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Anterior sensory organs in Sabellariidae (Annelida)

https://doi.org/10.1111/ivb.12153
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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.1206openalex-snapshot
The conservation status of Sabellaria alveolata (L.) (Polychaeta: Sabellariidae) reefs in the Bay of Mont‐Saint‐Michel
inferredcites →https://doi.org/10.1002/ece3.1556openalex-snapshot
Historical comparisons reveal multiple drivers of decadal change of an ecosystem engineer at the range edge
inferredcites →https://doi.org/10.1002/jmor.10605openalex-snapshot
Observations of serotonin and FMRFamide‐like immunoreactivity in palp sensory structures and the anterior nervous system of spionid polychaetes
inferredcites →https://doi.org/10.1002/jmor.10813openalex-snapshot
Ultrastructure of the extensively developed nuchal organs of Laonice bahusiensis (Annelida: Canalipalpata: Spionidae)
inferredcites →https://doi.org/10.1007/1-4020-3240-4_5openalex-snapshot
Sense organs in polychaetes (Annelida)
inferredcites →https://doi.org/10.1007/978-94-017-2887-4_14openalex-snapshot
Larval settlement of polychaetes
inferredcites →https://doi.org/10.1007/bf00351339openalex-snapshot
Settlement of the tube worm Hydroides dianthus (Polychaeta: Serpulidae): cues for gregarious settlement
inferredcites →https://doi.org/10.1007/bf00391588openalex-snapshot
Developmental studies of the post-settling stages of Sabellaria vulgaris (Polychaeta: Sabellariidae)
inferredcites →https://doi.org/10.1007/bf00393254openalex-snapshot
Spawning periodicity and habitat of the palolo worm Eunice viridis (Polychaeta: Eunicidae) in the Samoan Islands
inferredcites →https://doi.org/10.1007/bf00397571openalex-snapshot
Chemical induction of larval settlement and metamorphosis in the reef-building tube worm Phragmatopoma californica (Sabellariidae: Polychaeta)
inferredcites →https://doi.org/10.1007/bf00409012openalex-snapshot
Functional morphology of the larval tentacles of Phragmatopoma californica (Polychaeta: Sabellariidae): composite larval and adult organs of multifunctional significance
inferredcites →https://doi.org/10.1007/bf00409013openalex-snapshot
Ultrastructure and behavior of the larva of Phragmatopoma californica (Polychaeta: Sabellariidae): identification of sensory organs potentially involved in substrate selection
inferredcites →https://doi.org/10.1007/bf01016500openalex-snapshot
Chemically induced metamorphosis of polychaete larvae in both the laboratory and ocean environment
inferredcites →https://doi.org/10.1007/s10126-001-0069-3openalex-snapshot
Nucleotide Sequences of Ribosomal Internal Transcribed Spacers and Their Utility in Distinguishing Closely Related Perinereis Polychaets (Annelida; Polychaeta; Nereididae)
inferredcites →https://doi.org/10.1016/0967-0653(93)91415-9openalex-snapshot
10.1016/0967-0653(93)91415-9
inferredcites →https://doi.org/10.1016/0967-0653(93)91492-uopenalex-snapshot
10.1016/0967-0653(93)91492-u
inferredcites →https://doi.org/10.1016/b978-0-12-282503-3.50007-9openalex-snapshot
ANNELIDA: POLYCHAETA
inferredcites →https://doi.org/10.1016/j.csr.2009.05.002openalex-snapshot
Modelling larval dispersal and settlement of the reef-building polychaete Sabellaria alveolata: Role of hydroclimatic processes on the sustainability of biogenic reefs
inferredcites →https://doi.org/10.1016/j.jembe.2006.06.007openalex-snapshot
Sediment-associated cues for larval settlement of the infaunal spionid polychaetes Polydora cornuta and Streblospio benedicti
inferredcites →https://doi.org/10.1016/s0967-0653(97)82175-8openalex-snapshot
10.1016/s0967-0653(97)82175-8
inferredcites →https://doi.org/10.1017/s0025315400000576openalex-snapshot
Additional Observations On Larval Growth and Settlement of Sabellaria Alveolata
inferredcites →https://doi.org/10.1017/s0025315400025157openalex-snapshot
The distribution, development and settlement of the sabellarian polychaete Lygdamis muratus (Allen) Near Plymouth
inferredcites →https://doi.org/10.1017/s0025315400029787openalex-snapshot
The Larvæ of the British Sabellarians
inferredcites →https://doi.org/10.1017/s0025315400034561openalex-snapshot
The settlement behaviour of the larvae ofSabellaria alveolata(L.)
inferredcites →https://doi.org/10.1017/s0025315400055582openalex-snapshot
The Post-Larval Development of Loimia medusa Sav
inferredcites →https://doi.org/10.1023/a:1003704928668openalex-snapshot
Larval settlement of polychaetes
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/10.1080/00222930802140186openalex-snapshot
Caruncle inMegalommaJohansson, 1925 (Polychaeta: Sabellidae) and the description of a new species from the Eastern Tropical Pacific
inferredcites →https://doi.org/10.1080/00288330.2004.9517234openalex-snapshot
Morphology and biology of Polydora rickettsi (Polychaeta: Spionidae) from Chile
inferredcites →https://doi.org/10.1080/10635150600852011openalex-snapshot
Sequence-Based Species Delimitation for the DNA Taxonomy of Undescribed Insects
inferredcites →https://doi.org/10.1080/10635150701472164openalex-snapshot
Improvement of Phylogenies after Removing Divergent and Ambiguously Aligned Blocks from Protein Sequence Alignments
inferredcites →https://doi.org/10.1080/10635150802429642openalex-snapshot
A Rapid Bootstrap Algorithm for the RAxML Web Servers
inferredcites →https://doi.org/10.1080/11956860.1998.11682477openalex-snapshot
Timing of reproduction in marine polychaetes: The role of sex pheromones
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/molbev/mst197openalex-snapshot
MEGA6: Molecular Evolutionary Genetics Analysis Version 6.0
inferredcites →https://doi.org/10.1093/molbev/msu080openalex-snapshot
Illuminating the Base of the Annelid Tree Using Transcriptomics
inferredcites →https://doi.org/10.1109/ipdps.2002.1016585openalex-snapshot
TCS: estimating gene genealogies
inferredcites →https://doi.org/10.1111/j.1096-0031.2010.00341.xopenalex-snapshot
Phylogeny of Sabellidae (Annelida) and relationships with other taxa inferred from morphology and multiple genes
inferredcites →https://doi.org/10.1111/j.1096-3642.2011.00767.xopenalex-snapshot
Systematic revision of Sabellariidae (Polychaeta) and their relationships with other polychaetes using morphological and DNA sequence data
inferredcites →https://doi.org/10.1111/j.1463-6395.1997.tb01133.xopenalex-snapshot
Ultrastructure of Nuchal Organs in Polychaetes (Annelida) — New Results and Review
inferredcites →https://doi.org/10.1111/j.1525-142x.2008.00275.xopenalex-snapshot
Larval neurogenesis in Sabellaria alveolata reveals plasticity in polychaete neural patterning
inferredcites →https://doi.org/10.1111/zsc.12028openalex-snapshot
Cryptic diversity, intraspecific phenetic plasticity and recent geographical translocations inBranchiomma(Sabellidae, Annelida)
inferredcites →https://doi.org/10.1139/z76-241openalex-snapshot
Scanning electron microscopic observations of the larval development of the reef-building polychaete Phragmatopoma lapidosa
inferredcites →https://doi.org/10.1139/z83-065openalex-snapshot
Evolutionary radiation in polychaete ovaries and vitellogenic mechanisms: their possible role in life history patterns
inferredcites →https://doi.org/10.1139/z85-156openalex-snapshot
Larval development and metamorphosis of Sabellaria cementarium Moore, 1906 (Polychaeta: Sabellariidae)
inferredcites →https://doi.org/10.11646/zoosymposia.2.1.34openalex-snapshot
Distribution of Idanthyrsus cretus (Polychaeta: Sabellariidae) in the Tropical Eastern Pacific and application of PCR-RAPD for population analysis
inferredcites →https://doi.org/10.11646/zootaxa.3306.1.1openalex-snapshot
Revision of the Australian Sabellariidae (Polychaeta) and description of eight new species
inferredcites →https://doi.org/10.11646/zootaxa.4019.1.10openalex-snapshot
Sabellariidae from Lizard Island, Great Barrier Reef, including a new species of Lygdamis and notes on external morphology of the median organ
inferredcites →https://doi.org/10.11646/zootaxa.4052.5.3openalex-snapshot
Sabellaria jeramae, a new species (Annelida: Polychaeta: Sabellariidae) from the shallow waters of Malaysia, with a note on the ecological traits of reefs
inferredcites →https://doi.org/10.1242/jcs.s3-93.24.435openalex-snapshot
The Development and Structure of the Anterior Region of the Body in the Sabellariidae, with special reference to Phragmatopoma californica
inferredcites →https://doi.org/10.1575/1912/10280openalex-snapshot
Gregarious settlement by the larvae of Hydroides dianthus (Polychaeta, Serpulidae)
inferredcites →https://doi.org/10.1590/1678-476620141041513openalex-snapshot
Variação sazonal no recrutamento de Phragmatopoma caudata (Polychaeta, Sabellariidae) na costa sudeste do Brasil: biometria e validação de metodologia para categorização de classes etárias
inferredcites →https://doi.org/10.18475/cjos.v44i2.a10openalex-snapshot
The Ecological Importance of a Recently Discovered Intertidal Sabellariid Reef in St. Croix, U.S. Virgin Islands
inferredcites →https://doi.org/10.2307/1543088openalex-snapshot
Controlled Field Release of a Waterborne Chemical Signal Stimulates Planktonic Larvae to Settle
inferredcites →https://doi.org/10.2307/3593153openalex-snapshot
HolopelagicPoeobius meseres(“Poeobiidae,” Annelida) Is Derived From Benthic Flabelligerid Worms
inferredcites →https://doi.org/10.24199/j.mmv.2014.71.06openalex-snapshot
Oogenesis in Phragmatopoma (Polychaeta: Sabellariidae): Evidence for morphological distinction among geographically remote populations
inferredcites →https://doi.org/10.24199/j.mmv.2014.71.19openalex-snapshot
Systematics, evolution and phylogeny of Annelida – a morphological perspective
inferredcites →https://doi.org/10.2984/1534-6188(2007)61[399:nvnsap]2.0.co;2openalex-snapshot
Neosabellaria vitiensis, n. sp. (Annelida: Polychaeta: Sabellariidae), from Shallow Water of Suva Harbor, Fiji1
inferredcites →https://doi.org/10.3354/meps005069openalex-snapshot
Gregarious Settlement by the Larvae of Hydroides dianthus (Polychaeta: Serpulidae)
inferredcites →https://doi.org/10.3354/meps07011openalex-snapshot
Distribution and retention of Sabellaria alveolata larvae (Polychaeta: Sabellariidae) in the Bay of Mont-Saint-Michel, France
inferredcites →https://doi.org/10.3354/meps071245openalex-snapshot
Responses of planktonic larvae of the serpulid polychaete Spirobranchus polycerus var. augeneri to an alga, adult tubes and conspecific larvae
inferredcites →https://doi.org/10.3354/meps301159openalex-snapshot
Particle capture and processing mechanisms in Sabellaria alveolata (Polychaeta: Sabellariidae)
inferredcites →https://doi.org/10.3354/meps328295openalex-snapshot
Feeding mechanism of the polychaete Sabellaria alveolata revisited: comment on Dubois et al. (2005)
inferredcites →https://doi.org/10.3853/j.0067-1975.61.2009.1529openalex-snapshot
Review of the genus Megalomma (Polychaeta: Sabellidae) in Australia with description of three new species, new records and notes on certain features with phylogenetic implications
inferredcites →https://doi.org/10.3897/zookeys.223.3561openalex-snapshot
Reestablishment of Notopygos megalops McIntosh, description of N. caribea sp. n. from the Greater Caribbean and barcoding of “amphiamerican” Notopygos species (Annelida, Amphinomidae)
inferredcites →https://doi.org/10.3989/scimar.2011.75n2251openalex-snapshot
Revision of Hermodice Kinberg, 1857 (Polychaeta: Amphinomidae)
inferredcites →https://doi.org/10.7717/peerj.1201openalex-snapshot
Biological and ecological traits of marine species

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.4821.3.4zenodo-depositor-declared
Two new species of Sabellariidae (Annelida, Polychaeta) from the abyss of eastern Australia
inferred← citeshttps://doi.org/10.1002/jez.b.23192openalex-snapshot
Nuchal organs in the trochophore of Siboglinum fiordicum (Annelida, Siboglinidae)
inferred← citeshttps://doi.org/10.1002/jmor.70079openalex-snapshot
Morphological Organization, Sensory Structures and Catecholaminergic Nervous System of Lindrilus flavocapitatus (Annelida: Protodrilidae)
inferred← citeshttps://doi.org/10.1007/s00435-018-0422-yopenalex-snapshot
Anterior sense organs in Sabellaria alveolata (Annelida, Sedentaria, Spionida) with special reference to ultrastructure of photoreceptor elements presumably involved in shadow reflex
inferred← citeshttps://doi.org/10.1007/s13127-023-00603-0openalex-snapshot
Development and structure of the anterior nervous system and sense organs in the holopelagic annelid Tomopteris spp. (Phyllodocida, Errantia)
inferred← citeshttps://doi.org/10.1016/b978-0-12-809324-5.23775-9openalex-snapshot
Chemoreception in Aquatic Invertebrates
inferred← citeshttps://doi.org/10.1016/j.jcz.2026.08.002openalex-snapshot
Sensory structures and the organization of the nervous and muscle systems in Lindrilus flavocapitatus (Annelida: Protodrilidae)
inferred← citeshttps://doi.org/10.1016/j.marenvres.2023.106334openalex-snapshot
Body traits variation of a reef building polychaete across a latitudinal gradient
inferred← citeshttps://doi.org/10.1017/s002531541700087xopenalex-snapshot
Climate and environmental changes driving idiosyncratic shifts in the distribution of tropical and temperate worm reefs
inferred← citeshttps://doi.org/10.1093/chemse/bjae009openalex-snapshot
What are olfaction and gustation, and do all animals have them?
inferred← citeshttps://doi.org/10.1111/ivb.12412openalex-snapshot
Development and sexual dimorphism of branchiae in Streblospio benedicti
inferred← citeshttps://doi.org/10.1111/jbi.12938openalex-snapshot
Phylogeography of the reef‐building polychaetes of the genus Phragmatopoma in the western Atlantic Region
inferred← citeshttps://doi.org/10.1186/s12862-018-1263-5openalex-snapshot
Developmental studies provide new insights into the evolution of sense organs in Sabellariidae (Annelida)
inferred← citeshttps://doi.org/10.1186/s40850-021-00068-8openalex-snapshot
Ultrastructure and functional morphology of the appendages in the reef-building sedentary polychaete Sabellaria alveolata (Annelida, Sedentaria, Sabellida)
inferred← citeshttps://doi.org/10.1186/s40850-021-00094-6openalex-snapshot
May the palps be with you – new insights into the evolutionary origin of anterior appendages in Terebelliformia (Annelida)
inferred← citeshttps://doi.org/10.21203/rs.3.rs-60217/v1openalex-snapshot
Ultrastructure and Functional Morphology of the Appendages in the Reef-Building Sedentary Polychaete Sabellaria Alveolata (Annelida, Sedentaria, Sabellida)
inferred← citeshttps://doi.org/10.3389/fnins.2023.1310225openalex-snapshot
Palps across the tree – the neuronal innervation and development of sensory head appendages in Annelida
inferred← citeshttps://doi.org/10.4282/sosj.42.1openalex-snapshot
Description of a Reef-forming Neosabellaria upopoy sp. nov. (Annelida: Polychaeta: Sabellariidae) from Shallow Waters off Iburi, Hokkaido, Japan, with Notes on its Reproduction and Early Development
inferred← citeshttps://doi.org/10.53846/goediss-10255openalex-snapshot
The evolution of the head appendages in marine bristle worms
inferred← citeshttps://doi.org/10.6084/m9.figshare.14189840openalex-snapshot
Additional file 1 of Ultrastructure and functional morphology of the appendages in the reef-building sedentary polychaete Sabellaria alveolata (Annelida, Sedentaria, Sabellida)
inferred← citeshttps://doi.org/10.6084/m9.figshare.14189843openalex-snapshot
Additional file 2 of Ultrastructure and functional morphology of the appendages in the reef-building sedentary polychaete Sabellaria alveolata (Annelida, Sedentaria, Sabellida)
inferred← citeshttps://doi.org/10.6084/m9.figshare.14189846openalex-snapshot
Additional file 3 of Ultrastructure and functional morphology of the appendages in the reef-building sedentary polychaete Sabellaria alveolata (Annelida, Sedentaria, Sabellida)
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