Genetic structure and relatedness of brown trout () populations in the drainage basin of the Ölfusá river, South-Western Iceland.

Marcos Lagunas, Arnar Pálsson, Benóný Jónsson, Magnús Jóhannsson, Zophonías O Jónsson, Sigurður S Snorrason
Author Information
  1. Marcos Lagunas: Faculty of Life and Environmental Sciences, University of Iceland, Reykjavík, Iceland.
  2. Arnar Pálsson: Faculty of Life and Environmental Sciences, University of Iceland, Reykjavík, Iceland. ORCID
  3. Benóný Jónsson: Marine and Freshwater Research Institute, Selfoss, Iceland.
  4. Magnús Jóhannsson: Marine and Freshwater Research Institute, Selfoss, Iceland.
  5. Zophonías O Jónsson: Faculty of Life and Environmental Sciences, University of Iceland, Reykjavík, Iceland.
  6. Sigurður S Snorrason: Faculty of Life and Environmental Sciences, University of Iceland, Reykjavík, Iceland.

Abstract

Background: Lake Þingvallavatn in Iceland, a part of the river Ölfusá drainage basin, was presumably populated by brown trout soon after it formed at the end of the last Ice Age. The genetic relatedness of the brown trout in Þingvallavatn to other populations in the Ölfusá drainage basin is unknown. After the building of a dam at the outlet of the lake in 1959 brown trout catches declined, though numbers have now increased. The aim of this study was to assess effects of geographic isolation and potential downstream gene flow on the genetic structure and diversity in brown trout sampled in several locations in the western side of the watershed of River Ölfusá. We hypothesized that brown trout in Lake Þingvallavatn constituted several local spawning populations connected by occasional gene flow before the damming of the lake. We also estimated the effective population size (N) of some of these populations and tested for signs of a recent population bottleneck in Lake Þingvallavatn.
Methods: We sampled brown trout inhabiting four lakes and 12 rivers within and near the watershed of River Ölfusá by means of electro- and net- fishing. After stringent data filtering, 2,597 polymorphic loci obtained from ddRADseq data from 317 individuals were ascertained as putative neutral markers.
Results: Overall, the genetic relatedness of brown trout in the Ölfusá watershed reflected the connectivity and topography of the waterways. Ancestry proportion analyses and a phylogenetic tree revealed seven distinct clusters, some of which corresponded to small populations with reduced genetic diversity. There was no evidence of downstream gene flow from Lake Þingvallavatn, although gene flow was observed from much smaller mountain populations. Most locations showed low N values (., ~14.6 on average) while the putative anadromous trout from River Sog and the spawning population from River Öxará, that flows into Lake Þingvallavatn, showed notably higher N values (., 71.2 and 56.5, respectively). No signals of recent population bottlenecks were detected in the brown trout of Lake Þingvallavatn.
Discussion: This is the first time that the genetic structure and diversity of brown trout in the watershed of River Ölfusá have been assessed. Our results point towards the presence of a metapopulation in the watershed of Lake Þingvallavatn, which has been influenced by restoration efforts and is now dominated by a genetic component originated in River Öxará. Many of the locations studied represent different populations. Those that are isolated in headwater streams and lakes are genetically distinct presenting low genetic diversity, yet they can be important in increasing the genetic variation in downstream populations. These populations should be considered for conservation and direct management.

Keywords

References

  1. Mol Ecol. 2022 Dec;31(24):6422-6439 [PMID: 36170147]
  2. Heredity (Edinb). 2018 Mar;120(3):196-207 [PMID: 29269932]
  3. Nat Protoc. 2017 Dec;12(12):2640-2659 [PMID: 29189774]
  4. Heredity (Edinb). 2016 Oct;117(4):217-23 [PMID: 27005004]
  5. Mol Ecol. 2009 Mar;18(6):1100-11 [PMID: 19243511]
  6. J Med Entomol. 2020 Nov 13;57(6):1930-1941 [PMID: 32692366]
  7. Wellcome Open Res. 2021 May 13;6:108 [PMID: 34632087]
  8. Bioinformatics. 2011 Nov 1;27(21):3070-1 [PMID: 21926124]
  9. Bioinformatics. 2006 Nov 1;22(21):2688-90 [PMID: 16928733]
  10. Heredity (Edinb). 2012 Oct;109(4):246-53 [PMID: 22828900]
  11. Evolution. 1984 Nov;38(6):1358-1370 [PMID: 28563791]
  12. Genetics. 2012 Jun;191(2):579-92 [PMID: 22466040]
  13. Glob Chang Biol. 2016 Sep;22(9):3206-20 [PMID: 26936833]
  14. Evol Appl. 2010 May;3(3):244-62 [PMID: 25567922]
  15. Ecol Evol. 2012 Mar;2(3):562-73 [PMID: 22822435]
  16. Proc Natl Acad Sci U S A. 1979 Oct;76(10):5269-73 [PMID: 291943]
  17. Syst Biol. 2008 Oct;57(5):758-71 [PMID: 18853362]
  18. Proc Biol Sci. 2013 Aug 07;280(1768):20131339 [PMID: 23926150]
  19. Bioinformatics. 2012 Dec 15;28(24):3326-8 [PMID: 23060615]
  20. Science. 2011 Aug 19;333(6045):1024-6 [PMID: 21852500]
  21. Front Zool. 2009 Mar 30;6:6 [PMID: 19331654]
  22. G3 (Bethesda). 2011 Aug;1(3):171-82 [PMID: 22384329]
  23. Genetics. 1985 Nov;111(3):675-89 [PMID: 4054612]
  24. PLoS One. 2012;7(5):e37135 [PMID: 22675423]
  25. Mol Ecol Resour. 2011 Mar;11 Suppl 1:184-94 [PMID: 21429174]
  26. Genome Biol Evol. 2017 Aug 1;9(8):2057-2074 [PMID: 28903535]
  27. Mol Ecol Resour. 2015 Nov;15(6):1304-15 [PMID: 25783180]
  28. Mol Ecol. 1998 Aug;7(8):963-74 [PMID: 9711862]
  29. Ecol Evol. 2020 Feb 11;10(4):1929-1937 [PMID: 32128126]
  30. Mol Ecol. 2016 May;25(10):2176-94 [PMID: 26992010]
  31. Annu Rev Genet. 1995;29:305-27 [PMID: 8825477]
  32. PeerJ. 2014 Jun 10;2:e431 [PMID: 24949246]
  33. Genetics. 1996 Dec;144(4):2001-14 [PMID: 8978083]
  34. Bioinformatics. 2011 Aug 1;27(15):2156-8 [PMID: 21653522]
  35. Mol Ecol Resour. 2014 Jan;14(1):209-14 [PMID: 23992227]
  36. Genetics. 2014 Apr;196(4):973-83 [PMID: 24496008]
  37. Mol Ecol. 2018 Jul 10;: [PMID: 29987880]
  38. Bioinformatics. 2010 Nov 15;26(22):2867-73 [PMID: 20926424]
  39. Mol Ecol Resour. 2017 Jul;17(4):656-669 [PMID: 27762098]

MeSH Term

Iceland
Phylogeny
Drainage
Population Density
Genetic Structures

Word Cloud

Created with Highcharts 10.0.0troutbrownpopulationsÞingvallavatngeneticLakeÖlfusáRiverwatershedgeneflowdiversitypopulationIcelanddrainagebasinrelatednessdownstreamstructurelocationsNriverlakenowsampledseveralspawningrecentlakesdata2ddRADseqputativedistinctshowedlowvaluesÖxaráBackground:partpresumablypopulatedsoonformedendlastIceAgeunknownbuildingdamoutlet1959catchesdeclinedthoughnumbersincreasedaimstudyassesseffectsgeographicisolationpotentialwesternsidehypothesizedconstitutedlocalconnectedoccasionaldammingalsoestimatedeffectivesizetestedsignsbottleneckMethods:inhabitingfour12riverswithinnearmeanselectro-net-fishingstringentfiltering597polymorphiclociobtained317individualsascertainedneutralmarkersResults:OverallreflectedconnectivitytopographywaterwaysAncestryproportionanalysesphylogenetictreerevealedsevenclusterscorrespondedsmallreducedevidencealthoughobservedmuchsmallermountain~146averageanadromousSogflowsnotablyhigher71565respectivelysignalsbottlenecksdetectedDiscussion:firsttimeassessedresultspointtowardspresencemetapopulationinfluencedrestorationeffortsdominatedcomponentoriginatedManystudiedrepresentdifferentisolatedheadwaterstreamsgeneticallypresentingyetcanimportantincreasingvariationconsideredconservationdirectmanagementGeneticSouth-WesternBrownConservationHeadwatersIsolationLandlocked

Similar Articles

Cited By