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Journal articles on the topic 'Marenzelleria'

Author: Grafiati

Published: 4 June 2025

Last updated: 23 June 2025

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1

Radashevsky, Vasily I., Victoria V. Pankova, Vasily V. Malyar, José Cerca, and Torsten H. Struck. "A review of the worldwide distribution of Marenzelleria viridis, with new records for M. viridis, M. neglecta and Marenzelleria sp. (Annelida: Spionidae)." Zootaxa 5081, no. 3 (2021): 353–72. https://doi.org/10.11646/zootaxa.5081.3.3.

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Radashevsky, Vasily I., Pankova, Victoria V., Malyar, Vasily V., Cerca, José, Struck, Torsten H. (2021): A review of the worldwide distribution of Marenzelleria viridis, with new records for M. viridis, M. neglecta and Marenzelleria sp. (Annelida: Spionidae). Zootaxa 5081 (3): 353-372, DOI: 10.11646/zootaxa.5081.3.3

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2

Golubkov, Sergey M., and Mikhail S. Golubkov. "Dynamics of Marenzelleria spp. Biomass and Environmental Variability: A Case Study in the Neva Estuary (The Easternmost Baltic Sea)." Biology 13, no. 12 (2024): 974. http://dx.doi.org/10.3390/biology13120974.

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Predicting which non-indigenous species (NISs) will establish persistent invasive populations and cause significant ecosystem changes remains an important environmental challenge. We analyzed the spatial and temporal dynamics of the entire zoobenthos and the biomass of Marenzelleria spp., one of the most successful invaders in the Baltic Sea, in the Neva estuary in 2014–2023. A considerable decrease in Marenzelleria biomass was observed in the second half of the study period, which was accompanied by a sharp increase in the dominance of opportunistic oligochaete and chironomid species. Our one-way analysis of variance showed that communities with high Marenzelleria biomass had significantly higher diversity and biomass of native benthic crustaceans compared to communities with low alien polychaetes biomass. A high biomass of Marenzelleria was observed in biotopes characterized by low temperatures, high salinity, low plankton primary production and chlorophyll concentration. The results of PCA and one-way ANOVA indicated that these factors significantly influenced the spatial and temporal dynamics of the polychaete biomass. More detailed studies of the responses of NISs to environmental variables are needed to better understand and anticipate their dynamics in different regions of the Baltic Sea in relation to climate warming and anthropogenic impacts.

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3

RADASHEVSKY, VASILY I., VICTORIA V. PANKOVA, VASILY V. MALYAR, JOSÉ CERCA, and TORSTEN H. STRUCK. "A review of the worldwide distribution of Marenzelleria viridis, with new records for M. viridis, M. neglecta and Marenzelleria sp. (Annelida: Spionidae)." Zootaxa 5081, no. 3 (2021): 353–72. http://dx.doi.org/10.11646/zootaxa.5081.3.3.

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Marenzelleria Mesnil, 1896 is a small group of spionid polychaetes comprising five valid species, all of which appear similar to each other. The identification of worms based on morphological features is often confusing, and thus molecular data have been suggested as providing crucial additional diagnostic characters. Here we summarize and map available records of M. viridis (Verrill, 1873) worldwide, and, based on the analysis of fragment sequences of COI, 16S, 18S, 28S and Histone 3, report this species for the first time from Norway. We also summarize and map the records of Marenzelleria from North America, distinguishing those based on morphology and molecular data. We report new records for Marenzelleria sp. from Baffin Is., Nunavut, Canada, and for M. neglecta Sikorski & Bick, 2004 from Washington, USA.

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4

Atkins, S. M., A. M. Jones, and P. R. Garwood. "The ecology and reproductive cycle of a population of Marenzelleria viridis (Annelida: Polychaeta: Spionidae) in the Tay Estuary." Proceedings of the Royal Society of Edinburgh. Section B. Biological Sciences 92, no. 3-4 (1987): 311–22. http://dx.doi.org/10.1017/s0269727000004735.

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SynopsisThe occurrence of a population of the spionid polychaete Marenzelleria viridis (Verrill 1873) in the middle reaches of the Tay Estuary is reported. This is a new British and European record of a North American species, and its principal characteristics are described and compared with earlier accounts. Size frequency analysis of the population showed it to be dominated by large animals from July 1984 to May 1986. The population matured coelomic gametes during winter 1985–86 and spawned in March 1986 to produce a heavy settlement in May, which subsequently grew rapidly. The distribution of M. viridis in relation to other species, sediment and other ecological parameters is described from a single survey of the Invergowrie Bay mudflats. Marenzelleria population densities of up to 1500 m 2 were negatively correlated with all other species of a low diversity macrofaunal community dominated by predatory polychaetes and filter feeding bivalves. Marenzelleria was abundant down to sediment depths of 20–30 cm. The significance and origin of this population is discussed.

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5

Sarda, Rafael, Ivan Valiela, and Ken Foreman. "Life cycle, demography, and production of Marenzelleria viridis in a salt marsh of southern New England." Journal of the Marine Biological Association of the United Kingdom 75, no. 3 (1995): 725–38. http://dx.doi.org/10.1017/s0025315400039138.

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Population dynamics and production of the spionid polychaete Marenzelleria viridis were studied at Great Sippewissett salt marsh (Massachusetts, USA) for two years. Marenzelleria viridis was the main contributor in biomass and production to the macroinfaunal assemblages of the sandy organic sediments of the marsh. Marenzelleria viridis spawned during the cold part of the year and the appearance of settled larvae on sediments was observed from January to May. The density of M. viridis rose sharply from winter to late spring followed by a striking drop through summer. The estimated mean annual production of M. viridis was 60.0 g dry weight m2 during the first year and 26.3 g dry weight m2 during the second year. The population of M. viridis is affected by different processes during the year. The number of initial recruits seems to be largely governed by meteorological conditions. The numbers of recruits are then affected by competition for resources, and later, as predators become active, predation pressure determines the abundance of the population of M. viridis.

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6

Golubkov, Sergey, Alexei Tiunov, and Mikhail Golubkov. "Food-web modification in the eastern Gulf of Finland after invasion of Marenzelleria arctia (Spionidae, Polychaeta)." NeoBiota 66 (July 9, 2021): 75–94. http://dx.doi.org/10.3897/neobiota.66.63847.

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The paucity of data on non-indigenous marine species is a particular challenge for understanding the ecology of invasions and prioritising conservation and research efforts in marine ecosystems. Marenzelleria spp. are amongst the most successful non-native benthic species in the Baltic Sea during recent decades. We used stable isotope analysis (SIA) to test the hypothesis that the dominance of polychaete worm Marenzelleria arctia in the zoobenthos of the Neva Estuary after its invasion in the late 2000s is related to the position of this species in the benthic food webs. The trend towards a gradual decrease in the biomass of Marenzelleria worms was observed during 2014–2020, probably due to significant negative relationships between the biomass of oligochaetes and polychaetes, both of which, according to SIA, primarily use allochthonous organic carbon for their production. The biomass of benthic crustaceans practically did not change and remained very low. The SIA showed that, in contrast to the native crustacean Monoporeia affinis, polychates are practically not consumed either by the main invertebrate predator Saduria entomon, which preys on M. affinis, oligochaetes and larvae of chironomids or by benthivorous fish that prefer native benthic crustaceans. A hypothetical model for the position and functional role of M. arctia in the bottom food web is presented and discussed. According the model, the invasion of M. arctia has created an offshoot food chain in the Estuary food webs. The former dominant food webs, associated with native crustaceans, are now poorly developed. The lack of top-down control obviously contributes to the significant development of the Marenzelleria food chain, which, unlike native food chains, does not provide energy transfer from autochthonous and allochthonous organic matter to the upper trophic levels. The study showed that an alien species, without displacing native species, can significantly change the structure of food webs, creating blind offshoots of the food chain.

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7

Golubkov, Sergey, Alexei Tiunov, and Mikhail Golubkov. "Food-web modification in the eastern Gulf of Finland after invasion of Marenzelleria arctia (Spionidae, Polychaeta)." NeoBiota 66 (July 9, 2021): 75–94. https://doi.org/10.3897/neobiota.66.63847.

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The paucity of data on non-indigenous marine species is a particular challenge for understanding the ecology of invasions and prioritising conservation and research efforts in marine ecosystems. Marenzelleria spp. are amongst the most successful non-native benthic species in the Baltic Sea during recent decades. We used stable isotope analysis (SIA) to test the hypothesis that the dominance of polychaete worm Marenzelleria arctia in the zoobenthos of the Neva Estuary after its invasion in the late 2000s is related to the position of this species in the benthic food webs. The trend towards a gradual decrease in the biomass of Marenzelleria worms was observed during 2014–2020, probably due to significant negative relationships between the biomass of oligochaetes and polychaetes, both of which, according to SIA, primarily use allochthonous organic carbon for their production. The biomass of benthic crustaceans practically did not change and remained very low. The SIA showed that, in contrast to the native crustacean Monoporeia affinis, polychates are practically not consumed either by the main invertebrate predator Saduria entomon, which preys on M. affinis, oligochaetes and larvae of chironomids or by benthivorous fish that prefer native benthic crustaceans. A hypothetical model for the position and functional role of M. arctia in the bottom food web is presented and discussed. According the model, the invasion of M. arctia has created an offshoot food chain in the Estuary food webs. The former dominant food webs, associated with native crustaceans, are now poorly developed. The lack of top-down control obviously contributes to the significant development of the Marenzelleria food chain, which, unlike native food chains, does not provide energy transfer from autochthonous and allochthonous organic matter to the upper trophic levels. The study showed that an alien species, without displacing native species, can significantly change the structure of food webs, creating blind offshoots of the food chain.

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8

Sikorski, A. V., and A. Bick. "Revision of Marenzelleria Mesnil, 1896 (Spionidae, Polychaeta)." Sarsia 89, no. 4 (2004): 253–75. http://dx.doi.org/10.1080/00364820410002460.

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9

O’Reilly, M., and S. Nowacki. "First record of the non-native green palpworm Marenzelleria viridis (Annelida: Spionidae) in the Clyde Estuary." Glasgow Naturalist 27, no. 1 (2019): 45–48. http://dx.doi.org/10.37208/tgn27107.

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The non-native polychaete worm Marenzelleria viridis (Verrill, 1873) was found for the first time in the upper Clyde Estuary in 2016. This represents the first occurrence of this alien species on the west coast of Scotland. It appearsto be well established in low salinity waters at Govan Wharf where it dominated the biomass of riverbed infaunal invertebrates with densities of around 1,300 worms m-2.

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10

Bochert, R., and A. Bick. "Reproduction and larval development of Marenzelleria viridis (Polychaeta: Spionidae)." Marine Biology 123, no. 4 (1995): 763–73. http://dx.doi.org/10.1007/bf00349119.

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11

Teacă, Adrian, Tatiana Begun, Selma Menabit, and Mihaela Mureșan. "The First Record of Marenzelleria neglecta and the Spread of Laonome xeprovala in the Danube Delta–Black Sea Ecosystem." Diversity 14, no. 6 (2022): 423. http://dx.doi.org/10.3390/d14060423.

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Biological invasions can have major impacts on freshwater and marine ecosystems. Therefore, it is vital that non-indigenous species are accurately identified and reported when potential or confirmed invasions occur. The present study reports the first occurrence of Marenzelleria neglecta (Annelida, Spionidae) and the spread of Laonome xeprovala (Annelida, Sabellidae) in the Danube Delta–Black Sea ecosystem. Spionidae is one of the most diverse families of annelid worms and is a dominant group in terms of the number of species that have been introduced to non-native areas, while the members of Sabellidae are among the most visible polychaetes commonly found in fouling communities and are colonizing new geographic areas. Based on 20 samples collected in 2021, we provide an overview of the distribution of the investigated species and possible arrival pathways for Marenzelleria neglecta. Specimens were identified based on morphological descriptions. Both species have invasive behaviour, colonizing large areas in relatively short time periods and reaching relatively high densities (M. neglecta—1400 ind.m−2; L. xeprovala—40 ind.m−2). Due to their distribution and high abundances, the biology and ecology of these species in the Danube River–Danube Delta–Black Sea system need to be investigated further in order to assess their impact on ecosystem structure and functioning.

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12

Mikhailova, A. V., E. V. Popova, S. V. Shipulin, A. A. Maximov, I. S. Plotnikov, and N. V. Aladin. "ON THE INVASION OF THE GENUS MARENZELLERIA (POLYCHAETA, SPIONIDAE) REPRESENTATIVES INTO THE CASPIAN SEA BASIN." Russian Journal of Biological Invasions 14, no. 3 (2021): 45–49. http://dx.doi.org/10.35885/1996-1499-2021-14-3-45-49.

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In 2018, in the bottom fauna of the Caspian Sea, single specimens of a previously unknown species of polyhaetes were discovered. Since 2019, pelagic larvae of this species have been recorded in zooplankton samples. These worms are also found in the nutrition of migratory and semi-migratory fish species. According to morphological features, this polychaete species is identified as Marenzelleria arctia , an Arctic species dominating in the Gulf of Finland and probably invaded the Caspian along the Volga-Caspian invasion corridor.

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13

Radashevsky, Vasily, Victoria Pankova, Tatyana Neretina, and Alexander Tzetlin. "Canals and invasions: a review of the distribution of Marenzelleria (Annelida: Spionidae) in Eurasia, with a key to Marenzelleria species and insights on their relationships." Aquatic Invasions 17, no. 2 (2022): 186–206. http://dx.doi.org/10.3391/ai.2022.17.2.04.

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14

Bick, Andreas. "A new Spionidae (Polychaeta) from North Carolina, and a redescription of Marenzelleria wireni Augener, 1913, from Spitsbergen, with a key for all species of Marenzelleria." Helgoland Marine Research 59, no. 4 (2005): 265–72. http://dx.doi.org/10.1007/s10152-005-0002-7.

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15

Syomin, Vitaly, Andrey Sikorski, Ralf Bastrop, et al. "The invasion of the genus Marenzelleria (Polychaeta: Spionidae) into the Don River mouth and the Taganrog Bay: morphological and genetic study." Journal of the Marine Biological Association of the United Kingdom 97, no. 5 (2017): 975–84. http://dx.doi.org/10.1017/s0025315417001114.

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Alien polychaetes belonging to the genus Marenzelleria were recorded from the mouth of the Don River and Taganrog Bay in the Sea of Azov in February–March 2014. Morphological characteristics varied greatly and matched those of two species: M. neglecta and M. arctia. Some individuals did not match the descriptions of both species. A genetic study using different sequences (primarily COI, but also 16S, 28S, cytb and nuclear histone 3a) showed that only M. neglecta was present despite some morphological mismatches. A morphological description of the species according to the new data is presented, together with a revised table of variability of the key numeric characters. Since 2014, Marenzelleria has spread swiftly and become dominant in a considerable part of the Taganrog Bay, making up to 91% of the total abundance/biomass (6800 ind. m−2 and 31.2 g m−2, respectively). Monodominant sites were also present. Its occurrence is 100% in recent surveys. Such a sharp increase seems to be due to a lack of detritophages in the bay; this is supported by the fact that M. neglecta has not formed its specific assemblage. The community structure, if M. neglecta is excluded, is equal to that before the invasion. In the Sea of Azov itself, M. neglecta is not as abundant, but occurs up to the Strait of Kertch and at some sites in the Black Sea. Its spread further into the Black Sea seems possible, as well as into the Caspian Sea via the Volga-Don Canal.

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16

Bastrop, R., M. R�hner, and K. J�rss. "Are there two species of the polychaete genus Marenzelleria in Europe?" Marine Biology 121, no. 3 (1995): 509–16. http://dx.doi.org/10.1007/bf00349460.

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17

Quintana, Cintia Organo, Tanja Hansen, Matthieu Delefosse, Gary Banta, and Erik Kristensen. "Burrow ventilation and associated porewater irrigation by the polychaete Marenzelleria viridis." Journal of Experimental Marine Biology and Ecology 397, no. 2 (2011): 179–87. http://dx.doi.org/10.1016/j.jembe.2010.12.006.

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18

Selifonova, Zh P. "Current status of holo- and meroplankton of the Sea of Azov during the formation of the ice cover." Marine Biological Journal 4, no. 2 (2019): 63–70. http://dx.doi.org/10.21072/mbj.2019.04.2.07.

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The Sea of Azov is an inland freezing marine water basin. Winter season is considered to be one of the most important seasons for understanding patterns of functioning and formation of productivity of the ecosystem of the Sea of Azov. However, holo- and meroplankton during the formation of ice cover in the sea have not been studied enough. In recent years, several alien species, including Arctic species of polychaete worms, which in their development have the stage of pelagic larvae, have naturalized in the Sea of Azov. The aim of the work is to study the taxonomic composition and numerical abundance of winter holo- and meroplankton of the Sea of Azov in December 2018. Zooplankton sampling was conducted in the bays of the Sea of Azov, viz., Taganrog and Temryuk during the formation of seasonal ice cover. Zooplankton samples were collected from December 3 to 14 at temperatures from 0 to +3 °C at 14 stations, 9 of which were performed in the Taganrog Bay (the port area of Yeisk) in three replications, and 5 of which – in the Temryuk Bay (each sample – in one replication). Zooplankton was sampled throughout the water column at depths of 4–8 meter using a big-sized Juday net with an opening diameter of 37 cm (mesh size was 120 μm) by total catch. The material was fixed by 2–4 % neutral formaldehyde and treated in the laboratory by the conventional procedure. Calculations of biomass were made using the tables of the average mass of organisms. The results showed that under similar temperature conditions the density of holo- and meroplankton organisms in the Taganrog Bay was four times higher than in the Temryuk Bay. Winter subglacial zooplankton was represented by two groups of organisms – native eurythermic forms of holoplankton and polychaetes larvae. As before, calanoid copepod composition was dominated by euryhaline Ponto-Caspian species Eurytemora affinis (Poppe, 1880). However, the species composition of the winter meroplankton of the Sea of Azov changed significantly in comparison with that of the period up to 2014. Unusual high density (118–119.9 thousand ind.·m−3) of polychaete larvae of Marenzelleria genus, the recent invader in the Sea of Azov, was registered in the Taganrog Bay at a low water temperature of 0…+1.2 °C. The peak of zooplankton numerical density (128.9–136.7 thousand ind.·m−3) was observed in winter season for the first time. Winter subglacial maximum of abundance of the polychaetes larvae of Marenzelleria sp. was 4–6 times higher than the abundance of meroplankton, previously noted in June, the most productive month of the year. Naturalization of polychaete worms Marenzelleria sp. can lead to a radical restructuring of the Sea of Azov ecosystem and to an increase of its productivity. Further studies of the phenology of these polychaetes larval stages in this basin are needed.

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19

Bonaglia, S., M. Bartoli, JS Gunnarsson, et al. "Effect of reoxygenation and Marenzelleria spp. bioturbation on Baltic Sea sediment metabolism." Marine Ecology Progress Series 482 (May 22, 2013): 43–55. http://dx.doi.org/10.3354/meps10232.

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20

Kocheshkova, O. V., and E. E. Ezhova. "Polychaetes of Marenzelleria Genus (Spionidae) in the Southeastern Baltic Sea (Russian EEZ)." Russian Journal of Biological Invasions 9, no. 3 (2018): 219–27. http://dx.doi.org/10.1134/s2075111718030050.

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21

Kotta, J., and I. Kotta. "DISTRIBUTION AND INVASION ECOLOGY OF Marenzelleria viridis IN THE ESTONIAN COASTAL WATERS." Proceedings of the Estonian Academy of Sciences. Biology. Ecology 47, no. 3 (1998): 212. http://dx.doi.org/10.3176/biol.ecol.1998.3.04.

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22

Schneider, Anke. "Metabolic rate of the brackish water polychaete Marenzelleria viridis under reducing conditions." Thermochimica Acta 271 (January 1996): 31–40. http://dx.doi.org/10.1016/0040-6031(95)02592-8.

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23

Delefosse, M., GT Banta, P. Canal-Vergés, et al. "Macrobenthic community response to the Marenzelleria viridis (Polychaeta) invasion of a Danish estuary." Marine Ecology Progress Series 461 (August 8, 2012): 83–94. http://dx.doi.org/10.3354/meps09821.

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24

Lagzdins, G., and P. Pallo. "MARENZELLERIA VIRIDIS (VERRILL) (POLYCHAETA – SPIONIDAE) – A NEW SPECIES FOR THE GULF OF RIGA." Proceedings of the Estonian Academy of Sciences. Biology 43, no. 3 (1994): 184. http://dx.doi.org/10.3176/biol.1994.3.07.

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25

Hietanen, Susanna, Ari O. Laine, and Kaarina Lukkari. "The complex effects of the invasive polychaetes Marenzelleria spp. on benthic nutrient dynamics." Journal of Experimental Marine Biology and Ecology 352, no. 1 (2007): 89–102. http://dx.doi.org/10.1016/j.jembe.2007.07.018.

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26

GLASBY, CHRISTOPHER J., TARMO TIMM, ALEXANDER I. MUIR, and JOÃO GIL. "Catalogue of non-marine Polychaeta (Annelida) of the World." Zootaxa 2070, no. 1 (2009): 1–52. http://dx.doi.org/10.11646/zootaxa.2070.1.1.

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An annotated checklist and bibliography of 197 species (representing 78 genera and 26 families) of non-marine polychaetes of the world is presented, including synonymies, information on ecology, distribution, habitat, and references to the taxonomic and biological literature. Over half (57%) of the checklist species are represented by just three families as follows: Nereididae (61 species including Namanereis, Namalycastis, Neanthes and Hediste), Aeolosomatidae (27 species, mostly Aeolosoma) and Sabellidae (24 species including Caobangia and Manayunkia). Other well-represented taxa are the epizoic histriobdellid Stratiodrilus (11 species), the inland-sea-specialist ampharetid Hypania and related genera (5 species), and the freshwater-tolerant spionid Marenzelleria (5 species). One new combination is proposed for the nereidid Nereis tenuipalpa Pflugfelder, 1933, viz. Paraleonnates tenuipalpa n. comb.

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27

Naumenko, Elena Nikolaevna, Tat'yana Alekseevna Golubkova, Andrey Alexandrovich Gusev, and Liliya Vladimirovna Rudinskaya. "Biological invasions into planktonic and bottom communities of the Kaliningrad (Vistula) Lagoon of the Baltic Sea and their impact on the food supply and fish catches." Vestnik of Astrakhan State Technical University. Series: Fishing industry 2024, no. 3 (2024): 15–25. http://dx.doi.org/10.24143/2073-5529-2024-3-15-25.

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Uncontrolled dispersal of species in aquatic ecosystems has become one of the most important environmental problems. The main reason for the acceleration of this process is human economic activity. Aquatic ecosystems are particularly susceptible to attacks by alien species, and the main vector is the discharge of ballast water. Despite the fact that most alien species do not take root, there are species that successfully naturalize in recipient reservoirs. The impact of alien species on aboriginal communities is usually characterized by ambivalence. The Kaliningrad (Vistula) Lagoon, which has 5 ports in its water area, has also been attacked by alien species. The most powerful invasions occurred in 1988 (polychaetes of the genus Marenzelleria), in 1999 (predatory branchial crustaceans Cercopagis pengoi) and in 2010 (bivalves Rangia cuneata).These alien species had a multidirectional impact on food supply of commercial fish species. The first large-scale introduction of Marenzelleria spp. the structure of the bottom community has changed, the role of Chironomidae in the food supply has sharply decreased. The result was a decrease in the catch of Abramis brama, whose favorite food is of Chironomidae. The second large-scale invasion, of predatory Ponto-Caspian cladoceran C. pengoi, changed the structure of the planktonic community of the lagoon. There was a decrease in zooplankton biomass, as a result of which competition for feed resources turned out to be not in favor of the juvenile of Clupea harengus, the main planktophage. The third large-scale invasion of North American bivalve R. cuneata, the most powerful filter, affected the planktonic and bottom communities of the lagoon. The biomass of zooplankton decreased sharply, which created increased trophic conditions among planktophages fish and led to a decrease in catch. At the same time, the phenomenon of Atlantic rangia had a positive effect on other groups of the bottom community, which contributed to an increase in the catch of mollusk-eating fish, the main of which is of Rutilus rutilus.

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28

Jovanovic, Z., M. Larsen, C. Organo Quintana, E. Kristensen, and RN Glud. "Oxygen dynamics and porewater transport in sediments inhabited by the invasive polychaete Marenzelleria viridis." Marine Ecology Progress Series 504 (May 14, 2014): 181–92. http://dx.doi.org/10.3354/meps10737.

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29

Gastineau, Romain, Brygida Wawrzyniak-Wydrowska, Claude Lemieux, Monique Turmel, and Andrzej Witkowski. "Complete mitogenome of a Baltic Sea specimen of the non-indigenous polychaete Marenzelleria neglecta." Mitochondrial DNA Part B 4, no. 1 (2019): 581–82. http://dx.doi.org/10.1080/23802359.2018.1558125.

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30

Hubley, Mark J., Christopher D. A. Parks, and Juan Lin. "Temperature-induced changes in the locomotor capacity of juveniles of Marenzelleria viridis (Polychaeta, Spionidae)." Invertebrate Biology 120, no. 4 (2005): 372–77. http://dx.doi.org/10.1111/j.1744-7410.2001.tb00045.x.

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31

Quintana, Cintia O., Erik Kristensen, and Thomas Valdemarsen. "Impact of the invasive polychaete Marenzelleria viridis on the biogeochemistry of sandy marine sediments." Biogeochemistry 115, no. 1-3 (2012): 95–109. http://dx.doi.org/10.1007/s10533-012-9820-2.

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32

Mikhailova, A. V., E. V. Popova, S. V. Shipulin, A. A. Maximov, I. S. Plotnikov, and N. V. Aladin. "On the Invasion of the Genus Marenzelleria (Polychaeta, Spionidae) Representatives into the Caspian Sea Basin." Russian Journal of Biological Invasions 12, no. 4 (2021): 373–76. http://dx.doi.org/10.1134/s207511172104007x.

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Kauppi, L., A. Norkko, and J. Norkko. "Seasonal population dynamics of the invasive polychaete genus Marenzelleria spp. in contrasting soft-sediment habitats." Journal of Sea Research 131 (January 2018): 46–60. http://dx.doi.org/10.1016/j.seares.2017.10.005.

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34

Quintana, Cintia O., Caroline Raymond, Francisco J. A. Nascimento, et al. "Functional Performance of Three Invasive Marenzelleria Species Under Contrasting Ecological Conditions Within the Baltic Sea." Estuaries and Coasts 41, no. 6 (2018): 1766–81. http://dx.doi.org/10.1007/s12237-018-0376-9.

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35

Hedman, Jenny E., Jonas S. Gunnarsson, Göran Samuelsson, and Franck Gilbert. "Particle reworking and solute transport by the sediment-living polychaetes Marenzelleria neglecta and Hediste diversicolor." Journal of Experimental Marine Biology and Ecology 407, no. 2 (2011): 294–301. http://dx.doi.org/10.1016/j.jembe.2011.06.026.

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36

Gruszka, Piotr. "Marenzelleria viridis (Verrill, 1873) (Polychaeta: Spionidae)-a new component of shallow water benthic community in the Southern Baltic." Acta Ichthyologica et Piscatoria 21, S (1991): 57–65. http://dx.doi.org/10.3750/aip1991.21.s.07.

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Maximov, A. A., and V. A. Petukhov. "Role of macro- and meiobenthos in the bottom communities of the inner Gulf of Finland." Proceedings of the Zoological Institute RAS 315, no. 3 (2011): 289–310. http://dx.doi.org/10.31610/trudyzin/2011.315.3.289.

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Abstract:

The role of macro- and meiobenthos in the bottom communities of the inner Gulf of Finland was studied under different environmental conditions. In the shallow areas above 20 m isobath so-called principle of biocoenotic compensation was observed, that is, increase of meiobenthos quantitative characteristics with macrobenthos impoverishment. This principle was violated in the deeper areas, where bottom communities were wiped out periodically because of hypoxicanoxic events. The deep-water communities characterized by very unstable structure. The both studied benthos components were adversely af fected by hypoxia. In the following recovery succession macrobenthic polychaetes Marenzelleria spp. got advantage, which able to colonized quickly vacant bottoms because of presence of plankton larvae. The meiobenthos was typified by slower recovery. Thus, in the open waters of the Gulf of Finland meiobenthos can not compensate disappearance or strong impoverishment of macrozoobenthos in the case of near-bottom hypoxia formation, which in the last years became a common phenomenon for the most part of area of this water body.

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Maximov, A. A. "Large-scale invasion of Marenzelleria spp. (Polychaeta; Spionidae) in the eastern Gulf of Finland, Baltic Sea." Russian Journal of Biological Invasions 2, no. 1 (2011): 11–19. http://dx.doi.org/10.1134/s2075111711010036.

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Schiedek, Doris. "Marenzelleria viridis (Verrill, 1873) (Polychaeta), a new benthic species within European coastal waters Some metabolic features." Journal of Experimental Marine Biology and Ecology 211, no. 1 (1997): 85–101. http://dx.doi.org/10.1016/s0022-0981(96)02714-1.

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Fritzsche, D., and J. A. von Oertzen. "Metabolic responses to changing environmental conditions in the brackish water polychaetes Marenzelleria viridis and Hediste diversicolor." Marine Biology 121, no. 4 (1995): 693–99. http://dx.doi.org/10.1007/bf00349305.

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41

Eriksson Wiklund, A. K., and A. Andersson. "Benthic competition and population dynamics of Monoporeia affinis and Marenzelleria sp. in the northern Baltic Sea." Estuarine, Coastal and Shelf Science 144 (May 2014): 46–53. http://dx.doi.org/10.1016/j.ecss.2014.04.008.

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42

Bick, Andreas, and Roger Burckhardt. "Erstnachweis von Marenzelleria viridis (Polychaeta, Spionidae) für den Ostseeraum, mit einem Bestimmungsschlüssel der Spioniden der Ostsee." Mitteilungen aus dem Museum für Naturkunde in Berlin. Zoologisches Museum und Institut für Spezielle Zoologie (Berlin) 65, no. 2 (1989): 237–47. http://dx.doi.org/10.1002/mmnz.19890650208.

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43

Röhner, Matthias, Ralf Bastrop, and Karl Jürss. "Genetic differences between two allopatric populations (or sibling species) of the polychaete genus Marenzelleria in Europe." Comparative Biochemistry and Physiology Part B: Biochemistry and Molecular Biology 114, no. 2 (1996): 185–92. http://dx.doi.org/10.1016/0305-0491(96)00018-1.

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44

Neideman, R., J. Wenngren, and E. Ólafsson. "Competition between the introduced polychaete Marenzelleria sp. and the native amphipod Monoporeia affinis in Baltic soft bottoms." Marine Ecology Progress Series 264 (2003): 49–55. http://dx.doi.org/10.3354/meps264049.

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45

Maximov, A. A. "Changes in bottom communities of the eastern Gulf of Finland after introduction of the polychaete Marenzelleria neglecta." Russian Journal of Biological Invasions 1, no. 1 (2010): 11–16. http://dx.doi.org/10.1134/s2075111710010030.

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46

Maximov, Alexey, Erik Bonsdorff, Tatjana Eremina, Laura Kauppi, Alf Norkko, and Joanna Norkko. "Context-dependent consequences of Marenzelleria spp. (Spionidae: Polychaeta) invasion for nutrient cycling in the Northern Baltic Sea." Oceanologia 57, no. 4 (2015): 342–48. http://dx.doi.org/10.1016/j.oceano.2015.06.002.

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47

Gren, Ing-Marie, Antonia Nyström Sandman, and Johan Näslund. "Aquatic invasive species and ecosystem services: Economic effects of the worm Marenzelleria spp. in the Baltic Sea." Water Resources and Economics 24 (October 2018): 13–24. http://dx.doi.org/10.1016/j.wre.2018.02.003.

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48

Kocheshkova, O. V., and E. E. Ezhova. "On alien polychaete species of the Russian part of South-Eastern Baltic." Marine Biological Journal 3, no. 2 (2018): 53–63. http://dx.doi.org/10.21072/mbj.2018.03.2.04.

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Climatic changes and anthropogenic impact have resulted in numerous cases of introduction and range expansion of hydrobionts. In the late 20th century and in the early 21st century some species, previously not observed in the Vistula and Curonian lagoons (brackish waterbodies with well-developed port infrastructure and active navigation) were recorded more than once in the study area. The aim of this study was to characterize cases of alien polychaete introductions in the Russian part of the South-Eastern Baltic Sea, including shallow lagoons. Samples of zoobenthos, collected in the Russian exclusive economic zone in the South-Eastern Baltic Sea (139 sampling sites, 2001–2016), the North-Eastern Vistula Lagoon (45 s. s., 1997–2016) and the Southern Curonian Lagoon (24 s. s., 2001–2016), were studied. The material is stored in the IO RAS zoological collection. The south-western (Polish) part of the Vistula Lagoon and the northern (Lithuanian) part of the Curonian Lagoon were characterized using previously published data. In the Vistula Lagoon since the 1880s for over a century polychaetes were represented by the only species – Hediste diversicolor. Since the end of the 20th century, new species for the region have been registered: Marenzelleria neglecta (since 1988); Streblospio benedicti, Manayunkia aestuarina, Alkmaria romijni (since middle 1990s); Boccardiella ligerica (since 2008 in the Polish waters and since 2013 in the Russian waters); Laonome cf. calida (since 2014). In the Curonian Lagoon polychaetes (the only species, M. neglecta) occur in the northern (Lithuanian) part only. In the Russian part of the South-Eastern Baltic polychaetes of Marenzelleria genus have been registered since 1988, while M. arctia – since 2001, S. benedicti and B. ligerica have been recorded since the beginning of the 21st century. Thus, in the marine waters of the South-Eastern Baltic, three alien polychaete species have been recorded, while in the Vistula Lagoon – five, and in the Curonian Lagoon – one species. These introduced species belong to a group of estuarine, brackishwater infaunal organisms, whose native areals are in the Western or Eastern Atlantic and the south-western part of the Pacific Ocean. Salinity conditions have been shown to be the most favorable for aliens in the marine part of the study area, while trophic conditions – in the lagoons. The optimal combination of environmental factors for the aliens has been found to be in the shallow Vistula Lagoon due to an existence of the aria with bottom salinity not lower then 3.7–5.9 ‰, predominance of soft silty sediments, abundance of organic matter, and insignificant competition for food resources. Information on distribution, occurrence, abundance and status of alien populations is given.

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Renz, JR, and S. Forster. "Effects of bioirrigation by the three sibling species of Marenzelleria spp. on solute fluxes and porewater nutrient profiles." Marine Ecology Progress Series 505 (May 28, 2014): 145–59. http://dx.doi.org/10.3354/meps10756.

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Blank, M., R. Bastrop, M. Röhner, and K. Jürss. "Effect of salinity on spatial distribution and cell volume regulation in two sibling species of Marenzelleria (Polychaeta: Spionidae)." Marine Ecology Progress Series 271 (2004): 193–205. http://dx.doi.org/10.3354/meps271193.

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