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Phylogenetic Position and Floral Function of Siparuna (Siparunaceae: Laurales)
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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.1537-2197.1980.tb07699.xopenalex-snapshot
INFLORESCENCE AND FLOWER DEVELOPMENT IN THE PIPERACEAE. I. PEPEROMIA
inferredcites →https://doi.org/10.1002/j.1537-2197.1982.tb13314.xopenalex-snapshot
INFLORESCENCE AND FLOWER DEVELOPMENT IN THE PIPERACEAE. II. INFLORESCENCE DEVELOPMENT OF PIPER
inferredcites →https://doi.org/10.1002/j.1537-2197.1993.tb13780.xopenalex-snapshot
FUNCTIONAL SYNCARPY BY INTERCARPELLARY GROWTH OF POLLEN TUBES IN A PRIMITIVE APOCARPOUS ANGIOSPERM, ILLICIUM FLORIDANUM (ILLICIACEAE)
inferredcites →https://doi.org/10.1007/978-3-642-39417-1openalex-snapshot
Flowering plants, Eudicots : Malpighiales
inferredcites →https://doi.org/10.1007/bf00037152openalex-snapshot
Universal primers for amplification of three non-coding regions of chloroplast DNA
inferredcites →https://doi.org/10.1007/bf00984112openalex-snapshot
Diversity and evolutionary trends in the floral structure ofTambourissa (Monimiaceae)
inferredcites →https://doi.org/10.1007/bf00985351openalex-snapshot
Remarks on karyological differentiation patterns in tropical woody plants
inferredcites →https://doi.org/10.1007/bf00989009openalex-snapshot
The sporoderm ultrastructure inPersea, Nectandra, Hernandia, Gomortega and some other Lauralean genera
inferredcites →https://doi.org/10.1007/bf00989387openalex-snapshot
Synchronized dichogamy and dioecy in neotropicalLauraceae
inferredcites →https://doi.org/10.1007/bf01373439openalex-snapshot
�ber die Karpelle verschiedener Magnoliales. I
inferredcites →https://doi.org/10.1007/bf01373532openalex-snapshot
�ber die Karpelle verschiedener Magnoliales. VI.Gomortega keule (Gomortegaceae)
inferredcites →https://doi.org/10.1016/0031-9422(80)85004-7openalex-snapshot
Deviations from michaelis-menten behaviour of plant glutamate dehydrogenase with ammonium as variable substrate
inferredcites →https://doi.org/10.1038/344656a0openalex-snapshot
Chloroplast DNA sequence from a Miocene Magnolia species
inferredcites →https://doi.org/10.1080/00173138709429942openalex-snapshot
Pollen morphology ofPalmeria scandensandWilkiea huegeliana(Monimiaceae)
inferredcites →https://doi.org/10.1080/00173139009427751openalex-snapshot
Pollen types in the lauraceae
inferredcites →https://doi.org/10.1080/00173139009427752openalex-snapshot
Pollen morphology ofpeumus boldus(monimiaceae) — a comparison withpalmeria scandens
inferredcites →https://doi.org/10.1111/j.1095-8339.1989.tb01709.xopenalex-snapshot
The diversity of stamen structures and dehiscence patterns among Magnoliidae
inferredcites →https://doi.org/10.1111/j.1558-5646.1985.tb00420.xopenalex-snapshot
CONFIDENCE LIMITS ON PHYLOGENIES: AN APPROACH USING THE BOOTSTRAP
inferredcites →https://doi.org/10.1111/j.1756-1051.1987.tb00911.xopenalex-snapshot
A classification of the Monimiaceae
inferredcites →https://doi.org/10.1126/science.1523408openalex-snapshot
Carnivorous Plants: Phylogeny and Structural Evolution
inferredcites →https://doi.org/10.2307/2399135openalex-snapshot
A Monograph of the Monimiaceae (Laurales) in the Malagasy Region (Southwest Indian Ocean)
inferredcites →https://doi.org/10.2307/2399846openalex-snapshot
Phylogenetics of Seed Plants: An Analysis of Nucleotide Sequences from the Plastid Gene rbcL
inferredcites →https://doi.org/10.2307/2399848openalex-snapshot
Molecular Phylogenetics of the Magnoliidae: Cladistic Analyses of Nucleotide Sequences of the Plastid Gene rbcL
inferredcites →https://doi.org/10.2307/2399899openalex-snapshot
Integration of Morphological and Ribosomal RNA Data on the Origin of Angiosperms
inferredcites →https://doi.org/10.2307/2419537openalex-snapshot
Utility of Ontogenetic and Conventional Characters in Determining Phylogenetic Relationships of Saururaceae and Piperaceae (Piperales)
inferredcites →https://doi.org/10.5962/p.333933openalex-snapshot
The morphology and relationships of the Monimiaceae
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
inferred← citeshttps://doi.org/10.1590/2175-7860202576003zenodo-depositor-declared
Flora of Ceará: Siparunaceae
inferred← citeshttps://doi.org/10.1006/bojl.1997.0113openalex-snapshot
Gynoecium diversity and systematics of the Laurales
inferred← citeshttps://doi.org/10.1007/124_2022_61openalex-snapshot
Plant Evolution and Systematics 1982–2022: Changing Questions and Methods as Seen by a Participant
inferred← citeshttps://doi.org/10.1007/978-1-4020-9609-9_2openalex-snapshot
Class Magnoliopsida (Dicotyledons)
inferred← citeshttps://doi.org/10.1007/978-3-642-56849-7_14openalex-snapshot
Molecular Systematics: 1997–1999
inferred← citeshttps://doi.org/10.1007/bf02869011openalex-snapshot
The classification and geography of the flowering plants: Dicotyledons of the class Angiospermae
inferred← citeshttps://doi.org/10.1007/pl00013988openalex-snapshot
Embryology of Laurales: a Review and Perspectives
inferred← citeshttps://doi.org/10.1007/s10265-003-0091-9openalex-snapshot
Embryology of Siparunaceae (Laurales): characteristics and character evolution
inferred← citeshttps://doi.org/10.1016/j.cretres.2008.07.015openalex-snapshot
Lovellea wintonensis gen. et sp. nov.- Early Cretaceous (late Albian), anatomically preserved, angiospermous flowers and fruits from the Winton Formation, western Queensland, Australia
inferred← citeshttps://doi.org/10.1016/j.cretres.2021.104983openalex-snapshot
Reconstructing the Callianthus plant–An early aquatic angiosperm from the Lower Cretaceous of China
inferred← citeshttps://doi.org/10.1016/j.phytochem.2022.113291openalex-snapshot
Non-volatile constituents from Monimiaceae, Siparunaceae and Atherospermataceae plant species and their bioactivities: An up-date covering 2000–2021
inferred← citeshttps://doi.org/10.1016/s0031-9422(00)00222-3openalex-snapshot
Kaempferol glycosides from Siparuna apiosyce
inferred← citeshttps://doi.org/10.1016/s0034-6667(03)00120-9openalex-snapshot
First Cretaceous flowers from Antarctica
inferred← citeshttps://doi.org/10.1046/j.1095-8339.2003.00171.xopenalex-snapshot
Phylogenetic analysis of Magnoliales and Myristicaceae based on multiple data sets: implications for character evolution
inferred← citeshttps://doi.org/10.1046/j.1420-9101.2002.00414.xopenalex-snapshot
Evolution of syncarpy in angiosperms: theoretical and phylogenetic analyses of the effects of carpel fusion on offspring quantity and quality
inferred← citeshttps://doi.org/10.1071/sb04004openalex-snapshot
Structure and relationships of basal relictual angiosperms
inferred← citeshttps://doi.org/10.1078/1433-8319-00052openalex-snapshot
Phylogenetic affinities of Monimiaceae based on cpDNA gene and spacer sequences
inferred← citeshttps://doi.org/10.1080/03115518.2013.798765openalex-snapshot
Fruits and leaves with cuticle ofLaurelia otagoensissp. nov. (Atherospermataceae) from the early Miocene of Otago (New Zealand)
inferred← citeshttps://doi.org/10.1080/10412905.2010.9700338openalex-snapshot
Volatile Constituents of the Fruits ofSiparuna thecaphora(Siparunaceae) from Costa Rica
inferred← citeshttps://doi.org/10.1080/106351501753328820openalex-snapshot
Repeated Evolution of Dioecy from Monoecy in Siparunaceae (Laurales)
inferred← citeshttps://doi.org/10.1080/14786419.2013.843179openalex-snapshot
A new monoterpene glycoside fromSiparuna thecaphora
inferred← citeshttps://doi.org/10.1086/317572openalex-snapshot
Gynoecium Structure and Evolution in Basal Angiosperms
inferred← citeshttps://doi.org/10.1086/317574openalex-snapshot
What Is the Relationship among Hernandiaceae, Lauraceae, and Monimiaceae, and Why Is This Question So Difficult to Answer?
inferred← citeshttps://doi.org/10.1086/317584openalex-snapshot
Phylogeny of Basal Angiosperms: Analyses of Five Genes from Three Genomes
inferred← citeshttps://doi.org/10.1086/377063openalex-snapshot
Evolution of Floral Structures in Basal Angiosperms
inferred← citeshttps://doi.org/10.1086/593045openalex-snapshot
Comparative Gynoecium Structure and Development in Calycanthaceae (Laurales)
inferred← citeshttps://doi.org/10.1086/699281openalex-snapshot
Fruit Structure of Calycanthaceae (Laurales): Histology and Development
inferred← citeshttps://doi.org/10.1093/aob/mcr120openalex-snapshot
Angiosperm ovules: diversity, development, evolution
inferred← citeshttps://doi.org/10.1098/rstb.2009.0228openalex-snapshot
The evolution of floral biology in basal angiosperms
inferred← citeshttps://doi.org/10.1111/j.1096-0031.2010.00317.xopenalex-snapshot
Are monophyly and synapomorphy the same or different? Revisiting the role of morphology in phylogenetics
inferred← citeshttps://doi.org/10.1111/j.1469-8137.2011.03912.xopenalex-snapshot
Extra‐gynoecial pollen‐tube growth in apocarpous angiosperms is phylogenetically widespread and probably adaptive
inferred← citeshttps://doi.org/10.1111/j.1759-6831.2011.00171.xopenalex-snapshot
Deceit pollination and the effect of deforestation on reproduction in dioecious Schisandra sphenanthera (Schisandraceae) in central China
inferred← citeshttps://doi.org/10.1146/annurev.ecolsys.29.1.567openalex-snapshot
PHYLOGENY OF VASCULAR PLANTS
inferred← citeshttps://doi.org/10.11606/issn.2316-9052.v39p59-66openalex-snapshot
Flora da Serra do Cipó, Minas Gerais: Siparunaceae
inferred← citeshttps://doi.org/10.1554/02-445openalex-snapshot
CONVERGENCE AND COEVOLUTION IN A MUTUALISM: EVIDENCE FROM A MOLECULAR PHYLOGENY OF FICUS
inferred← citeshttps://doi.org/10.1590/s0102-695x2012005000040openalex-snapshot
Chemical constituents from three medicinal plants: Piper renitens, Siparuna guianensis and Alternanthera brasiliana
inferred← citeshttps://doi.org/10.2307/2656778openalex-snapshot
Circumscription and phylogeny of the Laurales: evidence from molecular and morphological data
inferred← citeshttps://doi.org/10.26879/386openalex-snapshot
Rare leaf fossils of Monimiaceae and Atherospermataceae (Laurales) from Eocene Patagonian rainforests and their biogeographic significance
inferred← citeshttps://doi.org/10.3389/fpls.2022.956193openalex-snapshot
Conspecific pollen advantage mediated by the extragynoecial compitum and its potential to resist interspecific reproductive interference between two Sagittaria species
inferred← citeshttps://doi.org/10.3390/plants11070974openalex-snapshot
Functional Differentiation of Floral Color and Scent in Gall Midge Pollination: A Study of a Schisandraceae Plant
inferred← citeshttps://doi.org/10.3732/ajb.0800047openalex-snapshot
Reconstructing the ancestral angiosperm flower and its initial specializations
inferred← citeshttps://doi.org/10.3732/ajb.1000077openalex-snapshot
Flower heating following anthesis and the evolution of gall midge pollination in Schisandraceae
inferred← citeshttps://doi.org/10.3732/ajb.1000299openalex-snapshot
Evolutionary diversification of the flowers in angiosperms
inferred← citeshttps://doi.org/10.3732/ajb.1100165openalex-snapshot
Intercarpellary growth of pollen tubes in the extragynoecial compitum and its contribution to fruit set in an apocarpous species, Schisandra sphenanthera (Schisandraceae)
inferred← citeshttps://doi.org/10.3732/ajb.1400359openalex-snapshot
Pollination of Vietnamese Aspidistra xuansonensis (Asparagaceae) by female Cecidomyiidi flies: Larvae of pollinator feed on fertile pollen in anthers of anthetic bisexual flowers
inferred← citeshttps://doi.org/10.3732/ajb.1500393openalex-snapshot
A mosaic Lauralean flower from the Early Cretaceous of Myanmar
inferred← citeshttps://doi.org/10.3732/ajb.92.9.1475openalex-snapshot
An extinct calycanthoid taxon, Jerseyanthus calycanthoides , from the Late Cretaceous of New Jersey
inferred← citeshttps://doi.org/10.3732/ajb.94.12.2041openalex-snapshot
Potomacanthus lobatus gen. et sp. nov., a new flower of probable Lauraceae from the Early Cretaceous (Early to Middle Albian) of eastern North America
inferred← citeshttps://doi.org/10.4067/s0716-078x2009000300007openalex-snapshot
Flower and fruit production and insect pollination of the endangered Chilean tree, Gomortega keule in native forest, exotic pine plantation and agricultural environments
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