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On the genus Spirobranchus (Annelida, Serpulidae) from the northern Red Sea, and a description of a new species

https://doi.org/10.1071/is17061
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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/aqc.666openalex-snapshot
Polychaete (Spirobranchus giganteus) loading on South African corals
inferredcites →https://doi.org/10.1002/iroh.199900019openalex-snapshot
Ecology and Biodiversity of Coral Reef Polychaetes of Guam and Saipan, Mariana Islands.
inferredcites →https://doi.org/10.1007/s00227-016-3058-9openalex-snapshot
A global invader or a complex of regionally distributed species? Clarifying the status of an invasive calcareous tubeworm Hydroides dianthus (Verrill, 1873) (Polychaeta: Serpulidae) using DNA barcoding
inferredcites →https://doi.org/10.1007/s00338-005-0084-3openalex-snapshot
A beneficial association between a polychaete worm and a scleractinian coral?
inferredcites →https://doi.org/10.1007/s00338-010-0601-xopenalex-snapshot
Coral mortality and serpulid infestations associated with red tide, in the Persian Gulf
inferredcites →https://doi.org/10.1007/s00338-015-1294-yopenalex-snapshot
Christmas tree worms of Indo-Pacific coral reefs: untangling the Spirobranchus corniculatus (Grube, 1862) complex
inferredcites →https://doi.org/10.1016/j.dsr2.2014.08.018openalex-snapshot
Polychaete-parasitizing copepods from the deep-sea Kuril–Kamchatka Trench (Pacific Ocean), with the description of a new Ophelicola species and comments on the currently known annelidicolous copepods
inferredcites →https://doi.org/10.1016/j.marpolbul.2016.04.055openalex-snapshot
Borehole density on the surface of living Porites corals as an indicator of sedimentation in Hong Kong
inferredcites →https://doi.org/10.1016/j.ode.2006.06.004openalex-snapshot
Phylogenetic relationships of Serpulidae (Annelida: Polychaeta) based on 18S rDNA sequence data, and implications for opercular evolution
inferredcites →https://doi.org/10.1016/j.ympev.2007.10.025openalex-snapshot
Yet another example of paraphyly in Annelida: Molecular evidence that Sabellidae contains Serpulidae
inferredcites →https://doi.org/10.1017/s0025315415000764openalex-snapshot
A new fouling Hydroides (Annelida, Sabellida, Serpulidae) from southern Gulf of California
inferredcites →https://doi.org/10.1071/is09003openalex-snapshot
Naming species with no morphological indicators: species status of Galeolaria caespitosa (Annelida : Serpulidae) inferred from nuclear and mitochondrial gene sequences and morphology
inferredcites →https://doi.org/10.1071/is12024openalex-snapshot
COI barcoding of Hydroides: a road from impossible to difficult
inferredcites →https://doi.org/10.1071/is15015openalex-snapshot
Is Hydroides brachyacantha (Serpulidae : Annelida) a widespread species?
inferredcites →https://doi.org/10.1071/zo9670201openalex-snapshot
Marine serpulidae (Annelida : Polychaeta) of eastern Queensland and New South Wales
inferredcites →https://doi.org/10.1073/pnas.76.4.1967openalex-snapshot
Rapid evolution of animal mitochondrial DNA.
inferredcites →https://doi.org/10.1080/00212210.1992.10688664openalex-snapshot
SERPULIDS (ANNELIDA: POLYCHAETA) ALONG THE MEDITERRANEAN COAST OF ISRAEL—NEW POPULATION BUILD-UPS OF LESSEPSIAN MIGRANTS
inferredcites →https://doi.org/10.1080/00785326.1998.10409381openalex-snapshot
Ecological correlates of arctic serpulidae (Annelida, Polychaeta) distributions
inferredcites →https://doi.org/10.1093/bioinformatics/btg180openalex-snapshot
MrBayes 3: Bayesian phylogenetic inference under mixed models
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/btm404openalex-snapshot
Clustal W and Clustal X version 2.0
inferredcites →https://doi.org/10.1093/bioinformatics/btp348openalex-snapshot
trimAl: a tool for automated alignment trimming in large-scale phylogenetic analyses
inferredcites →https://doi.org/10.1093/bioinformatics/btu531openalex-snapshot
AliView: a fast and lightweight alignment viewer and editor for large datasets
inferredcites →https://doi.org/10.1093/molbev/mss020openalex-snapshot
PartitionFinder: Combined Selection of Partitioning Schemes and Substitution Models for Phylogenetic Analyses
inferredcites →https://doi.org/10.1093/molbev/mst064openalex-snapshot
DAMBE5: A Comprehensive Software Package for Data Analysis in Molecular Biology and Evolution
inferredcites →https://doi.org/10.1093/oxfordjournals.molbev.a026241openalex-snapshot
Mitochondrial Genomes of Galathealinum, Helobdella, and Platynereis: Sequence and Gene Arrangement Comparisons Indicate that Pogonophora Is Not a Phylum and Annelida and Arthropoda Are Not Sister Taxa
inferredcites →https://doi.org/10.1093/oxfordjournals.molbev.a040143openalex-snapshot
Deuterostome phylogeny and the sister group of the chordates: evidence from molecules and morphology.
inferredcites →https://doi.org/10.1093/oxfordjournals.molbev.a040362openalex-snapshot
The small-subunit ribosomal RNA gene sequences from the hypotrichous ciliates Oxytricha nova and Stylonychia pustulata.
inferredcites →https://doi.org/10.1111/(issn)1096-3642openalex-snapshot
Zoological Journal of the Linnean Society
inferredcites →https://doi.org/10.1111/j.1096-3642.1984.tb01969.xopenalex-snapshot
Taxonomy and ecology of coral reef tube worms (Serpulidae, Spirorbidae) in the Sudanese Red Sea
inferredcites →https://doi.org/10.1111/j.1096-3642.1999.tb01376.xopenalex-snapshot
Redescription of Spirobranchus gaymardi (Quatrefages, 1866) (Polychaeta: Serpulidae) from the Indo-Pacific with remarks on the Spirobranchus giganteus complex
inferredcites →https://doi.org/10.1111/j.1463-6409.2006.00244.xopenalex-snapshot
Phylogenetic relationships within Serpulidae (Sabellida, Annelida) inferred from molecular and morphological data
inferredcites →https://doi.org/10.1111/zsc.12044openalex-snapshot
Cryptic polychaete diversity: a review
inferredcites →https://doi.org/10.1163/9789004629745_052openalex-snapshot
Red Sea Serpulids (Polychaeta) in the Eastern Mediterranean
inferredcites →https://doi.org/10.11646/zootaxa.2036.1.1openalex-snapshot
Taxonomy of Serpulidae (Annelida, Polychaeta): The state of affairs
inferredcites →https://doi.org/10.11646/zootaxa.2848.1.1openalex-snapshot
Serpulidae (Annelida: Polychaeta) from the Suez Canal—From a Lessepsian Migration Perspective (a Monograph)
inferredcites →https://doi.org/10.11646/zootaxa.3424.1.1openalex-snapshot
Serpulidae (Annelida: Polychaeta) from Hong Kong
inferredcites →https://doi.org/10.11646/zootaxa.4019.1.13openalex-snapshot
Serpulidae (Annelida) of Lizard Island, Great Barrier Reef, Australia
inferredcites →https://doi.org/10.1186/1471-2148-10-70openalex-snapshot
Fast evolving 18S rRNA sequences from Solenogastres (Mollusca) resist standard PCR amplification and give new insights into mollusk substitution rate heterogeneity
inferredcites →https://doi.org/10.1201/b11009-4openalex-snapshot
From microbes to people
inferredcites →https://doi.org/10.1201/crcocemarbioopenalex-snapshot
Oceanography and Marine Biology - An Annual Review
inferredcites →https://doi.org/10.1214/aos/1176344136openalex-snapshot
Estimating the Dimension of a Model
inferredcites →https://doi.org/10.12681/mms.194openalex-snapshot
Increasing Polychaete diversity as a consequence of increasing research effort in Greek waters: new records and exotic species
inferredcites →https://doi.org/10.12681/mms.195openalex-snapshot
Gametogenesis and spawning of Spirobranchus tetraceros (Polychaeta, Serpulidae) in Abu Kir Bay, Egypt
inferredcites →https://doi.org/10.1371/journal.pone.0043971openalex-snapshot
Extensive Pyrosequencing Reveals Frequent Intra-Genomic Variations of Internal Transcribed Spacer Regions of Nuclear Ribosomal DNA
inferredcites →https://doi.org/10.2307/3593153openalex-snapshot
HolopelagicPoeobius meseres(“Poeobiidae,” Annelida) Is Derived From Benthic Flabelligerid Worms
inferredcites →https://doi.org/10.25268/bimc.invemar.1995.24.0.379openalex-snapshot
SUCCESSIONAL PATTERNS ON FOULING PLATES IN THE BAY OF SANTA MARTA, COLOMBIAN CARIBBEAN
inferredcites →https://doi.org/10.3354/ab00444openalex-snapshot
Reef formation versus solitariness in two New Zealand serpulids does not involve cryptic species
inferredcites →https://doi.org/10.3391/ai.2006.1.4.6openalex-snapshot
Serpulid species (Polychaeta: Serpulidae) from the Levantine coast of Turkey (eastern Mediterranean), with special emphasis on alien species
inferredcites →https://doi.org/10.3853/j.0067-1975.61.2009.1489openalex-snapshot
Descriptions of new serpulid polychaetes from the Kimberleys of Australia and discussion of Australian and Indo-West Pacific species of Spirobranchus and superficially similar taxa
inferredcites →https://doi.org/10.3906/zoo-1405-72openalex-snapshot
Checklist of Annelida from the coasts of Turkey

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.4748.3.1zenodo-depositor-declared
A new species of the Spirobranchus kraussii-complex (Annelida, Serpulidae) from the Persian Gulf and Gulf of Oman
inferred← citeshttps://doi.org/10.11646/zootaxa.5040.1.2zenodo-depositor-declared
Spirobranchus bakau sp. nov. from Singapore: yet another species of S. kraussii-complex (Polychaeta: Serpulidae)
inferred← citeshttps://doi.org/10.3391/ai.2025.20.1.136400zenodo-depositor-declared
Not so Lessepsian migrants of the Spirobranchus tetraceros complex (Serpulidae, Annelida)
inferred← citeshttps://doi.org/10.1002/ecy.2668openalex-snapshot
Filamentous turf algae on tube worms intensify damage in massive Porites corals
inferred← citeshttps://doi.org/10.1002/njz2.70021openalex-snapshot
Exploring the Potential of Serpulid External Tube Morphology for Rapid Grouping Assessment in Ecological Research: A Case Study From Southern New Zealand
inferred← citeshttps://doi.org/10.1007/s00227-019-3504-6openalex-snapshot
Coral injuries caused by Spirobranchus opercula with and without epibiotic turf algae at Curaçao
inferred← citeshttps://doi.org/10.1007/s00227-026-04834-5openalex-snapshot
Drivers of Spirobranchus corniculatus (Grube, 1862) distribution on coral reefs in SE Sulawesi, Indonesia
inferred← citeshttps://doi.org/10.1016/j.ijpara.2023.09.002openalex-snapshot
Host specificity of coral-associated fauna and its relevance for coral reef biodiversity
inferred← citeshttps://doi.org/10.1016/j.rsma.2023.103184openalex-snapshot
Intertidal calcareous tubeworms (Annelida: Serpulidae) of the Persian Gulf and Gulf of Oman
inferred← citeshttps://doi.org/10.1080/07924259.2021.1932614openalex-snapshot
Early development of two species of Spirobranchus Blainville, 1818 (Polychaeta: Serpulidae) from the Southern Mexican Pacific
inferred← citeshttps://doi.org/10.11606/1807-0205/2020.60.05openalex-snapshot
Do Morphological Similarities and human-induced dispersal explain the non-native occurrence of Serpulidae (Annelida) in Southwest Atlantic? Taxonomic detailing is the key
inferred← citeshttps://doi.org/10.11606/1807-0205/2020.60.51openalex-snapshot
On a new species of Spirobranchus Blainville, 1818 (Annelida: Serpulidae) and considerations on the genus along the Brazilian coast
inferred← citeshttps://doi.org/10.12681/mms.21860openalex-snapshot
Non-indigenous polychaetes along the coasts of Italy: a critical review
inferred← citeshttps://doi.org/10.12911/22998993/186161openalex-snapshot
Water Quality Impact Christmas Tree Worms (Spirobranchus spp.) Distribution and Community Structure on Hard Corals At Sempu Island Nature Reserve, Malang, Indonesia
inferred← citeshttps://doi.org/10.13057/biodiv/d250445openalex-snapshot
Christmas tree worm Spirobranchus spp. (Annelida: Serpulidae) as indicators of coral health at Weh Island, Aceh Province, Indonesia
inferred← citeshttps://doi.org/10.2989/1814232x.2020.1831954openalex-snapshot
Spatial and temporal diversity of non-native biofouling species associated with marinas in two Angolan bays
inferred← citeshttps://doi.org/10.3161/15052249pje2023.71.4.002openalex-snapshot
Reef-Dwelling Christmas Tree Worms (Spirobranchus, Serpulidae, Polychaeta), on Porites Corals: Densities and Age Structure
inferred← citeshttps://doi.org/10.3390/d13030130openalex-snapshot
Fanworms: Yesterday, Today and Tomorrow
inferred← citeshttps://doi.org/10.3390/d14040241openalex-snapshot
The First Deep-Sea Stylasterid (Hydrozoa, Stylasteridae) of the Red Sea
inferred← citeshttps://doi.org/10.3390/d16050295openalex-snapshot
Stony Corals and Their Associated Fauna Residing in Marine Lakes under Extreme Environmental Conditions
inferred← citeshttps://doi.org/10.3853/j.2201-4349.74.2022.1820openalex-snapshot
A puzzle no more: the identity of Spirobranchus tetraceros (Schmarda, 1861) (Annelida, Serpulidae) is revealed
inferred← citeshttps://doi.org/10.3897/zookeys.1100.79569openalex-snapshot
A new species of the Spirobranchus kraussii complex, S. akitsushima (Annelida, Polychaeta, Serpulidae), from the rocky intertidal zone of Japan
inferred← citeshttps://doi.org/10.3989/scimar.04976.20aopenalex-snapshot
Following the Phoenician example: western Mediterranean colonization by Spirobranchus cf. tetraceros (Annelida: Serpulidae)
inferred← citeshttps://doi.org/10.4274/dir.2024.242652openalex-snapshot
Cortical and subcortical structural changes in pediatric patients with infratentorial tumors
inferred← citeshttps://doi.org/10.7717/peerj.11746openalex-snapshot
Molecular phylogenetic assessment ofSpirobranchus kraussii-complex (Annelida: Serpulidae) from the Japanese Archipelago
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