On the public citation graph

DNA sequences from three genomes reveal multiple long-distance dispersals and non-monophyly of sections in Australasian Plantago (Plantaginaceae)

0 signed · 134 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 See whether every reference in this work resolves to a known work and none has been retracted — and get a dated CiteStamped badge you can embed.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/tax.562028openalex-snapshot

Botanical names in Southern Hemisphere Veronica ( Plantaginaceae ): sect. Detzneria , sect. Hebe , and sect. Labiatoides

inferredcites →https://doi.org/10.1006/mpev.1999.0614openalex-snapshot

Phylogeny, Biogeography, and Processes of Molecular Differentiation in Quercus Subgenus Quercus (Fagaceae)

inferredcites →https://doi.org/10.1007/bf01734359openalex-snapshot

Evolutionary trees from DNA sequences: A maximum likelihood approach

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.tplants.2006.06.004openalex-snapshot

Reconstructing reticulate evolutionary histories of plants

inferredcites →https://doi.org/10.1016/j.ympev.2007.04.001openalex-snapshot

The relative performance of indel-coding methods in simulations

inferredcites →https://doi.org/10.1016/j.ympev.2007.12.019openalex-snapshot

Phylogeographic patterns in the Australasian genus Chionohebe (Veronica s.l., Plantaginaceae) based on AFLP and chloroplast DNA sequences

inferredcites →https://doi.org/10.1016/s0169-5347(02)02590-9openalex-snapshot

Plant dispersal N.E.W.S from New Zealand

inferredcites →https://doi.org/10.1016/s1055-7903(02)00210-5openalex-snapshot

The origins and evolution of the genus Myosotis L. (Boraginaceae)

inferredcites →https://doi.org/10.1038/nature07764openalex-snapshot

Phylogenetic biome conservatism on a global scale

inferredcites →https://doi.org/10.1046/j.1095-8339.2002.00070.xopenalex-snapshot

Phylogenetic relationships within Plantago (Plantaginaceae): evidence from nuclear ribosomal ITS and plastid trnL-F sequence data

inferredcites →https://doi.org/10.1046/j.1365-2699.1999.00392.xopenalex-snapshot

The importance of dispersal and recent speciation in the flora of New Zealand

inferredcites →https://doi.org/10.1046/j.1365-2699.2003.00895.xopenalex-snapshot

The biogeography of Gunnera L.: vicariance and dispersal

inferredcites →https://doi.org/10.1046/j.1365-2699.2003.00938.xopenalex-snapshot

Biogeography of temperate Australasian Polystichum ferns as inferred from chloroplast sequence and AFLP

inferredcites →https://doi.org/10.1071/sb01032openalex-snapshot

Phylogenetic analysis of ITS sequences suggests a Pliocene origin for the bipolar distribution of Scleranthus (Caryophyllaceae)

inferredcites →https://doi.org/10.1073/pnas.0408302101openalex-snapshot

Mitochondrial substitution rates are extraordinarily elevated and variable in a genus of flowering plants

inferredcites →https://doi.org/10.1073/pnas.84.24.9054openalex-snapshot

Rates of nucleotide substitution vary greatly among plant mitochondrial, chloroplast, and nuclear DNAs.

inferredcites →https://doi.org/10.1078/1439-6092-00005openalex-snapshot

The phylogeny of (Gentianaceae) and its colonization of the southern hemisphere as revealed by nuclear and chloroplast DNA sequence variation

inferredcites →https://doi.org/10.1080/0028825x.1971.10430222openalex-snapshot

Contributions to a Chromosome Atlas of the New Zealand Flora—15 Miscellaneous Families

inferredcites →https://doi.org/10.1080/0028825x.1973.10430272openalex-snapshot

Evolution of subalpine and alpine plant groups in New Zealand

inferredcites →https://doi.org/10.1080/0028825x.1988.10410121openalex-snapshot

Notes on New Zealand Plantago species

inferredcites →https://doi.org/10.1080/0028825x.1989.10410373openalex-snapshot

Contributions to a chromosome atlas of the New Zealand flora — 30 miscellaneous species

inferredcites →https://doi.org/10.1080/0028825x.1989.10414134openalex-snapshot

Are Plantago novae‐zelandiae L Moore and P. lanigera Hook. f. (Plantaginaceae) different?

inferredcites →https://doi.org/10.1080/0028825x.1998.9512581openalex-snapshot

Evolution and biogeography of the Hebe complex (Scrophulariaceae) inferred from ITS sequences

inferredcites →https://doi.org/10.1080/0028825x.1999.9512644openalex-snapshot

Phylogenetic relationships in Australasian Gnaphalieae (Compositae) inferred from ITS sequences

inferredcites →https://doi.org/10.1080/0028825x.2000.9512691openalex-snapshot

Patterns of diversification in chionohebe and parahebe (scrophulariaceae) inferred from ITS sequences

inferredcites →https://doi.org/10.1080/0028825x.2002.9512815openalex-snapshot

Molecular systematics of the New Zealand Pachycladon (Brassicaceae) complex: Generic circumscription and relationships to Arabidopsis sens. lat. and Arabis sens. lat.

inferredcites →https://doi.org/10.1080/0028825x.2004.9512937openalex-snapshot

Polyploidy, hybridization and evolution in Pratia (Campanulaceae)

inferredcites →https://doi.org/10.1080/03014220909510561openalex-snapshot

A review of genetic analyses of hybridisation in New Zealand

inferredcites →https://doi.org/10.1080/10635150116801openalex-snapshot

Failure of the ILD to Determine Data Combinability for Slow Loris Phylogeny

inferredcites →https://doi.org/10.1080/10635150290102474openalex-snapshot

New Zealand Kauri (Agathis australis (D.Don) Lindl., Araucariaceae) Survives Oligocene Drowning

inferredcites →https://doi.org/10.1080/10635150490423430openalex-snapshot

Southern Hemisphere Biogeography Inferred by Event-Based Models: Plant versus Animal Patterns

inferredcites →https://doi.org/10.1080/10635150490522304openalex-snapshot

Model Selection and Model Averaging in Phylogenetics: Advantages of Akaike Information Criterion and Bayesian Approaches Over Likelihood Ratio Tests

inferredcites →https://doi.org/10.1080/10635150701636412openalex-snapshot

The Drowning of New Zealand and the Problem of Agathis

inferredcites →https://doi.org/10.1086/421066openalex-snapshot

Clades, Clocks, and Continents: Historical and Biogeographical Analysis of Myrtaceae, Vochysiaceae, and Relatives in the Southern Hemisphere

inferredcites →https://doi.org/10.1086/526467openalex-snapshot

A Phylogeny for the African Restionaceae and New Perspectives on Morphology’s Role in Generating Complete Species Phylogenies for Large Clades

inferredcites →https://doi.org/10.1093/bib/5.2.150openalex-snapshot

MEGA3: Integrated software for Molecular Evolutionary Genetics Analysis and sequence alignment

inferredcites →https://doi.org/10.1093/bioinformatics/14.9.817openalex-snapshot

MODELTEST: testing the model of DNA substitution.

inferredcites →https://doi.org/10.1093/bioinformatics/17.8.754openalex-snapshot

MRBAYES: Bayesian inference of phylogenetic trees

inferredcites →https://doi.org/10.1093/jhered/92.4.371openalex-snapshot

DAMBE: Software Package for Data Analysis in Molecular Biology and Evolution

inferredcites →https://doi.org/10.1093/molbev/msj030openalex-snapshot

Application of Phylogenetic Networks in Evolutionary Studies

inferredcites →https://doi.org/10.1098/rspb.1995.0150openalex-snapshot

The Oligocene bottleneck and New Zealand biota: genetic record of a past environmental crisis

inferredcites →https://doi.org/10.1111/(issn)1095-8339openalex-snapshot

Botanical Journal of the Linnean Society

inferredcites →https://doi.org/10.1111/j.1095-8312.2006.00584.xopenalex-snapshot

The biogeography of the austral, subalpine genus Ourisia (Plantaginaceae) based on molecular phylogenetic evidence: South American origin and dispersal to New Zealand and Tasmania

inferredcites →https://doi.org/10.1111/j.1095-8339.1996.tb00484.xopenalex-snapshot

A phylogenetic study of the Plantaginaceae

inferredcites →https://doi.org/10.1111/j.1365-2699.2006.01643.xopenalex-snapshot

GUEST EDITORIAL: Hello New Zealand

inferredcites →https://doi.org/10.1111/j.1365-2699.2006.01655.xopenalex-snapshot

West Wind Drift revisited: testing for directional dispersal in the Southern Hemisphere using event‐based tree fitting

inferredcites →https://doi.org/10.1111/j.1365-2699.2007.01748.xopenalex-snapshot

Molecular evidence for long‐distance dispersal in the New Zealand pteridophyte flora

inferredcites →https://doi.org/10.1111/j.1365-2699.2007.01823.xopenalex-snapshot

Jordan’s and other ecogeographical rules, and the vertebral number in fishes

inferredcites →https://doi.org/10.1111/j.1365-2699.2007.01830.xopenalex-snapshot

Process and pattern in the biogeography of New Zealand – a global microcosm?

inferredcites →https://doi.org/10.1111/j.1756-1051.1984.tb01986.xopenalex-snapshot

Plantago sect. Oliganthos in southern South America, a taxonomic revision

inferredcites →https://doi.org/10.1126/science.1095210openalex-snapshot

Wind as a Long-Distance Dispersal Vehicle in the Southern Hemisphere

inferredcites →https://doi.org/10.1186/1471-2148-7-214openalex-snapshot

BEAST: Bayesian evolutionary analysis by sampling trees

inferredcites →https://doi.org/10.1371/journal.pbio.0030014openalex-snapshot

Relaxed Molecular Clock Provides Evidence for Long-Distance Dispersal of Nothofagus (Southern Beech)

inferredcites →https://doi.org/10.1371/journal.pbio.0030038openalex-snapshot

The Genomes of Oryza sativa: A History of Duplications

inferredcites →https://doi.org/10.1371/journal.pbio.0040088openalex-snapshot

Relaxed Phylogenetics and Dating with Confidence

inferredcites →https://doi.org/10.1600/0363644054223666openalex-snapshot

Origin of Veroniceae (Plantaginaceae, formerly Scrophulariaceae) on New Guinea

inferredcites →https://doi.org/10.1663/0007-196x(2007)59[129:mpamdo]2.0.co;2openalex-snapshot

Molecular phylogenetics and molecular dating of the New Zealand Gleicheniaceae

inferredcites →https://doi.org/10.1890/1540-9295(2006)004[0244:elsdvs]2.0.co;2openalex-snapshot

Extreme long-distance seed dispersal via sheep

inferredcites →https://doi.org/10.2165/00822942-200504010-00008openalex-snapshot

SeqState

inferredcites →https://doi.org/10.2307/2412908openalex-snapshot

Biogeography, the Vicariance Paradigm, and Continental Drift

inferredcites →https://doi.org/10.2307/25065417openalex-snapshot

Reconstructing patterns of reticulate evolution in angiosperms: what can we do?

inferredcites →https://doi.org/10.2307/25065860openalex-snapshot

Phylogeny and biogeography of Craspedia (Asteraceae: Gnaphalieae) based on ITS, ETS and psbA-trnH sequence data

inferredcites →https://doi.org/10.2307/25065861openalex-snapshot

Metteniusaceae, an early‐diverging family in the lamiid clade

inferredcites →https://doi.org/10.2307/2656781openalex-snapshot

Classification, origins, and patterns of diversification in New ZealandCarmichaelinae (Fabaceae)

inferredcites →https://doi.org/10.2307/2846036openalex-snapshot

The New Zealand Flora-Entirely Long-Distance Dispersal?

inferredcites →https://doi.org/10.2307/3298586openalex-snapshot

Phylogeny, Radiation, and Transoceanic Dispersal of New Zealand Alpine Buttercups: Molecular Evidence under Split Decomposition

inferredcites →https://doi.org/10.2307/3298656openalex-snapshot

Classification, Origin, and Diversification of the New Zealand Hebes (Scrophulariaceae)

inferredcites →https://doi.org/10.2307/3558433openalex-snapshot

Molecular systematics of Iridaceae: evidence from four plastid DNA regions

inferredcites →https://doi.org/10.26686/wgtn.16934719.v1openalex-snapshot

Evolution of Australasian Plantago (Plantaginaceae)

inferredcites →https://doi.org/10.3732/ajb.0800132openalex-snapshot

Molecular phylogeny and adaptive radiation of the endemic Hawaiian Plantago species (Plantaginaceae)

inferredcites →https://doi.org/10.3732/ajb.0800400openalex-snapshot

Molecular evidence of reticulate evolution in the subgenus Plantago (Plantaginaceae)

inferredcites →https://doi.org/10.3732/ajb.89.5.865openalex-snapshot

Patterns of diversification in New Zealand Stylidiaceae

inferredcites →https://doi.org/10.3732/ajb.90.1.123openalex-snapshot

Phylogeny of the sundews, Drosera (Droseraceae), based on chloroplast rbcL and nuclear 18S ribosomal DNA Sequences

inferredcites →https://doi.org/10.3732/ajb.90.3.429openalex-snapshot

Molecular systematics and biogeography of the amphibious genus Littorella (Plantaginaceae)

inferredcites →https://doi.org/10.3732/ajb.94.3.275openalex-snapshot

Comparison of whole chloroplast genome sequences to choose noncoding regions for phylogenetic studies in angiosperms: the tortoise and the hare III

inferredcites →https://doi.org/10.5860/choice.39-2183openalex-snapshot

MacClade 4.0: analysis of phylogeny and character evolution

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.306.1.6zenodo-depositor-declared

The intricate nomenclatural questions around Plantago holosteum (Plantaginaceae)

inferred← citeshttps://doi.org/10.11646/phytotaxa.316.1.1zenodo-depositor-declared

Contributions to the knowledge of the genus Plantago (Plantaginaceae) in the Central-West region of Brazil

inferred← citeshttps://doi.org/10.11646/phytotaxa.340.2.3zenodo-depositor-declared

Taxonomic and geographic novelties in the genus Plantago (Plantaginaceae) in Chile, including the description of a new species

inferred← citeshttps://doi.org/10.1002/tax.12035openalex-snapshot

Phylogenetic and morphometric analysis of Plantago section Coronopus (Plantaginaceae)

inferred← citeshttps://doi.org/10.1016/j.ympev.2012.05.008openalex-snapshot

A molecular phylogeny of the Lepidozia generic complex supports re-circumscription of the Lepidozioideae

inferred← citeshttps://doi.org/10.1016/j.ympev.2012.07.023openalex-snapshot

Phylogeny and colonization history of Pringlea antiscorbutica (Brassicaceae), an emblematic endemic from the South Indian Ocean Province

inferred← citeshttps://doi.org/10.1016/j.ympev.2019.05.013openalex-snapshot

The application of high-throughput sequencing for taxonomy: The case of Plantago subg. Plantago (Plantaginaceae)

inferred← citeshttps://doi.org/10.1016/j.ympev.2021.107217openalex-snapshot

Plastomes from tribe Plantagineae (Plantaginaceae) reveal infrageneric structural synapormorphies and localized hypermutation for Plantago and functional loss of ndh genes from Littorella

inferred← citeshttps://doi.org/10.1016/j.ympev.2025.108469openalex-snapshot

Resolving reticulate evolutionary histories of polyploid species of Azorella (Apiaceae) endemic to New Zealand

inferred← citeshttps://doi.org/10.1038/s41598-021-92114-1openalex-snapshot

The composition of Australian Plantago seeds highlights their potential as nutritionally-rich functional food ingredients

inferred← citeshttps://doi.org/10.1071/sb09040_eropenalex-snapshot

Erratum to : DNA sequences from three genomes reveal multiple long-distance dispersals and non-monophyly of sections in Australasian Plantago (Plantaginaceae)

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/10.1071/sb10028openalex-snapshot

Tasmanian and Victorian populations of the fern Asplenium hookerianum result from independent dispersals from New Zealand

inferred← citeshttps://doi.org/10.1071/sb11023openalex-snapshot

An expanded molecular phylogeny of the southern bluebells (Wahlenbergia, Campanulaceae) from Australia and New Zealand

inferred← citeshttps://doi.org/10.1071/sb11032openalex-snapshot

Morphological and molecular data reveal three rather than one species of Sicyos (Cucurbitaceae) in Australia, New Zealand and Islands of the South West Pacific

inferred← citeshttps://doi.org/10.1071/sb12006openalex-snapshot

Molecular phylogeny and systematics of Prostanthera (Lamiaceae)

inferred← citeshttps://doi.org/10.1073/pnas.1011361108openalex-snapshot

Gradual disintegration of the floral symmetry gene network is implicated in the evolution of a wind-pollination syndrome

inferred← citeshttps://doi.org/10.1080/0028825x.2010.515598openalex-snapshot

New chromosome counts in New Zealand species of Plantago (Plantaginaceae)

inferred← citeshttps://doi.org/10.1080/0028825x.2010.518318openalex-snapshot

Testing species limits of New Zealand Plantago (Plantaginaceae) using internal transcribed spacer (ITS) DNA sequences

inferred← citeshttps://doi.org/10.1080/0028825x.2012.671179openalex-snapshot

A taxonomic revision of native New Zealand Plantago (Plantaginaceae)

inferred← citeshttps://doi.org/10.1080/0028825x.2012.698624openalex-snapshot

Phylogenetic relationships and species delimitation of New Zealand bluebells ( Wahlenbergia, Campanulaceae) based on analyses of AFLP data

inferred← citeshttps://doi.org/10.1080/0028825x.2014.898664openalex-snapshot

In situ hybridization with genomic and rDNA probes reveals complex origins for polyploid New Zealand species of Plantago (Plantaginaceae)

inferred← citeshttps://doi.org/10.1080/00837792.2017.1349066openalex-snapshot

Nomenclatural and taxonomic notes on Mediterranean narrow-leaved plantains (Plantago section Maritima, Plantaginaceae)

inferred← citeshttps://doi.org/10.1080/03036758.2019.1676797openalex-snapshot

The importance and prevalence of allopolyploidy in Aotearoa New Zealand

inferred← citeshttps://doi.org/10.1080/17550874.2021.2012849openalex-snapshot

Plant speciation in the Quaternary

inferred← citeshttps://doi.org/10.1086/657657openalex-snapshot

Amplified Fragment Length Polymorphism Data Reveal a History of Auto- and Allopolyploidy in New Zealand Endemic Species of Plantago (Plantaginaceae): New Perspectives on a Taxonomically Challenging Group

inferred← citeshttps://doi.org/10.1086/658183openalex-snapshot

New World Origins of Southwest Pacific Gesneriaceae: Multiple Movements Across and Within the South Pacific

inferred← citeshttps://doi.org/10.1093/dnares/dsad013openalex-snapshot

Genome assembly of the pioneer speciesPlantago majorL. (Plantaginaceae) provides insight into its global distribution and adaptation to metal-contaminated soil

inferred← citeshttps://doi.org/10.1093/jhered/ess049openalex-snapshot

Variable Changes in Genome Size Associated with Different Polyploid Events in Plantago (Plantaginaceae)

inferred← citeshttps://doi.org/10.1101/2020.07.31.230813openalex-snapshot

How to map a plantain: phylogeny of the diverse Plantagineae (Lamiales)

inferred← citeshttps://doi.org/10.1111/geb.12389openalex-snapshot

Palaeoendemic plants provide evidence for persistence of open, well‐watered vegetation since the C retaceous

inferred← citeshttps://doi.org/10.1111/j.1095-8312.2012.01946.xopenalex-snapshot

Are the liverworts really that old? Cretaceous origins and Cenozoic diversifications in Lepidoziaceae reflect a recurrent theme in liverwort evolution

inferred← citeshttps://doi.org/10.1111/j.1365-2699.2011.02522.xopenalex-snapshot

Phylogeography of the pademelons (Marsupialia: Macropodidae: Thylogale) in New Guinea reflects both geological and climatic events during the Plio-Pleistocene

inferred← citeshttps://doi.org/10.1111/j.1469-8137.2011.03681.xopenalex-snapshot

Parental effects modulate seed longevity: exploring parental and offspring phenotypes to elucidate pre‐zygotic environmental influences

inferred← citeshttps://doi.org/10.1111/jbi.12952openalex-snapshot

Around the pole: evolution of sub‐Antarctic Ranunculus

inferred← citeshttps://doi.org/10.1111/jbi.13525openalex-snapshot

Ancestral range reconstruction of remote oceanic island species of Plantago (Plantaginaceae) reveals differing scales and modes of dispersal

inferred← citeshttps://doi.org/10.1111/mec.14875openalex-snapshot

Going under down under? Lineage ages argue for extensive survival of the Oligocene marine transgression on Zealandia

inferred← citeshttps://doi.org/10.1111/nph.14544openalex-snapshot

Evolutionary priority effects persist in anthropogenically created habitats, but not through nonnative plant invasion

inferred← citeshttps://doi.org/10.1111/nph.17095openalex-snapshot

The goo‐d stuff: Plantago as a myxospermous model with modern utility

inferred← citeshttps://doi.org/10.12705/663.14openalex-snapshot

Typification of the Linnaean names Plantago serraria and P. subulata ( Plantago subgenus Coronopus , Plantaginaceae)

inferred← citeshttps://doi.org/10.15560/11.4.1667openalex-snapshot

First record of Plantago commersoniana (Plantaginaceae), a rare and threatened species, in the Central-West region of Brazil

inferred← citeshttps://doi.org/10.1600/036364414x680960openalex-snapshot

Plantago rahniana (Plantaginaceae): A Narrow Endemic, New Species from Southern Brazil

inferred← citeshttps://doi.org/10.22092/ijb.2020.343166.1287openalex-snapshot

تنوع ژنتیکی و ساختار جمعیتی بارهنگ Plantago major L. در ایران (پلانتاجیناسه)

inferred← citeshttps://doi.org/10.26686/nzsr.v73i3-4.8536openalex-snapshot

Integrative, next-generation, collaborative vascular plant systematics in New Zealand

inferred← citeshttps://doi.org/10.26686/wgtn.16970986openalex-snapshot

The Evolution of Wahlenbergia (Campanulaceae) in Australasia

inferred← citeshttps://doi.org/10.26686/wgtn.16970986.v1openalex-snapshot

The Evolution of Wahlenbergia (Campanulaceae) in Australasia

inferred← citeshttps://doi.org/10.26686/wgtn.17151437openalex-snapshot

Repeated patterns in the evolution of size in island plants

inferred← citeshttps://doi.org/10.26686/wgtn.17151437.v1openalex-snapshot

Repeated patterns in the evolution of size in island plants

inferred← citeshttps://doi.org/10.3159/torrey-d-14-00029.1openalex-snapshot

Plantago corvensis(Plantaginaceae): a new narrowly endemic species from rocky cliffs in southern Brazil1

inferred← citeshttps://doi.org/10.3159/torrey-d-14-00070openalex-snapshot

The use of potential distribution models in the study of the distribution and conservation status of plants: The case of Plantago L. (Plantaginaceae) in Brazil1

inferred← citeshttps://doi.org/10.3390/plants10112299openalex-snapshot

Molecular and Morphological Data Improve the Classification of Plantagineae (Lamiales)

inferred← citeshttps://doi.org/10.3390/plants13192691openalex-snapshot

Comparative Plastomics of Plantains (Plantago, Plantaginaceae) as a Tool for the Development of Species-Specific DNA Barcodes

inferred← citeshttps://doi.org/10.3410/f.9742956.10430054openalex-snapshot

Faculty Opinions recommendation of Gradual disintegration of the floral symmetry gene network is implicated in the evolution of a wind-pollination syndrome.

inferred← citeshttps://doi.org/10.3417/2018272openalex-snapshot

Typification ofPlantagoNames (Plantagineae, Plantaginaceae) Linked to the Flora of Argentina

inferred← citeshttps://doi.org/10.4013/nbc.2017.122.08openalex-snapshot

Plantago trinitatis Rahn (Plantaginaceae): New sites of occurrence and altitudinal variation at Trindade Island, Brazil

inferred← citeshttps://doi.org/10.5007/2175-7925.2014v27n2p57openalex-snapshot

Descrição da espécie nova Plantago aparadensis (Plantaginaceae), endêmica dos Aparados da Serra Geral, sul do Brasil

inferred← citeshttps://doi.org/10.7717/peerj.2050openalex-snapshot

Yet another new species from one of the best-studied neotropical areas: Plantago humboldtiana (Plantaginaceae), an extremely narrow endemic new species from a waterfall in southern Brazil

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.