi.org/10.1016/j.flora.2025.152861openalex-snapshot
In praise of bracteoles
inferred← citeshttps://doi.org/10.1016/j.ppees.2026.125952openalex-snapshot
Heterochronic shifts and modular organization underlie the evolution of floral morphotypes in Eperua (Detarioideae, Leguminosae)
inferred← citeshttps://doi.org/10.1080/23818107.2024.2303750openalex-snapshot
Perianth phyllotaxis and symmetry in Lamiales
inferred← citeshttps://doi.org/10.1080/23818107.2026.2673404openalex-snapshot
Modeling physical pressure in floral development
inferred← citeshttps://doi.org/10.1093/aob/mcaf167openalex-snapshot
Hygroscopic awns and inflorescence architecture in a wind-pollinated Australian monocot: functional convergence with grasses
inferred← citeshttps://doi.org/10.3389/fpls.2022.1081981openalex-snapshot
Reproductive development of common buckwheat (Fagopyrum esculentum Moench) and its wild relatives provides insights into their evolutionary biology
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