On the public citation graph
Larval Ontogenetic Stages of Chaetopterus: Developmental Heterochrony in the Evolution of Chaetopterid Polychaetes
0 signed · 78 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.
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known work and none has been retracted — and get a dated CiteStamped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.
What this work says
Outgoing claims: the papers this work cites, builds on, or argues with.
inferredcites →https://doi.org/10.1002/jez.1400030202openalex-snapshot
Observations and experiments concerning the elementary phenomena of embryonic development in Chætopterus
inferredcites →https://doi.org/10.1002/jmor.1050130202openalex-snapshot
The early development of marine annelids
inferredcites →https://doi.org/10.1002/jmor.1050200306openalex-snapshot
A study of the life‐history and habits of Chætopterus variopedatus, renier et claparede
inferredcites →https://doi.org/10.1002/jmor.1051810205openalex-snapshot
The nervous system of the tube‐worm Chaetopterus variopedatus (Polychaeta)
inferredcites →https://doi.org/10.1006/bijl.1998.0278openalex-snapshot
Trochophore concepts: ciliary bands and the evolution of larvae in spiralian Metazoa
inferredcites →https://doi.org/10.1006/dbio.1999.9541openalex-snapshot
Expression Patterns of Anterior Hox Genes in the Polychaete Chaetopterus: Correlation with Morphological Boundaries
inferredcites →https://doi.org/10.1007/bf00456106openalex-snapshot
The role of unequal cleavage and the polar lobe in the segregation of developmental potential during first cleavage in the embryo of Ch�topterus variopedatus
inferredcites →https://doi.org/10.1007/bf02438937openalex-snapshot
Removal of the polar lobe leads to the formation of functionally deficient photocytes in the annelidChaetopterus variopedatus
inferredcites →https://doi.org/10.1016/0012-1606(85)90078-8openalex-snapshot
The spatial distribution of maternal mRNA is determined by a cortical cytoskeletal domain in Chaetopterus eggs
inferredcites →https://doi.org/10.1016/s0070-2153(08)60222-7openalex-snapshot
1 Cytoskeleton, Cellular Signals, and Cytoplasmic Localization in Chaetopterus Embryos
inferredcites →https://doi.org/10.1017/s0025315400056010openalex-snapshot
The Larval Development of Ophelia Bicornis Savigny
inferredcites →https://doi.org/10.1073/pnas.94.10.5162openalex-snapshot
The origin and evolution of animal appendages
inferredcites →https://doi.org/10.1080/00785326.1969.10419288openalex-snapshot
Reproduction and larval development ofPolydorafrom Northern New England (Polychaeta: spionidae)
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/10.1083/jcb.62.1.175openalex-snapshot
GROWTH AND LABILITY OF CHAETOPTERUS OOCYTE MITOTIC SPINDLES ISOLATED IN THE PRESENCE OF PORCINE BRAIN TUBULIN
inferredcites →https://doi.org/10.1093/mind/xci.363.321openalex-snapshot
Description and Identification
inferredcites →https://doi.org/10.1111/j.1463-6395.1966.tb00738.xopenalex-snapshot
The Comparative Embryology of the Polychaeta
inferredcites →https://doi.org/10.1111/j.1463-6409.1997.tb00411.xopenalex-snapshot
Polychaete systematics: Past and present
inferredcites →https://doi.org/10.1111/j.1463-6409.1997.tb00412.xopenalex-snapshot
Cladistics and polychaetes
inferredcites →https://doi.org/10.1111/j.1469-7998.1962.tb01837.xopenalex-snapshot
THE POLYCHAETE STOMODEUM AND THE INTER‐RELATIONSHIPS OF THE FAMILIES OF POLYCHAETA
inferredcites →https://doi.org/10.1242/jcs.s2-78.312.543openalex-snapshot
The Development of the Sabellid Branchiomma vesiculosum
inferredcites →https://doi.org/10.2307/1537850openalex-snapshot
THE METHOD OF FEEDING OF CHAETOPTERUS
inferredcites →https://doi.org/10.2307/1539840openalex-snapshot
TUBE-BUILDING AND FEEDING IN CHAETOPTERID POLYCHAETES
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/10.5962/bhl.part.75135openalex-snapshot
Quelques stades larvaires d'un Chétoptère
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
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/bies.10409openalex-snapshot
The polychaete Platynereis dumerilii (Annelida): a laboratory animal with spiralian cleavage, lifelong segment proliferation and a mixed benthic/pelagic life cycle
inferred← citeshttps://doi.org/10.1002/dvdy.628openalex-snapshot
Future research directions of the model marine tubeworm Hydroides elegans and synthesis of developmental staging of the complete life cycle
inferred← citeshttps://doi.org/10.1002/jez.b.20001openalex-snapshot
Trochophora larvae: Cell‐lineages, ciliary bands, and body regions. 1. Annelida and Mollusca
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/10.1006/dbio.1999.9475openalex-snapshot
Bilaterian Origins: Significance of New Experimental Observations
inferred← citeshttps://doi.org/10.1006/dbio.1999.9541openalex-snapshot
Expression Patterns of Anterior Hox Genes in the Polychaete Chaetopterus: Correlation with Morphological Boundaries
inferred← citeshttps://doi.org/10.1006/dbio.2001.0309openalex-snapshot
The Spatial and Temporal Expression of Ch-en, the engrailed Gene in the Polychaete Chaetopterus, Does Not Support a Role in Body Axis Segmentation
inferred← citeshttps://doi.org/10.1007/s00239-001-0046-5openalex-snapshot
Cloning and Molecular Characterization of the First Innexin of the Phylum Annelida—Expression of the Gene During Development
inferred← citeshttps://doi.org/10.1007/s00239-003-0023-2openalex-snapshot
Specificity of Cellular Expression of C. variopedatus Polychaete Innexin in the Developing Embryo: Evolutionary Aspects of Innexins? Heterogeneous Gene Structures
inferred← citeshttps://doi.org/10.1007/s00427-006-0119-yopenalex-snapshot
Hox gene expression in larval development of the polychaetes Nereis virens and Platynereis dumerilii (Annelida, Lophotrochozoa)
inferred← citeshttps://doi.org/10.1007/s13127-022-00553-zopenalex-snapshot
Loss of complexity from larval towards adult nervous systems in Chaetopteridae (Chaetopteriformia, Annelida) unveils evolutionary patterns in Annelida
inferred← citeshttps://doi.org/10.1016/j.mod.2009.06.653openalex-snapshot
15-P009 Heterochronic shifts explain variations in a sequentially developing repeated pattern: Palatal ridges of muroid rodents
inferred← citeshttps://doi.org/10.1016/j.ode.2005.11.002openalex-snapshot
A multigene framework for polychaete phylogenetic studies
inferred← citeshttps://doi.org/10.1017/s002531542510091xopenalex-snapshot
Impact of monsoon waves on the deposition of chitin tubes of polychaetes along the central-eastern Arabian Sea
inferred← citeshttps://doi.org/10.1038/s41586-022-05636-7openalex-snapshot
Annelid functional genomics reveal the origins of bilaterian life cycles
inferred← citeshttps://doi.org/10.1073/pnas.97.9.4487openalex-snapshot
Quantitative assessment of Hox complex expression in the indirect development of the polychaete annelid Chaetopterus sp.
inferred← citeshttps://doi.org/10.1080/0022293031000155395openalex-snapshot
Reproduction and morphology of Polydorella (Polychaeta: Spionidae), including the description of a new species from the Philippines
inferred← citeshttps://doi.org/10.1080/11035897.2012.752762openalex-snapshot
Ghosts from the past – ancestral features reflected in the jaw ontogeny of the polychaetous annelidsMarphysa fauchaldi(Eunicidae) andDiopatra aciculata(Onuphidae)
inferred← citeshttps://doi.org/10.1093/icb/41.3.640openalex-snapshot
Comparative Analysis of Hox Gene Expression in the PolychaeteChaetopterus: Implications for the Evolution of Body Plan Regionalization
inferred← citeshttps://doi.org/10.1093/icb/42.3.678openalex-snapshot
Unsegmented Annelids? Possible Origins of Four Lophotrochozoan Worm Taxa
inferred← citeshttps://doi.org/10.1101/2022.10.24.513551openalex-snapshot
Developmental staging and future research directions of the model marine tubeworm Hydroides elegans
inferred← citeshttps://doi.org/10.1111/ivb.12034openalex-snapshot
The importance of larval eyes in the polychaete Capitella teleta: effects of larval eye deletion on formation of the adult eye
inferred← citeshttps://doi.org/10.1111/j.0022-1112.2005.00914.xopenalex-snapshot
Early ontogenetic ecology of sofie Chondrostoma toxostoma: an integrated approach to organism‐environment relationships
inferred← citeshttps://doi.org/10.1111/j.1096-3642.2011.00800.xopenalex-snapshot
Branching out: a remarkable new branching syllid (Annelida) living in a Petrosia sponge (Porifera: Demospongiae)
inferred← citeshttps://doi.org/10.1111/j.1525-142x.2005.05061.xopenalex-snapshot
caudal and even‐skipped in the annelid Platynereis dumerilii and the ancestry of posterior growth
inferred← citeshttps://doi.org/10.1111/j.1525-142x.2009.00348.xopenalex-snapshot
Heterochronic shifts explain variations in a sequentially developing repeated pattern: palatal ridges of muroid rodents
inferred← citeshttps://doi.org/10.1111/j.1525-142x.2009.00386.xopenalex-snapshot
Integrative analysis of polychaete ontogeny: cell proliferation patterns and myogenesis in trochophore larvae of Sabellaria alveolata
inferred← citeshttps://doi.org/10.1111/j.1525-142x.2010.00457.xopenalex-snapshot
The segmental pattern of otx, gbx, and Hox genes in the annelid Platynereis dumerilii
inferred← citeshttps://doi.org/10.1111/j.1744-7410.2012.00257.xopenalex-snapshot
Morphological comparison of the regeneration process in S abella spallanzanii and B ranchiomma luctuosum ( A nnelida, S abellida)
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/10.1186/1742-9994-7-31openalex-snapshot
The normal development of Platynereis dumerilii (Nereididae, Annelida)
inferred← citeshttps://doi.org/10.1186/2041-9139-1-2openalex-snapshot
Expression of FoxA and GATA transcription factors correlates with regionalized gut development in two lophotrochozoan marine worms: Chaetopterus (Annelida) and Themiste lageniformis (Sipuncula)
inferred← citeshttps://doi.org/10.1186/2041-9139-4-14openalex-snapshot
Expression of Hox genes during regeneration of nereid polychaete Alitta (Nereis) virens (Annelida, Lophotrochozoa)
inferred← citeshttps://doi.org/10.1186/s12983-021-00426-9openalex-snapshot
Myogenesis of Siboglinum fiordicum sheds light on body regionalisation in beard worms (Siboglinidae, Annelida)
inferred← citeshttps://doi.org/10.1186/s13227-020-00161-yopenalex-snapshot
Activin/Nodal signaling mediates dorsal–ventral axis formation before third quartet formation in embryos of the annelid Chaetopterus pergamentaceus
inferred← citeshttps://doi.org/10.1387/ijdb.103151ahopenalex-snapshot
Mark Q. Martindale: shedding new light on developmental diversity
inferred← citeshttps://doi.org/10.1387/ijdb.140095mbopenalex-snapshot
Sipuncula: an emerging model of spiralian development and evolution
inferred← citeshttps://doi.org/10.1387/ijdb.140148gbopenalex-snapshot
Segment formation in Annelids: patterns, processes and evolution
inferred← citeshttps://doi.org/10.1387/ijdb.14756337openalex-snapshot
Time's arrow: heterochrony and the evolution of development
inferred← citeshttps://doi.org/10.15298/invertzool.22.4.05openalex-snapshot
Localization and distribution dynamics of total maternal RNA in oocytes and early embryos of Platynereis dumerilii (Annelida)
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/10.1668/0003-1569(2001)041[0640:caohge]2.0.co;2openalex-snapshot
Comparative Analysis of Hox Gene Expression in the PolychaeteChaetopterus: Implications for the Evolution of Body Plan Regionalization1
inferred← citeshttps://doi.org/10.2108/zsj.18.285openalex-snapshot
Segmentation in Annelids: Cellular and Molecular Basis for Metameric Body Plan
inferred← citeshttps://doi.org/10.2307/25066579openalex-snapshot
Description and Relationships ofChaetopterus pugaporcinus, an Unusual Pelagic Polychaete (Annelida, Chaetopteridae)
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/10.3390/jdb9030037openalex-snapshot
Maternal Transcripts of Hox Genes Are Found in Oocytes of Platynereis dumerilii (Annelida, Nereididae)
inferred← citeshttps://doi.org/10.53846/goediss-10255openalex-snapshot
The evolution of the head appendages in marine bristle worms
inferred← citeshttps://doi.org/10.64898/2026.02.04.703583openalex-snapshot
Annelid eye evolution revealed by developmental, ultrastructural, and connectome analyses of cerebral eyes in Malacoceros fuliginosus
showing the first 52 of 53 · page through all 53
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.