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Description and Relationships ofChaetopterus pugaporcinus, an Unusual Pelagic Polychaete (Annelida, Chaetopteridae)
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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/(sici)1097-4687(199810)238:1<93::aid-jmor8>3.0.co;2-oopenalex-snapshot
Giant pelagic larvae of Phyllodocidae (Polychaeta, Annelida)
inferredcites →https://doi.org/10.1006/jmbi.2000.4042openalex-snapshot
T-coffee: a novel method for fast and accurate multiple sequence alignment 1 1Edited by J. Thornton
inferredcites →https://doi.org/10.1007/978-94-017-0655-1_26openalex-snapshot
Identification of adults and larvae in Spiochaetopterus (Polychaeta, Chaetopteridae): consequences for larval transport and recruitment
inferredcites →https://doi.org/10.1007/978-94-017-2864-5_3openalex-snapshot
The spreading potential of polychaete larvae does not predict adult distributions; consequences for conditions of recruitment
inferredcites →https://doi.org/10.1007/bf02106180openalex-snapshot
Dinoflagellates in evolution. A molecular phylogenetic analysis of large subunit ribosomal RNA
inferredcites →https://doi.org/10.1016/0378-1119(88)90066-2openalex-snapshot
The characterization of enzymatically amplified eukaryotic 16S-like rRNA-coding regions
inferredcites →https://doi.org/10.1016/0967-0637(94)00021-jopenalex-snapshot
Pelagic and benthic ecology of the lower interface of the Eastern Tropical Pacific oxygen minimum zone
inferredcites →https://doi.org/10.1016/s0022-0981(96)02693-7openalex-snapshot
Control of position in the water column by the larvae of Poecilochaetus serpens, (Polychaeta): the importance of mucus secretion
inferredcites →https://doi.org/10.1017/s002531540001290xopenalex-snapshot
Studies on Chaetopterus variopedatus (Renier). I. The light-producing glands
inferredcites →https://doi.org/10.1017/s002531540100368xopenalex-snapshot
Spiochaetopterus nonatoi, a new species of Chaetopteridae (Polychaeta) from Brazil: biogeographical consequences
inferredcites →https://doi.org/10.1017/s002531540200588xopenalex-snapshot
Mesochaetopterus sagittarius: an example of a biogeography discrepancy between larval and adult boundaries: implication for recruitment studies
inferredcites →https://doi.org/10.1023/a:1017073409259openalex-snapshot
The spreading potential of polychaete larvae does not predict adult distributions; consequences for conditions of recruitment
inferredcites →https://doi.org/10.1023/a:1026165419638openalex-snapshot
Identification of adults and larvae in Spiochaetopterus (Polychaeta, Chaetopteridae): consequences for larval transport and recruitment
inferredcites →https://doi.org/10.1080/00785236.1999.10409420openalex-snapshot
Planktonic larvae ofSpiochaetopterusin the Gulf of California: New evidence that the geographic distribution of species with a long planktonic larval life is relatively restricted
inferredcites →https://doi.org/10.1080/00785326.1994.10430579openalex-snapshot
Redescription ofSpiochaetopterus solitarius(Rioja, 1917), with notes on tube structure and comments on the generic status (Polychaeta: Chaetopteridae)
inferredcites →https://doi.org/10.1080/10635150118469openalex-snapshot
Selecting the Best-Fit Model of Nucleotide Substitution
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/oso/9780198549567.001.0001openalex-snapshot
The Biology of the Deep Ocean
inferredcites →https://doi.org/10.1109/tac.1974.1100705openalex-snapshot
A new look at the statistical model identification
inferredcites →https://doi.org/10.1111/j.1469-7998.1904.tb08291.xopenalex-snapshot
The Polychaeta of the Maldive Archipelago from the Collections made by J. Stanley Gnrdiner in 1899
inferredcites →https://doi.org/10.1126/science.1104279openalex-snapshot
The Cryptic Filtering House of an Invertebrate Larva
inferredcites →https://doi.org/10.1126/science.176.4040.1239openalex-snapshot
Free-Floating Mucus Webs: A Novel Feeding Adaptation for the Open Ocean
inferredcites →https://doi.org/10.2307/1537850openalex-snapshot
THE METHOD OF FEEDING OF CHAETOPTERUS
inferredcites →https://doi.org/10.2307/1541164openalex-snapshot
LUMINESCENCE CONTROL IN THE TUBE-WORMCHAETOPTERUS VARIOPEDATUS: ROLE OF NERVE CORD AND PHOTOGENIC GLAND
inferredcites →https://doi.org/10.2307/1542786openalex-snapshot
Larval Ontogenetic Stages of Chaetopterus: Developmental Heterochrony in the Evolution of Chaetopterid Polychaetes
inferredcites →https://doi.org/10.3989/scimar.2003.67n199openalex-snapshot
Spiochaetopterus creoceanae, a new species of Chaetopteridae (Polychaeta) from the Persian Gulf belonging to the costarum complex
inferredcites →https://doi.org/10.4319/lo.1975.20.6.0907openalex-snapshot
Underwater observations of gelatinous zooplankton: Sampling problems, feeding biology, and behavior1
inferredcites →https://doi.org/10.5281/zenodo.15145663openalex-snapshot
Table 1 in A new Gammarus species from Xinjiang Uygur Autonomous Region (China) with a key to Xinjiang freshwater gammarids (Crustacea, Amphipoda, Gammaridae)
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/zootaxa.3974.4.2zenodo-depositor-declared
A new species of Mesochaetopterus (Annelida, Chaetopteridae) from Hong Kong, with comments on the phylogeny of the family
inferred← citeshttps://doi.org/10.11646/zootaxa.4323.1.3zenodo-depositor-declared
Cutting a Gordian knot of tubeworms with DNA data: the story of the Hydroides operculata-complex (Annelida, Serpulidae)
inferred← citeshttps://doi.org/10.11646/zootaxa.4571.4.7zenodo-depositor-declared
A new species of Flabelligeridae (Annelida), Trophoniella radesiensis n. sp., from Tunisia
inferred← citeshttps://doi.org/10.11646/zootaxa.4821.3.4zenodo-depositor-declared
Two new species of Sabellariidae (Annelida, Polychaeta) from the abyss of eastern Australia
inferred← citeshttps://doi.org/10.11646/zootaxa.5529.2.2zenodo-depositor-declared
A twin of Polydora hoplura (Annelida: Spionidae) from the Arabian (Persian) Gulf, with review of primers used for barcoding of Spionidae
inferred← citeshttps://doi.org/10.11646/zootaxa.5613.1.3zenodo-depositor-declared
A new species of an unusual polychaete genus Ctenophoricola (Phyllodocida, Phyllodocidae, Alciopini) from the Indian Ocean
inferred← citeshttps://doi.org/10.11646/zootaxa.5632.1.1zenodo-depositor-declared
Holopelagic Annelida from the Red Sea off the Central Saudi Arabian coast
inferred← citeshttps://doi.org/10.11646/zootaxa.5673.2.2zenodo-depositor-declared
Parahesione dudahamra sp. nov., an eye-catching symbiotic worm from the Red Sea, with complementary description and notes on Leocrates giardi Gravier, 1900 (Annelida: Phyllodocida: Hesionidae)
inferred← citeshttps://doi.org/10.5852/ejt.2020.643zenodo-depositor-declared
Hidden in plain sight, Chaetopterus dewysee sp. nov. (Chaetopteridae, Annelida) – A new species from Southern California
inferred← citeshttps://doi.org/10.5852/ejt.2020.720.1111zenodo-depositor-declared
A new species of Chaetopterus (Annelida: Chaetopteridae) from eastern Canada, with a redescription of Chaetopterus norvegicus M. Sars, 1835
inferred← citeshttps://doi.org/10.1002/9780470455203.ch2openalex-snapshot
Annelid Phylogeny—Molecular Analysis with an Emphasis on Model Annelids
inferred← citeshttps://doi.org/10.1002/jez.b.22492openalex-snapshot
Temporal Plasticity in Annelid Development—Ontogeny of Phyllodoce groenlandica (Phyllodocidae, Annelida) Reveals Heterochronous Patterns
inferred← citeshttps://doi.org/10.1007/s00227-009-1296-9openalex-snapshot
Eurythoe complanata (Polychaeta: Amphinomidae), the ‘cosmopolitan’ fireworm, consists of at least three cryptic species
inferred← citeshttps://doi.org/10.1007/s00227-026-04852-3openalex-snapshot
Haplotype diversity in a two-year survey of the invasive calcareous tubeworm Ficopomatus enigmaticus (Annelida: Serpulidae) in a subtropical estuary with high shipping traffic
inferred← citeshttps://doi.org/10.1007/s00343-016-5256-1openalex-snapshot
A new species of Phyllochaetopterus Grube, 1863 (Polychaeta: Chaetopteridae) from Hainan Island, South China Sea
inferred← citeshttps://doi.org/10.1007/s00343-019-8022-3openalex-snapshot
Catalogue of Polychaete species (Annelida) described from China Seas during 2008–2017
inferred← citeshttps://doi.org/10.1007/s12526-015-0355-3openalex-snapshot
On the taxonomy and phylogeny of Ctenodrilus (Annelida: Cirratulidae) with a first report from South Africa
inferred← citeshttps://doi.org/10.1007/s12526-016-0619-6openalex-snapshot
Extension of the geographical distribution of the crab Asthenognathus atlanticus Monod, 1932, in the eastern English Channel through its commensal relationship with the polychaete Chaetopterus variopedatus (Renier, 1804)
inferred← citeshttps://doi.org/10.1007/s13127-010-0033-zopenalex-snapshot
Establishing species and species boundaries in Sabellastarte Krøyer, 1856 (Annelida: Sabellidae): an integrative approach
inferred← citeshttps://doi.org/10.1016/j.jcz.2026.06.007openalex-snapshot
Revision of Typhloscolecidae (Annelida, Errantia) with the description of three new Typhloscolex species
inferred← citeshttps://doi.org/10.1016/j.tree.2026.03.004openalex-snapshot
Marine conservation: linking taxonomy, Red Listing, and public engagement
inferred← citeshttps://doi.org/10.1016/j.ympev.2008.05.042openalex-snapshot
Multiple origins of pelagicism within Flabelligeridae (Annelida)
inferred← citeshttps://doi.org/10.1016/j.ympev.2018.06.021openalex-snapshot
Barcoding and multi-locus phylogeography of the globally distributed calcareous tubeworm genus Hydroides Gunnerus, 1768 (Annelida, Polychaeta, Serpulidae)
inferred← citeshttps://doi.org/10.1017/s1477200009990168openalex-snapshot
Evolution of the unique freshwater cave‐dwelling tube worm Marifugia cavatica (Annelida: Serpulidae)
inferred← citeshttps://doi.org/10.1038/s41598-021-89459-yopenalex-snapshot
Morphological convergence and adaptation in cave and pelagic scale worms (Polynoidae, Annelida)
inferred← citeshttps://doi.org/10.1071/is08011openalex-snapshot
Phylogeny of the Serpula–Crucigera–Hydroides clade (Serpulidae : Annelida) using molecular and morphological data: implications for operculum evolution
inferred← citeshttps://doi.org/10.1071/is21081openalex-snapshot
Citizen science and integrative taxonomy reveal a great diversity within Caribbean Chaetopteridae (Annelida), with the description of one new species
inferred← citeshttps://doi.org/10.1080/17451000802317683openalex-snapshot
Discrete genetic boundaries of threeStreblospio(Spionidae, Annelida) species and the status ofS. shrubsolii
inferred← citeshttps://doi.org/10.1093/icb/icm086openalex-snapshot
A brief review of holopelagic annelids
inferred← citeshttps://doi.org/10.1093/icb/icx017openalex-snapshot
Glowing Worms: Biological, Chemical, and Functional Diversity of Bioluminescent Annelids
inferred← citeshttps://doi.org/10.1111/j.1096-3642.2007.00342.xopenalex-snapshot
Description of a new species of Mesochaetopterus (Annelida, Polychaeta, Chaetopteridae), with redescription of Mesochaetopterus xerecus and an approach to the phylogeny of the family
inferred← citeshttps://doi.org/10.1111/j.1463-6409.2010.00418.xopenalex-snapshot
Origins of holopelagic Typhloscolecidae and Lopadorhynchidae within Phyllodocidae (Phyllodocida, Annelida)
inferred← citeshttps://doi.org/10.1111/j.1463-6409.2010.00460.xopenalex-snapshot
Phylogenetics of Acrocirridae and Flabelligeridae (Cirratuliformia, Annelida)
inferred← citeshttps://doi.org/10.1111/mec.14286openalex-snapshot
Vertical gradients in species richness and community composition across the twilight zone in the North Pacific Subtropical Gyre
inferred← citeshttps://doi.org/10.1111/php.13221openalex-snapshot
Chaetopterus variopedatus Bioluminescence: A Review of Light Emission within a Species Complex
inferred← citeshttps://doi.org/10.1111/zsc.12238openalex-snapshot
Phylogenetic analyses of Chaetopteridae (Annelida)
inferred← citeshttps://doi.org/10.1134/s2075111725050017openalex-snapshot
First Record of Polychates Dodecaceria concharum Örsted, 1843 (Polychaeta: Cirratulidae) in Shells of Scallop Chlamys islandica O. F. Müller, 1776 (Bivalvia: Pectinidae) in the Barents Sea
inferred← citeshttps://doi.org/10.1146/annurev-marine-010814-020007openalex-snapshot
Diet of Worms Emended: An Update of Polychaete Feeding Guilds
inferred← citeshttps://doi.org/10.1186/s40851-022-00188-0openalex-snapshot
Ultrastructure of cerebral eyes in Oweniidae and Chaetopteridae (Annelida) – implications for the evolution of eyes in Annelida
inferred← citeshttps://doi.org/10.1371/journal.pone.0011842openalex-snapshot
The Biodiversity of the Mediterranean Sea: Estimates, Patterns, and Threats
inferred← citeshttps://doi.org/10.1371/journal.pone.0207249openalex-snapshot
Pelagic shrimp play dead in deep oxygen minima
inferred← citeshttps://doi.org/10.1635/053.158.0113openalex-snapshot
ChaetopterusandMesochaetopterus(Polychaeta: Chaetopteridae) from the Galapagos Islands, with Descriptions of Four New Species
inferred← citeshttps://doi.org/10.21411/cbm.a.42737680openalex-snapshot
A new species of Phyllochaetopterus (Annelida: Chaetopteridae) from deep-sea hydrothermal Ashadze-1 vent field, Mid-Atlantic Ridge: taxonomical description and partial COI DNA sequence
inferred← citeshttps://doi.org/10.21805/bzn.v67i4.a8openalex-snapshot
Case 3525Tricoelia variopedataRenier, [1804] (currentlyChaetopterus variopedatus; Annelida, Polychaeta): proposed conservation of the specific name
inferred← citeshttps://doi.org/10.24075/brsmu.2021.049openalex-snapshot
Similarities and differences between the Chaetopterus variopedatus polychaete luciferases depending on the type of habitat
inferred← citeshttps://doi.org/10.24075/vrgmu.2021.049openalex-snapshot
Skhodstvo i razlichiya lyuciferaz polihet Chaetopterus variopedatus v zavisimosti ot mesta ih obitaniya
inferred← citeshttps://doi.org/10.24199/j.mmv.2014.71.23openalex-snapshot
A new species of Chaetopterus (Annelida, Chaetopteridae) from Hong Kong
inferred← citeshttps://doi.org/10.2988/0006-324x-126.4.287openalex-snapshot
First whale fall chaetopterid; a gigantic new species of Phyllochaetopterus (Chaetopteridae: Annelida) from the deep sea off California
inferred← citeshttps://doi.org/10.3389/fmars.2024.1382212openalex-snapshot
Unraveling the phylogeny of Chaetopteridae (Annelida) through mitochondrial genome analysis
inferred← citeshttps://doi.org/10.3390/d15030398openalex-snapshot
Phylogeny of Serpulidae (Annelida, Polychaeta) Inferred from Morphology and DNA Sequences, with a New Classification
inferred← citeshttps://doi.org/10.3390/d17050366openalex-snapshot
The Diversity and Phylogenetic Relationships of a Chaetopterus Symbiont Community in Djibouti, with Redescription of Chaetopterus djiboutiensis Gravier, 1906 Stat. Nov. (Annelida: Chaetopteridae)
inferred← citeshttps://doi.org/10.3800/pbr.15.228openalex-snapshot
Bioluminescent properties of Mesochaetopterus japonicus (Polychaeta: Chaetopteridae) with comparison to Chaetopterus
inferred← citeshttps://doi.org/10.3897/zookeys.1015.54387openalex-snapshot
Molecular identification and larval morphology of spionid polychaetes (Annelida, Spionidae) from northeastern Japan
inferred← citeshttps://doi.org/10.3897/zookeys.614.8346openalex-snapshot
New species of Trophoniella from Shimoda, Japan (Annelida, Flabelligeridae)
inferred← citeshttps://doi.org/10.5670/oceanog.2017.421openalex-snapshot
The Coevolution of Midwater Research and ROV Technology at MBARI
inferred← citeshttps://doi.org/10.5670/oceanog.2017.422openalex-snapshot
Insights into the Biodiversity, Behavior, and Bioluminescence of Deep-Sea Organisms Using Molecular and Maritime Technology
inferred← citeshttps://doi.org/10.7287/peerj.13909v0.1/reviews/1openalex-snapshot
Peer Review #1 of "Phylogenetic position of the enigmatic genus Atherospio and description of Atherospio aestuarii sp. nov. (Annelida: Spionidae) from Japan (v0.1)"
inferred← citeshttps://doi.org/10.7287/peerj.13909v0.1/reviews/2openalex-snapshot
Peer Review #2 of "Phylogenetic position of the enigmatic genus Atherospio and description of Atherospio aestuarii sp. nov. (Annelida: Spionidae) from Japan (v0.1)"
inferred← citeshttps://doi.org/10.7287/peerj.13909v0.1/reviews/3openalex-snapshot
Peer Review #3 of "Phylogenetic position of the enigmatic genus Atherospio and description of Atherospio aestuarii sp. nov. (Annelida: Spionidae) from Japan (v0.1)"
inferred← citeshttps://doi.org/10.7287/peerj.13909v0.2/reviews/1openalex-snapshot
Peer Review #1 of "Phylogenetic position of the enigmatic genus Atherospio and description of Atherospio aestuarii sp. nov. (Annelida: Spionidae) from Japan (v0.2)"
inferred← citeshttps://doi.org/10.7287/peerj.13909v0.2/reviews/3openalex-snapshot
Peer Review #3 of "Phylogenetic position of the enigmatic genus Atherospio and description of Atherospio aestuarii sp. nov. (Annelida: Spionidae) from Japan (v0.2)"
inferred← citeshttps://doi.org/10.7717/peerj.13909openalex-snapshot
Phylogenetic position of the enigmatic genus Atherospio and description of Atherospio aestuarii sp. nov. (Annelida: Spionidae) from Japan
inferred← citeshttps://doi.org/10.7717/peerj.2930openalex-snapshot
Do syntopic host species harbour similar symbiotic communities? The case of Chaetopterus spp. (Annelida: Chaetopteridae)
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