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Evaluating the Utility of Single-Locus DNA Barcoding for the Identification of Ribbon Worms (Phylum Nemertea)
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What this work says
Outgoing claims: the papers this work cites, builds on, or argues with.
inferredcites →https://doi.org/10.1016/j.ympev.2006.11.021openalex-snapshot
A comprehensive DNA sequence library is essential for identification with DNA barcodes
inferredcites →https://doi.org/10.1017/s002531541300146xopenalex-snapshot
A new nemertean species: what are the useful characters for ribbon worm descriptions?
inferredcites →https://doi.org/10.1046/j.1365-294x.2000.01020.xopenalex-snapshot
TCS: a computer program to estimate gene genealogies
inferredcites →https://doi.org/10.1080/10635150500431239openalex-snapshot
Statistical Approaches for DNA Barcoding
inferredcites →https://doi.org/10.1080/10635150802406343openalex-snapshot
The Use of Mean Instead of Smallest Interspecific Distances Exaggerates the Size of the “Barcoding Gap” and Leads to Misidentification
inferredcites →https://doi.org/10.1080/17451000510018962openalex-snapshot
What can biological barcoding do for marine biology?
inferredcites →https://doi.org/10.1093/acprof:osobl/9780199587100.001.0001openalex-snapshot
Ecological Speciation
inferredcites →https://doi.org/10.1093/bioinformatics/btl446openalex-snapshot
RAxML-VI-HPC: maximum likelihood-based phylogenetic analyses with thousands of taxa and mixed models
inferredcites →https://doi.org/10.1093/bioinformatics/btt499openalex-snapshot
A general species delimitation method with applications to phylogenetic placements
inferredcites →https://doi.org/10.1093/icb/25.1.5openalex-snapshot
The Need for a Standard Approach to Taxonomic Descriptions of Nemerteans
inferredcites →https://doi.org/10.1093/jhered/esl036openalex-snapshot
A Genomic Perspective on the Shortcomings of Mitochondrial DNA for “Barcoding” Identification
inferredcites →https://doi.org/10.1093/molbev/mst010openalex-snapshot
MAFFT Multiple Sequence Alignment Software Version 7: Improvements in Performance and Usability
inferredcites →https://doi.org/10.1093/sysbio/syt033openalex-snapshot
Delimiting Species Using Single-Locus Data and the Generalized Mixed Yule Coalescent Approach: A Revised Method and Evaluation on Simulated Data Sets
inferredcites →https://doi.org/10.1098/rsbl.2003.0025openalex-snapshot
Barcoding animal life: cytochrome c oxidase subunit 1 divergences among closely related species
inferredcites →https://doi.org/10.1098/rsbl.2007.0307openalex-snapshot
Things fall apart: biological species form unconnected parsimony networks
inferredcites →https://doi.org/10.1098/rspb.2002.2218openalex-snapshot
Biological identifications through DNA barcodes
inferredcites →https://doi.org/10.1098/rspb.2007.1290openalex-snapshot
Character-based DNA barcoding allows discrimination of genera, species and populations in Odonata
inferredcites →https://doi.org/10.1098/rstb.2005.1714openalex-snapshot
DNA barcoding for effective biodiversity assessment of a hyperdiverse arthropod group: the ants of Madagascar
inferredcites →https://doi.org/10.1098/rstb.2005.1722openalex-snapshot
The unholy trinity: taxonomy, species delimitation and DNA barcoding
inferredcites →https://doi.org/10.1111/1755-0998.12046openalex-snapshot
The seven deadly sins of DNA barcoding
inferredcites →https://doi.org/10.1111/j.1095-8312.2009.01310.xopenalex-snapshot
Polymorphism hides cryptic species in Oerstedia dorsalis (Nemertea, Hoplonemertea)
inferredcites →https://doi.org/10.1111/j.1096-0031.2003.00008.xopenalex-snapshot
Myth of the molecule: DNA barcodes for species cannot replace morphology for identification and classification
inferredcites →https://doi.org/10.1111/j.1096-0031.2011.00370.xopenalex-snapshot
On the inappropriate use of Kimura‐2‐parameter (K2P) divergences in the DNA‐barcoding literature
inferredcites →https://doi.org/10.1111/j.1096-3642.1976.tb00828.xopenalex-snapshot
Freshwater nemerteans
inferredcites →https://doi.org/10.1111/j.1096-3642.2010.00650.xopenalex-snapshot
Systematics and phylogeny of the hoplonemertean genus Diplomma (Nemertea) based on molecular and morphological evidence
inferredcites →https://doi.org/10.1111/j.1365-294x.2010.04720.xopenalex-snapshot
An integrative approach to species discovery in odonates: from character‐based DNA barcoding to ecology
inferredcites →https://doi.org/10.1111/j.1439-0469.2010.00568.xopenalex-snapshot
Nemertean taxonomy - time to change lane?
inferredcites →https://doi.org/10.1111/j.1461-0248.2004.00715.xopenalex-snapshot
Ecological speciation
inferredcites →https://doi.org/10.1111/j.1469-7998.1979.tb03952.xopenalex-snapshot
Statistical analysis of variation in characters in Tetrastemma laminariae (Nemertini), with a redescription of the species
inferredcites →https://doi.org/10.1111/j.1469-7998.1981.tb05768.xopenalex-snapshot
The Geonemertes problem (Nemertea)
inferredcites →https://doi.org/10.1111/j.1469-7998.1993.tb02687.xopenalex-snapshot
Intraspecific variation in nemerteans (Nemertea): synonymization of genera Paroerstedia and Oerstediella with Oerstedia
inferredcites →https://doi.org/10.1111/j.1471-8286.2006.01641.xopenalex-snapshot
DNA barcoding using chitons (genus Mopalia)
inferredcites →https://doi.org/10.1111/j.1471-8286.2007.01996.xopenalex-snapshot
DNA BARCODING: Barcoding corals: limited by interspecific divergence, not intraspecific variation
inferredcites →https://doi.org/10.1111/j.1755-0998.2008.02235.xopenalex-snapshot
caos software for use in character‐based DNA barcoding
inferredcites →https://doi.org/10.1111/j.1755-0998.2009.02774.xopenalex-snapshot
DNA barcoding should accompany taxonomy – the case of Cerebratulus spp (Nemertea)
inferredcites →https://doi.org/10.1111/j.1755-0998.2011.03032.xopenalex-snapshot
Comparing and combining distance‐based and character‐based approaches for barcoding turtles
inferredcites →https://doi.org/10.1186/1471-2105-11-206openalex-snapshot
Comparative performances of DNA barcoding across insect orders
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.0030422openalex-snapshot
DNA Barcoding: Error Rates Based on Comprehensive Sampling
inferredcites →https://doi.org/10.1899/09-183.1openalex-snapshot
First audit of macroinvertebrate samples from an EU Water Framework Directive monitoring program: human error greatly lowers precision of assessment results
inferredcites →https://doi.org/10.3109/19401736.2010.529905openalex-snapshot
Barcoding, types and theHirudofiles: Using information content to critically evaluate the identity of DNA barcodes
inferredcites →https://doi.org/10.3109/19401736.2014.984166openalex-snapshot
Does a global DNA barcoding gap exist in Annelida?
inferredcites →https://doi.org/10.5860/choice.45-2365openalex-snapshot
The Light and Smith manual: intertidal invertebrates from central California to Oregon
inferredcites →https://doi.org/10.6084/m9.figshare.1568234openalex-snapshot
Does a global DNA barcoding gap exist in Annelida?
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
inferred← citeshttps://doi.org/10.11646/zootaxa.4691.4.2zenodo-depositor-declared
Molecular systematics of the heteronemertean genus Dushia (Nemertea, Pilidiophora), with descriptions of D. wijnhoffae sp. nov. and D. nigra species complex comb. nov.
inferred← citeshttps://doi.org/10.11646/zootaxa.4722.2.4zenodo-depositor-declared
A re-examination of the taxonomic status of Prostoma jenningsi—a Freshwater Nemertean
inferred← citeshttps://doi.org/10.11646/zootaxa.4808.2.10zenodo-depositor-declared
A histology-free description of a new species of the genus Tetrastemma (Nemertea: Hoplonemertea: Monostilifera) from Hawaii and India
inferred← citeshttps://doi.org/10.11646/zootaxa.5249.5.6zenodo-depositor-declared
Species description and phylogenetics of Oerstedia fuscosparsa sp. nov. (Nemertea: Monostilifera: Oerstediidae) from Japan
inferred← citeshttps://doi.org/10.11646/zootaxa.5646.4.1zenodo-depositor-declared
A taxonomic revision of the freshwater monostiliferous hoplonemertean genus Prostoma Dugès, 1828 (Nemertea: Eumonostilifera): a radical solution or an over-lumping?
inferred← citeshttps://doi.org/10.12782/specdiv.30.71zenodo-depositor-declared
Species Diversity of Tetranemertes (Nemertea: Monostilifera) in Japan
inferred← citeshttps://doi.org/10.31610/trudyzin/2023.327.1.41zenodo-depositor-declared
Nemertean fauna (Nemertea) of the White Sea: 140 years of study
inferred← citeshttps://doi.org/10.3897/zookeys.1204.117869zenodo-depositor-declared
Ribbon worms (phylum Nemertea) from Bodega Bay, California: A largely undescribed diversity
inferred← citeshttps://doi.org/10.5324/fn.v39i0.2734zenodo-depositor-declared
Resolving a 200-year-old taxonomic conundrum: neotype designation for Cephalothrix linearis (Nemertea: Palaeonemertea) based on a topotype from Bergen, Norway
inferred← citeshttps://doi.org/10.5852/ejt.2022.845.1959zenodo-depositor-declared
Cutting the ribbon: bathyal Nemertea from seeps along the Costa Rica margin, with descriptions of 2 new genera and 9 new species
inferred← citeshttps://doi.org/10.1002/arch.22070openalex-snapshot
DNA barcoding of the genus Gampsocleis (Orthoptera, Tettigoniidae) from China
inferred← citeshttps://doi.org/10.1007/s00300-018-2298-1openalex-snapshot
A new member of the genus Antarctonemertes (Hoplonemertea, Nemertea) from Antarctic waters
inferred← citeshttps://doi.org/10.1007/s00300-018-2438-7openalex-snapshot
Species identity and genetic structure of nemerteans of the “Lineus ruber–viridis” complex (Muller, 1774) from Arctic waters
inferred← citeshttps://doi.org/10.1007/s00300-023-03117-9openalex-snapshot
DNA barcoding reveals hidden nemertean diversity from the marine protected area Namuncurá–Burdwood Bank, Southwestern Atlantic
inferred← citeshttps://doi.org/10.1007/s00300-025-03395-5openalex-snapshot
Nemertean diversity at the end of the world: histology-free description of three new species and evidence of genetic isolation between Antarctica and South America
inferred← citeshttps://doi.org/10.1007/s12526-026-01642-4openalex-snapshot
Comparative mitogenomics and biodiversity studies of Nemertea
inferred← citeshttps://doi.org/10.1007/s13205-018-1092-7openalex-snapshot
Assessment of three plastid DNA barcode markers for identification of Clinacanthus nutans (Acanthaceae)
inferred← citeshttps://doi.org/10.1016/j.dsr.2024.104439openalex-snapshot
Descriptions of two new deep-sea nemertean species from the genera Alvinonemertes and Sagornya gen. nov. (Hoplonemertea, Oerstediina) with discussion on close genetic relationship between deep-sea species
inferred← citeshttps://doi.org/10.1016/j.dsr.2025.104549openalex-snapshot
Deep-sea nemerteans collected along the Japan Trench and the southern Kuril-Kamchatka Trench onboard the R/V Hakuho-maru with descriptions of two new species in Hoplonemertea
inferred← citeshttps://doi.org/10.1016/j.dsr2.2022.105081openalex-snapshot
Nemerteans collected in the Bering Sea during the research cruises aboard the R/V Akademik M.A. Lavrentyev in 2016, 2018, and 2021 with an analysis of deep-sea heteronemertean and hoplonemertean species
inferred← citeshttps://doi.org/10.1016/j.jcz.2022.10.003openalex-snapshot
A new oerstediid discovered from wood falls in the Sea of Kumano, Japan: Description of Rhombonemertes rublinea gen. et sp. nov. (Nemertea: Eumonostilifera)
inferred← citeshttps://doi.org/10.1071/is17029openalex-snapshot
Genetic diversity of marine oligochaetous clitellates in selected areas of the South Atlantic as revealed by DNA barcoding
inferred← citeshttps://doi.org/10.1071/is18080openalex-snapshot
Cephalotrichella echinicola, sp. nov. (Palaeonemertea : Cephalotrichellidae), a new nemertean associated with sea urchins from Nha Trang Bay (South China Sea)
inferred← citeshttps://doi.org/10.1071/is20048openalex-snapshot
Species delimitation integrative approach reveals three new species in the Nemertopsis bivittata complex
inferred← citeshttps://doi.org/10.1071/is20057openalex-snapshot
A new nemertean with a branched proboscis, Gorgonorhynchus citrinus sp. nov. (Nemertea: Pilidiophora), with molecular systematics of the genus
inferred← citeshttps://doi.org/10.1071/is20061openalex-snapshot
Evaluation of the taxonomic position of the genus Carinina (Nemertea : Palaeonemertea), with descriptions of two new species
inferred← citeshttps://doi.org/10.1071/is22066openalex-snapshot
At the edge of the sea: the supralittoral nemertean, Acteonemertes orientalis sp. nov. (Nemertea: Eumonostilifera: Plectonemertidae) from Japan
inferred← citeshttps://doi.org/10.1080/00222933.2022.2118642openalex-snapshot
Histology-free description and phylogenetics of Tetrastemma parallelos sp. nov. (Nemertea: Eumonostilifera) from Japan
inferred← citeshttps://doi.org/10.1080/14772000.2017.1317672openalex-snapshot
Taxonomy and phylogeny ofLineus torquatusand allies (Nemertea, Lineidae) with descriptions of a new genus and a new cryptic species
inferred← citeshttps://doi.org/10.1080/14772000.2025.2504484openalex-snapshot
Ribbon worms living on deep-sea trees: Alvinonemertes daitoensis sp. nov. (Nemertea, Monostilifera) associated with the glass sponge Walteria leukarti (Porifera, Hexactinellida)
inferred← citeshttps://doi.org/10.1080/17451000.2025.2553517openalex-snapshot
Species composition of the genus Baseodiscus Diesing, 1850 (Pilidiophora: Valenciniidae) in Japan and the Philippines with turbotaxonomy of two new species
inferred← citeshttps://doi.org/10.1080/24701394.2017.1357709openalex-snapshot
Estimating the barcoding gap in a global dataset of cox1 sequences for Odonata: close, but no cigar
inferred← citeshttps://doi.org/10.1080/24701394.2025.2602435openalex-snapshot
Nemerteans Emplectonema ex gr. gracile (Johnston 1837) (Hoplonemertea, Monostilifera) from the Sea of Okhotsk, Sea of Japan, and Yellow Sea
inferred← citeshttps://doi.org/10.1093/jcbiol/ruaa060openalex-snapshot
Two species of Carcinonemertes Coe, 1902 (Nemertea: Carcinonemertidae) infesting the Caribbean spiny lobster, Panulirus argus (Latreille, 1804) (Decapoda: Achelata: Palinuridae), in Saint Kitts, West Indies
inferred← citeshttps://doi.org/10.1093/zoolinnean/zlac015openalex-snapshot
Exploring the basal topology of the heteronemertean tree of life: establishment of a new family, along with turbotaxonomy of Valenciniidae (Nemertea: Pilidiophora: Heteronemertea)
inferred← citeshttps://doi.org/10.1098/rsbl.2025.0744openalex-snapshot
Genomic evidence reveals a record-breaking range in Tubulanus lutescens (Nemertea) from shallow coasts to deep-sea seeps
inferred← citeshttps://doi.org/10.1111/ivb.12363openalex-snapshot
Hoplonemertean larvae are planktonic predators that capture and devour active animal prey
inferred← citeshttps://doi.org/10.1111/jzs.12266openalex-snapshot
Assessing the diversity and distribution ofCephalothrixspecies (Nemertea: Palaeonemertea) in European waters by comparing different species delimitation methods
inferred← citeshttps://doi.org/10.1134/s1063074025700476openalex-snapshot
The First Barcoding Analysis of Symbiotic Nemerteans of the Genus Malacobdella Blainville, 1827 (Hoplonemertea, Monostilifera) from the Far Eastern Seas of Russia
inferred← citeshttps://doi.org/10.1139/gen-2020-0140openalex-snapshot
Barcoding a can of worms: testing cox1 performance as a DNA barcode of Nematoda
inferred← citeshttps://doi.org/10.11606/t.41.2022.tde-09062022-173135openalex-snapshot
Nemertopsis bivittata (Hoplonemertea), Lineus sanguineus (Heteronemertea) e Perinereis ponteni (Polychaeta): validade das espécies, fluxo gênico e diversidade genética na costa brasileira
inferred← citeshttps://doi.org/10.1186/s12862-019-1404-5openalex-snapshot
Singleton molecular species delimitation based on COI-5P barcode sequences revealed high cryptic/undescribed diversity for Chinese katydids (Orthoptera: Tettigoniidae)
inferred← citeshttps://doi.org/10.1186/s12862-025-02468-7openalex-snapshot
Unrecognized species-level diversity of terrestrial nemerteans in the UNESCO world heritage Ogasawara Islands revealed by mitogenomics
inferred← citeshttps://doi.org/10.1186/s13071-017-2457-1openalex-snapshot
Cytochrome c oxidase subunit 1 gene as a DNA barcode for discriminating Trypanosoma cruzi DTUs and closely related species
inferred← citeshttps://doi.org/10.12782/specdiv.25.183openalex-snapshot
A New Species of Bathyal Nemertean, Proamphiporus kaimeiae sp. nov., off Tohoku, Japan, and Molecular Systematics of the Genus (Nemertea: Monostilifera)
inferred← citeshttps://doi.org/10.12782/specdiv.25.251openalex-snapshot
Three Species of Ribbon Worms (Nemertea) from Cebu, the Philippines
inferred← citeshttps://doi.org/10.12782/specdiv.28.199openalex-snapshot
A Sponge-dwelling Ribbon Worm, Tetrastemma carneum sp. nov. (Nemertea: Monostilifera) Collected off Ofunato, Japan
inferred← citeshttps://doi.org/10.15560/16.2.265openalex-snapshot
New record of the monostiliferous hoplonemertean Gurjanovella littoralis Uschakov, 1926 from Japan (Nemertea, Hoplonemertea, Monostilifera)
inferred← citeshttps://doi.org/10.2108/zs210075openalex-snapshot
Description of Tubulanus misakiensis sp. nov. (Nemertea: Palaeonemertea) from Sagami Bay, Japan
inferred← citeshttps://doi.org/10.2108/zs240094openalex-snapshot
A New Species of Prosadenoporus (Nemertea: Eumonostilifera) from the North-East Coast of the Bay of Bengal, India
inferred← citeshttps://doi.org/10.25268/bimc.invemar.2022.51.1.1066openalex-snapshot
Gen Citocromo Oxidasa I confirma la presencia del nemertino Carcinonemertes conanobrieni, parásito de la langosta espinosa del Caribe (Panulirus argus) en Colombia
inferred← citeshttps://doi.org/10.29215/pecen.v3i2.1264openalex-snapshot
First record of the marine nemertean Evelineus mcintoshii (Langerhans, 1880) (Heteronemertea, Lineidae) in Northeastern Brazil
inferred← citeshttps://doi.org/10.3389/fevo.2024.1356316openalex-snapshot
Delimiting the polymorphic congeners of the genus Oerstedia Quatrefages, 1864 (Nemertea, Hoplonemertea), and descriptions of three new species from the Northwest Pacific
inferred← citeshttps://doi.org/10.3389/fmars.2022.1009536openalex-snapshot
Diversity of interstitial nemerteans of the genus Ototyphlonemertes (Nemertea: Monostilifera: Ototyphlonemertidae) in the South China Sea, with a comment on the distribution pattern of the genus
inferred← citeshttps://doi.org/10.3389/fmars.2022.906383openalex-snapshot
Molecular Phylogeny of the Genus Nipponnemertes (Nemertea: Monostilifera: Cratenemertidae) and Descriptions of 10 New Species, With Notes on Small Body Size in a Newly Discovered Clade
inferred← citeshttps://doi.org/10.3390/ecologies7010027openalex-snapshot
Conservation Significance of Forest Remnants for Urban Biodiversity: Parks as a Refuge for the Wood Cricket, Nemobius sylvestris (Insecta: Orthoptera: Trigonidiidae)
inferred← citeshttps://doi.org/10.3390/w15040809openalex-snapshot
Distribution and Phylogenetic Position of the Antarctic Ribbon Worm Heteronemertes longifissa (Nemertea, Pilidiophora)
inferred← citeshttps://doi.org/10.3897/zookeys.1146.95004openalex-snapshot
Three new species in Tetrastemma Ehrenberg, 1828 (Nemertea, Monostilifera) from sublittoral to upper bathyal zones of the northwestern Pacific
inferred← citeshttps://doi.org/10.3897/zookeys.1181.109521openalex-snapshot
Seven new species of Tetranemertes Chernyshev, 1992 (Monostilifera, Hoplonemertea, Nemertea) from the Caribbean Sea, western Pacific, and Arabian Sea, and revision of the genus
inferred← citeshttps://doi.org/10.3897/zookeys.693.12015openalex-snapshot
Nipponnemertes incainca sp. n. Adoption of the new taxonomic proposal for nemerteans (Nemertea, Cratenemertidae)
inferred← citeshttps://doi.org/10.5821/dissertation-2117-120993openalex-snapshot
An onto-phylogenetic journey through the life history of flying squids (Cephalopoda: Ommastrephidae)
inferred← citeshttps://doi.org/10.7717/peerj.13857openalex-snapshot
First eumonostiliferous nemertean from the Nishi-Shichito Ridge, Genrokunemertes obesa gen. et sp. nov. (Eumonostilifera, Nemertea)
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