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A few‐gene plastid phylogenetic framework for mycoheterotrophic monocots

https://doi.org/10.3732/ajb.1500412
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What this work says

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

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Pigment composition of putatively achlorophyllous angiosperms
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Plant mitochondrial DNA evolved rapidly in structure, but slowly in sequence
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Phylogenetic analysis using parsimony and likelihood methods
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raxmlGUI: a graphical front-end for RAxML
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Missing data and the design of phylogenetic analyses
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Myco-heterotroph/epiparasitic plant interactions with ectomycorrhizal and arbuscular mycorrhizal fungi
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Why are plastid genomes retained in non-photosynthetic organisms?
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New insights in the long-debated evolutionary history of Triuridaceae (Pandanales)
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Basic Local Alignment Search Tool
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Oldest known fossils of monocotyledons
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Gene transfer to the nucleus and the evolution of chloroplasts
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Gene transfer from parasitic to host plants
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Molecular phylogenetics: principles and practice
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An update of the Angiosperm Phylogeny Group classification for the orders and families of flowering plants: APG II
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A Phylogenetic Analysis of the Plastid matK Gene with Emphasis on Melanthiaceae sensu lato
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A phylogeny inferred from large-subunit (26S) ribosomal DNA sequences suggests that Burmanniales are polyphyletic
inferredcites →https://doi.org/10.1073/pnas.0709121104openalex-snapshot
Analysis of 81 genes from 64 plastid genomes resolves relationships in angiosperms and identifies genome-scale evolutionary patterns
inferredcites →https://doi.org/10.1073/pnas.0905845106openalex-snapshot
A DNA barcode for land plants
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Fine-scale mergers of chloroplast and mitochondrial genes create functional, transcompartmentally chimeric mitochondrial genes
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Comparative analysis of a large dataset indicates that internal transcribed spacer (ITS) should be incorporated into the core barcode for seed plants
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Factors mediating plastid dependency and the origins of parasitism in apicomplexans and their close relatives
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Rates of nucleotide substitution vary greatly among plant mitochondrial, chloroplast, and nuclear DNAs.
inferredcites →https://doi.org/10.1073/pnas.89.22.10648openalex-snapshot
Function and evolution of a minimal plastid genome from a nonphotosynthetic parasitic plant.
inferredcites →https://doi.org/10.1080/0028825x.2003.9512828openalex-snapshot
A phylogenetic analysis of large‐subunit (26S) ribosome DNA sequences suggests that the Corsiaceae are polyphyletic
inferredcites →https://doi.org/10.1080/10635150117959openalex-snapshot
Bias in Phylogenetic Estimation and Its Relevance to the Choice between Parsimony and Likelihood Methods
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An Approximately Unbiased Test of Phylogenetic Tree Selection
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Increased Taxon Sampling Is Advantageous for Phylogenetic Inference
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Can Incomplete Taxa Rescue Phylogenetic Analyses from Long-Branch Attraction?
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Branch-Length Prior Influences Bayesian Posterior Probability of Phylogeny
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Resolution of Phylogenetic Conflict in Large Data Sets by Increased Taxon Sampling
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Taxonomic Sampling, Phylogenetic Accuracy, and Investigator Bias
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Microstructural Changes in Noncoding Chloroplast DNA: Interpretation, Evolution, and Utility of Indels and Inversions in Basal Angiosperm Phylogenetic Inference
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Myco-heterotrophy: when fungi host plants
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CONSEL: for assessing the confidence of phylogenetic tree selection
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RAxML-VI-HPC: maximum likelihood-based phylogenetic analyses with thousands of taxa and mixed models
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Sequencing and Analysis of Plastid Genome in Mycoheterotrophic Orchid Neottia nidus-avis
inferredcites →https://doi.org/10.1093/gbe/evu001openalex-snapshot
The Plastid Genome of Mycoheterotrophic Monocot Petrosavia stellaris Exhibits Both Gene Losses and Multiple Rearrangements
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Exploring the Limits for Reduction of Plastid Genomes: A Case Study of the Mycoheterotrophic Orchids Epipogium aphyllum and Epipogium roseum
inferredcites →https://doi.org/10.1093/gbe/evv134openalex-snapshot
The Highly Reduced Plastome of MycoheterotrophicSciaphila(Triuridaceae) Is Colinear with Its Green Relatives and Is under Strong Purifying Selection
inferredcites →https://doi.org/10.1093/gbe/evv251openalex-snapshot
The Plastomes of Two Species in the Endoparasite GenusPilostyles(Apodanthaceae) Each Retain Just Five or Six Possibly Functional Genes
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How Meaningful Are Bayesian Support Values?
inferredcites →https://doi.org/10.1093/molbev/msm267openalex-snapshot
Functional Gene Losses Occur with Minimal Size Reduction in the Plastid Genome of the Parasitic Liverwort Aneura mirabilis
inferredcites →https://doi.org/10.1093/molbev/msr028openalex-snapshot
Rampant Gene Loss in the Underground Orchid Rhizanthella gardneri Highlights Evolutionary Constraints on Plastid Genomes
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PartitionFinder: Combined Selection of Partitioning Schemes and Substitution Models for Phylogenetic Analyses
inferredcites →https://doi.org/10.1093/molbev/mss075openalex-snapshot
Bayesian Phylogenetics with BEAUti and the BEAST 1.7
inferredcites →https://doi.org/10.1093/molbev/msu051openalex-snapshot
Possible Loss of the Chloroplast Genome in the Parasitic Flowering Plant Rafflesia lagascae (Rafflesiaceae)
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Investigating the Path of Plastid Genome Degradation in an Early-Transitional Clade of Heterotrophic Orchids, and Implications for Heterotrophic Angiosperms
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Cases in which Parsimony or Compatibility Methods will be Positively Misleading
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General Inconsistency Conditions for Maximum Parsimony: Effects of Branch Lengths and Increasing Numbers of Taxa
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Is the Felsenstein Zone a Fly Trap?
inferredcites →https://doi.org/10.1093/sysbio/49.2.369openalex-snapshot
Gaps as Characters in Sequence-Based Phylogenetic Analyses
inferredcites →https://doi.org/10.1093/sysbio/syu044openalex-snapshot
Maximum Likelihood Inference of Small Trees in the Presence of Long Branches
inferredcites →https://doi.org/10.1098/rspb.2005.3067openalex-snapshot
Repeated evolution of net venation and fleshy fruits among monocots in shaded habitats confirms a priori predictions: evidence from an ndhF phylogeny
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Potential Functional Replacement of the Plastidic Acetyl-CoA Carboxylase Subunit (accD) Gene by Recent Transfers to the Nucleus in Some Angiosperm Lineages
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A Plastid without a Genome: Evidence from the Nonphotosynthetic Green Algal Genus Polytomella
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The Rice Nuclear Genome Continuously Integrates, Shuffles, and Eliminates the Chloroplast Genome to Cause Chloroplast–Nuclear DNA Flux
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Mechanisms of Functional and Physical Genome Reduction in Photosynthetic and Nonphotosynthetic Parasitic Plants of the Broomrape Family
inferredcites →https://doi.org/10.1105/tpc.7.10.1713openalex-snapshot
The stroma of higher plant plastids contain ClpP and ClpC, functional homologs of Escherichia coli ClpP and ClpA: an archetypal two-component ATP-dependent protease.
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Familial relationships of the monocot order Liliales based on a molecular phylogenetic analysis using four plastid loci:matK,rbcL,atpBandatpF-H
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Monocot fossils suitable for molecular dating analyses
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An update of the Angiosperm Phylogeny Group classification for the orders and families of flowering plants: APG III
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The biology of myco‐heterotrophic (‘saprophytic’) plants
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Evolution of mycoheterotrophy in plants: a phylogenetic perspective
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Testing candidate plant barcode regions in the Myristicaceae
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.1931-0846.2007.tb00409.xopenalex-snapshot
The Fall Line: a Physiographic‐Forest Vegetation Boundary
inferredcites →https://doi.org/10.1111/jbi.12486openalex-snapshot
Ancient Gondwana break‐up explains the distribution of the mycoheterotrophic family Corsiaceae (Liliales)
inferredcites →https://doi.org/10.1111/nph.13784openalex-snapshot
Massive intracellular gene transfer during plastid genome reduction in nongreen Orobanchaceae
inferredcites →https://doi.org/10.1126/science.1094786openalex-snapshot
Complete Genome Sequence of the Apicomplexan, Cryptosporidium parvum
inferredcites →https://doi.org/10.1126/science.1100671openalex-snapshot
Host-to-Parasite Gene Transfer in Flowering Plants: Phylogenetic Evidence from Malpighiales
inferredcites →https://doi.org/10.1126/science.1187145openalex-snapshot
Horizontal Gene Transfer by the Parasitic Plant Striga hermonthica
inferredcites →https://doi.org/10.1139/b09-093openalex-snapshot
Inference of phylogenetic relationships among the subfamilies of grasses (Poaceae: Poales) using meso-scale exemplar-based sampling of the plastid genome
inferredcites →https://doi.org/10.1146/annurev.ecolsys.36.102003.152633openalex-snapshot
Model Selection in Phylogenetics
inferredcites →https://doi.org/10.1146/annurev.ge.22.120188.002513openalex-snapshot
PHYLOGENIES FROM MOLECULAR SEQUENCES: INFERENCE AND RELIABILITY
inferredcites →https://doi.org/10.1186/1471-2148-14-23openalex-snapshot
From algae to angiosperms–inferring the phylogeny of green plants (Viridiplantae) from 360 plastid genomes
inferredcites →https://doi.org/10.1186/1471-2148-8-178openalex-snapshot
Diversification of myco-heterotrophic angiosperms: evidence from Burmanniaceae
inferredcites →https://doi.org/10.1186/1471-2164-12-211openalex-snapshot
Building a model: developing genomic resources for common milkweed (Asclepias syriaca) with low coverage genome sequencing
inferredcites →https://doi.org/10.1186/1471-2229-7-57openalex-snapshot
Complete plastid genome sequences suggest strong selection for retention of photosynthetic genes in the parasitic plant genus Cuscuta
inferredcites →https://doi.org/10.1214/aos/1176344136openalex-snapshot
Estimating the Dimension of a Model
inferredcites →https://doi.org/10.1371/journal.pone.0002802openalex-snapshot
Multiple Multilocus DNA Barcodes from the Plastid Genome Discriminate Plant Species Equally Well
inferredcites →https://doi.org/10.1371/journal.pone.0005982openalex-snapshot
Parallel Loss of Plastid Introns and Their Maturase in the Genus Cuscuta
inferredcites →https://doi.org/10.1371/journal.pone.0007891openalex-snapshot
Long-Branch Attraction Bias and Inconsistency in Bayesian Phylogenetics
inferredcites →https://doi.org/10.1371/journal.pone.0019254openalex-snapshot
Choosing and Using a Plant DNA Barcode
inferredcites →https://doi.org/10.1371/journal.pone.0042925openalex-snapshot
Highly Incomplete Taxa Can Rescue Phylogenetic Analyses from the Negative Impacts of Limited Taxon Sampling
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/10.1600/036364408785679806openalex-snapshot
Iridaceae 'Out of Australasia'? Phylogeny, Biogeography, and Divergence Time Based on Plastid DNA Sequences
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Recircumscription of the monocotyledonous family Petrosaviaceae to include Japonolirion
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/10.2307/2412923openalex-snapshot
Cases in which Parsimony or Compatibility Methods Will be Positively Misleading
inferredcites →https://doi.org/10.2307/2419691openalex-snapshot
Corsiopsis chinensis gen. et sp. nov. (Corsiaceae): First Record of the Family in Asia
inferredcites →https://doi.org/10.2307/2656749openalex-snapshot
Utility of 17 chloroplast genes for inferring the phylogeny of the basal angiosperms
inferredcites →https://doi.org/10.2307/2666142openalex-snapshot
The Evolution of Non-Coding Chloroplast DNA and Its Application in Plant Systematics
inferredcites →https://doi.org/10.2307/2992015openalex-snapshot
An Ordinal Classification for the Families of Flowering Plants
inferredcites →https://doi.org/10.2307/2992396openalex-snapshot
A Framework for the Quantitative Study of Evolutionary Trees
inferredcites →https://doi.org/10.2307/3558433openalex-snapshot
Molecular systematics of Iridaceae: evidence from four plastid DNA regions
inferredcites →https://doi.org/10.3417/2010023openalex-snapshot
Assembling the Tree of the Monocotyledons: Plastome Sequence Phylogeny and Evolution of Poales 1
inferredcites →https://doi.org/10.3724/sp.j.1002.2008.08016openalex-snapshot
Taxon sampling and the accuracy of phylogenetic analyses
inferredcites →https://doi.org/10.3732/ajb.1000404openalex-snapshot
Angiosperm phylogeny: 17 genes, 640 taxa
inferredcites →https://doi.org/10.3732/ajb.1200256openalex-snapshot
The plastid genome of the mycoheterotrophic Corallorhiza striata (Orchidaceae) is in the relatively early stages of degradation
inferredcites →https://doi.org/10.3732/ajb.89.12.1940openalex-snapshot
Triuridaceae fossil flowers from the Upper Cretaceous of New Jersey
inferredcites →https://doi.org/10.3732/ajb.90.12.1758openalex-snapshot
Angiosperm phylogeny based on <011>mat K sequence information
inferredcites →https://doi.org/10.3732/ajb.91.6.997openalex-snapshot
Amborella not a “basal angiosperm”? Not so fast
inferredcites →https://doi.org/10.3732/ajb.93.11.1684openalex-snapshot
Phylogeny and evolution of Burmanniaceae (Dioscoreales) based on nuclear and mitochondrial data
inferredcites →https://doi.org/10.3732/ajb.95.4.498openalex-snapshot
Relationships and evolution of matK in a group of leafless orchids (Corallorhiza and Corallorhizinae; Orchidaceae: Epidendroideae)
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

What points at this work

Incoming claims: where this work appears in other papers’ reference lists and arguments.

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Seychellaria barbata (Triuridaceae), a new species from Marojejy National Park, Madagascar
inferred← citeshttps://doi.org/10.11646/phytotaxa.441.3.1zenodo-depositor-declared
A revision of the family Thismiaceae (Dioscoreales) in Cambodia, Laos and Vietnam
inferred← citeshttps://doi.org/10.11646/phytotaxa.548.2.10zenodo-depositor-declared
How many species are there in the monocot order Petrosaviales? Synonymization of Petrosavia amamiensis with P. sakuraii
inferred← citeshttps://doi.org/10.11646/phytotaxa.564.2.5zenodo-depositor-declared
Thismia petasiformis (Thismiaceae), a new fairy lantern species from the Brazilian Amazon Forest
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Phylogenetic and biogeographical analyses of Thismia (Thismiaceae) support T. malipoensis as the eighth species in China
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Phylogenomic inference in extremis: A case study with mycoheterotroph plastomes
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Monocot plastid phylogenomics, timeline, net rates of species diversification, the power of multi‐gene analyses, and a functional model for the origin of monocots
inferred← citeshttps://doi.org/10.1002/ajb2.1397openalex-snapshot
Organellomic data sets confirm a cryptic consensus on (unrooted) land‐plant relationships and provide new insights into bryophyte molecular evolution
inferred← citeshttps://doi.org/10.1002/ajb2.16084openalex-snapshot
Phylogenomics and plastome evolution of a Brazilian mycoheterotrophic orchid, Pogoniopsis schenckii
inferred← citeshttps://doi.org/10.1002/ajb2.70267openalex-snapshot
Placing very long branch taxa in the plant tree of life: A case study with Dioscoreales mycoheterotrophs
inferred← citeshttps://doi.org/10.1002/ppp3.26openalex-snapshot
Oxygyne: An extraordinarily elusive flower
inferred← citeshttps://doi.org/10.1002/tax.12769openalex-snapshot
Phylogeny and historical biogeography of the Panama‐hat family (Cyclanthaceae, Pandanales)
inferred← citeshttps://doi.org/10.1007/s12225-023-10124-wopenalex-snapshot
Afrothismiaceae (Dioscoreales), a new fully mycoheterotrophic family endemic to tropical Africa
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The first complete plastid genome of Burmannia disticha L. from the mycoheterotrophic monocot family Burmanniaceae
inferred← citeshttps://doi.org/10.1071/bt22075openalex-snapshot
Retention of an apparently functional plastome in an apparently mycoheterotrophic orchid, Dipodium roseum D.L.Jones & M.A.Clem. (Orchidaceae)
inferred← citeshttps://doi.org/10.1071/bt22075_coopenalex-snapshot
Corrigendum to : Retention of an apparently functional plastome in an apparently mycoheterotrophic orchid, Dipodium roseum D.L.Jones & M.A.Clem. (Orchidaceae)
inferred← citeshttps://doi.org/10.1071/sb18028openalex-snapshot
Evolution of Geosiris (Iridaceae): historical biogeography and plastid-genome evolution in a genus of non-photosynthetic tropical rainforest herbs disjunct across the Indian Ocean
inferred← citeshttps://doi.org/10.1093/botlinnean/boaa017openalex-snapshot
Phylogenetics of the mycoheterotrophic genus Thismia (Thismiaceae: Dioscoreales) with a focus on the Old World taxa: delineation of novel natural groups and insights into the evolution of morphological traits
inferred← citeshttps://doi.org/10.1093/botlinnean/boag020openalex-snapshot
Phylogeny, morphological evolution, and taxonomic diversity of the mycoheterotrophic genus Epirixanthes (Polygalaceae)
inferred← citeshttps://doi.org/10.1093/gbe/evac183openalex-snapshot
Phylotranscriptomic Analyses of Mycoheterotrophic Monocots Show a Continuum of Convergent Evolutionary Changes in Expressed Nuclear Genes From Three Independent Nonphotosynthetic Lineages
inferred← citeshttps://doi.org/10.1093/gbe/evy064openalex-snapshot
Genome Reports: Contracted Genes and Dwarfed Plastome in Mycoheterotrophic Sciaphila thaidanica (Triuridaceae, Pandanales)
inferred← citeshttps://doi.org/10.1111/cla.12417openalex-snapshot
A bi‐organellar phylogenomic study of Pandanales: inference of higher‐order relationships and unusual rate‐variation patterns
inferred← citeshttps://doi.org/10.1111/nph.14398openalex-snapshot
Plastomes on the edge: the evolutionary breakdown of mycoheterotroph plastid genomes
inferred← citeshttps://doi.org/10.1111/nph.14681openalex-snapshot
On the brink: the highly reduced plastomes of nonphotosynthetic Ericaceae
inferred← citeshttps://doi.org/10.1111/nph.18335openalex-snapshot
Mitochondrial genomic data are effective at placing mycoheterotrophic lineages in plant phylogeny
inferred← citeshttps://doi.org/10.11606/d.41.2022.tde-02082022-195122openalex-snapshot
Diversidade e filogenia do complexo Laurencia (Ceramiales, Rhodophyta) no Atlântico tropical e subtropical com ênfase na costa da Venezuela
inferred← citeshttps://doi.org/10.11606/t.41.2019.tde-11012019-145936openalex-snapshot
Systematics of Cyclanthaceae
inferred← citeshttps://doi.org/10.1186/s12870-023-04302-yopenalex-snapshot
Habitat-related plastome evolution in the mycoheterotrophic Neottia listeroides complex (Orchidaceae, Neottieae)
inferred← citeshttps://doi.org/10.1186/s12915-021-01166-2openalex-snapshot
Plastid phylogenomic insights into relationships of all flowering plant families
inferred← citeshttps://doi.org/10.15553/c2017v722a2openalex-snapshot
First record of Geosiris (Iridaceae: Geosiridoideae) from Australasia : a new record and a new species from the Wet Tropics of Queensland, Australia
inferred← citeshttps://doi.org/10.3389/fpls.2020.00022openalex-snapshot
Plastome Evolution and Phylogeny of Orchidaceae, With 24 New Sequences
inferred← citeshttps://doi.org/10.3389/fpls.2020.00729openalex-snapshot
Insights Into Chloroplast Genome Evolution Across Opuntioideae (Cactaceae) Reveals Robust Yet Sometimes Conflicting Phylogenetic Topologies
inferred← citeshttps://doi.org/10.3389/fpls.2021.602598openalex-snapshot
Comparative Analysis of Plastid Genomes in the Non-photosynthetic Genus Thismia Reveals Ongoing Gene Set Reduction
inferred← citeshttps://doi.org/10.3389/fpls.2022.876779openalex-snapshot
Phylogenomic resolution of order- and family-level monocot relationships using 602 single-copy nuclear genes and 1375 BUSCO genes
inferred← citeshttps://doi.org/10.3389/fpls.2023.1160446openalex-snapshot
Evolutionary differences in gene loss and pseudogenization among mycoheterotrophic orchids in the tribe Vanilleae (subfamily Vanilloideae)
inferred← citeshttps://doi.org/10.3389/fpls.2025.1511582openalex-snapshot
Resolving phylogenetic conflicts in Pandanales: the dual roles of gene flow and whole-genome duplication
inferred← citeshttps://doi.org/10.3732/ajb.1600042openalex-snapshot
Drastic reduction of plastome size in the mycoheterotrophic Thismia tentaculata relative to that of its autotrophic relative Tacca chantrieri
inferred← citeshttps://doi.org/10.3732/apps.1700079openalex-snapshot
Using Herbarium‐Derived DNAs to Assemble a Large‐Scale DNA Barcode Library for the Vascular Plants of Canada
inferred← citeshttps://doi.org/10.6084/m9.figshare.16900939openalex-snapshot
Additional file 10 of Plastid phylogenomic insights into relationships of all flowering plant families
inferred← citeshttps://doi.org/10.6084/m9.figshare.16900945openalex-snapshot
Additional file 11 of Plastid phylogenomic insights into relationships of all flowering plant families
inferred← citeshttps://doi.org/10.6084/m9.figshare.16900948openalex-snapshot
Additional file 12 of Plastid phylogenomic insights into relationships of all flowering plant families
inferred← citeshttps://doi.org/10.6084/m9.figshare.16900951openalex-snapshot
Additional file 13 of Plastid phylogenomic insights into relationships of all flowering plant families
inferred← citeshttps://doi.org/10.6084/m9.figshare.16900957openalex-snapshot
Additional file 14 of Plastid phylogenomic insights into relationships of all flowering plant families
inferred← citeshttps://doi.org/10.6084/m9.figshare.16900960openalex-snapshot
Additional file 15 of Plastid phylogenomic insights into relationships of all flowering plant families
inferred← citeshttps://doi.org/10.6084/m9.figshare.16900963openalex-snapshot
Additional file 1 of Plastid phylogenomic insights into relationships of all flowering plant families
inferred← citeshttps://doi.org/10.6084/m9.figshare.16900966openalex-snapshot
Additional file 2 of Plastid phylogenomic insights into relationships of all flowering plant families
inferred← citeshttps://doi.org/10.6084/m9.figshare.16900972openalex-snapshot
Additional file 3 of Plastid phylogenomic insights into relationships of all flowering plant families
inferred← citeshttps://doi.org/10.6084/m9.figshare.16900975openalex-snapshot
Additional file 4 of Plastid phylogenomic insights into relationships of all flowering plant families
inferred← citeshttps://doi.org/10.6084/m9.figshare.16900978openalex-snapshot
Additional file 5 of Plastid phylogenomic insights into relationships of all flowering plant families
inferred← citeshttps://doi.org/10.6084/m9.figshare.16900984openalex-snapshot
Additional file 6 of Plastid phylogenomic insights into relationships of all flowering plant families
inferred← citeshttps://doi.org/10.6084/m9.figshare.16900987openalex-snapshot
Additional file 7 of Plastid phylogenomic insights into relationships of all flowering plant families
inferred← citeshttps://doi.org/10.6084/m9.figshare.16900990openalex-snapshot
Additional file 8 of Plastid phylogenomic insights into relationships of all flowering plant families
inferred← citeshttps://doi.org/10.6084/m9.figshare.16900996openalex-snapshot
Additional file 9 of Plastid phylogenomic insights into relationships of all flowering plant families
inferred← citeshttps://doi.org/10.6084/m9.figshare.23250662openalex-snapshot
Additional file 1 of Habitat-related plastome evolution in the mycoheterotrophic Neottia listeroides complex (Orchidaceae, Neottieae)
inferred← citeshttps://doi.org/10.64898/2026.10.07.757398openalex-snapshot
Unexpected excess heterozygosity in a threatened, mycoheterotrophic, self-pollinating orchid
inferred← citeshttps://doi.org/10.7287/peerj.6896v0.1/reviews/1openalex-snapshot
Peer Review #1 of "Chemodiversity of Calophyllum inophyllum L. oil bioactive components related to their specific geographical distribution in the South Pacific region (v0.1)"
inferred← citeshttps://doi.org/10.7287/peerj.6896v0.1/reviews/2openalex-snapshot
Peer Review #2 of "Chemodiversity of Calophyllum inophyllum L. oil bioactive components related to their specific geographical distribution in the South Pacific region (v0.1)"
inferred← citeshttps://doi.org/10.7287/peerj.6896v0.1/reviews/3openalex-snapshot
Peer Review #3 of "Chemodiversity of Calophyllum inophyllum L. oil bioactive components related to their specific geographical distribution in the South Pacific region (v0.1)"
inferred← citeshttps://doi.org/10.7287/peerj.6896v0.2/reviews/1openalex-snapshot
Peer Review #1 of "Chemodiversity of Calophyllum inophyllum L. oil bioactive components related to their specific geographical distribution in the South Pacific region (v0.2)"
inferred← citeshttps://doi.org/10.7287/peerj.6896v0.2/reviews/2openalex-snapshot
Peer Review #2 of "Chemodiversity of Calophyllum inophyllum L. oil bioactive components related to their specific geographical distribution in the South Pacific region (v0.2)"
inferred← citeshttps://doi.org/10.7287/peerj.6896v0.2/reviews/3openalex-snapshot
Peer Review #3 of "Chemodiversity of Calophyllum inophyllum L. oil bioactive components related to their specific geographical distribution in the South Pacific region (v0.2)"
inferred← citeshttps://doi.org/10.7717/peerj.6896openalex-snapshot
Chemodiversity of Calophyllum inophyllum L. oil bioactive components related to their specific geographical distribution in the South Pacific region
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.