Ocean current connectivity propelling the secondary spread of a marine invasive comb jelly across western Eurasia
Aim: Invasive species are of increasing global concern. Nevertheless, the mechanisms driving further distribution after the initial establishment of non‐native species remain largely unresolved, especially in marine systems. Ocean currents can be a major driver governing range occupancy, but this ha...
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creator | Jaspers, Cornelia Huwer, Bastian Antajan, Elvire Hosia, Aino Hinrichsen, Hans-Harald Biastoch, Arne Angel, Dror Asmus, Ragnhild Augustin, Christina Bagheri, Siamak Beggs, Steven E Balsby, Thorsten J.S Boersma, Maarten Bonnet, Delphine Christensen, Jens T Dänhardt, Andreas Delpy, Floriane Falkenhaug, Tone Finenko, Galina Fleming, Nicholas E.C Fuentes, Veronica Galil, Bella S Gittenberger, Arjan Griffin, Donal C Haslob, Holger Javidpour, Jamileh Kamburska, Lyudmila Kube, Sandra Langenberg, Victor Lehtiniemi, Maiju Lombard, Fabien Malzahn, Arne Marambio, Macarena Mihneva, Veselina Møller, Lene Friis Niermann, Ulrich Okyar, Melek Isinibilir Ôzdemir, Zekiye Birinci Pitois, Sophie Reusch, Thorsten B.H Robbens, Johan Stefanova, Kremena Thibault, Delphine van der Veer, Henk W Vansteenbrugge, Lies van Walraven, Lodewijk Woźniczka, Adam |
description | Aim: Invasive species are of increasing global concern. Nevertheless, the mechanisms driving further distribution after the initial establishment of non‐native species remain largely unresolved, especially in marine systems. Ocean currents can be a major driver governing range occupancy, but this has not been accounted for in most invasion ecology studies so far. We investigate how well initial establishment areas are interconnected to later occupancy regions to test for the potential role of ocean currents driving secondary spread dynamics in order to infer invasion corridors and the source–sink dynamics of a non‐native holoplanktonic biological probe species on a continental scale. Location: Western Eurasia. Time period: 1980s–2016. Major taxa studied: ‘Comb jelly’ Mnemiopsis leidyi. Methods: Based on 12,400 geo‐referenced occurrence data, we reconstruct the invasion history of M. leidyi in western Eurasia. We model ocean currents and calculate their stability to match the temporal and spatial spread dynamics with large‐scale connectivity patterns via ocean currents. Additionally, genetic markers are used to test the predicted connectivity between subpopulations. Results: Ocean currents can explain secondary spread dynamics, matching observed range expansions and the timing of first occurrence of our holoplanktonic non‐native biological probe species, leading to invasion corridors in western Eurasia. In northern Europe, regional extinctions after cold winters were followed by rapid recolonizations at a speed of up to 2,000 km per season. Source areas hosting year‐round populations in highly interconnected regions can re‐seed genotypes over large distances after local extinctions. Main conclusions: Although the release of ballast water from container ships may contribute to the dispersal of non‐native species, our results highlight the importance of ocean currents driving secondary spread dynamics. Highly interconnected areas hosting invasive species are crucial for secondary spread dynamics on a continental scale. Invasion risk assessments should consider large‐scale connectivity patterns and the potential source regions of non‐native marine species. |
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Nevertheless, the mechanisms driving further distribution after the initial establishment of non‐native species remain largely unresolved, especially in marine systems. Ocean currents can be a major driver governing range occupancy, but this has not been accounted for in most invasion ecology studies so far. We investigate how well initial establishment areas are interconnected to later occupancy regions to test for the potential role of ocean currents driving secondary spread dynamics in order to infer invasion corridors and the source–sink dynamics of a non‐native holoplanktonic biological probe species on a continental scale. Location: Western Eurasia. Time period: 1980s–2016. Major taxa studied: ‘Comb jelly’ Mnemiopsis leidyi. Methods: Based on 12,400 geo‐referenced occurrence data, we reconstruct the invasion history of M. leidyi in western Eurasia. We model ocean currents and calculate their stability to match the temporal and spatial spread dynamics with large‐scale connectivity patterns via ocean currents. Additionally, genetic markers are used to test the predicted connectivity between subpopulations. Results: Ocean currents can explain secondary spread dynamics, matching observed range expansions and the timing of first occurrence of our holoplanktonic non‐native biological probe species, leading to invasion corridors in western Eurasia. In northern Europe, regional extinctions after cold winters were followed by rapid recolonizations at a speed of up to 2,000 km per season. Source areas hosting year‐round populations in highly interconnected regions can re‐seed genotypes over large distances after local extinctions. Main conclusions: Although the release of ballast water from container ships may contribute to the dispersal of non‐native species, our results highlight the importance of ocean currents driving secondary spread dynamics. Highly interconnected areas hosting invasive species are crucial for secondary spread dynamics on a continental scale. Invasion risk assessments should consider large‐scale connectivity patterns and the potential source regions of non‐native marine species.</description><language>eng</language><publisher>Wiley</publisher><subject>biological invasions ; gelatinous zooplankton ; invasion corridors ; invasive species ; jellyfish ; marine connectivity ; Mnemiopsis leidyi ; range expansion ; source populations ; source–sink dynamics</subject><creationdate>2018</creationdate><rights>info:eu-repo/semantics/openAccess</rights><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>230,780,885,26567</link.rule.ids><linktorsrc>$$Uhttp://hdl.handle.net/1956/19124$$EView_record_in_NORA$$FView_record_in_$$GNORA$$Hfree_for_read</linktorsrc></links><search><creatorcontrib>Jaspers, Cornelia</creatorcontrib><creatorcontrib>Huwer, Bastian</creatorcontrib><creatorcontrib>Antajan, Elvire</creatorcontrib><creatorcontrib>Hosia, Aino</creatorcontrib><creatorcontrib>Hinrichsen, Hans-Harald</creatorcontrib><creatorcontrib>Biastoch, Arne</creatorcontrib><creatorcontrib>Angel, Dror</creatorcontrib><creatorcontrib>Asmus, Ragnhild</creatorcontrib><creatorcontrib>Augustin, Christina</creatorcontrib><creatorcontrib>Bagheri, Siamak</creatorcontrib><creatorcontrib>Beggs, Steven E</creatorcontrib><creatorcontrib>Balsby, Thorsten J.S</creatorcontrib><creatorcontrib>Boersma, Maarten</creatorcontrib><creatorcontrib>Bonnet, Delphine</creatorcontrib><creatorcontrib>Christensen, Jens T</creatorcontrib><creatorcontrib>Dänhardt, Andreas</creatorcontrib><creatorcontrib>Delpy, Floriane</creatorcontrib><creatorcontrib>Falkenhaug, Tone</creatorcontrib><creatorcontrib>Finenko, Galina</creatorcontrib><creatorcontrib>Fleming, Nicholas E.C</creatorcontrib><creatorcontrib>Fuentes, Veronica</creatorcontrib><creatorcontrib>Galil, Bella S</creatorcontrib><creatorcontrib>Gittenberger, Arjan</creatorcontrib><creatorcontrib>Griffin, Donal C</creatorcontrib><creatorcontrib>Haslob, Holger</creatorcontrib><creatorcontrib>Javidpour, Jamileh</creatorcontrib><creatorcontrib>Kamburska, Lyudmila</creatorcontrib><creatorcontrib>Kube, Sandra</creatorcontrib><creatorcontrib>Langenberg, Victor</creatorcontrib><creatorcontrib>Lehtiniemi, Maiju</creatorcontrib><creatorcontrib>Lombard, Fabien</creatorcontrib><creatorcontrib>Malzahn, Arne</creatorcontrib><creatorcontrib>Marambio, Macarena</creatorcontrib><creatorcontrib>Mihneva, Veselina</creatorcontrib><creatorcontrib>Møller, Lene Friis</creatorcontrib><creatorcontrib>Niermann, Ulrich</creatorcontrib><creatorcontrib>Okyar, Melek Isinibilir</creatorcontrib><creatorcontrib>Ôzdemir, Zekiye Birinci</creatorcontrib><creatorcontrib>Pitois, Sophie</creatorcontrib><creatorcontrib>Reusch, Thorsten B.H</creatorcontrib><creatorcontrib>Robbens, Johan</creatorcontrib><creatorcontrib>Stefanova, Kremena</creatorcontrib><creatorcontrib>Thibault, Delphine</creatorcontrib><creatorcontrib>van der Veer, Henk W</creatorcontrib><creatorcontrib>Vansteenbrugge, Lies</creatorcontrib><creatorcontrib>van Walraven, Lodewijk</creatorcontrib><creatorcontrib>Woźniczka, Adam</creatorcontrib><title>Ocean current connectivity propelling the secondary spread of a marine invasive comb jelly across western Eurasia</title><description>Aim: Invasive species are of increasing global concern. Nevertheless, the mechanisms driving further distribution after the initial establishment of non‐native species remain largely unresolved, especially in marine systems. Ocean currents can be a major driver governing range occupancy, but this has not been accounted for in most invasion ecology studies so far. We investigate how well initial establishment areas are interconnected to later occupancy regions to test for the potential role of ocean currents driving secondary spread dynamics in order to infer invasion corridors and the source–sink dynamics of a non‐native holoplanktonic biological probe species on a continental scale. Location: Western Eurasia. Time period: 1980s–2016. Major taxa studied: ‘Comb jelly’ Mnemiopsis leidyi. Methods: Based on 12,400 geo‐referenced occurrence data, we reconstruct the invasion history of M. leidyi in western Eurasia. We model ocean currents and calculate their stability to match the temporal and spatial spread dynamics with large‐scale connectivity patterns via ocean currents. Additionally, genetic markers are used to test the predicted connectivity between subpopulations. Results: Ocean currents can explain secondary spread dynamics, matching observed range expansions and the timing of first occurrence of our holoplanktonic non‐native biological probe species, leading to invasion corridors in western Eurasia. In northern Europe, regional extinctions after cold winters were followed by rapid recolonizations at a speed of up to 2,000 km per season. Source areas hosting year‐round populations in highly interconnected regions can re‐seed genotypes over large distances after local extinctions. Main conclusions: Although the release of ballast water from container ships may contribute to the dispersal of non‐native species, our results highlight the importance of ocean currents driving secondary spread dynamics. Highly interconnected areas hosting invasive species are crucial for secondary spread dynamics on a continental scale. Invasion risk assessments should consider large‐scale connectivity patterns and the potential source regions of non‐native marine species.</description><subject>biological invasions</subject><subject>gelatinous zooplankton</subject><subject>invasion corridors</subject><subject>invasive species</subject><subject>jellyfish</subject><subject>marine connectivity</subject><subject>Mnemiopsis leidyi</subject><subject>range expansion</subject><subject>source populations</subject><subject>source–sink dynamics</subject><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2018</creationdate><recordtype>article</recordtype><sourceid>3HK</sourceid><recordid>eNqFjDsOwkAMRNNQIOAKaC5AEX4SNQLR0dBHZmPAKHiDvQnK7dmCnmZeMW9mXLzPgUkROjPWhBBVOSTpJQ1oLbbcNKJ3pAfDObc12QBvjalGvIHwIhNliPbk0nN-eF3xzLMBFCy648Oe2BSHzrJC02J0o8Z59uOkmB8Pl_1pEUw8iVYajapyt9nmKJfr1V_hC2Y1Qrk</recordid><startdate>2018</startdate><enddate>2018</enddate><creator>Jaspers, Cornelia</creator><creator>Huwer, Bastian</creator><creator>Antajan, Elvire</creator><creator>Hosia, Aino</creator><creator>Hinrichsen, Hans-Harald</creator><creator>Biastoch, Arne</creator><creator>Angel, Dror</creator><creator>Asmus, Ragnhild</creator><creator>Augustin, Christina</creator><creator>Bagheri, Siamak</creator><creator>Beggs, Steven E</creator><creator>Balsby, Thorsten J.S</creator><creator>Boersma, Maarten</creator><creator>Bonnet, Delphine</creator><creator>Christensen, Jens T</creator><creator>Dänhardt, Andreas</creator><creator>Delpy, Floriane</creator><creator>Falkenhaug, Tone</creator><creator>Finenko, Galina</creator><creator>Fleming, Nicholas E.C</creator><creator>Fuentes, Veronica</creator><creator>Galil, Bella S</creator><creator>Gittenberger, Arjan</creator><creator>Griffin, Donal C</creator><creator>Haslob, Holger</creator><creator>Javidpour, Jamileh</creator><creator>Kamburska, Lyudmila</creator><creator>Kube, Sandra</creator><creator>Langenberg, Victor</creator><creator>Lehtiniemi, Maiju</creator><creator>Lombard, Fabien</creator><creator>Malzahn, Arne</creator><creator>Marambio, Macarena</creator><creator>Mihneva, Veselina</creator><creator>Møller, Lene Friis</creator><creator>Niermann, Ulrich</creator><creator>Okyar, Melek Isinibilir</creator><creator>Ôzdemir, Zekiye Birinci</creator><creator>Pitois, Sophie</creator><creator>Reusch, Thorsten B.H</creator><creator>Robbens, Johan</creator><creator>Stefanova, Kremena</creator><creator>Thibault, Delphine</creator><creator>van der Veer, Henk W</creator><creator>Vansteenbrugge, Lies</creator><creator>van Walraven, Lodewijk</creator><creator>Woźniczka, Adam</creator><general>Wiley</general><scope>3HK</scope></search><sort><creationdate>2018</creationdate><title>Ocean current connectivity propelling the secondary spread of a marine invasive comb jelly across western Eurasia</title><author>Jaspers, Cornelia ; Huwer, Bastian ; Antajan, Elvire ; Hosia, Aino ; Hinrichsen, Hans-Harald ; Biastoch, Arne ; Angel, Dror ; Asmus, Ragnhild ; Augustin, Christina ; Bagheri, Siamak ; Beggs, Steven E ; Balsby, Thorsten J.S ; Boersma, Maarten ; Bonnet, Delphine ; Christensen, Jens T ; Dänhardt, Andreas ; Delpy, Floriane ; Falkenhaug, Tone ; Finenko, Galina ; Fleming, Nicholas E.C ; Fuentes, Veronica ; Galil, Bella S ; Gittenberger, Arjan ; Griffin, Donal C ; Haslob, Holger ; Javidpour, Jamileh ; Kamburska, Lyudmila ; Kube, Sandra ; Langenberg, Victor ; Lehtiniemi, Maiju ; Lombard, Fabien ; Malzahn, Arne ; Marambio, Macarena ; Mihneva, Veselina ; Møller, Lene Friis ; Niermann, Ulrich ; Okyar, Melek Isinibilir ; Ôzdemir, Zekiye Birinci ; Pitois, Sophie ; Reusch, Thorsten B.H ; Robbens, Johan ; Stefanova, Kremena ; Thibault, Delphine ; van der Veer, Henk W ; Vansteenbrugge, Lies ; van Walraven, Lodewijk ; Woźniczka, Adam</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-cristin_nora_1956_191243</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2018</creationdate><topic>biological invasions</topic><topic>gelatinous zooplankton</topic><topic>invasion corridors</topic><topic>invasive species</topic><topic>jellyfish</topic><topic>marine connectivity</topic><topic>Mnemiopsis leidyi</topic><topic>range expansion</topic><topic>source populations</topic><topic>source–sink dynamics</topic><toplevel>online_resources</toplevel><creatorcontrib>Jaspers, Cornelia</creatorcontrib><creatorcontrib>Huwer, Bastian</creatorcontrib><creatorcontrib>Antajan, Elvire</creatorcontrib><creatorcontrib>Hosia, Aino</creatorcontrib><creatorcontrib>Hinrichsen, Hans-Harald</creatorcontrib><creatorcontrib>Biastoch, Arne</creatorcontrib><creatorcontrib>Angel, Dror</creatorcontrib><creatorcontrib>Asmus, Ragnhild</creatorcontrib><creatorcontrib>Augustin, 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Archives</collection></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext_linktorsrc</fulltext></delivery><addata><au>Jaspers, Cornelia</au><au>Huwer, Bastian</au><au>Antajan, Elvire</au><au>Hosia, Aino</au><au>Hinrichsen, Hans-Harald</au><au>Biastoch, Arne</au><au>Angel, Dror</au><au>Asmus, Ragnhild</au><au>Augustin, Christina</au><au>Bagheri, Siamak</au><au>Beggs, Steven E</au><au>Balsby, Thorsten J.S</au><au>Boersma, Maarten</au><au>Bonnet, Delphine</au><au>Christensen, Jens T</au><au>Dänhardt, Andreas</au><au>Delpy, Floriane</au><au>Falkenhaug, Tone</au><au>Finenko, Galina</au><au>Fleming, Nicholas E.C</au><au>Fuentes, Veronica</au><au>Galil, Bella S</au><au>Gittenberger, Arjan</au><au>Griffin, Donal C</au><au>Haslob, Holger</au><au>Javidpour, Jamileh</au><au>Kamburska, Lyudmila</au><au>Kube, Sandra</au><au>Langenberg, Victor</au><au>Lehtiniemi, Maiju</au><au>Lombard, Fabien</au><au>Malzahn, Arne</au><au>Marambio, Macarena</au><au>Mihneva, Veselina</au><au>Møller, Lene Friis</au><au>Niermann, Ulrich</au><au>Okyar, Melek Isinibilir</au><au>Ôzdemir, Zekiye Birinci</au><au>Pitois, Sophie</au><au>Reusch, Thorsten B.H</au><au>Robbens, Johan</au><au>Stefanova, Kremena</au><au>Thibault, Delphine</au><au>van der Veer, Henk W</au><au>Vansteenbrugge, Lies</au><au>van Walraven, Lodewijk</au><au>Woźniczka, Adam</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Ocean current connectivity propelling the secondary spread of a marine invasive comb jelly across western Eurasia</atitle><date>2018</date><risdate>2018</risdate><abstract>Aim: Invasive species are of increasing global concern. Nevertheless, the mechanisms driving further distribution after the initial establishment of non‐native species remain largely unresolved, especially in marine systems. Ocean currents can be a major driver governing range occupancy, but this has not been accounted for in most invasion ecology studies so far. We investigate how well initial establishment areas are interconnected to later occupancy regions to test for the potential role of ocean currents driving secondary spread dynamics in order to infer invasion corridors and the source–sink dynamics of a non‐native holoplanktonic biological probe species on a continental scale. Location: Western Eurasia. Time period: 1980s–2016. Major taxa studied: ‘Comb jelly’ Mnemiopsis leidyi. Methods: Based on 12,400 geo‐referenced occurrence data, we reconstruct the invasion history of M. leidyi in western Eurasia. We model ocean currents and calculate their stability to match the temporal and spatial spread dynamics with large‐scale connectivity patterns via ocean currents. Additionally, genetic markers are used to test the predicted connectivity between subpopulations. Results: Ocean currents can explain secondary spread dynamics, matching observed range expansions and the timing of first occurrence of our holoplanktonic non‐native biological probe species, leading to invasion corridors in western Eurasia. In northern Europe, regional extinctions after cold winters were followed by rapid recolonizations at a speed of up to 2,000 km per season. Source areas hosting year‐round populations in highly interconnected regions can re‐seed genotypes over large distances after local extinctions. Main conclusions: Although the release of ballast water from container ships may contribute to the dispersal of non‐native species, our results highlight the importance of ocean currents driving secondary spread dynamics. Highly interconnected areas hosting invasive species are crucial for secondary spread dynamics on a continental scale. Invasion risk assessments should consider large‐scale connectivity patterns and the potential source regions of non‐native marine species.</abstract><pub>Wiley</pub><oa>free_for_read</oa></addata></record> |
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subjects | biological invasions gelatinous zooplankton invasion corridors invasive species jellyfish marine connectivity Mnemiopsis leidyi range expansion source populations source–sink dynamics |
title | Ocean current connectivity propelling the secondary spread of a marine invasive comb jelly across western Eurasia |
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