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Age structure and spawning of a Northumberland population of Melinna cristata (Polychaeta: Ampharetidae)

https://doi.org/10.1007/bf00367988
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What this work says

Outgoing claims: the papers this work cites, builds on, or argues with.

inferredcites →https://doi.org/10.1007/bf00346914openalex-snapshot
Reproduction of a Northumberland population of the polychaete Cirratulus cirratus
inferredcites →https://doi.org/10.1007/bf00355223openalex-snapshot
Ovary structure and oogenesis in Cirratulus cirratus (Polychaeta: Cirratulidae)
inferredcites →https://doi.org/10.1007/bf00367986openalex-snapshot
Gametogenesis in a Northumberland population of the polychaete Melinna cristata
inferredcites →https://doi.org/10.1007/bf01613354openalex-snapshot
Untersuchungen am pazifischen PalolowurmEunice viridis (Polychaeta) in Samoa
inferredcites →https://doi.org/10.1016/0016-6480(65)90067-5openalex-snapshot
Evidence for a feedback mechanism influencing spermatogonial division in the lugworm (Arenicola marina L.)
inferredcites →https://doi.org/10.1016/0016-6480(73)90125-1openalex-snapshot
The regulation of ovary function in Cirratulus cirratus (Polychaeta)
inferredcites →https://doi.org/10.1016/0022-0981(68)90004-xopenalex-snapshot
Egg numbers, metabolic efficiency of egg production and fecundity; Local and regional variations in a number of common cirripedes
inferredcites →https://doi.org/10.1016/0025-326x(81)90086-2openalex-snapshot
Advances in marine biology Vol. 18
inferredcites →https://doi.org/10.1017/s0025315400001582openalex-snapshot
The Spawning of Arenicola Marina (L.) II. Spawning Under Experimental Conditions
inferredcites →https://doi.org/10.1017/s0025315400006172openalex-snapshot
The spawning of Arenicola marina (L). I. The breeding season
inferredcites →https://doi.org/10.1017/s0025315400011450openalex-snapshot
The Growth Of Balanus Balanoides (L.) and B. Crenatus Brug. Under Varying Conditions Of Submersion
inferredcites →https://doi.org/10.1017/s0025315400012613openalex-snapshot
Notes on the reproduction and early development of the cirratulid Tharyx marioni (St Joseph)
inferredcites →https://doi.org/10.1017/s0025315400016295openalex-snapshot
The spawning ofArenicola marina(L.) III. Maturation and shedding of the Ova
inferredcites →https://doi.org/10.1017/s0025315400035232openalex-snapshot
Gametogenesis and Breeding in a Natural Population of Nereis Virens
inferredcites →https://doi.org/10.1029/ar005p0039openalex-snapshot
Reproductive periodicities in several contrasting populations ofOdontaster ValidusKoehler, A common Antarctic asteroid
inferredcites →https://doi.org/10.1146/annurev.ph.21.030159.002555openalex-snapshot
Comparative Physiology: Annual Reproductive Cycles of Marine Invertebrates
inferredcites →https://doi.org/10.1515/znb-1955-1109openalex-snapshot
Photoperiodizität als Ursache des von der Mondphase abhängigen Metamorphose-Rhythmus bei dem Polychaeten Platynereis Dumerilii
inferredcites →https://doi.org/10.2307/1538379openalex-snapshot
AN ANNUAL HISTORY OF A POPULATION OF NEREIS DIVERSICOLOR O. F. MULLER
inferredcites →https://doi.org/10.2307/1538381openalex-snapshot
EXISTENCE OF PHYSIOLOGICALLY-DIFFERENT RACES OF OYSTERS, CRASSOSTREA VIRGINICA
inferredcites →https://doi.org/10.2307/1539324openalex-snapshot
GAMETOGENESIS AND SPAWNING OF THE EUROPEAN OYSTER, O. EDULIS, IN WATERS OF MAINE
inferredcites →https://doi.org/10.2307/1539954openalex-snapshot
REPRODUCTION AND EARLY DEVELOPMENT OF THE SPIONID POLYCHAETE, SCOLECOLEPIDES VIRIDIS (VERRILL)
inferredcites →https://doi.org/10.2307/1540291openalex-snapshot
REPRODUCTIVE PHYSIOLOGICAL VARIATION IN LATITUDINALLY SEPARATED POPULATIONS OF THE BAY SCALLOP,AEQUIPECTEN IRRADIANSLAMARCK
inferredcites →https://doi.org/10.2307/3564971openalex-snapshot
The Bottom Fauna Communities and Their Sediment Relationships off the Coast of Northumberland
inferredcites →https://doi.org/10.5281/zenodo.16152091openalex-snapshot
On the Life History of Nereis grubei (Kinberg), a Polychaete Annelid from California
inferredcites →https://doi.org/10.5281/zenodo.16199287openalex-snapshot
Studien über den Körperbau der Anneliden
inferredcites →https://doi.org/10.5281/zenodo.16432083openalex-snapshot
A review of the family Ampharetidae (Polychaeta)
inferredcites →https://doi.org/10.5962/bhl.title.7234openalex-snapshot
The American Arbacia and other sea urchins

What points at this work

Incoming claims: where this work appears in other papers’ reference lists and arguments.

inferred← citeshttps://doi.org/10.3853/j.2201-4349.75.2023.1803zenodo-depositor-declared
New species of Melinna (Melinnidae, Annelida) from the Australian abyss with comments on M. albicincta, M. cristata and M. elisabethae
inferred← citeshttps://doi.org/10.1007/978-1-4899-4995-0_17openalex-snapshot
Growth Lines in Polychaete Jaws (Teeth)
inferred← citeshttps://doi.org/10.1007/bf00388934openalex-snapshot
A population study of the polychaete Capitella capitata at plymouth
inferred← citeshttps://doi.org/10.1007/bf00391119openalex-snapshot
Ultrastructure of oogenesis in the holopelagic polychaetes Rhynchonerella angelini and Alciopa reynaudii (Polychaeta: Alciopidae)
inferred← citeshttps://doi.org/10.1007/bf00391202openalex-snapshot
Population dynamics and secondary production in Melinna palmata (Polychaeta: Ampharetidae)
inferred← citeshttps://doi.org/10.1007/bf00396284openalex-snapshot
Dynamics and biological cycle of a Melinna palmata (Ampharetidae) population during the recolonisation of a dredged area in the vicinity of the harbour of Brest (France)
inferred← citeshttps://doi.org/10.1007/bf00406827openalex-snapshot
Reproductive success, relative abundance and population structure of two species of Nephtys in an estuarine beach
inferred← citeshttps://doi.org/10.1007/bf00508259openalex-snapshot
Population dynamics and secondary production in an estuarine population of Nephtys hombergii (Polychaeta: Nephtyidae)
inferred← citeshttps://doi.org/10.1007/bf01313511openalex-snapshot
Demography and reproductive biology ofMelinna palmata (Ampharetidae: Polychaeta) in Inner Galway Bay on the west coast of Ireland
inferred← citeshttps://doi.org/10.1016/0022-0981(90)90134-xopenalex-snapshot
Reproductive biology of the polychaete Owenia fusiformis Delle Chiaje in the Bay of Seine (eastern English Channel)
inferred← citeshttps://doi.org/10.1016/0272-7714(86)90051-xopenalex-snapshot
Temporal heterogeneity in deep-water soft-sediment benthos—an attempt to reveal temporal structure
inferred← citeshttps://doi.org/10.1016/b978-0-12-282503-3.50007-9openalex-snapshot
ANNELIDA: POLYCHAETA
inferred← citeshttps://doi.org/10.1016/j.dsr2.2016.08.017openalex-snapshot
Paramytha ossicola sp. nov. (Polychaeta, Ampharetidae) from mammal bones: Reproductive biology and population structure
inferred← citeshttps://doi.org/10.1016/s0924-7963(96)00053-xopenalex-snapshot
Does a pulsed food supply to the benthos affect polychaete recruitment patterns in the Northeast Water Polynya?
inferred← citeshttps://doi.org/10.1017/s0025315400015964openalex-snapshot
Reproductive biology ofEulalia viridis(Müller) (Polychaeta: Phyllodocidae) in the north eastern U.K.
inferred← citeshttps://doi.org/10.1111/j.1744-7410.2002.tb00133.xopenalex-snapshot
Do life history traits account for diversity of polychaete annelids?
inferred← citeshttps://doi.org/10.1575/1912/5263openalex-snapshot
Development and planktonic larvae of common benthic invertebrates of the Woods Hole, Massachusetts region: summary of existing data and bibliographic sources
inferred← citeshttps://doi.org/10.21608/ejabf.2006.1876openalex-snapshot
SPERM MORPHOLOGY AND SPERMATOGENESIS IN THE TUBE-WORM POMATOLEIOS KRASSII (POLYCHAETA: SPIROBRANCHINAE) FROM THE SUEZ BAY, EGYPT.
inferred← citeshttps://doi.org/10.2331/fishsci.65.48openalex-snapshot
Use of Annual Density Banding to Estimate Longevity of Infauna of Massive Corals
inferred← citeshttps://doi.org/10.3390/d13020060openalex-snapshot
The Terebelliformia-Recent Developments and Future Directions
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