On the public citation graph
Delimitation of Sauropus (Phyllanthaceae) Based on Plastid matK and Nuclear Ribosomal ITS DNA Sequence Data
0 signed · 61 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.
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known work and none has been retracted — and get a dated CiteStamped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.
What this work says
Outgoing claims: the papers this work cites, builds on, or argues with.
inferredcites →https://doi.org/10.1007/pl00013970openalex-snapshot
Ovules and Seeds in Subfamily Phyllanthoideae (Euphorbiaceae): Structure and Systematic Implications
inferredcites →https://doi.org/10.1016/0168-9525(90)90186-aopenalex-snapshot
PCR protocols — A guide to methods and applications
inferredcites →https://doi.org/10.1016/0968-0004(90)90252-7openalex-snapshot
PCR protocols — A guide to methods and applications
inferredcites →https://doi.org/10.1016/b978-0-12-372180-8.50042-1openalex-snapshot
AMPLIFICATION AND DIRECT SEQUENCING OF FUNGAL RIBOSOMAL RNA GENES FOR PHYLOGENETICS
inferredcites →https://doi.org/10.1016/j.ympev.2004.12.002openalex-snapshot
Molecular phylogenetics of Phyllanthaceae inferred from five genes (plastid atpB, matK, 3′ndhF, rbcL, and nuclear PHYC)
inferredcites →https://doi.org/10.1046/j.1095-8339.2003.t01-1-00158.xopenalex-snapshot
An update of the Angiosperm Phylogeny Group classification for the orders and families of flowering plants: APG II
inferredcites →https://doi.org/10.1073/pnas.0837153100openalex-snapshot
An obligate pollination mutualism and reciprocal diversification in the tree genus Glochidion (Euphorbiaceae)
inferredcites →https://doi.org/10.1080/00173130310016464openalex-snapshot
Pollen morphology of the Flueggeinae (Euphorbiaceae, Phyllanthoideae)
inferredcites →https://doi.org/10.1093/bioinformatics/17.8.754openalex-snapshot
MRBAYES: Bayesian inference of phylogenetic trees
inferredcites →https://doi.org/10.1093/bioinformatics/btg180openalex-snapshot
MrBayes 3: Bayesian phylogenetic inference under mixed models
inferredcites →https://doi.org/10.1093/sysbio/20.4.406openalex-snapshot
Toward Defining the Course of Evolution: Minimum Change for a Specific Tree Topology
inferredcites →https://doi.org/10.1111/boj.12385openalex-snapshot
An update of the Angiosperm Phylogeny Group classification for the orders and families of flowering plants: APG IV
inferredcites →https://doi.org/10.1111/j.1095-8339.1987.tb01041.xopenalex-snapshot
Wood anatomy of the Euphorbiaceae, in particular of the subfamily Phyllanthoideae
inferredcites →https://doi.org/10.1111/j.1365-2699.2004.01149.xopenalex-snapshot
Phytogeography, range size and richness of Australian endemic Sauropus (Euphorbiaceae)
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/10.1159/000156416openalex-snapshot
Interactive Analysis of Phylogeny and Character Evolution Using the Computer Program MacClade
inferredcites →https://doi.org/10.2307/2399139openalex-snapshot
Systematic Foliar Morphology of Phyllanthoideae (Euphorbiaceae). I. Conspectus
inferredcites →https://doi.org/10.2307/2399909openalex-snapshot
Synopsis of the Genera and Suprageneric Taxa of Euphorbiaceae
inferredcites →https://doi.org/10.2307/2412116openalex-snapshot
Toward Defining the Course of Evolution: Minimum Change for a Specific Tree Topology
inferredcites →https://doi.org/10.2307/4110024openalex-snapshot
A Partial Synopsis of the Euphorbiaceae-Platylobeae of Australia (Excluding Phyllanthus, Euphorbia and Calycopeplus)
inferredcites →https://doi.org/10.3732/ajb.91.11.1882openalex-snapshot
Molecular phylogenetic analysis of Phyllanthaceae (Phyllanthoideae pro parte, Euphorbiaceae sensu lato) using plastid RBCL DNA sequences
inferredcites →https://doi.org/10.3732/ajb.91.9.1319openalex-snapshot
Obligate pollination mutualism in Breynia (Phyllanthaceae): further documentation of pollination mutualism involving Epicephala moths (Gracillariidae)
inferredcites →https://doi.org/10.3732/ajb.92.1.132openalex-snapshot
Molecular phylogenetics of Phyllanthaceae: evidence from plastid MATK and nuclear PHYC sequences
inferredcites →https://doi.org/10.3732/ajb.93.4.637openalex-snapshot
Phylogenetics of tribe Phyllantheae (Phyllanthaceae; Euphorbiaceae sensu lato) based on nrITS and plastid matK DNA sequence data
inferredcites →https://doi.org/10.3767/000651903x675017openalex-snapshot
Revision of the Malesian and Thai species of Sauropus (Euphorbiaceae: Phyllanthoideae)
inferredcites →https://doi.org/10.5860/choice.39-2183openalex-snapshot
MacClade 4.0: analysis of phylogeny and character evolution
inferredcites →https://doi.org/10.5962/bhl.title.115427openalex-snapshot
Bijdragen tot de flora van Nederlandsch Indie
inferredcites →https://doi.org/10.5962/bhl.title.116758openalex-snapshot
Fragmenta phytographiae australiae
inferredcites →https://doi.org/10.5962/p.365847openalex-snapshot
Four new rare species of Sauropus Blume (Euphorbiaceae: Phyllantheae) from north Queensland
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
inferred← citeshttps://doi.org/10.1002/tax.12424zenodo-depositor-declared
Molecular phylogenetics of Phyllanthus sensu lato (Phyllanthaceae): Towards coherent monophyletic taxa
inferred← citeshttps://doi.org/10.11646/phytotaxa.319.2.3zenodo-depositor-declared
Phyllanthus eremitus (Phyllanthaceae), a narrowly endemic new species from Santa Catarina, southern Brazil, and lectotypification and range extension of P. hyssopifolioides
inferred← citeshttps://doi.org/10.11646/phytotaxa.706.2.3zenodo-depositor-declared
Synonymization of the name Cathetus roeperianus (Phyllanthaceae) with an emended description and lectotypification of Cathetus fasciculata from the collections of India
inferred← citeshttps://doi.org/10.1002/njb.05025openalex-snapshot
Breynia phuongiana (Phyllanthaceae), a new species from the Central Highlands of Vietnam
inferred← citeshttps://doi.org/10.1002/tax.12887openalex-snapshot
The challenges of classifying big genera such asIpomoea
inferred← citeshttps://doi.org/10.1002/tax.70170openalex-snapshot
A phylogenomic framework for species delimitation in Kirganelia (Phyllanthaceae): Tracing a history of reticulate evolution
inferred← citeshttps://doi.org/10.1007/978-4-431-56532-1_4openalex-snapshot
Diversity of Phyllanthaceae Plants
inferred← citeshttps://doi.org/10.1007/s10709-025-00249-0openalex-snapshot
Comparative plastomes and phylogenetic relationships of Breynia, Glochidion, Phyllanthus, Sauropus, and Synostemon from plastomes and ITS
inferred← citeshttps://doi.org/10.1016/j.japb.2025.09.003openalex-snapshot
Chloroplast genome sequencing of the medicinal plant Flueggea suffruticosa and phylogenetic analysis of Phyllanthaceae
inferred← citeshttps://doi.org/10.1071/sb11005openalex-snapshot
Phylogeny and proposed circumscription of Breynia, Sauropus and Synostemon (Phyllanthaceae), based on chloroplast and nuclear DNA sequences
inferred← citeshttps://doi.org/10.1071/sb14034openalex-snapshot
Molecular data consistently recover a ‘Queensland clade’ of Synostemon (Phyllanthaceae, Phyllantheae) with distinctive floral morphology
inferred← citeshttps://doi.org/10.1071/sb16008openalex-snapshot
Morphological and molecular data show Synostemon trachyspermus (Phyllanthaceae, Phyllantheae) to be a heterogeneous species assemblage
inferred← citeshttps://doi.org/10.1071/sb18029openalex-snapshot
Morphological and molecular data show an enlarged tropical Australian radiation in Synostemon (Phyllanthaceae, Phyllantheae) previously concealed by heteromorphic species concepts
inferred← citeshttps://doi.org/10.1080/00837792.2018.1452370openalex-snapshot
Phyllanthus timboënsis(Phyllanthaceae), a new species from Santa Catarina, southern Brazil
inferred← citeshttps://doi.org/10.1080/13102818.2016.1224978openalex-snapshot
Molecular study of intraspecific differences among Sauropus androgynus (L.) Merr. from Indonesia revealed by ITS region variability
inferred← citeshttps://doi.org/10.1086/706454openalex-snapshot
Phylogenetic Relationships and Character Evolution in NeotropicalPhyllanthus(Phyllanthaceae), with a Focus on the Cuban and Caribbean Taxa
inferred← citeshttps://doi.org/10.1093/botlinnean/boaf037openalex-snapshot
Molecular phylogeny of Phyllanthus L. sect. Phyllanthus (Phyllantheae: Phyllanthaceae) reveals the need for a reclassification of Phyllanthus subg. Phyllanthus
inferred← citeshttps://doi.org/10.1111/j.1438-8677.2011.00455.xopenalex-snapshot
Classification and differentiation of the genus Peganum indigenous to China based on chloroplast trnL‐F and psbA‐trnH sequences and seed coat morphology
inferred← citeshttps://doi.org/10.1111/j.1442-1984.2009.00266.xopenalex-snapshot
Evolution of obligate pollination mutualism in the tribe Phyllantheae (Phyllanthaceae)
inferred← citeshttps://doi.org/10.1111/jbi.12517openalex-snapshot
Historical biogeography of Breynia (Phyllanthaceae): what caused speciation?
inferred← citeshttps://doi.org/10.1111/njb.01072openalex-snapshot
Systematic wood anatomy of the tribe Phyllantheae (Phyllanthaceae, Euphorbiaceae s.l.) from India: implication in reinstatement of Phyllanthus, Glochidion and allies
inferred← citeshttps://doi.org/10.1111/njb.04635openalex-snapshot
Breynia enchengensis (Phyllanthaceae), a new species from limestone areas of southwestern Guangxi, China
inferred← citeshttps://doi.org/10.1371/journal.pone.0019219openalex-snapshot
Gelechiidae Moths Are Capable of Chemically Dissolving the Pollen of Their Host Plants: First Documented Sporopollenin Breakdown by an Animal
inferred← citeshttps://doi.org/10.1600/036364409789271263openalex-snapshot
More Miocene Dispersal Between Africa and Asia—the Case of Bridelia (Phyllanthaceae)
inferred← citeshttps://doi.org/10.3329/bjpt.v19i2.13125openalex-snapshot
Nineteen new combinations and a new name in Breynia J.R. Forst. & G. Forst. (Phyllanthaceae) from Indian subcontinent
inferred← citeshttps://doi.org/10.3767/blumea.2018.63.02.14openalex-snapshot
Subgeneric delimitation of the plant genus Phyllanthus (Phyllanthaceae)
inferred← citeshttps://doi.org/10.3767/blumea.2019.64.03.05openalex-snapshot
A taxonomic revision of Phyllanthus subgenus Macraea (Phyllanthaceae)
inferred← citeshttps://doi.org/10.3897/phytokeys.206.85241openalex-snapshot
Breynia hiemalis (Phyllanthaceae, Phyllantheae), a new species from Yunnan, south-west China
inferred← citeshttps://doi.org/10.3897/phytokeys.225.99506openalex-snapshot
Parallel developments in floral adaptations to obligate moth pollination mutualism in tribe Phyllantheae (Phyllanthaceae)
inferred← citeshttps://doi.org/10.5282/ubm/epub.14660openalex-snapshot
Gelechiidae Moths Are Capable of Chemically Dissolving the Pollen of Their Host Plants
inferred← citeshttps://doi.org/10.58828/nuy00735openalex-snapshot
Synostemon hamersleyensis (Phyllanthaceae), a new species endemic to the Pilbara, Western Australia
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.