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Anterior regeneration in the polychaeteMarenzelleria viridis(Annelida: Spionidae)
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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/jmor.20316openalex-snapshot
Structure and anterior regeneration of musculature and nervous system inCirratuluscf.cirratus(Cirratulidae, Annelida)
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/10.1006/ecss.1997.0322openalex-snapshot
The Impact of Epifaunal Predation on the Structure of Macroinfaunal Invertebrate Communities of Tidal Saltmarsh Creeks
inferredcites →https://doi.org/10.1007/978-94-017-2887-4_4openalex-snapshot
Reproduction and larval development of the spioniform Polychaeta with application to systematics and phylogeny
inferredcites →https://doi.org/10.1007/bf00349119openalex-snapshot
Reproduction and larval development of Marenzelleria viridis (Polychaeta: Spionidae)
inferredcites →https://doi.org/10.1007/bf00419279openalex-snapshot
Die entwicklung der larvalsegmente bei den anneliden
inferredcites →https://doi.org/10.1007/bf02334787openalex-snapshot
Distribution and life cycle of the North American Spionid polychaeteMarenzelleria viridis (Verrill, 1873) in the Ems estuary
inferredcites →https://doi.org/10.1007/s00227-005-1595-8openalex-snapshot
The “piece-by-piece predation” of Eteone longa on Scolelepis squamata (Polychaetes )—traces on the sediment documenting chase, defence and mutilation
inferredcites →https://doi.org/10.1007/s00227-006-0274-8openalex-snapshot
Effects of simulated sublethal predation on the growth and regeneration rates of a spionid polychaete in laboratory flumes
inferredcites →https://doi.org/10.1007/s00227-006-0431-0openalex-snapshot
Anterior regeneration in the spionid polychaetes Dipolydora quadrilobata and Pygospio elegans
inferredcites →https://doi.org/10.1007/s002270050213openalex-snapshot
Prey selection by the hogchoker, Trinectes maculatus (Pisces: Soleidae), along summer salinity gradients in Chesapeake Bay, USA
inferredcites →https://doi.org/10.1007/s00427-015-0496-1openalex-snapshot
Vasa, PL10, and Piwi gene expression during caudal regeneration of the polychaete annelid Alitta virens
inferredcites →https://doi.org/10.1007/s00436-015-4734-2openalex-snapshot
First documentation and molecular confirmation of three trematode species (Platyhelminthes: Trematoda) infecting the polychaete Marenzelleria viridis (Annelida: Spionidae)
inferredcites →https://doi.org/10.1007/s10152-008-0142-7openalex-snapshot
Broad-scale patterns of abundance of non-indigenous soft-bottom invertebrates in Denmark
inferredcites →https://doi.org/10.1007/s10530-005-6186-6openalex-snapshot
Multiple Invasions – A Polychaete Genus Enters the Baltic Sea
inferredcites →https://doi.org/10.1016/0022-0981(85)90197-2openalex-snapshot
The effects of sublethal predation on reproduction in the spionid polychaete Polydora ligni Webster
inferredcites →https://doi.org/10.1016/0077-7579(79)90037-1openalex-snapshot
Annual food intake by plaice and flounder in a tidal flat area in the dutch wadden sea, with special reference to consumption of regenerating parts of macrobenthic prey
inferredcites →https://doi.org/10.1016/j.tree.2009.08.005openalex-snapshot
Evolution of animal regeneration: re-emergence of a field
inferredcites →https://doi.org/10.1016/s1385-1101(01)00088-0openalex-snapshot
Ecological consequence of the introduction of the polychaete Marenzelleria cf. viridis into a shallow-water biotope of the northern Baltic Sea
inferredcites →https://doi.org/10.1017/s0025315400055594openalex-snapshot
Regeneration in the polychæt Chætopterus variopedatus
inferredcites →https://doi.org/10.1017/s0025315403007227hopenalex-snapshot
Life history, morphology and distribution of Dipolydora armata (Polychaeta: Spionidae)
inferredcites →https://doi.org/10.1023/a:1003784324125openalex-snapshot
Reproduction and larval development of the spioniform Polychaeta with application to systematics and phylogeny
inferredcites →https://doi.org/10.1023/a:1009903521182openalex-snapshot
Population dynamics, growth and production of the neozoon Marenzelleria cf. viridis (Verrill, 1873) (Polychaeta: Spionidae) in a coastal water of the southern Baltic Sea
inferredcites →https://doi.org/10.1023/a:1009967807978openalex-snapshot
Bibliography on the genus Marenzelleria and its geographical distribution, principal topics and nomenclature
inferredcites →https://doi.org/10.1029/ar039p0205openalex-snapshot
Polychaetes of the family Spionidae from South America, Antarctica, and adjacent seas and islands
inferredcites →https://doi.org/10.1038/1711161a0openalex-snapshot
Asexual Reproduction in Pygospio elegans Claparède (Polychæta sedentaria)
inferredcites →https://doi.org/10.1046/j.1463-6395.2001.00078.xopenalex-snapshot
The morphology and ecology of Dipolydora armata (Polychaeta, Spionidae) from the western Mediterranean Sea
inferredcites →https://doi.org/10.1080/0022293031000155395openalex-snapshot
Reproduction and morphology of Polydorella (Polychaeta: Spionidae), including the description of a new species from the Philippines
inferredcites →https://doi.org/10.1080/00222933.2012.679323openalex-snapshot
Morphology and natural history of the cryptogenic sponge associate Polydora colonia Moore, 1907 (Polychaeta: Spionidae)
inferredcites →https://doi.org/10.1080/00288330.2003.9517204openalex-snapshot
Morphogenesis during sexual and asexual reproduction in Amphipolydora vestalis (Polychaeta: Spionidae)
inferredcites →https://doi.org/10.1080/00364820410002460openalex-snapshot
Revision of Marenzelleria Mesnil, 1896 (Spionidae, Polychaeta)
inferredcites →https://doi.org/10.1080/00785326.1973.10430115openalex-snapshot
Systematics and ecology of the Isefjord marine fauna (Denmark)
inferredcites →https://doi.org/10.1080/00785326.1996.10432467openalex-snapshot
Variation in the reproductive status, larval occurrence and recruitment in an estuarine population ofMarenzelleria viridis(Polychaeta: Spionidae)
inferredcites →https://doi.org/10.1080/07924259.2011.638404openalex-snapshot
Asexual reproduction and anterior regeneration under high and low temperatures in the sponge associate Polydora colonia (Polychaeta: Spionidae)
inferredcites →https://doi.org/10.1093/icb/icj051openalex-snapshot
Distribution of segment regeneration ability in the Annelida
inferredcites →https://doi.org/10.1093/icb/icq099openalex-snapshot
Frequency of Injury and the Ecology of Regeneration in Marine Benthic Invertebrates
inferredcites →https://doi.org/10.1093/icb/icq118openalex-snapshot
Evolutionary Loss of Animal Regeneration: Pattern and Process
inferredcites →https://doi.org/10.1093/icb/icu109openalex-snapshot
Early Events in Annelid Regeneration: A Cellular Perspective
inferredcites →https://doi.org/10.1093/molbev/msu080openalex-snapshot
Illuminating the Base of the Annelid Tree Using Transcriptomics
inferredcites →https://doi.org/10.1111/cla.12015openalex-snapshot
Phylogenomics of A nnelida revisited: a cladistic approach using genome‐wide expressed sequence tag data mining and examining the effects of missing data
inferredcites →https://doi.org/10.1111/j.1440-169x.2004.00763.xopenalex-snapshot
Nerve development, growth and differentiation during regeneration inEnchytraeus fragmentosusandStylaria lacustris(Oligochaeta)
inferredcites →https://doi.org/10.1111/j.1463-6395.2007.00275.xopenalex-snapshot
Reproductive Biology and Phylogeny of Annelida
inferredcites →https://doi.org/10.1111/j.1469-185x.2007.00020.xopenalex-snapshot
Leave it all behind: a taxonomic perspective of autotomy in invertebrates
inferredcites →https://doi.org/10.1111/j.1525-142x.2010.00458.xopenalex-snapshot
Evolution of a novel developmental trajectory: fission is distinct from regeneration in the annelid Pristina leidyi
inferredcites →https://doi.org/10.1111/j.1744-7410.2007.00114.xopenalex-snapshot
Morphology of anterior regeneration in two spionid polychaete species: implications for feeding efficiency
inferredcites →https://doi.org/10.1111/j.1744-7410.2010.00216.xopenalex-snapshot
Reproductive cycles of the sympatric excavating sponges Cliona celata and Cliona viridis in the Mediterranean Sea
inferredcites →https://doi.org/10.1111/j.1744-7410.2011.00234.xopenalex-snapshot
Palp growth, regeneration, and longevity of the obligate hermit crab symbiont Dipolydora commensalis (Annelida: Spionidae)
inferredcites →https://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)
inferredcites →https://doi.org/10.1111/maec.12361openalex-snapshot
The influence of hypo‐osmotic stress on the regenerative capacity of the invasive polychaete Marenzelleria viridis from its native range
inferredcites →https://doi.org/10.11646/zootaxa.1064.1.1openalex-snapshot
On adult and larval morphology of Polydora cornuta Bosc, 1802 (Annelida: Spionidae)
inferredcites →https://doi.org/10.11646/zootaxa.1353.1.1openalex-snapshot
Morphology and biology of Polydora species (Polychaeta: Spionidae) boring into oyster shells in South America, with the description of a new species
inferredcites →https://doi.org/10.11646/zootaxa.1459.1.1openalex-snapshot
New records and description of four new species of spionids (Annelida: Polychaeta: Spionidae) from the Philippines: the genera Dispio, Malacoceros, Polydora, and Scolelepis, with notes on palp ciliation patterns of the genus Scolelepis
inferredcites →https://doi.org/10.11646/zootaxa.3152.1.1openalex-snapshot
Spionidae (Annelida) from shallow waters around the British Islands: an identification guide for the NMBAQC Scheme with an overview of spionid morphology and biology
inferredcites →https://doi.org/10.11646/zootaxa.4019.1.22openalex-snapshot
Spionidae (Annelida) from Lizard Island, Great Barrier Reef, Australia: the genera Aonides, Dipolydora, Polydorella, Prionospio, Pseudopolydora, Rhynchospio, and Tripolydora
inferredcites →https://doi.org/10.1186/2041-9139-4-1openalex-snapshot
Comparative gene expression supports the origin of the incisor and molar process from a single endite in the mandible of the red flour beetle Tribolium castaneum
inferredcites →https://doi.org/10.1186/2041-9139-4-13openalex-snapshot
Hox gene expression during postlarval development of the polychaete Alitta virens
inferredcites →https://doi.org/10.1186/2041-9139-4-14openalex-snapshot
Expression of Hox genes during regeneration of nereid polychaete Alitta (Nereis) virens (Annelida, Lophotrochozoa)
inferredcites →https://doi.org/10.1201/9781482280159openalex-snapshot
Reproductive Biology and Phylogeny of Annelida
inferredcites →https://doi.org/10.1242/dev.128.14.2781openalex-snapshot
Evolution of regeneration and fission in annelids: insights fromengrailed- andorthodenticle-class gene expression
inferredcites →https://doi.org/10.2307/1351559openalex-snapshot
Nocturnal Swimming of Scolecolepides viridis (Polychaeta: Spionidae)
inferredcites →https://doi.org/10.2307/1352000openalex-snapshot
Sediment Transport, Biotic Modifications and Selection of Grain Size in a Surface Deposit-Feeder
inferredcites →https://doi.org/10.2307/1542705openalex-snapshot
Morphogenesis during asexual reproduction in Pygospio elegans Claparede (Annelida, Polychaeta)
inferredcites →https://doi.org/10.2307/1543524openalex-snapshot
Asexual Reproduction in Pygospio elegans Claparède (Annelida, Polychaeta) in Relation to Parasitism by Lepocreadium setiferoides (Miller and Northup) (Platyhelminthes, Trematoda)
inferredcites →https://doi.org/10.3354/meps09821openalex-snapshot
Macrobenthic community response to the Marenzelleria viridis (Polychaeta) invasion of a Danish estuary
inferredcites →https://doi.org/10.5281/zenodo.209619openalex-snapshot
Spionidae (Annelida) from shallow waters around the British Islands: an identification guide for the NMBAQC Scheme with an overview of spionid morphology and biology
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.5081.3.3zenodo-depositor-declared
A review of the worldwide distribution of Marenzelleria viridis, with new records for M. viridis, M. neglecta and Marenzelleria sp. (Annelida: Spionidae)
inferred← citeshttps://doi.org/10.1017/s0025315421000163openalex-snapshot
A new record of a cryptogenic Dipolydora species (Annelida: Spionidae) in South Africa
inferred← citeshttps://doi.org/10.1111/ivb.12412openalex-snapshot
Development and sexual dimorphism of branchiae in Streblospio benedicti
inferred← citeshttps://doi.org/10.1134/s2075111721040068openalex-snapshot
About Regeneration of Alien Polychaete Polydora websteri (Annelida: Spionidae)
inferred← citeshttps://doi.org/10.3390/biology12111412openalex-snapshot
Mass Start or Time Trial? Structure of the Nervous System and Neuroregeneration in Pygospio elegans (Spionidae, Annelida)
inferred← citeshttps://doi.org/10.35885/1996-1499-2021-14-3-24-31openalex-snapshot
ABOUT REGENERATION OF ALIEN POLYCHAETE POLYDORA WEBSTERI (ANNELIDA: SPIONIDAE)
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