Phylogeography of the veined squid, Loligo forbesii, in European waters

The veined squid, Loligo forbesii Steenstrup, 1856, occurs at the European Shelf areas including the Azores and represents a valuable resource for the European commercial fishery in the North East Atlantic. However, very little is known about its population structure and phylogeography. This lack of...

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Published in:Scientific Reports
Main Authors: Göpel, A. (Anika), Oesterwind, D. (Daniel), Barret, C. (Cristopher), Cannas, R. (Rita), Silva, L. (Luis), Sobrino, I. (Ignacio), Santos, M.B. (María Begoña)
Format: Article in Journal/Newspaper
Language:English
Published: Centro Oceanográfico de Cádiz 2022
Subjects:
Online Access:http://hdl.handle.net/10508/15702
https://doi.org/10.1038/s41598-022-11530-z
id ftieo:oai:repositorio.ieo.es:10508/15702
record_format openpolar
institution Open Polar
collection Instituto Español de Oceanografía: e-IEO
op_collection_id ftieo
language English
topic Loligo forbesii
Phylogeography
European waters
fish
report literature
shelf seas
classification
outflow
spellingShingle Loligo forbesii
Phylogeography
European waters
fish
report literature
shelf seas
classification
outflow
Göpel, A. (Anika)
Oesterwind, D. (Daniel)
Barret, C. (Cristopher)
Cannas, R. (Rita)
Silva, L. (Luis)
Sobrino, I. (Ignacio)
Santos, M.B. (María Begoña)
Phylogeography of the veined squid, Loligo forbesii, in European waters
topic_facet Loligo forbesii
Phylogeography
European waters
fish
report literature
shelf seas
classification
outflow
description The veined squid, Loligo forbesii Steenstrup, 1856, occurs at the European Shelf areas including the Azores and represents a valuable resource for the European commercial fishery in the North East Atlantic. However, very little is known about its population structure and phylogeography. This lack of knowledge also impedes the development of sustainable fishery management for this species. The present study combined the use of two types of markers that retrieve patterns of gene flow in different time spans; the analysis of 16 nuclear microsatellites and sequencing of the mitochondrial cytochrome oxidase subunit I (COI). Whereas the high mutation rate of microsatellites allows the description of recent patterns of connectivity in species, the lower mutation rate of COI provides phylogeographic patterns on a longer timescale. A total of 347 individuals of L. forbesii were investigated from nearly the entire distribution range of the species, including the North East Atlantic Shelf, the Azores and the Mediterranean. Individuals from the Western and Eastern Mediterranean Sea have never been included in a genetic study before. We were able to analyse COI sequences from all 12 sampling areas and define three clades of L. forbesii. Due to our large sampling area, we are presenting 13 COIhaplotypes that were previously unknown. The microsatellite analysis does not include the Azores but three main clades could be identified at the remaining 11 sampling sites. Low FST values indicate gene flow over large geographical distances. However, the genetically significant differences and an additional slight grouping in the microsatellite structure reveal that geographical barriers seem to influence the population structure and reduce gene flow. Furthermore, both markers provide strong evidence that the observed phylogeographic pattern reflects the geographical history of the Azores and the Mediterranean Sea. Postprint
format Article in Journal/Newspaper
author Göpel, A. (Anika)
Oesterwind, D. (Daniel)
Barret, C. (Cristopher)
Cannas, R. (Rita)
Silva, L. (Luis)
Sobrino, I. (Ignacio)
Santos, M.B. (María Begoña)
author_facet Göpel, A. (Anika)
Oesterwind, D. (Daniel)
Barret, C. (Cristopher)
Cannas, R. (Rita)
Silva, L. (Luis)
Sobrino, I. (Ignacio)
Santos, M.B. (María Begoña)
author_sort Göpel, A. (Anika)
title Phylogeography of the veined squid, Loligo forbesii, in European waters
title_short Phylogeography of the veined squid, Loligo forbesii, in European waters
title_full Phylogeography of the veined squid, Loligo forbesii, in European waters
title_fullStr Phylogeography of the veined squid, Loligo forbesii, in European waters
title_full_unstemmed Phylogeography of the veined squid, Loligo forbesii, in European waters
title_sort phylogeography of the veined squid, loligo forbesii, in european waters
publisher Centro Oceanográfico de Cádiz
publishDate 2022
url http://hdl.handle.net/10508/15702
https://doi.org/10.1038/s41598-022-11530-z
op_coverage Océan atlantique
Atlantique Nord
Atlantic Ocean
Atlántico Norte
Océano Atlántico
ICES
North Atlantic
genre North Atlantic
North East Atlantic
genre_facet North Atlantic
North East Atlantic
op_relation https://www.nature.com/articles/s41598-022-11530-z
http://hdl.handle.net/10508/15702
Scientific Reports.Nature, 12. 2022: Phylogeography of the veined squid, Loligo forbesii, in European waters Anika Göpel1,2, Daniel Oesterwind1*, Christopher Barrett3, Rita Cannas8, Luis Silva Caparro10, Pierluigi Carbonara9, Marilena Donnaloia9, Maria Cristina Follesa8, Angela Larivain6, Vladimir Laptikhovsky3, Evgenia Lefkaditou4, Jean‑Paul Robin6, Maria Begoña Santos11, Ignacio Sobrino10, Julio Valeiras11, Maria Valls7, Hugo C. Vieira12, Kai Wieland5 & Ralf Bastrop2 The veined squid, Loligo forbesii Steenstrup, 1856, occurs at the European Shelf areas including the Azores and represents a valuable resource for the European commercial fishery in the North East Atlantic. However, very little is known about its population structure and phylogeography. This lack of knowledge also impedes the development of sustainable fishery management for this species. The present study combined the use of two types of markers that retrieve patterns of gene flow in different time spans; the analysis of 16 nuclear microsatellites and sequencing of the mitochondrial cytochrome oxidase subunit I (COI). Whereas the high mutation rate of microsatellites allows the description of recent patterns of connectivity in species, the lower mutation rate of COI provides phylogeographic patterns on a longer timescale. A total of 347 individuals of L. forbesii were investigated from nearly the entire distribution range of the species, including the North East Atlantic Shelf, the Azores and the Mediterranean. Individuals from the Western and Eastern Mediterranean Sea have never been included in a genetic study before. We were able to analyse COI sequences from all 12 sampling areas and define three clades of L. forbesii. Due to our large sampling area, we are presenting 13 COIhaplotypes that were previously unknown. The microsatellite analysis does not include the Azores but three main clades could be identified at the remaining 11 sampling sites. Low FST values indicate gene flow over large geographical distances. However, the genetically significant differences and an additional slight grouping in the microsatellite structure reveal that geographical barriers seem to influence the population structure and reduce gene flow. Furthermore, both markers provide strong evidence that the observed phylogeographic pattern reflects the geographical history of the Azores and the Mediterranean Sea. Within the last decades biomass of various cephalopod populations and commercial catches increased worldwide1. Especially in the Atlantic Ocean, the commercial importance of the loliginids has grown2,3. Loliginids landings reached about 12,000 t3 in 2017 showing a fivefold increase between 2000 and 2017 in the entire Northeast Atlantic, which illustrates the growing socio-economic importance. Among the loliginids, the veined squid Loligo forbesii Steenstrup, 1856 is one of the most important species for the European fishery3. This species is neritic, associated to the shelf and equally distributed on the lower shelf (80–200 m) and the upper slope OPEN 1Thünen Institute of Baltic Sea Fisheries, Alter Hafen Süd 2, 18069 Rostock, Germany. 2Institute of Biological Sciences, University of Rostock, Albert‑Einstein‑Str. 3, 18059 Rostock, Germany. 3Cefas Laboratory, Pakefield Rd, Lowestoft NR33 0HT, UK. 4Hellenic Centre for Marine Research, Institute of Marine Biological Resources and Inland Waters, 576 SideRD Vouliagmenis Ave, 16452 Athens, Greece. 5Technical University of Denmark, National Institute of Aquatic Resources, Nordsøen Forskerpark, Willemoesvej 2, 9850 Hirtshals, Denmark. 6University of Caen Normandy, CS 14032, 14032 Caen Cedex 05, France. 7Centre Oceanográfic de les Balears s/n, Instituto Español de Oceanografía (IEO), 07015 Palma, Spain. 8Department of Life and Environmental Sciences, University of Cagliari, Cagliari, Italy. 9COISPA Tecnologia & Ricerca, Via dei Trulli, 18‑20, Bari, Italy. 10Centro Oceanográfico de Cádiz, Instituto Español de Oceanografía, Puerto Pesquero, Muelle de Levante S/N, 11006 Cádiz, Spain. 11Centro Oceanográfico de Vigo, Instituto Español de Oceanografía (IEO), Subida a Radio Faro, 50, 36390 Vigo, Spain. 12CESAM ‑ Centre for Environmental and Marine Studies, Department of Biology, University of Aveiro, Campus de Santiago, 3810‑193 Aveiro, Portugal. *email: daniel.oesterwind@thuenen.de-53. Göpel, A. Populationsgenetik und Phylogeographie des Nordischen Kalmars Loligo forbesii Steenstrup, 1856 in Europäischen Gewässern. Masterthesis, Univ. Rostock in German, 76pp (2020). 54. Oesterwind, D. et al. Biology and meso-scale distribution patterns of North Sea cephalopods. Fish. Res. 106, 141–150 (2010). 55. Sauer, W. H. H. et al. Tag recapture studies of the chokka squid Loligo vulgaris reynaudii d’Orbigny, 1845 on inshore spawning grounds on the south-east coast of South Africa. Fish. Res. 45, 283–289 (2000). 56. Knowlton, N. & Weigt, L. A. New dates and new rates for divergence across the Isthmus of Panama. Proc. R. Soc. B Biol. Sci. 265, 2257–2263 (1998). 57. Pérez-Losada, M. et al. Testing hypotheses of population structuring in the Northeast Atlantic Ocean and Mediterranean Sea using the common cuttlefish Sepia officinalis. Mol. Ecol. 16, 2667–2679 (2007). 58. O’Dor, R. K. Can understanding squid life-history strategies and recruitment improve management?. South African J. Mar. Sci. 7615, 193–206 (1998). 59. Izquierdo, A. et al. Modelling in the Strait of Gibraltar: From operational oceanography to scale interactions. Fundam. i Prikl. Gidrofiz. 9, 15–24 (2016). 60. Clarke, M. & Hart, M. Treatise Online no. 102: Part M, Chapter 11: Statoliths and coleoid evolution. Treatise Online (2018). 61. Hsü, K. J. et al. Late Miocene desiccation of the mediterranean. Nature 242, 240–244 (1973). 62. Garcia-Castellanos, D. et al. Catastrophic flood of the Mediterranean after the Messinian salinity crisis. Nature 462, 778–781 (2009). 63. Thunell, R. C. et al. Atlantic-mediterranean water exchange during the late neocene. Paleoceanography 2(6), 661 (1987). 64. Green, C. P. et al. Combining statolith element composition and fourier shape data allows discrimination of spatial and temporal stock structure of arrow squid (Nototodarus gouldi). Can. J. Fish. Aquat. Sci. 72, 1609–1618 (2015). Acknowledgements This project has been partly funded by the EU through the European Maritime and Fisheries Fund (EMFF) within the Spanish National Program of collection, management and use of data in the fisheries sector and support for scientific advice regarding the Common Fisheries Policy and genetic sampling was supported by the Cephs and Chefs INTERREG project. Sampling in the Azores was funded by CESAM (UIDP/50017/2020+UIDB/50 017/2020+LA/P/0094/2020) that is financed by FCT/MCTES through national funds. We thank Christopher Zimmermann for the funding support of the study, Matthias Kloppmann and his crew for his considerate cruise lead during sampling in the North Sea and Nicholas Badouvas, Nikolaos Fotiadis, for their sample preparation at HCMR. We also thank Lukas Krebes and Sören Möller from the University of Rostock for sharing their experiences with the microsatellite analysis. Last but not least, we would like to thank the students Vivian Fischbach and Chantal Petong for their valuable lab work, two anonymous reviewers for their very constructive comments and especially the editor (Raquel Godinho) for her patient management of the review process and her huge support to get this manuscript published. Author contributions A.G.: Performed the laboratory analysis and statistics and wrote the draft manuscript and led the revision; D.O.: conceived the study project, organized samples and contributed to the drafting of the manuscript and led the revisions; R.B.: supervised lab work and statistics and contributed to the drafting of the manuscript and to the revisions; C.B., R.C., L.S.C., P.C., M.D., M.C.F., A.L., V.L., E.L., J.-P.R., M.B.S., I.S., J.V., M.V., K.W.: prepared samples and reviewed the draft manuscript and the revisions. H.C.V. prepared Azorean samples and contributed to the revisions of the manuscript. All authors read and approved the manuscript. Funding Open Access funding enabled and organized by Projekt DEAL. Competing interests The authors declare no competing interests. Additional information Supplementary Information The online version contains supplementary material available at https:// doi. org/ 10. 1038/ s41598- 022- 11530-z. Correspondence and requests for materials should be addressed to D.O. Reprints and permissions information is available at www.nature.com/reprints. Publisher’s note Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations. Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http:// creat iveco mmons. org/ licen ses/ by/4. 0/.
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spelling ftieo:oai:repositorio.ieo.es:10508/15702 2023-05-15T17:36:21+02:00 Phylogeography of the veined squid, Loligo forbesii, in European waters Göpel, A. (Anika) Oesterwind, D. (Daniel) Barret, C. (Cristopher) Cannas, R. (Rita) Silva, L. (Luis) Sobrino, I. (Ignacio) Santos, M.B. (María Begoña) Océan atlantique Atlantique Nord Atlantic Ocean Atlántico Norte Océano Atlántico ICES North Atlantic 2022-05-12 http://hdl.handle.net/10508/15702 https://doi.org/10.1038/s41598-022-11530-z eng eng Centro Oceanográfico de Cádiz https://www.nature.com/articles/s41598-022-11530-z http://hdl.handle.net/10508/15702 Scientific Reports.Nature, 12. 2022: Phylogeography of the veined squid, Loligo forbesii, in European waters Anika Göpel1,2, Daniel Oesterwind1*, Christopher Barrett3, Rita Cannas8, Luis Silva Caparro10, Pierluigi Carbonara9, Marilena Donnaloia9, Maria Cristina Follesa8, Angela Larivain6, Vladimir Laptikhovsky3, Evgenia Lefkaditou4, Jean‑Paul Robin6, Maria Begoña Santos11, Ignacio Sobrino10, Julio Valeiras11, Maria Valls7, Hugo C. Vieira12, Kai Wieland5 & Ralf Bastrop2 The veined squid, Loligo forbesii Steenstrup, 1856, occurs at the European Shelf areas including the Azores and represents a valuable resource for the European commercial fishery in the North East Atlantic. However, very little is known about its population structure and phylogeography. This lack of knowledge also impedes the development of sustainable fishery management for this species. The present study combined the use of two types of markers that retrieve patterns of gene flow in different time spans; the analysis of 16 nuclear microsatellites and sequencing of the mitochondrial cytochrome oxidase subunit I (COI). Whereas the high mutation rate of microsatellites allows the description of recent patterns of connectivity in species, the lower mutation rate of COI provides phylogeographic patterns on a longer timescale. A total of 347 individuals of L. forbesii were investigated from nearly the entire distribution range of the species, including the North East Atlantic Shelf, the Azores and the Mediterranean. Individuals from the Western and Eastern Mediterranean Sea have never been included in a genetic study before. We were able to analyse COI sequences from all 12 sampling areas and define three clades of L. forbesii. Due to our large sampling area, we are presenting 13 COIhaplotypes that were previously unknown. The microsatellite analysis does not include the Azores but three main clades could be identified at the remaining 11 sampling sites. Low FST values indicate gene flow over large geographical distances. However, the genetically significant differences and an additional slight grouping in the microsatellite structure reveal that geographical barriers seem to influence the population structure and reduce gene flow. Furthermore, both markers provide strong evidence that the observed phylogeographic pattern reflects the geographical history of the Azores and the Mediterranean Sea. Within the last decades biomass of various cephalopod populations and commercial catches increased worldwide1. Especially in the Atlantic Ocean, the commercial importance of the loliginids has grown2,3. Loliginids landings reached about 12,000 t3 in 2017 showing a fivefold increase between 2000 and 2017 in the entire Northeast Atlantic, which illustrates the growing socio-economic importance. Among the loliginids, the veined squid Loligo forbesii Steenstrup, 1856 is one of the most important species for the European fishery3. This species is neritic, associated to the shelf and equally distributed on the lower shelf (80–200 m) and the upper slope OPEN 1Thünen Institute of Baltic Sea Fisheries, Alter Hafen Süd 2, 18069 Rostock, Germany. 2Institute of Biological Sciences, University of Rostock, Albert‑Einstein‑Str. 3, 18059 Rostock, Germany. 3Cefas Laboratory, Pakefield Rd, Lowestoft NR33 0HT, UK. 4Hellenic Centre for Marine Research, Institute of Marine Biological Resources and Inland Waters, 576 SideRD Vouliagmenis Ave, 16452 Athens, Greece. 5Technical University of Denmark, National Institute of Aquatic Resources, Nordsøen Forskerpark, Willemoesvej 2, 9850 Hirtshals, Denmark. 6University of Caen Normandy, CS 14032, 14032 Caen Cedex 05, France. 7Centre Oceanográfic de les Balears s/n, Instituto Español de Oceanografía (IEO), 07015 Palma, Spain. 8Department of Life and Environmental Sciences, University of Cagliari, Cagliari, Italy. 9COISPA Tecnologia & Ricerca, Via dei Trulli, 18‑20, Bari, Italy. 10Centro Oceanográfico de Cádiz, Instituto Español de Oceanografía, Puerto Pesquero, Muelle de Levante S/N, 11006 Cádiz, Spain. 11Centro Oceanográfico de Vigo, Instituto Español de Oceanografía (IEO), Subida a Radio Faro, 50, 36390 Vigo, Spain. 12CESAM ‑ Centre for Environmental and Marine Studies, Department of Biology, University of Aveiro, Campus de Santiago, 3810‑193 Aveiro, Portugal. *email: daniel.oesterwind@thuenen.de-53. Göpel, A. Populationsgenetik und Phylogeographie des Nordischen Kalmars Loligo forbesii Steenstrup, 1856 in Europäischen Gewässern. Masterthesis, Univ. Rostock in German, 76pp (2020). 54. Oesterwind, D. et al. Biology and meso-scale distribution patterns of North Sea cephalopods. Fish. Res. 106, 141–150 (2010). 55. Sauer, W. H. H. et al. Tag recapture studies of the chokka squid Loligo vulgaris reynaudii d’Orbigny, 1845 on inshore spawning grounds on the south-east coast of South Africa. Fish. Res. 45, 283–289 (2000). 56. Knowlton, N. & Weigt, L. A. New dates and new rates for divergence across the Isthmus of Panama. Proc. R. Soc. B Biol. Sci. 265, 2257–2263 (1998). 57. Pérez-Losada, M. et al. Testing hypotheses of population structuring in the Northeast Atlantic Ocean and Mediterranean Sea using the common cuttlefish Sepia officinalis. Mol. Ecol. 16, 2667–2679 (2007). 58. O’Dor, R. K. Can understanding squid life-history strategies and recruitment improve management?. South African J. Mar. Sci. 7615, 193–206 (1998). 59. Izquierdo, A. et al. Modelling in the Strait of Gibraltar: From operational oceanography to scale interactions. Fundam. i Prikl. Gidrofiz. 9, 15–24 (2016). 60. Clarke, M. & Hart, M. Treatise Online no. 102: Part M, Chapter 11: Statoliths and coleoid evolution. Treatise Online (2018). 61. Hsü, K. J. et al. Late Miocene desiccation of the mediterranean. Nature 242, 240–244 (1973). 62. Garcia-Castellanos, D. et al. Catastrophic flood of the Mediterranean after the Messinian salinity crisis. Nature 462, 778–781 (2009). 63. Thunell, R. C. et al. Atlantic-mediterranean water exchange during the late neocene. Paleoceanography 2(6), 661 (1987). 64. Green, C. P. et al. Combining statolith element composition and fourier shape data allows discrimination of spatial and temporal stock structure of arrow squid (Nototodarus gouldi). Can. J. Fish. Aquat. Sci. 72, 1609–1618 (2015). Acknowledgements This project has been partly funded by the EU through the European Maritime and Fisheries Fund (EMFF) within the Spanish National Program of collection, management and use of data in the fisheries sector and support for scientific advice regarding the Common Fisheries Policy and genetic sampling was supported by the Cephs and Chefs INTERREG project. Sampling in the Azores was funded by CESAM (UIDP/50017/2020+UIDB/50 017/2020+LA/P/0094/2020) that is financed by FCT/MCTES through national funds. We thank Christopher Zimmermann for the funding support of the study, Matthias Kloppmann and his crew for his considerate cruise lead during sampling in the North Sea and Nicholas Badouvas, Nikolaos Fotiadis, for their sample preparation at HCMR. We also thank Lukas Krebes and Sören Möller from the University of Rostock for sharing their experiences with the microsatellite analysis. Last but not least, we would like to thank the students Vivian Fischbach and Chantal Petong for their valuable lab work, two anonymous reviewers for their very constructive comments and especially the editor (Raquel Godinho) for her patient management of the review process and her huge support to get this manuscript published. Author contributions A.G.: Performed the laboratory analysis and statistics and wrote the draft manuscript and led the revision; D.O.: conceived the study project, organized samples and contributed to the drafting of the manuscript and led the revisions; R.B.: supervised lab work and statistics and contributed to the drafting of the manuscript and to the revisions; C.B., R.C., L.S.C., P.C., M.D., M.C.F., A.L., V.L., E.L., J.-P.R., M.B.S., I.S., J.V., M.V., K.W.: prepared samples and reviewed the draft manuscript and the revisions. H.C.V. prepared Azorean samples and contributed to the revisions of the manuscript. All authors read and approved the manuscript. Funding Open Access funding enabled and organized by Projekt DEAL. Competing interests The authors declare no competing interests. Additional information Supplementary Information The online version contains supplementary material available at https:// doi. org/ 10. 1038/ s41598- 022- 11530-z. Correspondence and requests for materials should be addressed to D.O. Reprints and permissions information is available at www.nature.com/reprints. Publisher’s note Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations. Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http:// creat iveco mmons. org/ licen ses/ by/4. 0/. 2045-2322 doi:10.1038/s41598-022-11530-z Atribución-NoComercial-SinDerivadas 3.0 España http://creativecommons.org/licenses/by-nc-nd/3.0/es/ openAccess CC-BY-NC-ND Loligo forbesii Phylogeography European waters fish report literature shelf seas classification outflow article 2022 ftieo https://doi.org/10.1038/s41598-022-11530-z 2022-09-20T23:46:50Z The veined squid, Loligo forbesii Steenstrup, 1856, occurs at the European Shelf areas including the Azores and represents a valuable resource for the European commercial fishery in the North East Atlantic. However, very little is known about its population structure and phylogeography. This lack of knowledge also impedes the development of sustainable fishery management for this species. The present study combined the use of two types of markers that retrieve patterns of gene flow in different time spans; the analysis of 16 nuclear microsatellites and sequencing of the mitochondrial cytochrome oxidase subunit I (COI). Whereas the high mutation rate of microsatellites allows the description of recent patterns of connectivity in species, the lower mutation rate of COI provides phylogeographic patterns on a longer timescale. A total of 347 individuals of L. forbesii were investigated from nearly the entire distribution range of the species, including the North East Atlantic Shelf, the Azores and the Mediterranean. Individuals from the Western and Eastern Mediterranean Sea have never been included in a genetic study before. We were able to analyse COI sequences from all 12 sampling areas and define three clades of L. forbesii. Due to our large sampling area, we are presenting 13 COIhaplotypes that were previously unknown. The microsatellite analysis does not include the Azores but three main clades could be identified at the remaining 11 sampling sites. Low FST values indicate gene flow over large geographical distances. However, the genetically significant differences and an additional slight grouping in the microsatellite structure reveal that geographical barriers seem to influence the population structure and reduce gene flow. Furthermore, both markers provide strong evidence that the observed phylogeographic pattern reflects the geographical history of the Azores and the Mediterranean Sea. Postprint Article in Journal/Newspaper North Atlantic North East Atlantic Instituto Español de Oceanografía: e-IEO Scientific Reports 12 1