The devil is in the details: exploring how functionally distinct round goby is among native fish in the Baltic Sea
Authors/Creators
- 1. Technical University of Denmark, Kongens Lyngby, Denmark
- 2. Swedish University of Agricultural Sciences, Öregrund, Sweden
Description
Understanding the characteristics and conditions that make non-indigenous species (NIS) successful at establishing in recipient communities is a key in determining their potential impacts on native species, as well as to improve management actions such as prevention of future invasions. The round goby (Neogobius melanostomus) is one of the most widespread non-indigenous fish species in the Northern Hemisphere, including the coastal zones of the Baltic Sea. The impacts of round goby in the Baltic Sea are pronounced and multifaceted, yet our knowledge regarding the underlying assembly processes determining its establishment is limited. To overcome this knowledge gap, we applied a trait-based approach to assess the degree of niche overlap and functional (trait) similarity between round goby and native fish species in coastal areas from the Baltic Sea, based on the functional distinctiveness metric. Our results show that round goby is generally quite similar (or not dissimilar) to the native fish of the regional species pool, at least in terms of its overall trait composition. Conversely, round goby demonstrates pronounced differences compared to the native community in its display of parental care and territorial behaviour. Such differences in individual traits could play an important role in round goby's invasion success in the Baltic Sea, including its interactions with native species (e.g. competition). Our results and their potential implications may be highly relevant for conservation and management if integrated within existing risk assessment tools for biological invasions in order to prioritise and enhance the effectiveness of preventative actions towards the expansion of round goby.
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References
- Ah-King M, Kvarnemo C, Tullberg BS (2005) The influence of territoriality and mating system on the evolution of male care: A phylogenetic study on fish. Journal of Evolutionary Biology 18(2): 371–382. https://doi.org/10.1111/j.1420-9101.2004.00823.x
- Almqvist G, Strandmark AK, Appelberg M (2010) Has the invasive round goby caused new links in Baltic food webs? Environmental Biology of Fishes 89(1): 79–93. https://doi.org/10.1007/s10641-010-9692-z
- Anton A, Geraldi NR, Lovelock CE, Apostolaki ET, Bennett S, Cebrian J, Krause-Jensen D, Marbà N, Martinetto P, Pandolfi JM, Santana-Garcon J, Duarte CM (2019) Global ecological impacts of marine exotic species. Nature Ecology & Evolution 3(5): 787–800. https://doi.org/10.1038/s41559-019-0851-0
- Azour F, van Deurs M, Behrens J, Carl H, Hüssy K, Greisen K, Ebert R, Møller P (2015) Invasion rate and population characteristics of the round goby Neogobius melanostomus: Effects of density and invasion history. Aquatic Biology 24(1): 41–52. https://doi.org/10.3354/ab00634
- Backström T, Winkelmann C (2022) Invasive round goby shows higher sensitivity to salinization than native European perch. NeoBiota 75: 23–38. https://doi.org/10.3897/neobiota.75.86528
- Balshine S, Verma A, Chant V, Theysmeyer T (2005) Competitive Interactions between Round Gobies and Logperch. Journal of Great Lakes Research 31(1): 68–77. https://doi.org/10.1016/S0380-1330(05)70238-0
- Bax N, Williamson A, Aguero M, Gonzalez E, Geeves W (2003) Marine invasive alien species: A threat to global biodiversity. Marine Policy 27(4): 313–323. https://doi.org/10.1016/S0308-597X(03)00041-1
- Behrens JW, van Deurs M, Christensen EAF (2017) Evaluating dispersal potential of an invasive fish by the use of aerobic scope and osmoregulation capacity. PLoS ONE 12(4): e0176038. https://doi.org/10.1371/journal.pone.0176038
- Behrens JW, Ryberg MP, Einberg H, Eschbaum R, Florin A-B, Grygiel W, Herrmann JP, Huwer B, Hüssy K, Knospina E, Nõomaa K, Oesterwind D, Polte P, Smoliński S, Ustups D, van Deurs M, Ojaveer H (2022) Seasonal depth distribution and thermal experience of the non-indigenous round goby Neogobius melanostomus in the Baltic Sea: Implications to key trophic relations. Biological Invasions 24(2): 527–541. https://doi.org/10.1007/s10530-021-02662-w
- Belmaker J, Parravicini V, Kulbicki M (2013) Ecological traits and environmental affinity explain Red Sea fish introduction into the Mediterranean. Global Change Biology 19(5): 1373–1382. https://doi.org/10.1111/gcb.12132
- de Bello F, Botta-Dukát Z, Lepš J, Fibich P (2021) Towards a more balanced combination of multiple traits when computing functional differences between species. Methods in Ecology and Evolution 12: 443–448. https://doi.org/10.1111/2041-210X.13537
- Beukhof E, Dencker TS, Pecuchet L, Lindegren M (2019a) Spatio-temporal variation in marine fish traits reveals community-wide responses to environmental change. Marine Ecology Progress Series 610: 205–222. https://doi.org/10.3354/meps12826
- Beukhof E, Frelat R, Pecuchet L, Maureaud A, Dencker TS, Sólmundsson J, Punzón A, Primicerio R, Hidalgo M, Möllmann C, Lindegren M (2019b) Marine fish traits follow fast-slow continuum across oceans. Scientific Reports 9(1): 17878. https://doi.org/10.1038/s41598-019-53998-2
- Blackburn TM, Pyšek P, Bacher S, Carlton JT, Duncan RP, Jarošík V, Wilson JRU, Richardson DM (2011) A proposed unified framework for biological invasions. Trends in Ecology & Evolution 26(7): 333–339. https://doi.org/10.1016/j.tree.2011.03.023
- Breiman L (2001) Random Forests. Machine Learning 45: 5–32. https://doi.org/10.1023/A:1010933404324
- Cadotte MW, Campbell SE, Li S, Sodhi DS, Mandrak NE (2018) Preadaptation and naturalization of nonnative species: Darwin's two fundamental insights into species invasion. Annual Review of Plant Biology 69(1): 661–684. https://doi.org/10.1146/annurev-arplant-042817-040339
- Chapple DG, Simmonds SM, Wong BBM (2012) Can behavioral and personality traits influence the success of unintentional species introductions? Trends in Ecology & Evolution 27(1): 57–64. https://doi.org/10.1016/j.tree.2011.09.010
- Christensen EAF, Norin T, Tabak I, van Deurs M, Behrens JW (2021) Effects of temperature on physiological performance and behavioral thermoregulation in an invasive fish, the round goby. Journal of Experimental Biology 224 (1): jeb.237669. https://doi.org/10.1242/jeb.237669
- Cleland EE (2011) Trait divergence and the ecosystem impacts of invading species. The New Phytologist 189(3): 649–652. https://doi.org/10.1111/j.1469-8137.2010.03607.x
- Coulon N, Lindegren M, Goberville E, Toussaint A, Receveur A, Auber A (2023) Threatened fish species in the Northeast Atlantic are functionally rare. Global Ecology and Biogeography 32(10): 1827–1845. https://doi.org/10.1111/geb.13731
- Dencker TS, Pecuchet L, Beukhof E, Richardson K, Payne MR, Lindegren M (2017) Temporal and spatial differences between taxonomic and trait biodiversity in a large marine ecosystem: Causes and consequences. PLoS ONE 12(12): e0189731. https://doi.org/10.1371/journal.pone.0189731
- Dubs DOL, Corkum LD (1996) Behavioral Interactions Between Round Gobies (Neogobius melanostomus) and Mottled Sculpins (Cottus bairdi). Journal of Great Lakes Research 22(4): 838–844. https://doi.org/10.1016/S0380-1330(96)71005-5
- El-Barougy RF, Elgamal I, Rohr RP, Probert AF, Khedr AA, Bacher S (2020) Functional similarity and dissimilarity facilitate alien plant invasiveness along biotic and abiotic gradients in an arid protected area. Biological Invasions 22(6): 1997–2016. https://doi.org/10.1007/s10530-020-02235-3
- Ericsson P, Persson A, Behrens JW, Brodin T, Hirsch PE, Sundelin A, van Deurs M, von Friesen LW, Nilsson PA (2021) Personality-dependent inter- and intraspecific foraging competition in the invasive round goby, Neogobius melanostomus. Journal of Fish Biology 98(5): 1234–1241. https://doi.org/10.1111/jfb.14652
- Erlandsson M, Fredriksson R, Bergström U (2021) Kartering av uppväxtområden för fisk i grunda områden i Östersjön. Aqua reports. https://res.slu.se/id/publ/113831 [April 25, 2023]
- Escoriza D, Ruhí A (2016) Functional distance to recipient communities may favour invasiveness: Insights from two invasive frogs. Diversity & Distributions 22(5): 519–533. https://doi.org/10.1111/ddi.12421
- Ferrari SLP, Cribari-Neto F (2004) Beta regression for modelling rates and proportions. Journal of Applied Statistics 31(7): 799–815. https://doi.org/10.1080/0266476042000214501
- Gallien L, Carboni M (2017) The community ecology of invasive species: Where are we and what's next? Ecography 40(2): 335–352. https://doi.org/10.1111/ecog.02446
- Gallien L, Carboni M, Münkemüller T (2014) Identifying the signal of environmental filtering and competition in invasion patterns - a contest of approaches from community ecology. Methods in Ecology and Evolution 5(10): 1002–1011. https://doi.org/10.1111/2041-210X.12257
- Gallien L, Mazel F, Lavergne S, Renaud J, Douzet R, Thuiller W (2015) Contrasting the effects of environment, dispersal and biotic interactions to explain the distribution of invasive plants in alpine communities. Biological Invasions 17(5): 1407–1423. https://doi.org/10.1007/s10530-014-0803-1
- Geraldi NR, Anton A, Santana-Garcon J, Bennett S, Marbà N, Lovelock CE, Apostolaki ET, Cebrian J, Krause-Jensen D, Martinetto P, Pandolfi JM, Duarte CM (2020) Ecological effects of non-native species in marine ecosystems relate to co-occurring anthropogenic pressures. Global Change Biology 26(3): 1248–1258. https://doi.org/10.1111/gcb.14930
- Gower JC (1971) 27 A general coefficient of similarity and some of its properties. Biometrics 27(4): 857–871. https://doi.org/10.2307/2528823
- Grenié M, Denelle P, Tucker CM, Munoz F, Violle C (2017) funrar: An R package to characterize functional rarity. Diversity & Distributions 23(12): 1365–1371. https://doi.org/10.1111/ddi.12629
- HELCOM (2018) Status of coastal fish communities in the Baltic Sea during 2011–2016 - the third thematic assessment.
- HELCOM (2019) Guidelines for coastal fish monitoring. https://helcom.fi/wp-content/uploads/2020/01/HELCOM-Guidelines-for-coastal-fish-monitoring-2019.pdf [June 21, 2023]
- HELCOM (2023) Thematic assessment of hazardous substances, marine litter, underwater noise and non-indigenous species 2016–2021. Helsinki Commission (HELCOM). 190.
- Hess S, Fischer S, Taborsky B (2016) Territorial aggression reduces vigilance but increases aggression towards predators in a cooperatively breeding fish. Animal Behaviour 113: 229–235. https://doi.org/10.1016/j.anbehav.2016.01.008
- Hillebrand H, Bennett DM, Cadotte MW (2008) Consequences of dominance: A review of evenness effects on local and regional ecosystem processes. Ecology 89(6): 1510–1520. https://doi.org/10.1890/07-1053.1
- Hirsch PE, N'Guyen A, Adrian-Kalchhauser I, Burkhardt-Holm P (2016) What do we really know about the impacts of one of the 100 worst invaders in Europe? A reality check. Ambio 45(3): 267–279. https://doi.org/10.1007/s13280-015-0718-9
- Huntingford FA (1976) The relationship between anti-predator behaviour and aggression among conspecifics in the three-spined stickleback, Gasterosteus Aculeatus. Animal Behaviour 24(2): 245–260. https://doi.org/10.1016/S0003-3472(76)80034-6
- ICES (2022a) Baltic Sea Ecoregion – Ecosystem overview. ICES Advice: Ecosystem Overviews, 24 pp. https://doi.org/10.17895/ICES.ADVICE.21725438
- ICES (2022b) Workshop on stickleback and round goby in the Baltic Sea (WKSTARGATE). ICES Scientific Reports. [report] https://doi.org/10.17895/ices.pub.21345291.v2
- IPBES (2023) Summary for Policymakers of the Thematic Assessment Report on Invasive Alien Species and their Control of the Intergovernmental Science-Policy Platform on Biodiversity and Ecosystem Services. IPBES secretariat. https://doi.org/10.5281/zenodo.3553579
- Jones JC, Reynolds JD (1999) Costs of egg ventilation for male common gobies breeding in conditions of low dissolved oxygen. Animal Behaviour 57(1): 181–188. https://doi.org/10.1006/anbe.1998.0939
- Jude DJ (1997) Round gobies: Cyberfish of the third millennium. Great Lakes Research Review 3: 27–34.
- Karlson AML, Almqvist G, Skóra KE, Appelberg M (2007) Indications of competition between non-indigenous round goby and native flounder in the Baltic Sea. ICES Journal of Marine Science 64(3): 479–486. https://doi.org/10.1093/icesjms/fsl049
- Katsanevakis S, Wallentinus I, Zenetos A, Leppäkoski E, Çinar ME, Oztürk B, Grabowski M, Golani D, Cardoso AC (2014) Impacts of invasive alien marine species on ecosystem services and biodiversity: A pan-European review. Aquatic Invasions 9(4): 391–423. https://doi.org/10.3391/ai.2014.9.4.01
- Kornis MS, Mercado-Silva N, Vander Zanden MJ (2012) Twenty years of invasion: A review of round goby Neogobius melanostomus biology, spread and ecological implications. Journal of Fish Biology 80(2): 235–285. https://doi.org/10.1111/j.1095-8649.2011.03157.x
- Kotta J, Nurkse K, Puntila R, Ojaveer H (2016) Shipping and natural environmental conditions determine the distribution of the invasive non-indigenous round goby Neogobius melanostomus in a regional sea. Estuarine, Coastal and Shelf Science 169: 15–24. https://doi.org/10.1016/j.ecss.2015.11.029
- Kraft NJB, Adler PB, Godoy O, James EC, Fuller S, Levine JM (2015) Community assembly, coexistence and the environmental filtering metaphor. Functional Ecology 29: 592–599. https://doi.org/10.1111/1365-2435.12345
- Kruze E, Avotins A, Rozenfelde L, Putnis I, Sics I, Briekmane L, Olsson J (2023) The population development of the invasive round goby Neogobius melanostomus in latvian waters of the Baltic Sea. Fishes 8(6): 305. https://doi.org/10.3390/fishes8060305
- Leppäkoski E, Gollasch S, Gruszka P, Ojaveer H, Olenin S, Panov V (2002) The Baltic - A sea of invaders. Canadian Journal of Fisheries and Aquatic Sciences 59(7): 1175–1188. https://doi.org/10.1139/f02-089
- Liaw A, Wiener M (2002) Classification and Regression by randomForest. R News: 2.
- Lindegren M, Thomas MK, Jónasdóttir SH, Nielsen TG, Munk P (2020) Environmental niche separation promotes coexistence among ecologically similar zooplankton species—North Sea copepods as a case study. Limnology and Oceanography 65(3): 545–556. https://doi.org/10.1002/lno.11322
- Lindegren M, Gabellini AP, Munk P, Edelvang K, Hansen FT (2022) Identifying key processes and drivers affecting the presence of non-indigenous marine species in coastal waters. Biological Invasions 24(9): 2835–2850. https://doi.org/10.1007/s10530-022-02802-w
- Litchman E, Klausmeier CA (2008) Trait-based community ecology of phytoplankton. Annual Review of Ecology, Evolution, and Systematics 39(1): 615–639. https://doi.org/10.1146/annurev.ecolsys.39.110707.173549
- Litchman E, Ohman MD, Kiørboe T (2013) Trait-based approaches to zooplankton communities. Journal of Plankton Research 35(3): 473–484. https://doi.org/10.1093/plankt/fbt019
- Lodge DM, Simonin PW, Burgiel SW, Keller RP, Bossenbroek JM, Jerde CL, Kramer AM, Rutherford ES, Barnes MA, Wittmann ME, Chadderton WL, Apriesnig JL, Beletsky D, Cooke RM, Drake JM, Egan SP, Finnoff DC, Gantz CA, Grey EK, Hoff MH, Howeth JG, Jensen RA, Larson ER, Mandrak NE, Mason DM, Martinez FA, Newcomb TJ, Rothlisberger JD, Tucker AJ, Warziniack TW, Zhang H (2016) Risk Analysis and Bioeconomics of Invasive Species to Inform Policy and Management. Annual Review of Environment and Resources 41(1): 453–488. https://doi.org/10.1146/annurev-environ-110615-085532
- Matern S, Herrmann J-P, Temming A (2021) Differences in diet compositions and feeding strategies of invasive round goby Neogobius melanostomus and native black goby Gobius niger in the Western Baltic Sea. Aquatic Invasions 16(2): 314–328. https://doi.org/10.3391/ai.2021.16.2.07
- Mathakutha R, Steyn C, Roux PC le, Blom IJ, Chown SL, Daru BH, Ripley BS, Louw A, Greve M (2019) Invasive species differ in key functional traits from native and non‐invasive alien plant species. Journal of Vegetation Science 30: 994–1006. https://doi.org/10.1111/jvs.12772
- Meunier B, Yavno S, Ahmed S, Corkum LD (2009) First documentation of spawning and nest guarding in the laboratory by the invasive fish, the round goby (Neogobius melanostomus). Journal of Great Lakes Research 35(4): 608–612. https://doi.org/10.1016/j.jglr.2009.08.012
- Millennium Ecosystem Assessment (Program) [Ed.] (2005) Ecosystems and human well-being: wetlands and water synthesis: a report of the Millennium Ecosystem Assessment. World Resources Institute, Washington, DC, 68 pp.
- Momigliano P, Denys GPJ, Jokinen H, Merilä J (2018) Platichthys solemdali sp. nov. (Actinopterygii, Pleuronectiformes): A New Flounder Species From the Baltic Sea. Frontiers in Marine Science 5: 225. https://doi.org/10.3389/fmars.2018.00225
- Montanyès M, Weigel B, Lindegren M (2023) Community assembly processes and drivers shaping marine fish community structure in the North Sea. Ecography 2023(10): e06642. https://doi.org/10.1111/ecog.06642
- Nõomaa K, Kotta J, Szava-Kovats R, Herkül K, Eschbaum R, Vetemaa M (2022) Novel fish predator causes sustained changes in its prey populations. Frontiers in Marine Science 9: 849878. https://doi.org/10.3389/fmars.2022.849878
- Ojaveer H, Jaanus A, Mackenzie BR, Martin G, Olenin S, Radziejewska T, Telesh I, Zettler ML, Zaiko A (2010) Status of biodiversity in the Baltic sea. PLoS ONE 5(9): 1–19. https://doi.org/10.1371/journal.pone.0012467
- Ojaveer H, Olenin S, Narščius A, Florin A-B, Ezhova E, Gollasch S, Jensen KR, Lehtiniemi M, Minchin D, Normant-Saremba M, Strāke S (2017) Dynamics of biological invasions and pathways over time: A case study of a temperate coastal sea. Biological Invasions 19(3): 799–813. https://doi.org/10.1007/s10530-016-1316-x
- Olenin S, Gollasch S, Lehtiniemi M, Sapota M, Zaiko A (2017) Biological invasions. In: Snoeijs-Leijonmalm P, Schubert H, Radziejewska T (Eds) Biological Oceanography of the Baltic Sea. Springer Netherlands, Dordrecht, 193–232. https://doi.org/10.1007/978-94-007-0668-2_5
- Olsson J (2019) Past and current trends of coastal predatory fish in the Baltic Sea with a focus on perch, pike, and pikeperch. Fishes 4(1): 7. https://doi.org/10.3390/fishes4010007
- Olsson J, Bergström L, Gårdmark A (2012) Abiotic drivers of coastal fish community change during four decades in the Baltic Sea. ICES Journal of Marine Science 69(6): 961–970. https://doi.org/10.1093/icesjms/fss072
- Paavola M, Olenin S, Leppäkoski E (2005) Are invasive species most successful in habitats of low native species richness across European brackish water seas? Estuarine, Coastal and Shelf Science 64(4): 738–750. https://doi.org/10.1016/j.ecss.2005.03.021
- Pavoine S, Vallet J, Dufour AB, Gachet S, Daniel H (2009) On the challenge of treating various types of variables: Application for improving the measurement of functional diversity. Oikos 118(3): 391–402. https://doi.org/10.1111/j.1600-0706.2008.16668.x
- Pecuchet L, Törnroos A, Lindegren M (2016) Patterns and drivers of fish community assembly in a large marine ecosystem. Marine Ecology Progress Series 546: 239–248. https://doi.org/10.3354/meps11613
- Pecuchet L, Lindegren M, Hidalgo M, Delgado M, Esteban A, Fock HO, Gil de Sola L, Punzón A, Sólmundsson J, Payne MR (2017) From traits to life-history strategies: Deconstructing fish community composition across European seas. Global Ecology and Biogeography 26(7): 812–822. https://doi.org/10.1111/geb.12587
- Puntila-Dodd R, Florin A-B, Naddafi R, Behrens JW, Kotta J, Smolinski S, Wozniczka A (2018) Abundance and distribution of round goby (Neogobius melanostomus).
- Puntila-Dodd R, Bekkevold D, Behrens JW (2021) Estimating salinity stress via hsp70 expression in the invasive round goby (Neogobius melanostomus): Implications for further range expansion. Hydrobiologia 848(2): 421–429. https://doi.org/10.1007/s10750-020-04449-x
- Quell F, Schratzberger M, Beauchard O, Bruggeman J, Webb T (2021) Biological trait profiles discriminate between native and non-indigenous marine invertebrates. Aquatic Invasions 16(4): 571–600. https://doi.org/10.3391/ai.2021.16.4.01
- R Core Team (2021) R: A language and environment for statistical computing. R Foundation for Statistical Computing, Vienna, Austria. [URL] http://www. R-project.org
- Reusch TBH, Dierking J, Andersson HC, Bonsdorff E, Carstensen J, Casini M, Czajkowski M, Hasler B, Hinsby K, Hyytiäinen K, Johannesson K, Jomaa S, Jormalainen V, Kuosa H, Kurland S, Laikre L, MacKenzie BR, Margonski P, Melzner F, Oesterwind D, Ojaveer H, Refsgaard JC, Sandström A, Schwarz G, Tonderski K, Winder M, Zandersen M (2018) The Baltic Sea as a time machine for the future coastal ocean. Science Advances 4(5): eaar8195. https://doi.org/10.1126/sciadv.aar8195
- Ricciardi A, Hoopes MF, Marchetti MP, Lockwood JL (2013) Progress toward understanding the ecological impacts of nonnative species. Ecological Monographs 83(3): 263–282. https://doi.org/10.1890/13-0183.1
- Ricotta C, Godefroid S, Rocchini D (2010) Patterns of native and exotic species richness in the urban flora of Brussels: rejecting the 'rich get richer' model. Biological Invasions 12: 233–240. https://doi.org/10.1007/s10530-009-9445-0
- Rilov G, Crooks JA (2009) 204 Biological Invasions in Marine Ecosystems. https://doi.org/10.1007/978-3-540-79236-9
- Schwartzbach A, Behrens JW, Svendsen JC, Nielsen P, van Deurs M (2020) Size-dependent predation of round goby Neogobius melanostomus on blue mussels Mytilus edulis. Fisheries Management and Ecology 27(3): 215–218. https://doi.org/10.1111/fme.12400
- Skabeikis A, Morkūnė R, Bacevičius E, Lesutienė J, Morkūnas J, Poškienė A, Šiaulys A (2019) Effect of round goby (Neogobius melanostomus) invasion on blue mussel (Mytilus edulis trossulus) population and winter diet of the long-tailed duck (Clangula hyemalis). Biological Invasions 21(3): 911–923. https://doi.org/10.1007/s10530-018-1869-y
- Skóra KE, Stolarski J (1993) Neogobius melanostomus (Pallas 1811) a new immigrant species in Baltic Sea. Proceedings of the Second International Estuary Symposium held in Gdańsk, 18–22.
- Steger J, Bošnjak M, Belmaker J, Galil BS, Zuschin M, Albano PG (2022) Non-indigenous molluscs in the Eastern Mediterranean have distinct traits and cannot replace historic ecosystem functioning. Global Ecology and Biogeography 31(1): 89–102. https://doi.org/10.1111/geb.13415
- Törnroos A, Bonsdorff E (2012) Developing the multitrait concept for functional diversity: Lessons from a system rich in functions but poor in species. Ecological Applications 22(8): 2221–2236. https://doi.org/10.1890/11-2042.1
- Törnroos A, Bonsdorff E, Bremner J, Blomqvist M, Josefson AB, Garcia C, Warzocha J (2015) Marine benthic ecological functioning over decreasing taxonomic richness. Journal of Sea Research 98: 49–56. https://doi.org/10.1016/j.seares.2014.04.010
- Törnroos A, Pecuchet L, Olsson J, Gårdmark A, Blomqvist M, Lindegren M, Bonsdorff E (2019) Four decades of functional community change reveals gradual trends and low interlinkage across trophic groups in a large marine ecosystem. Global Change Biology 25(4): 1235–1246. https://doi.org/10.1111/gcb.14552
- van Deurs M, Moran NP, Schreiber Plet-Hansen K, Dinesen GE, Azour F, Carl H, Møller PR, Behrens JW (2021) Impacts of the invasive round goby (Neogobius melanostomus) on benthic invertebrate fauna: A case study from the Baltic Sea. NeoBiota 68: 19–30. https://doi.org/10.3897/neobiota.68.67340
- Viana IG, Siriwardane-de Zoysa R, Willette DA, Gillis LG (2019) Exploring how non-native seagrass species could provide essential ecosystems services: A perspective on the highly invasive seagrass Halophila stipulacea in the Caribbean Sea. Biological Invasions 21: 1461–1472. https://doi.org/10.1007/s10530-019-01924-y
- Violle C, Navas M-L, Vile D, Kazakou E, Fortunel C, Hummel I, Garnier E (2007) Let the concept of trait be functional! Oikos 116(5): 882–892. https://doi.org/10.1111/j.0030-1299.2007.15559.x
- Violle C, Thuiller W, Mouquet N, Munoz F, Kraft NJB, Cadotte MW, Livingstone SW, Mouillot D (2017) Functional rarity: The ecology of outliers. Trends in Ecology & Evolution 32(5): 356–367. https://doi.org/10.1016/j.tree.2017.02.002
- Vitousek PM, D'Antonio CM, Loope LL, Westbrooks R (1996) Biological invasions as Global Environmental Change.
- Vivó-Pons A, Alós J, Tomas F (2020) Invasion by an ecosystem engineer shifts the abundance and distribution of fish but does not decrease diversity. Marine Pollution Bulletin 160: 111586. https://doi.org/10.1016/j.marpolbul.2020.111586
- Vivó-Pons A, Blomqvist M, Törnroos A, Lindegren M (2023) A trait-based approach to assess niche overlap and functional distinctiveness between non-indigenous and native species. Ecology Letters 26(11): 1911–1925. https://doi.org/10.1111/ele.14315
- Voipio A (1981) 30 The Baltic Sea. Elsevier B. V., Helsinki, 418 pp.
- Wallin-Kihlberg I, Florin A-B, Lundström K, Östman Ö (2023) Detection of multiple fish species in the diet of the invasive round goby reveals new trophic interactions in the Baltic Sea. Aquatic Invasions 18(2): 141–162. https://doi.org/10.3391/ai.2023.18.2.104960
- Wickett RG, Corkum LD (1998) Nest defense by the non-indigenous fish, the round goby, Neogobius melanostomus (Gobiidae), on a shipwreck in western Lake Erie. Canadian Field Naturalist 112: 653–656.
- Wood SN (2017) Generalized Additive Models: An Introduction with R, Second Edition Generalized additive models: An introduction with R, 2nd edn. CRC Press, 476 pp. https://doi.org/10.1201/9781315370279
- Xu M, Li S, Dick JTA, Gu D, Fang M, Yang Y, Hu Y, Mu X (2022) Exotic fishes that are phylogenetically close but functionally distant to native fishes are more likely to establish. Global Change Biology 28(19): 5683–5694. https://doi.org/10.1111/gcb.16360
- Zobel M (1997) The relative role of species pools in determining plant species richness: An alternative explanation of species coexistence? Trends in Ecology & Evolution 12(7): 266–269. https://doi.org/10.1016/S0169-5347(97)01096-3