Carlton, J. T. & Geller, J. B. Ecological roulette: The global transport of non-indigenous marine organisms. Sciences 261, 78–82 (1993).
Google Scholar
Ruiz, G. M., Fofonov, P. & Hines, A. H. Non-indigenous species as stressors in estuarine and marine communities: Assessing invasion impacts and interactions. Limnol. Oceanogr. 44, 950–972 (1999).
Google Scholar
Mack, R. N. et al. Biotic invasions: Causes, epidemiology, global consequences, and control. Ecol. Appl. 10, 689–710 (2000).
Google Scholar
Tsiamis, K. et al. Non-indigenous species refined national baseline inventories: A synthesis in the context of the European Union’s Marine Strategy Framework Directive. Mar. Pollut. Bull. 145, 429–435 (2019).
Google Scholar
Gollasch, S. Overview on introduced aquatic species in European navigational and adjacent waters. Helgol. Mar. Res. 60(2), 84–89 (2006).
Google Scholar
Zenetos, A. et al. Alien species in the Mediterranean Sea by 2010 A contribution to the application of European Union’ Marine Strategy Framework Directive (MSFD) Part I. Spatial distribution. Mediterr. Mar. Sci. 11, 381–493 (2010).
Google Scholar
Zenetos, A. et al. Uncertainties and validation of alien species catalogues: The Mediterranean as an example. Est. Coast. Shelf. Sci. 191, 171–187 (2017).
Google Scholar
Uttieri, M. et al. Towards a EURopean OBservatory of the non-indigenous calanoid copepod Pseudodiaptomus marinUS. Biol. Invasions 22(3), 885–906. https://doi.org/10.1007/s10530-019-02174-8 (2020).
Google Scholar
Vidjak, O. et al. Zooplankton in Adriatic port environments: Indigenous communities and non-indigenous species. Mar. Pollut. Bull. 147, 133–149. https://doi.org/10.1016/j.marpolbul.2018.06.055 (2019).
Google Scholar
Malej, A. et al. Mnemiopsis leidyi in the northern Adriatic: Here to stay?. J. Sea Res. 124, 10–16. https://doi.org/10.1016/j.seares.2017.04.010 (2017).
Google Scholar
Marchini, A., Ferrario, J., Sfriso, A. & Occhipinti-Ambrogi, A. Current status and trends of biological invasions in the Lagoon of Venice, a hotspot of marine NIS introductions in the Mediterranean Sea. Biol. Invasions 17, 2943–2962. https://doi.org/10.1007/s10530-015-0922-3 (2015).
Google Scholar
Galliene, C. P. & Robins, D. B. Is Oithona the most important copepod in the world’s oceans?. J. Plankton Res. 23(12), 1421–1432 (2001).
Google Scholar
Saiz, E., Calbet, A. & Broglio, E. Effects of small-scale turbolence on copepods: The case of Oithona davisae. Limnol. Oceanogr. 48, 1304–1311. https://doi.org/10.4319/lo.2003.48.3.1304 (2003).
Google Scholar
Turner, T. The importance of small planktonic copepods and their roles in pelagic marine food webs. Zool. Stud. 43(2), 255–266 (2004).
Hwang, I. S., Kumar, R., Dahms, H. U., Tseng, L. C. & Chen, Q. C. Mesh size affects abundance estimates of Oithona spp. (Copepoda, Cyclopoida). Crustaceana 80(7), 827–837 (2007).
Google Scholar
Nishida, S., Tanaka, O. & Omori, M. Cyclopoid copepods of the family Oithonidae in Suruga bay and adjacent waters. Bull. Plankton Soc. Japan 24, 120–157 (1977).
Uye, S. I. & Sano, K. Seasonal reproductive biology of the small cyclopoid copepod Oithona davisae in a temperate eutrophic inlet. Mar. Ecol. Prog. Ser. 118, 121–128 (1995).
Google Scholar
Zagami, G. et al. Biogeographical distribution and ecology of the planktonic copepod Oithona davisae: Rapid invasion in Lakes Faro and Ganzirri (Central Mediterranean Sea). In Trends in Copepod Studies-Distribution, Biology and Ecology (ed. Uttieri, M.) 59–82 (Nova Science Publisher, New York, 2018).
Cornils, A. & Wend-Heckmann, B. First report of the planktonic copepod Oithona davisae in the northern Wadden Sea (North Sea): Evidence for recent invasion?. Helgol. Mar. Res. 69, 243–248. https://doi.org/10.1007/s10152-015-0426-7 (2015).
Google Scholar
Uye, S. I. & Sano, K. Seasonal variations in biomass, growth rate and production rate of the small cyclopoid copepod Oithona davisae in a temperate eutrophic inlet. Mar. Ecol. Progr. Ser. 163, 37–44 (1998).
Google Scholar
Ferrari, F. D. & Orsi, J. Oithona davisae, new species, and Limnoithona sinensis (Burckhardt, 1912) (Copepoda, Oithonidae) from the Sacramento San-Joaquin Estuary, California. J. Crustac. Biol. 4, 106–126. https://doi.org/10.2307/1547900 (1984).
Google Scholar
Cordell, J. R. et al. Factors influencing densities of non-indigenous species in the ballast water of ships arriving at ports in Puget Sound, Washington, United States. Aquat. Conserv. Mar. Freshw. Ecosyst. 19, 322–343. https://doi.org/10.1002/aqc.986 (2009).
Google Scholar
Dexter, E., Bollens, S. M., Cordell, J. & Rollwagen-Bollenseric, G. Zooplankton invasion on a grand scale: Insights from a 20-yr time series across 38 Northeast Pacific estuaries. Ecosphere 11(5), e03040 (2020).
Google Scholar
Temnykh, A. & Nishida, S. New record of the planktonic copepod Oithona davisae Ferrari and Orsi in the Black Sea with notes on the identity of Oithona brevicornis. Aquat. Invasions 7, 425–431 (2012).
Google Scholar
Uriarte, I., Villate, F. & Iriarte, A. Zooplankton recolonization of the inner estuary of Bilbao: Influence of pollution abatement, climate and non-indigenous species. J. Plankton Res. 38, 718–731. https://doi.org/10.1093/plankt/fbv060 (2015).
Google Scholar
Isinibilir, M., Svetlichny, L. & Hubareva, E. Competitive advantage of the invasive copepod Oithona davisae over the indigenous copepod Oithona nana in the Marmara Sea and Golden Horn Estuary. Mar. Freshw. Behav. Physiol. 49(6), 391–405. https://doi.org/10.1080/10236244.2016.1236528 (2016).
Google Scholar
Terbıyık Kurt, T. & Beşiktepe, Ş. First distribution record of the invasive copepod Oithona davisae Ferrari and Orsi, 1984, in the coastal waters of the Aegean Sea. Mar. Ecol. 40(3), e12548. https://doi.org/10.1111/maec.12548 (2019).
Google Scholar
Cucco, A. & Umgiesser, G. Modeling the Venice Lagoon residence time. Ecol. Model. 193, 34–51 (2006).
Google Scholar
Gačić, M. et al. Temporal variations of water flow between the Venetian lagoon and the open sea. J. Mar. Syst. 51, 33–47. https://doi.org/10.1016/j.jmarsys.2004.05.025 (2004).
Google Scholar
Zuliani, A., Zaggia, L., Collavini, F. & Zonta, R. Freshwater discharge from the drainage basin to the Venice Lagoon (Italy). Environ. Int. 31, 929–938 (2005).
Google Scholar
Sigovini, M. Multiscale dynamics of zoobenthic communities and relationships with environmental factors in the Lagoon of Venice. 207 pp (2011).
Zirino, A. et al. Salinity and its variability in the Lagoon of Venice, 2000–2009. Adv. Oceanogr. Limnol. 5, 41–59. https://doi.org/10.1080/19475721.2014.900113 (2014).
Google Scholar
Amos, C. L., Umgiesser, G., Ghezzo, M., Kassem, H. & Ferrarin, C. Sea Surface Temperature Trends in Venice Lagoon and the Adjacent Waters. J. Coast. Res. 33(2), 385–395. https://doi.org/10.2112/JCOASTRES-D-16-00017.1 (2016).
Google Scholar
Ravera, O. The Lagoon of Venice: The result of both natural factors and human influence. J. Limnol. 59, 19–30 (2000).
Google Scholar
Solidoro, C. et al. Response of the Venice Lagoon ecosystem to natural and anthropogenic pressures over the last 50 years. In Coastal lagoons: Critical habitats of environmental change (eds Kennish, M. J. & Paerl, H. W.) 483–511 (CRC Press, New York, 2010).
Camatti, E., Pansera, M. & Bergamasco, A. The copepod Acartia tonsa Dana in a microtidal Mediterranean lagoon: History of a successful invasion. Water 11(6), 1200. https://doi.org/10.3390/w11061200 (2019).
Google Scholar
Schroeder, A. et al. DNA metabarcoding and morphological analysis-Assessment of zooplankton biodiversity in transitional waters. Mar. Environ. Res. https://doi.org/10.1016/j.marenvres.2020.104946 (2020).
Google Scholar
Camatti, E. et al. Analisi dei popolamenti zooplanctonici nella laguna di Venezia dal 1975 al 2004. Biol. Mar. Mediterr. 13, 46–53 (2006).
Riccardi, N. Selectivity of plankton nets over mesozooplankton taxa: Implications for abundance, biomass and diversity estimation. J. Limnol. 69(2), 287–296. https://doi.org/10.3274/JL10-69-2-10 (2010).
Google Scholar
Pansera, M. et al. How does mesh-size selection reshape the description of zooplankton community structure in coastal lakes?. Est. Coast. Shelf. Sci. 151, 221–235 (2014).
Google Scholar
Harris, R., Wiebe, P., Lenz, J., Skjoldal, H. R. & Huntley, M. ICES Zooplankton methodology manual (Elsevier, New York, 2000).
Clarke, K.R. & Gorley, R.N. PRIMERv6: User Manual/Tutorial. PRIMER-E, Plymouth, 192 pp (2006).
Legendre, L. & Legendre, P. Ecologie numerique, Tome 2: La structure de données écologiques. Québec, Canada Masson, Paris, France and Presses de l’Univ. du (1984).
Tokeshi, M. Niche apportionment or random assortment e species abundance patterns revisited. J. Anim. Ecol. 59, 1129–1146 (1990).
Google Scholar
Tokeshi, M. Species abundance patterns and community structure. Adv. Ecol. Res. 24, 111–186 (1993).
Google Scholar
Fesl, C. Niche-oriented species-abundance models: Different approaches of their application to larval chironomid (Diptera) assemblages in a large river. J. Anim. Ecol. 71, 1085–1094 (2002).
Google Scholar
Spatharis, S., Orfanidis, S., Panayotidis, P. & Tsirtsis, G. Assembly processes in upper subtidal macroalgae: The effect of wave exposure. Est. Coast. Shelf. Sci. 91(2), 298–305. https://doi.org/10.1016/j.ecss.2010.10.032 (2011).
Google Scholar
Ferreira, F. C. & Petrere, J. M. Comments about some species abundance patterns: Classic, neutral, and niche partitioning models. Braz. J. Biol. 68(4), 1003–1012. https://doi.org/10.1590/S1519-69842008000500008 (2008).
Google Scholar
Spatharis, S., Mouillot, D., Do Chi, T., Danielidis, D. B. & Tsirtsis, G. A niche-based modeling approach to phytoplankton community assembly rules. Oecol. 159(1), 171–180. https://doi.org/10.1007/s00442-008-1178-8 (2009).
Google Scholar
Johansson, F., Englund, G., Brodin, T. & Gardfjell, H. Species abundance models and patterns in dragonfly communities: Effects of fish predators. Oikos 114(1), 27–36 (2006).
Google Scholar
Anderson, B. J. & Mouillot, D. Influence of scale and resolution on niche apportionment rules in saltmeadow vegetation. Aquat. Biol. 1(2), 195–204. https://doi.org/10.3354/ab00017 (2007).
Google Scholar
Tokeshi, M. Power fraction: A new explanation of relative abundance patterns in species-rich assemblages. Oikos 75, 543–550 (1996).
Google Scholar
Seebens, H., Gastner, M. T., Blasius, B. & Courchamp, F. The risk of marine bioinvasion caused by global shipping. Ecol. Lett. 16(6), 782–790. https://doi.org/10.1111/ele.12111 (2013).
Google Scholar
Casal, C. M. V. Global documentation of fish introductions: The growing crisis and recommendations for actions. Biol. Invasions 8, 3–11 (2006).
Google Scholar
Giani, M. et al. Recent changes in the marine ecosystems of the northern Adriatic Sea. Estuar. Coast. Shelf. Sci. 115, 1–13. https://doi.org/10.1016/j.ecss.2012.08.023 (2012).
Google Scholar
Schroeder, K. et al. Rapid response to climate change in a marginal sea. Sci. Rep. 7(1), 1–7. https://doi.org/10.1038/s41598-017-04455-5 (2017).
Google Scholar
Elliott, M. Biological pollutants and biological pollution — an increasing cause for concern. Mar. Pollut. Bull. 46, 275–280 (2003).
Google Scholar
Elton, C. S. The Ecology of Invasions by Animals and Plants (Methuen, London, 1958).
Gubanova, A., Garbazey, O. A., Popova, E. V., Altukhov, D. A. & Mukhanov, V. S. Oithona davisae: Naturalization in the Black Sea, interannual and seasonal dynamics, and effect on the structure of the planktonic copepod community. Oceanol. 59(6), 912–919. https://doi.org/10.31857/S0030-15745961008-1015 (2019).
Google Scholar
Altukhov, D. A., Gubanova, A. D. & Mukhanov, V. S. New invasive copepod Oithona davisae, Ferrari and Orsi, 1984: Seasonal dynamics in Sevastopol Bay and expansion along the Black Sea coasts. Mar. Ecol. 35, 28–34 (2014).
Google Scholar
Svetlichny, L. et al. Adaptive strategy of thermophilic Oithona davisae in the cold Black Sea environment. Turk. J. Fish. Aquat. Sci. 16(1), 077–090. https://doi.org/10.4194/1303-2712-v16_1_09 (2016).
Google Scholar
Hubareva, E. & Svetlichny, L. Salinity and temperature tolerance of alien copepods Acartia tonsa and Oithona davisae in the Black Sea. Rapp. Comm. Int. Mer. Mediterr. 40, 742. https://doi.org/10.13140/2.1.1145.3445 (2013).
Google Scholar
Svetlichny, L., Hubareva, E. & İşi̇ni̇bi̇li̇r, M. ,. Population dynamics of the copepod invader Oithona davisae in the Black Sea. Turk. J. Zool. 42(6), 684–693. https://doi.org/10.3906/zoo-1804-48 (2018).
Google Scholar
Uye, S. I. Replacement of large copepods by small ones with eutrophication of embayments: Cause and consequence. Hydrobiol. 292(293), 513–519. https://doi.org/10.1007/BF00229979 (1994).
Google Scholar
Saiz, E., Griffell, K., Calbet, A. & Isari, S. Feeding rates and prey: Predator size ratios of the nauplii and adult females of the marine cyclopoid copepod Oithona davisae. Limnol. Oceanography 59(6), 2077–2088 (2014).
Google Scholar
Cheng, W., Akiba, T., Omura, T. & Tanaka, Y. On the foraging and feeding ability of Oithona davisae (Crustacea, Copepoda). Hydrobiol. 741(1), 167–176. https://doi.org/10.1007/s10750-014-1867-8 (2014).
Google Scholar
Khanaychenko, A., Mukhanov, V., Aganesova, L., Besiktepe, S. & Gavrilova, N. Grazing and feeding selectivity of Oithona davisae in the Black Sea: Importance of cryptophytes. Turk. J. Fish. Aquat. Sci. 18(8), 937–949. https://doi.org/10.4194/1303-2712-v18_8_02 (2018).
Google Scholar
Uchima, M. Gut content analysis of neritic copepods Acartia omorii and Oithona davisae by a new method. Mar. Ecol. Prog. Ser. 48(1), 93–97 (1988).
Google Scholar
Uchima, M. & Hirano, R. Swimming behavior of the marine copepod Oithona davisae: Internal control and search for environment. Mar. Biol. 99(1), 47–56 (1988).
Google Scholar
Bernardi Aubry, F., Acri, F., Bianchi, F. & Pugnetti, A. Looking for patterns in the phytoplankton community of the Mediterranean microtidal Venice Lagoon: Evidence from ten years of observations. Sci. Mar. 77(1), 47–60. https://doi.org/10.3989/scimar.03638.21A (2013).
Google Scholar
Facca, C. et al. Description of a Multimetric Phytoplankton Index (MPI) for the assessment of transitional waters. Mar. Pollut. Bull. 79(1–2), 145–154. https://doi.org/10.1016/j.marpolbul.2013.12.025 (2014).
Google Scholar
Acri, F., Braga, F. & Bernardi Aubry, F. Long-term dynamics in nutrients, chlorophyll a and water quality parameters in the Lagoon of Venice. Sci. Mar. https://doi.org/10.3989/scimar.05022.30A (2020).
Google Scholar
Bandelj, V. et al. Analysis of multitrophic plankton assemblages in the Lagoon of Venice. Mar. Ecol. Prog. Ser. 368, 23–40. https://doi.org/10.3354/meps07565 (2008).
Google Scholar
Gubanova, A. et al. Species composition of Black Sea marine planktonic copepods. J. Mar. Syst. 135, 44–52. https://doi.org/10.1016/j.jmarsys.2013.12.004 (2014).
Google Scholar
Sacca, A., Guglielmo, L. & Bruni, V. Vertical and temporal microbial community patterns in a meromictic coastal lake influenced by the Straits of Messina upwelling system. Hydrobiology 600(1), 89–104 (2008).
Google Scholar
Tagliapietra, D., Zanon, V., Frangipane, G., Umgiesser, G. & Sigovini, M. Physiographic zoning of the Venetian Lagoon. In Scientific Research and Safeguarding of Venice (ed. Campostrini, P.) 161–164 (2010).
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