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Marine and Freshwater Research Marine and Freshwater Research Society
Advances in the aquatic sciences
RESEARCH ARTICLE

Soft-bottom polychaetes in a chronic eutrophic bay on the coast of Alexandria

Noha Elebiary https://orcid.org/0000-0003-1056-3061 A * , Faiza Abd Elnaby https://orcid.org/0000-0002-1457-2363 A , Mohamed M. Dorgham https://orcid.org/0000-0002-9239-8241 B , Amira M. Hamdan B and Rasha Hamdy B
+ Author Affiliations
- Author Affiliations

A National Institute of Oceanography and Fisheries (NIOF), Alexandria, Egypt.

B Oceanography Department, Faculty of Science, Alexandria University, Alexandria, Egypt.

* Correspondence to: nohahassan8853@yahoo.com

Handling Editor: Jill Chiu

Marine and Freshwater Research 74(4) 347-356 https://doi.org/10.1071/MF22204
Submitted: 30 September 2022  Accepted: 28 December 2022   Published: 30 January 2023

© 2023 The Author(s) (or their employer(s)). Published by CSIRO Publishing

Abstract

Context: The polychaetes are the major benthos in the soft bottom of the eutrophic Eastern Harbour of Alexandria, Egypt.

Aim: Investigate the quantitative and qualitative dynamics of polychaete community in the Harbour.

Methods: Polychaetes were collected bimonthly from August 2018 to June 2019, by using a 29- × 16-cm grab.

Key results: In total, 54 polychaete species were identified, belonging to 27 families and 51 genera. The family Syllidae was represented by eight species, Spionidae by five species, and Cirratulidae by five species, against one to three species from all other families. Eleven alien species were recorded, including four new to the Mediterranean Sea (Caulleriella cristata, Armandia casuarina, Spio blakei and Prionospio lighti). The polychaete community displayed pronounced temporal variations in both species diversity and numerical abundance at the two sampled sites.

Conclusion: This study showed high diversity and abundance of polychaetes in such eutrophic basin.

Implications: The eutrophication may play a role in the structure and count of polychaetes in the Eastern Harbour.

Keywords: Alexandria coast, alien species, diversity, Eastern Harbour, Egypt, eutrophic, indicator species, Mediterranean, new record, polychaetes, soft bottom.


References

Abd Elnaby, FA, and Abdelsalam, KM (2021). New records of marine Annelida (Polychaeta) in the Egyptian coast, eastern Mediterranean Sea. Egyptian Journal of Aquatic Biology and Fisheries 25, 953–965.
New records of marine Annelida (Polychaeta) in the Egyptian coast, eastern Mediterranean Sea.Crossref | GoogleScholarGoogle Scholar |

Abd-Elnaby, FA (2007). Some polychaete species from the soft bottom of the Eastern Harbour of Alexandria, Egypt, with special reference to orbiniids and paraonids habitats. Egyptian Journal of Aquatic Research 33, 185–201.

Abd-Elnaby FA (2013) Polychaeta from the Eastern Harbour of Alexandria. (National Institute of Oceanography and Fisheries) Available at https://www.gbif.org/dataset/0c27b712-832d-4f0e-8e03-97af404e83ff [Verified 6 Janury 2023]

Abd-Elnaby, FA, and Gab-Alla, AF (2007). New records of Pettiboneia and Protodorvillea (Polychaeta: Dorvilleidae) from the Eastern Harbour of Alexandria. Journal of the Egyptian German Society of Zoology – D. Invertebrate Zoology and Parasitology 54, 159–174.

Abdelnaby, FA (2020). Alien Polychaete species and the first record of Branchiomma bairdi (McIntosh, 1885) from the Suez Canal and the Mediterranean coast of Egypt. Egyptian Journal of Aquatic Biology and Fisheries 24, 13–32.
Alien Polychaete species and the first record of Branchiomma bairdi (McIntosh, 1885) from the Suez Canal and the Mediterranean coast of Egypt.Crossref | GoogleScholarGoogle Scholar |

Bartels-Hardege, HD, and Zeeck, E (1990). Reproductive behaviour of Nereis diversicolor (Annelida: Polychaeta). Marine Biology 106, 409–412.
Reproductive behaviour of Nereis diversicolor (Annelida: Polychaeta).Crossref | GoogleScholarGoogle Scholar |

Bentley, M, and Pacey, A (1992). Physiological and environmental control of reproduction in polychaetes. Oceanography and Marine Biology: An Annual Review 30, 443–481.

Blake, JA (2016). Kirkegaardia (Polychaeta, Cirratulidae), new name for Monticellina Laubier, preoccupied in the Rhabdocoela, together with new records and descriptions of eight previously known and sixteen new species from the Atlantic, Pacific, and Southern Oceans. Zootaxa 4166, 1–93.
Kirkegaardia (Polychaeta, Cirratulidae), new name for Monticellina Laubier, preoccupied in the Rhabdocoela, together with new records and descriptions of eight previously known and sixteen new species from the Atlantic, Pacific, and Southern Oceans.Crossref | GoogleScholarGoogle Scholar |

Buruaem, LM, Petti, MAV, and Abessa, DMS (2015). Soft-bottom polychaetes from the Brazilian harbors of Mucuripe and Pecém (state of Ceará) and Santos (state of São Paulo). Check List 11, 1721.
Soft-bottom polychaetes from the Brazilian harbors of Mucuripe and Pecém (state of Ceará) and Santos (state of São Paulo).Crossref | GoogleScholarGoogle Scholar |

Chariton AA, Pettigrove VJ, Baird DJ (2016) Ecological assessment. In ‘Sediment quality assessment: a practical guide’. (Eds SL Simpson, GE Batley) pp. 195–236. (CSIRO Publishing: Melbourne, Vic., Australia) https://doi.org/10.1071/9781486303854

Chu, J-W, and Levin, LA (1989). Photoperiod and temperature regulation of growth and reproduction in Streblospio benedicti (Polychaeta: Spionidae). Invertebrate Reproduction & Development 15, 131–142.
Photoperiod and temperature regulation of growth and reproduction in Streblospio benedicti (Polychaeta: Spionidae).Crossref | GoogleScholarGoogle Scholar |

Çinar, ME (2009). Alien polychaete species (Annelida: Polychaeta) on the southern coast of Turkey (Levantine Sea, Eastern Mediterranean), with 13 new records for the Mediterranean Sea. Journal of Natural History 43, 2283–2328.
Alien polychaete species (Annelida: Polychaeta) on the southern coast of Turkey (Levantine Sea, Eastern Mediterranean), with 13 new records for the Mediterranean Sea.Crossref | GoogleScholarGoogle Scholar |

Danulat, E, Muniz, P, García-Alonso, J, and Yannicelli, B (2002). First assessment of the highly contaminated harbour of Montevideo, Uruguay. Marine Pollution Bulletin 44, 554–565.
First assessment of the highly contaminated harbour of Montevideo, Uruguay.Crossref | GoogleScholarGoogle Scholar |

Dean, HK (2008). The use of polychaetes (Annelida) as indicator species of marine pollution: a review. Revista de Biología Tropical 56, 11–38.

Dorgham, MM, Hamdy, R, El-Rashidy, HH, and Atta, MM (2013). First records of polychaetes new to Egyptian Mediterranean waters. Oceanologia 55, 235–267.
First records of polychaetes new to Egyptian Mediterranean waters.Crossref | GoogleScholarGoogle Scholar |

Dorgham, MM, Hamdy, R, EL Rashidy, HH, Atta, MM, and Musco, L (2014). Distribution patterns of shallow water polychaetes (Annelida) along the Alexandria coast, Egypt (eastern Mediterranean). Mediterranean Marine Science 15, 635–649.
Distribution patterns of shallow water polychaetes (Annelida) along the Alexandria coast, Egypt (eastern Mediterranean).Crossref | GoogleScholarGoogle Scholar |

Elsayed, RH, and Dorgham, MM (2019). Macrofauna associated with a recently described bryozoan species in the Eastern Harbour of Alexandria, Egypt. Mediterranean Marine Science 20, 248–259.
Macrofauna associated with a recently described bryozoan species in the Eastern Harbour of Alexandria, Egypt.Crossref | GoogleScholarGoogle Scholar |

Elías, R, Vallarino, EA, Scagliola, M, and Isla, FI (2004). Macrobenthic distribution patterns at a sewage disposal site in the inner shelf off Mar del Plata (SW Atlantic). Journal of Coastal Research 204, 1176–1182.
Macrobenthic distribution patterns at a sewage disposal site in the inner shelf off Mar del Plata (SW Atlantic).Crossref | GoogleScholarGoogle Scholar |

Elías, R, Palacios, JR, Rivero, MS, and Vallarino, EA (2005). Short-term responses to sewage discharge and storms of subtidal sand-bottom macrozoobenthic assemblages off Mar del Plata City, Argentina (SW Atlantic). Journal of Sea Research 53, 231–242.
Short-term responses to sewage discharge and storms of subtidal sand-bottom macrozoobenthic assemblages off Mar del Plata City, Argentina (SW Atlantic).Crossref | GoogleScholarGoogle Scholar |

Erdoğan-Dereli, D, Çinar, ME, and Dağlı, E (2017). Cirrophorus species (Annelida: Polychaeta: Paraonidae) in the Sea of Marmara, with description of a new species. Zootaxa 4347, 137–150.
Cirrophorus species (Annelida: Polychaeta: Paraonidae) in the Sea of Marmara, with description of a new species.Crossref | GoogleScholarGoogle Scholar |

Fauchald, K, and Jumars, PA (1979). The diet of worms: a study of polychaete feeding guilds. Oceanography and Marine Biology Annual Review 17, 193–284.

Fauvel P (1923) ‘Faune de France 5. Polychètes Errantes.’ (Ed. Fédération des sociétés françaises de sciences naturelles) (Le Chevalier: Paris, France)

Fauvel P (1927) ‘Faune de France 16. Polychètes Sédentaires addenda aux errantes, archiannélides, myzostomaires.’ (Ed. Fédération des sociétés françaises de sciences naturelles) (Le Chevalier: Paris, France)

Folk, RL, and Ward, WC (1957). Brazos River bar [Texas]; a study in the significance of grain size parameters. Journal of Sedimentary Research 27, 3–26.
Brazos River bar [Texas]; a study in the significance of grain size parameters.Crossref | GoogleScholarGoogle Scholar |

Grall, J, and Glémarec, M (1997). Using biotic indices to estimate macrobenthic community perturbations in the Bay of Brest. Estuarine, Coastal and Shelf Science 44, 43–53.
Using biotic indices to estimate macrobenthic community perturbations in the Bay of Brest.Crossref | GoogleScholarGoogle Scholar |

Guerra-García, JM, and García-Gómez, JC (2004). Polychaete assemblages and sediment pollution in a harbour with two opposing entrances. Helgoland Marine Research 58, 183–191.
Polychaete assemblages and sediment pollution in a harbour with two opposing entrances.Crossref | GoogleScholarGoogle Scholar |

Hamdy, R, and Dorgham, M (2018). Intermittent study of benthic fauna in the Eastern Harbour of Alexandria, Egypt. Egyptian Journal of Aquatic Biology and Fisheries 22, 209–223.
Intermittent study of benthic fauna in the Eastern Harbour of Alexandria, Egypt.Crossref | GoogleScholarGoogle Scholar |

Hamdy, R, and Ibrahim, HG (2019). Recent changes in polychaete community along the Alexandria coast, Egypt. Egyptian Journal of Aquatic Biology and Fisheries 23, 1–12.
Recent changes in polychaete community along the Alexandria coast, Egypt.Crossref | GoogleScholarGoogle Scholar |

Hamdy, R, Khalil, AEN, Atta, MM, and Ibrahim, HG (2018). Diversity and distribution of polychaetes associated with macroalgae along the Alexandria Coast, Egypt. Journal of King Abdulaziz University: Marine Science 28, 67–79.
Diversity and distribution of polychaetes associated with macroalgae along the Alexandria Coast, Egypt.Crossref | GoogleScholarGoogle Scholar |

Holmer, M, Forbes, VE, and Forbes, TL (1997). Impact of the polychaete Capitella sp. I on microbial activity in an organic-rich marine sediment contaminated with the polycyclic aromatic hydrocarbon fluoranthene. Marine Biology 128, 679–688.
Impact of the polychaete Capitella sp. I on microbial activity in an organic-rich marine sediment contaminated with the polycyclic aromatic hydrocarbon fluoranthene.Crossref | GoogleScholarGoogle Scholar |

Hosokawa, S, Naito, R, and Nakamura, Y (2020). Spatial patterns of concentrations of Cu, Zn, Cd, and Pb in marine sediments from Japanese port areas. Regional Studies in Marine Science 35, 101135.
Spatial patterns of concentrations of Cu, Zn, Cd, and Pb in marine sediments from Japanese port areas.Crossref | GoogleScholarGoogle Scholar |

Hosokawa, S, Momota, K, Chariton, AA, Naito, R, and Nakamura, Y (2021). The use of diversity indices for local assessment of marine sediment quality. Scientific Reports 11, 14991.
The use of diversity indices for local assessment of marine sediment quality.Crossref | GoogleScholarGoogle Scholar |

Hsieh, TC, Ma, KH, and Chao, A (2016). iNEXT: an R package for rarefaction and extrapolation of species diversity (Hill numbers). Methods in Ecology and Evolution 7, 1451–1456.
iNEXT: an R package for rarefaction and extrapolation of species diversity (Hill numbers).Crossref | GoogleScholarGoogle Scholar |

Johnston, EL, and Roberts, DA (2009). Contaminants reduce the richness and evenness of marine communities: a review and meta-analysis. Environmental Pollution 157, 1745–1752.
Contaminants reduce the richness and evenness of marine communities: a review and meta-analysis.Crossref | GoogleScholarGoogle Scholar |

Jouin-Toulmond, C, and Gambi, MC (2007). Description of Saccocirrus goodrichi sp. nov. (Annelida: Polychaeta: Saccocirridae), a new Mediterranean species and new data on the chaetae of S. papillocercus and S. major. Cahiers de Biologie Marine 48, 381–390.

Lardicci, C, Abbiati, M, Crema, R, Morri, C, Bianchi, CN, and Castelli, A (1993). The distribution of polychaetes along environmental gradients: an example from the Or betel I o Lagoon, Italy. Marine Ecology 14, 35–52.
The distribution of polychaetes along environmental gradients: an example from the Or betel I o Lagoon, Italy.Crossref | GoogleScholarGoogle Scholar |

Lawrence, AJ, and Soame, JM (2004). The effects of climate change on the reproduction of coastal invertebrates. International Journal of Avian Science 146, 29–39.
The effects of climate change on the reproduction of coastal invertebrates.Crossref | GoogleScholarGoogle Scholar |

Mistri, M, Fano, EA, Ghion, F, and Rossi, R (2002). Disturbance and community pattern of polychaetes inhabiting Valle Magnavacca (Valli di Comacchio, northern Adriatic Sea, Italy). Marine Ecology 23, 31–49.
Disturbance and community pattern of polychaetes inhabiting Valle Magnavacca (Valli di Comacchio, northern Adriatic Sea, Italy).Crossref | GoogleScholarGoogle Scholar |

Moreira, J, and Parapar, J (2017). New data on the Opheliidae (Annelida) from Lizard Island (Great Barrier Reef, Australia): five new species of the genus Armandia Filippi, 1861. Zootaxa 4290, 483–502.
New data on the Opheliidae (Annelida) from Lizard Island (Great Barrier Reef, Australia): five new species of the genus Armandia Filippi, 1861.Crossref | GoogleScholarGoogle Scholar |

Murugesan P, Sarathy PP, Muthuvelu S, Mahadevan G (2018) Diversity and distribution of polychaetes in mangroves of east coast of India. In ‘Mangrove ecosystem ecology and function’. (Ed. S Sharma) pp. 107–130. (IntechOpen: UK) https://doi.org/10.5772/intechopen.78332

Nessim RB, Tadros HRZ, Abou-Taleb AE (2006) Pore water characteristics of Alexandria Eastern Harbour Sediments (Oct. 2004–Oct. 2005). Environmental impacts, environmental impact assessment. Technical Report, National Institute of Oceanography, Egypt.

Nesto, N, Simonini, R, Prevedelli, D, and Da Ros, L (2012). Effects of diet and density on growth, survival and gametogenesis of Hediste diversicolor (O.F.Müller, 1776) (Nereididae, Polychaeta). Aquaculture 362–363, 1–9.
Effects of diet and density on growth, survival and gametogenesis of Hediste diversicolor (O.F.Müller, 1776) (Nereididae, Polychaeta).Crossref | GoogleScholarGoogle Scholar |

Nicolaidou, A, and Papadopoulou, K-N (1989). Factors affecting the distribution and diversity of polychaetes in Amivrakikos Bay, Greece. Marine Ecology 10, 193–204.
Factors affecting the distribution and diversity of polychaetes in Amivrakikos Bay, Greece.Crossref | GoogleScholarGoogle Scholar |

Pearson, TH, and Rosenberg, R (1978). Macrobenthic succession in relation to organic enrichment and pollution of the marine environment. Oceanography and Marine Biology – An Annual Review 16, 229–311.

Pocklington, P, and Wells, PG (1992). Polychaetes Key taxa for marine environmental quality monitoring. Marine Pollution Bulletin 24, 593–598.
Polychaetes Key taxa for marine environmental quality monitoring.Crossref | GoogleScholarGoogle Scholar |

Qian, P-Y, and Chia, F-S (1991). Fecundity and egg size are mediated by food quality in the polychaete worm Capitella sp. Journal of Experimental Marine Biology and Ecology 148, 11–25.
Fecundity and egg size are mediated by food quality in the polychaete worm Capitella sp.Crossref | GoogleScholarGoogle Scholar |

Rasha, H, Noha, E, Faiza, AE, Mohamed, D, Giorgos, C, and Amira, H (2022). Dynamics of polychaete communities in the intertidal soft bottom of Alexandria coast, Egypt. Regional Studies in Marine Science 56, 102645.
Dynamics of polychaete communities in the intertidal soft bottom of Alexandria coast, Egypt.Crossref | GoogleScholarGoogle Scholar |

Rivero, MS, Elías, R, and Vallarino, EA (2005). First survey of macroinfauna in the Mar del Plata Harbor (Argentina), and the use of polychaetes as pollution indicators. Revista de Biología Marina y Oceanografía 40, 101–108.
First survey of macroinfauna in the Mar del Plata Harbor (Argentina), and the use of polychaetes as pollution indicators.Crossref | GoogleScholarGoogle Scholar |

San Martin G (1984) Estudio biogeografico, faunistico y sistematico de los poliquetos de la familia silidos (Syllidae: Polychaeta) en Baleares. PhD Thesis, Universidad Complutense de Madrid, Spain.

Selim SA (1978) Systematic and distributional studies of polychaetes in the Eastern Harbour, Alexandria. MSc Thesis, Alexandria University, Alexandria, Egypt.

Selim, SA (1997). Assessment of polychaete fauna in the Eastern Harbour of Alexandria, Egypt. Bulletin of High Institute of Public Health 27, 131–146.

Sigamani, S, Perumal, M, Arumugam, S, Preetha Mini Jose, HM, and Veeraiyan, B (2015). AMBI indices and multivariate approach to assess the ecological health of Vellar–Coleroon estuarine system undergoing various human activities. Marine Pollution Bulletin 100, 334–343.
AMBI indices and multivariate approach to assess the ecological health of Vellar–Coleroon estuarine system undergoing various human activities.Crossref | GoogleScholarGoogle Scholar |

Sigamani, S, Samikannu, M, and Alagiri, TG (2019). Assessment of effluent stressed ecosystem of Cuddalore coastal waters – a bio-indicator approach. Thalassas: An International Journal of Marine Sciences 35, 437–449.
Assessment of effluent stressed ecosystem of Cuddalore coastal waters – a bio-indicator approach.Crossref | GoogleScholarGoogle Scholar |

Sivadas, S, Ingole, B, and Nanajkumar, M (2010). Benthic polychaetes as good indicator of anthropogenic impacts. Indian Journal of Marine Sciences 39, 201–211.

Sivaraj, S, Murugesan, P, Muthuvelu, S, Vivekanandan, KE, and Vijayalakshmi, S (2014). AMBI and M-AMBI indices as a robust tool for assessing the effluent stressed ecosystem in Nandgaon Coastal waters, Maharashtra, India. Estuarine, Coastal and Shelf Science 146, 60–67.
AMBI and M-AMBI indices as a robust tool for assessing the effluent stressed ecosystem in Nandgaon Coastal waters, Maharashtra, India.Crossref | GoogleScholarGoogle Scholar |

Surugiu, V (2005). The use of polychaetes as indicators of eutrophication and organic enrichment of coastal waters: a study case – Romanian Black Sea coast. Analele Ştiinţifice ale Universităţii ‘Al. I. Cuza’ Iaşi, s. Biologie Animală 51, 55–62.

Vanosmael, C, Willems, KA, Claeys, D, Vincx, M, and Heip, C (1982). Macrobenthos of a sublittoral sandbank in the Southern Bight of the North Sea. Journal of the Marine Biological Association of the United Kingdom 62, 521–534.
Macrobenthos of a sublittoral sandbank in the Southern Bight of the North Sea.Crossref | GoogleScholarGoogle Scholar |

Walkley, A, and Black, IA (1934). An examination of the Degtjareff method for determining soil organic matter, and a proposed modification of the chromic acid titration method. Soil Science 37, 29–38.
An examination of the Degtjareff method for determining soil organic matter, and a proposed modification of the chromic acid titration method.Crossref | GoogleScholarGoogle Scholar |

Yokoyama, H (2002). Impact of fish and pearl farming on the benthic environments in Gokasho bay: evaluation from seasonal fluctuations of the macrobenthos. Fisheries Science 68, 258–268.
Impact of fish and pearl farming on the benthic environments in Gokasho bay: evaluation from seasonal fluctuations of the macrobenthos.Crossref | GoogleScholarGoogle Scholar |