On the public citation graph

Fascicles and Filamentous Structures: Comparative Ontogeny of Morphological Novelties in Triuridaceae

https://doi.org/10.1086/590476
0 signed · 106 inferred · view as graph

Inferred edges come from two machine sources: sweeps of open repository metadata (mostly SSRN and Zenodo), and a bulk OpenAlex citation snapshot. Every row below is labelled with the one it came from. Neither is a complete citation index — absence here is not evidence of absence.

Is this your work? Sign in with ORCID and put your name on the claims that are yours.
Claim with ORCID
Reference health. See whether every reference in this work resolves to a known work and none has been retracted — and get a dated CiteStamped badge you can embed.
See reference health

What this work says

Outgoing claims: the papers this work cites, builds on, or argues with.

inferredcites →https://doi.org/10.1002/fedr.20001110313openalex-snapshot
Floral morphology and development in Dioscoreales
inferredcites →https://doi.org/10.1002/j.1537-2197.1931.tb09580.xopenalex-snapshot
THE VASCULAR ANATOMY OF THE FLOWER WITH REFUTATION OF THE THEORY OF CARPEL POLYMORPHISM
inferredcites →https://doi.org/10.1002/j.1537-2197.1937.tb09167.xopenalex-snapshot
THE PHYLOGENY OF THE STAMEN
inferredcites →https://doi.org/10.1002/j.1537-2197.1942.tb10277.xopenalex-snapshot
THE TELOME THEORY AND THE ORIGIN OF THE STAMEN
inferredcites →https://doi.org/10.1002/j.1537-2197.1988.tb11234.xopenalex-snapshot
HOMEOSIS IN PLANTS
inferredcites →https://doi.org/10.1002/jez.1063openalex-snapshot
Origins of flower morphology
inferredcites →https://doi.org/10.1006/anbo.1997.0474openalex-snapshot
The Fundamental Relevance of Morphology and Morphogenesis to Plant Research
inferredcites →https://doi.org/10.1006/bojl.1997.0113openalex-snapshot
Gynoecium diversity and systematics of the Laurales
inferredcites →https://doi.org/10.1007/978-3-7091-6910-0_12openalex-snapshot
Flowers in Magnoliidae and the origin of flowers in other subclasses of the angiosperms. I. The relationships between flowers of Magnoliidae and Alismatidae
inferredcites →https://doi.org/10.1007/bf00024964openalex-snapshot
Aspects of floral development
inferredcites →https://doi.org/10.1007/bf01373364openalex-snapshot
Entwicklungsgeschichtliche Untersuchungen am Androeceum der Alismatales
inferredcites →https://doi.org/10.1007/bf01845744openalex-snapshot
Classification and the new morphology
inferredcites →https://doi.org/10.1007/bf02860852openalex-snapshot
The origin of angiosperms
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/s00606-007-0559-5openalex-snapshot
Flower structure and development in Tupidanthus calyptratus (Araliaceae): an extreme case of polymery among asterids
inferredcites →https://doi.org/10.1071/9780643090149openalex-snapshot
Monocots: Systematics and Evolution
inferredcites →https://doi.org/10.1086/314279openalex-snapshot
Floral Organogenesis in Some Species of Tradescantia and Callisia (Commelinaceae)
inferredcites →https://doi.org/10.1086/317571openalex-snapshot
The Reproductive Structures of the Basal AngiospermAmborella Trichopoda(Amborellaceae)
inferredcites →https://doi.org/10.1086/317572openalex-snapshot
Gynoecium Structure and Evolution in Basal Angiosperms
inferredcites →https://doi.org/10.1086/368235openalex-snapshot
Inside‐Out Flowers Characteristic ofLacandonia schismaticaEvolved at Least before Its Divergence from a Closely Related Taxon,Triuris brevistylis
inferredcites →https://doi.org/10.1086/376878openalex-snapshot
The Evolutionary Significance of Homeosis in Flowers: A Morphological Perspective
inferredcites →https://doi.org/10.1086/376879openalex-snapshot
Monocot Pseudanthia Revisited: Floral Structure of the Mycoheterotrophic Family Triuridaceae
inferredcites →https://doi.org/10.1086/588071openalex-snapshot
The Branching Stamens ofRicinusand the Homologies of the Angiosperm Stamen Fascicle
inferredcites →https://doi.org/10.1093/aob/mcm091openalex-snapshot
The Discovery of Polyandry in Curculigo (Hypoxidaceae): Implications for Androecium Evolution of Asparagoid Monocotyledons
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/oxfordjournals.aob.a085801openalex-snapshot
Androecial Development in Six Polyandrous Genera Representing Five Major Groups of Palms
inferredcites →https://doi.org/10.1093/oxfordjournals.aob.a090303openalex-snapshot
The Early Evolution of the Angiosperms1
inferredcites →https://doi.org/10.1104/pp.010867openalex-snapshot
The Regulation of Compound Leaf Development
inferredcites →https://doi.org/10.1104/pp.117.3.771openalex-snapshot
Overexpression of a Homeobox Gene, LeT6, Reveals Indeterminate Features in the Tomato Compound Leaf1
inferredcites →https://doi.org/10.1105/tpc.11.1.69openalex-snapshot
FILAMENTOUS FLOWER Controls the Formation and Development of Arabidopsis Inflorescences and Floral Meristems
inferredcites →https://doi.org/10.1105/tpc.7.5.529openalex-snapshot
UFO: An Arabidopsis Gene Involved in Both Floral Meristem and Floral Organ Development
inferredcites →https://doi.org/10.1105/tpc.7.9.1485openalex-snapshot
UNUSUAL FLORAL ORGANS Controls Meristem Identity and Organ Primordia Fate in Arabidopsis.
inferredcites →https://doi.org/10.1111/j.1095-8339.1907.tb01074.xopenalex-snapshot
On the Origin of Angiosperms.
inferredcites →https://doi.org/10.1111/j.1095-8339.1978.tb01396.xopenalex-snapshot
Floral organogenesis of Echinodorus amazonicus Rataj and floral construction of the Alismatales
inferredcites →https://doi.org/10.1111/j.1095-8339.1999.tb00528.xopenalex-snapshot
Gynoecium diversity and systematics of the basal eudicots
inferredcites →https://doi.org/10.1111/j.1095-8339.2001.tb00555.xopenalex-snapshot
Gynoecium diversity and systematics in basal monocots
inferredcites →https://doi.org/10.1111/j.1438-8677.1964.tb03493.xopenalex-snapshot
3. G. Bosian: Der Peltier‐Effekt im Einsatz zur Küvettenklima‐Regulierung
inferredcites →https://doi.org/10.1111/j.1756-1051.1987.tb00936.xopenalex-snapshot
The distribution and the systematic relevance of the androecial characters oligomery and polymery in the Magnoliophytina
inferredcites →https://doi.org/10.1111/j.1756-1051.1992.tb01839.xopenalex-snapshot
Complex polyandry in the Magnoliatae: definition, distribution and systematic value
inferredcites →https://doi.org/10.1126/science.283.5409.1911openalex-snapshot
Signaling of Cell Fate Decisions by CLAVATA3 in Arabidopsis Shoot Meristems
inferredcites →https://doi.org/10.1139/b72-076openalex-snapshot
Floral development of Alisma triviale
inferredcites →https://doi.org/10.1139/b73-138openalex-snapshot
Nonspiral androecium and gynoecium of Sagittaria latifolia
inferredcites →https://doi.org/10.1139/b73-314openalex-snapshot
Floral development of Hydrocleis nymphoides
inferredcites →https://doi.org/10.1139/b74-026openalex-snapshot
Floral development of Butomus umbellatus
inferredcites →https://doi.org/10.1139/b77-126openalex-snapshot
Floral organogenesis of Limnocharis flava
inferredcites →https://doi.org/10.1139/b77-127openalex-snapshot
Development of the inflorescence and flower of Sagittaria cuneata
inferredcites →https://doi.org/10.1139/b77-128openalex-snapshot
Floral development of Aponogeton natans and A. undulatus
inferredcites →https://doi.org/10.1139/b89-375openalex-snapshot
Floral development in Arabidopsis thaliana: a comparison of the wild type and the homeotic pistillata mutant
inferredcites →https://doi.org/10.1139/b90-296openalex-snapshot
Leaves and epiphyllous shoots in Chisocheton (Meliaceae): a continuum of woody leaf and stem axes
inferredcites →https://doi.org/10.1139/b94-088openalex-snapshot
Expression of shoot features in early leaf development of Murraya paniculata (Rutaceae)
inferredcites →https://doi.org/10.1139/b99-106openalex-snapshot
Studies in the Alismataceae. XI. Development of the inflorescence and flowers of Wiesneria triandra (Dalzell) Micheli
inferredcites →https://doi.org/10.1139/cjb-77-11-1569openalex-snapshot
Studies in the Alismataceae. XI. Development of the inflorescence and flowers of Wiesneria triandra (Dalzell) Micheli
inferredcites →https://doi.org/10.1242/dev.119.2.397openalex-snapshot
CLAVATA1, a regulator of meristem and flower development in Arabidopsis
inferredcites →https://doi.org/10.1242/dev.121.7.2057openalex-snapshot
CLAVATA3 is a specific regulator of shoot and floral meristem development affecting the same processes as CLAVATA1
inferredcites →https://doi.org/10.1600/0363644041744365openalex-snapshot
A Phylogeny of the Monocots, as Inferred from rbcL and atpA Sequence Variation, and a Comparison of Methods for Calculating Jackknife and Bootstrap Values
inferredcites →https://doi.org/10.1600/036364406777585766openalex-snapshot
Morphological Phylogenetic Analysis of Pandanales: Testing Contrasting Hypotheses of Floral Evolution
inferredcites →https://doi.org/10.1663/0006-8101(2002)068[0488:ufsaie]2.0.co;2openalex-snapshot
Unique Floral Structures and Iterative Evolutionary Themes in Asparagales: Insights from a Morphological Cladistic Analysis
inferredcites →https://doi.org/10.2307/1222385openalex-snapshot
The Role of Scent Glands in Pollination: On the Structure and Function of Osmophores
inferredcites →https://doi.org/10.2307/2399935openalex-snapshot
Pollen Development and Fertilization in Lacandonia schismatica (Lacandoniaceae)
inferredcites →https://doi.org/10.2307/2482553openalex-snapshot
Morphology of the Angiosperms.
inferredcites →https://doi.org/10.2307/2483907openalex-snapshot
Fundamentals of Phytomorphology.
inferredcites →https://doi.org/10.2307/2807789openalex-snapshot
Monocotyledons: Systematics and Evolution.
inferredcites →https://doi.org/10.2307/4111207openalex-snapshot
Kupeaeae, a New Tribe of Triuridaceae from Africa
inferredcites →https://doi.org/10.3732/ajb.93.1.15openalex-snapshot
Comparative developmental series of the Mexican triurids support a euanthial interpretation for the unusual reproductive axes of Lacandonia schismatica (Triuridaceae)
inferredcites →https://doi.org/10.3732/ajb.94.7.1073openalex-snapshot
Morphology of Hydatellaceae, an anomalous aquatic family recently recognized as an early‐divergent angiosperm lineage
inferredcites →https://doi.org/10.5962/bhl.title.127448openalex-snapshot
Versuch die Metamorphose der Pflanzen zu erklaren
inferredcites →https://doi.org/10.5962/p.185558openalex-snapshot
Centrifugal Stamens
inferredcites →https://doi.org/10.7016/bbas.200401.0033openalex-snapshot
Evolution of Apocarpy in Alismatidae Using Phylogenetic Evidence from Chloroplast rbcL Gene Sequence Data

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.268.4.1zenodo-depositor-declared
Seychellaria barbata (Triuridaceae), a new species from Marojejy National Park, Madagascar
inferred← citeshttps://doi.org/10.1002/tax.621005openalex-snapshot
Comparative fruit structure in Hydatellaceae (Nymphaeales) reveals specialized pericarp dehiscence in some early–divergent angiosperms with ascidiate carpels
inferred← citeshttps://doi.org/10.1007/978-1-4614-5209-6_2openalex-snapshot
Taxonomy and Classification
inferred← citeshttps://doi.org/10.1007/s12229-026-09339-wopenalex-snapshot
Heterochrony Underpins the Diversity of Ontogenetic Patterns in Monocot Flowers
inferred← citeshttps://doi.org/10.1016/j.aspen.2017.06.011openalex-snapshot
Seed dispersal by ants in the fully mycoheterotrophic plant Sciaphila secundiflora (Triuridaceae)
inferred← citeshttps://doi.org/10.1016/j.pbi.2009.09.019openalex-snapshot
All in a spin: centrifugal organ formation and floral patterning
inferred← citeshttps://doi.org/10.1016/j.tplants.2009.03.004openalex-snapshot
The key role of morphology in modelling inflorescence architecture
inferred← citeshttps://doi.org/10.1017/cbo9781139002950.014openalex-snapshot
Anther, ovule and embryological characters in Velloziaceae in relation to the systematics of Pandanales
inferred← citeshttps://doi.org/10.1071/sb10015openalex-snapshot
Development of reproductive structures in the sole Indian species of Hydatellaceae, Trithuria konkanensis, and its morphological differences from Australian taxa
inferred← citeshttps://doi.org/10.1080/23818107.2024.2373433openalex-snapshot
Jean-Baptiste Payer (1818–1860), prolific botanist and enlightened French citizen: his legacy in flower development and a need for a new, global compendium
inferred← citeshttps://doi.org/10.1086/653132openalex-snapshot
Homologies of Floral Structures in Velloziaceae with Particular Reference to the Corona
inferred← citeshttps://doi.org/10.1086/676817openalex-snapshot
Comparative Anatomy of Reproductive Structures in Cyclanthaceae (Pandanales)
inferred← citeshttps://doi.org/10.1093/aob/mcs246openalex-snapshot
Racemose inflorescences of monocots: structural and morphogenetic interaction at the flower/inflorescence level
inferred← citeshttps://doi.org/10.1093/aob/mct009openalex-snapshot
Towards an ontogenetic understanding of inflorescence diversity
inferred← citeshttps://doi.org/10.1093/aob/mcu224openalex-snapshot
Current trends and future directions in flower development research
inferred← citeshttps://doi.org/10.1093/jxb/erae080openalex-snapshot
My favourite flowering image: the remarkable inside-out flowers of Lacandonia
inferred← citeshttps://doi.org/10.1093/jxb/erm028openalex-snapshot
Flowering Newsletter bibliography for 2006
inferred← citeshttps://doi.org/10.1093/jxb/erp154openalex-snapshot
Flowering Newsletter bibliography for 2008
inferred← citeshttps://doi.org/10.1093/jxb/ers024openalex-snapshot
When ABC becomes ACB
inferred← citeshttps://doi.org/10.1098/rstb.2009.0234openalex-snapshot
Defining the limits of flowers: the challenge of distinguishing between the evolutionary products of simple versus compound strobili
inferred← citeshttps://doi.org/10.1105/tpc.109.069153openalex-snapshot
B-Function Expression in the Flower Center Underlies the Homeotic Phenotype of Lacandonia schismatica (Triuridaceae)
inferred← citeshttps://doi.org/10.1111/boj.12099openalex-snapshot
Multicarpellate gynoecia in angiosperms: occurrence, development, organization and architectural constraints
inferred← citeshttps://doi.org/10.1111/boj.12188openalex-snapshot
Flower morphology and relationships ofSchefflera subintegra(Araliaceae, Apiales): an evolutionary step towards extreme floral polymery
inferred← citeshttps://doi.org/10.1134/s1062360411040084openalex-snapshot
Morphogenetic lability of the Ruppia maritima (Ruppiaceae, Alismatales) reproductive organs: From two lateral flowers to a terminal flower
inferred← citeshttps://doi.org/10.1134/s1062360419060080openalex-snapshot
One Upward, Two Steps Down: Order of Floral Organ Initiation
inferred← citeshttps://doi.org/10.1139/b2012-060openalex-snapshot
Complex patterns of morphogenesis, embryology, and reproduction in Triuris brevistylis, a species of Triuridaceae (Pandanales) closely related to Lacandonia schismatica
inferred← citeshttps://doi.org/10.1663/0006-8101(2007)73[67:aucotc]2.0.co;2openalex-snapshot
An Updated Classification of the Class Magnoliopsida (“Angiospermae”)
inferred← citeshttps://doi.org/10.29038/2617-4723-2016-332-7-12-16openalex-snapshot
Загальна організація та мерність квітки Однодольних у зв’язку із систематикою
inferred← citeshttps://doi.org/10.3390/plants12244138openalex-snapshot
Patterns of Carpel Structure, Development, and Evolution in Monocots
inferred← citeshttps://doi.org/10.3417/2009142openalex-snapshot
Evolutionary History of the Monocot Flower 1
inferred← citeshttps://doi.org/10.3732/ajb.0800027openalex-snapshot
Nonflowers near the base of extant angiosperms? Spatiotemporal arrangement of organs in reproductive units of Hydatellaceae and its bearing on the origin of the flower
inferred← citeshttps://doi.org/10.3732/ajb.0900074openalex-snapshot
Morphology and development of the gynoecium in Centrolepidaceae: The most remarkable range of variation in Poales
inferred← citeshttps://doi.org/10.3732/ajb.1000299openalex-snapshot
Evolutionary diversification of the flowers in angiosperms
inferred← citeshttps://doi.org/10.3732/ajb.1300355openalex-snapshot
Comparative development of rare cases of a polycarpellate gynoecium in an otherwise monocarpellate family, Leguminosae
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
inferred← citeshttps://doi.org/10.7717/peerj.1653openalex-snapshot
Inside-out flowers of Lacandonia brasiliana (Triuridaceae) provide new insights into fundamental aspects of floral patterning
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.