Population stock structure of leatherback turtles (Dermochelyscoriacea) in the Atlantic revealed using mtDNA and microsatellite markers

This study presents a comprehensive genetic analysis of stock structure for leatherback turtles ( Dermochelys coriacea ), combining 17 microsatellite loci and 763 bp of the mtDNA control region. Recently discovered eastern Atlantic nesting populations of this critically endangered species were absen...

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Published in:Conservation genetics Vol. 14; no. 3; pp. 625 - 636
Main Authors: Dutton, Peter H., Roden, Suzanne E., Stewart, Kelly R., LaCasella, Erin, Tiwari, Manjula, Formia, Angela, Thomé, Joao Carlos, Livingstone, Suzanne R., Eckert, Scott, Chacon-Chaverri, Didiher, Rivalan, Philippe, Allman, Phil
Format: Journal Article
Language:English
Published: Dordrecht Springer Netherlands 01.06.2013
Springer Nature B.V
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ISSN:1566-0621, 1572-9737
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Abstract This study presents a comprehensive genetic analysis of stock structure for leatherback turtles ( Dermochelys coriacea ), combining 17 microsatellite loci and 763 bp of the mtDNA control region. Recently discovered eastern Atlantic nesting populations of this critically endangered species were absent in a previous survey that found little ocean-wide mtDNA variation. We added rookeries in West Africa and Brazil and generated longer sequences for previously analyzed samples. A total of 1,417 individuals were sampled from nine nesting sites in the Atlantic and SW Indian Ocean. We detected additional mtDNA variation with the longer sequences, identifying ten polymorphic sites that resolved a total of ten haplotypes, including three new variants of haplotypes previously described by shorter sequences. Population differentiation was substantial between all but two adjacent rookery pairs, and F ST values ranged from 0.034 to 0.676 and 0.004 to 0.205 for mtDNA and microsatellite data respectively, suggesting that male-mediated gene flow is not as widespread as previously assumed. We detected weak ( F ST  = 0.008 and 0.006) but significant differentiation with microsatellites between the two population pairs that were indistinguishable with mtDNA data. POWSIM analysis showed that our mtDNA marker had very low statistical power to detect weak structure ( F ST  < 0.005), while our microsatellite marker array had high power. We conclude that the weak differentiation detected with microsatellites reflects a fine scale level of demographic independence that warrants recognition, and that all nine of the nesting colonies should be considered as demographically independent populations for conservation. Our findings illustrate the importance of evaluating the power of specific genetic markers to detect structure in order to correctly identify the appropriate population units to conserve.
AbstractList This study presents a comprehensive genetic analysis of stock structure for leatherback turtles ( Dermochelys coriacea ), combining 17 microsatellite loci and 763 bp of the mtDNA control region. Recently discovered eastern Atlantic nesting populations of this critically endangered species were absent in a previous survey that found little ocean-wide mtDNA variation. We added rookeries in West Africa and Brazil and generated longer sequences for previously analyzed samples. A total of 1,417 individuals were sampled from nine nesting sites in the Atlantic and SW Indian Ocean. We detected additional mtDNA variation with the longer sequences, identifying ten polymorphic sites that resolved a total of ten haplotypes, including three new variants of haplotypes previously described by shorter sequences. Population differentiation was substantial between all but two adjacent rookery pairs, and F ST values ranged from 0.034 to 0.676 and 0.004 to 0.205 for mtDNA and microsatellite data respectively, suggesting that male-mediated gene flow is not as widespread as previously assumed. We detected weak ( F ST  = 0.008 and 0.006) but significant differentiation with microsatellites between the two population pairs that were indistinguishable with mtDNA data. POWSIM analysis showed that our mtDNA marker had very low statistical power to detect weak structure ( F ST  < 0.005), while our microsatellite marker array had high power. We conclude that the weak differentiation detected with microsatellites reflects a fine scale level of demographic independence that warrants recognition, and that all nine of the nesting colonies should be considered as demographically independent populations for conservation. Our findings illustrate the importance of evaluating the power of specific genetic markers to detect structure in order to correctly identify the appropriate population units to conserve.
This study presents a comprehensive genetic analysis of stock structure for leatherback turtles (Dermochelys coriacea), combining 17 microsatellite loci and 763 bp of the mtDNA control region. Recently discovered eastern Atlantic nesting populations of this critically endangered species were absent in a previous survey that found little ocean-wide mtDNA variation. We added rookeries in West Africa and Brazil and generated longer sequences for previously analyzed samples. A total of 1,417 individuals were sampled from nine nesting sites in the Atlantic and SW Indian Ocean. We detected additional mtDNA variation with the longer sequences, identifying ten polymorphic sites that resolved a total of ten haplotypes, including three new variants of haplotypes previously described by shorter sequences. Population differentiation was substantial between all but two adjacent rookery pairs, and F ^sub ST^ values ranged from 0.034 to 0.676 and 0.004 to 0.205 for mtDNA and microsatellite data respectively, suggesting that male-mediated gene flow is not as widespread as previously assumed. We detected weak (F ^sub ST^ = 0.008 and 0.006) but significant differentiation with microsatellites between the two population pairs that were indistinguishable with mtDNA data. POWSIM analysis showed that our mtDNA marker had very low statistical power to detect weak structure (F ^sub ST^ < 0.005), while our microsatellite marker array had high power. We conclude that the weak differentiation detected with microsatellites reflects a fine scale level of demographic independence that warrants recognition, and that all nine of the nesting colonies should be considered as demographically independent populations for conservation. Our findings illustrate the importance of evaluating the power of specific genetic markers to detect structure in order to correctly identify the appropriate population units to conserve.[PUBLICATION ABSTRACT]
This study presents a comprehensive genetic analysis of stock structure for leatherback turtles (Dermochelys coriacea), combining 17 microsatellite loci and 763 bp of the mtDNA control region. Recently discovered eastern Atlantic nesting populations of this critically endangered species were absent in a previous survey that found little ocean-wide mtDNA variation. We added rookeries in West Africa and Brazil and generated longer sequences for previously analyzed samples. A total of 1,417 individuals were sampled from nine nesting sites in the Atlantic and SW Indian Ocean. We detected additional mtDNA variation with the longer sequences, identifying ten polymorphic sites that resolved a total of ten haplotypes, including three new variants of haplotypes previously described by shorter sequences. Population differentiation was substantial between all but two adjacent rookery pairs, and F sub(ST) values ranged from 0.034 to 0.676 and 0.004 to 0.205 for mtDNA and microsatellite data respectively, suggesting that male-mediated gene flow is not as widespread as previously assumed. We detected weak (F sub(ST) = 0.008 and 0.006) but significant differentiation with microsatellites between the two population pairs that were indistinguishable with mtDNA data. POWSIM analysis showed that our mtDNA marker had very low statistical power to detect weak structure (F sub(ST) < 0.005), while our microsatellite marker array had high power. We conclude that the weak differentiation detected with microsatellites reflects a fine scale level of demographic independence that warrants recognition, and that all nine of the nesting colonies should be considered as demographically independent populations for conservation. Our findings illustrate the importance of evaluating the power of specific genetic markers to detect structure in order to correctly identify the appropriate population units to conserve.
This study presents a comprehensive genetic analysis of stock structure for leatherback turtles (Dermochelys coriacea), combining 17 microsatellite loci and 763 bp of the mtDNA control region. Recently discovered eastern Atlantic nesting populations of this critically endangered species were absent in a previous survey that found little ocean-wide mtDNA variation. We added rookeries in West Africa and Brazil and generated longer sequences for previously analyzed samples. A total of 1,417 individuals were sampled from nine nesting sites in the Atlantic and SW Indian Ocean. We detected additional mtDNA variation with the longer sequences, identifying ten polymorphic sites that resolved a total of ten haplotypes, including three new variants of haplotypes previously described by shorter sequences. Population differentiation was substantial between all but two adjacent rookery pairs, and F ST values ranged from 0.034 to 0.676 and 0.004 to 0.205 for mtDNA and microsatellite data respectively, suggesting that male-mediated gene flow is not as widespread as previously assumed. We detected weak (F ST = 0.008 and 0.006) but significant differentiation with microsatellites between the two population pairs that were indistinguishable with mtDNA data. POWSIM analysis showed that our mtDNA marker had very low statistical power to detect weak structure (F ST < 0.005), while our microsatellite marker array had high power. We conclude that the weak differentiation detected with microsatellites reflects a fine scale level of demographic independence that warrants recognition, and that all nine of the nesting colonies should be considered as demographically independent populations for conservation. Our findings illustrate the importance of evaluating the power of specific genetic markers to detect structure in order to correctly identify the appropriate population units to conserve. © 2013 Springer Science+Business Media Dordrecht (outside the USA).
Author Thomé, Joao Carlos
LaCasella, Erin
Formia, Angela
Eckert, Scott
Tiwari, Manjula
Chacon-Chaverri, Didiher
Stewart, Kelly R.
Dutton, Peter H.
Livingstone, Suzanne R.
Rivalan, Philippe
Allman, Phil
Roden, Suzanne E.
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  organization: Protected Resources Division, Southwest Fisheries Science Center, National Marine Fisheries Service, National Oceanic and Atmospheric Administration
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  surname: Stewart
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  organization: Protected Resources Division, Southwest Fisheries Science Center, National Marine Fisheries Service, National Oceanic and Atmospheric Administration
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  surname: Livingstone
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  organization: College of Medical, Veterinary & Life Sciences, Institute of Biodiversity, Animal Health & Comparative Medicine, University of Glasgow
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  fullname: Eckert, Scott
  organization: Biology and Natural Resources Department, Principia College
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  fullname: Allman, Phil
  organization: Department of Biological Studies, Florida Gulf Coast University
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Issue 3
Keywords Microsatellites
Recovery plan
Mitochondrial DNA
Demographically independent populations
Management
Sea turtle
Conservation genetics
Language English
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  year: 2013
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PublicationTitle Conservation genetics
PublicationTitleAbbrev Conserv Genet
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LaCasella EL, Dutton PH (2008) Longer mtDNA sequences resolve leatherback stock structure. In: Rees AF, Frick M, Panagopoulou A, Williams K (eds.) Proceedings of the twenty-seventh annual symposium on sea turtle biology and conservation, p 128–129. NOAA technical memorandum NMFS-SEFSC-569. NOAA, Miami, p 262
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References_xml – reference: Martinez LS, Barragan AR (2011) Importance of networks for conservation of the Pacific leatherback turtle: the case of “Projecto Laud” in Mexico. In: Dutton PH, Squires D, Mahfuzuddin A (eds) Conservation and sustainable management of sea turtles in the Pacific Ocean. University of Hawaii Press, Hawaii, pp 120–131
– reference: HoelzelARDoverGAGenetic differentiation between sympatric Killer whale populationsHeredity19916619119510.1038/hdy.1991.24
– reference: FitzSimmonsNNMoritzCLimpusCJPopeLPrinceRITGeographic structure of the mitochondrial and nuclear gene polymorphisms in Australian green turtle populations and male-biased gene flowGenetics19971471843185494098401:CAS:528:DyaK1cXivFGqsQ%3D%3D
– reference: WittMJBongunoEABroderickACCoyneMSFormiaAGibudiAMounguenguiGAMMoussoundaCNsafouMNougessonoSParnellRJSounguetG-PVerhageSGodleyBJTracking leatherback turtles from the world’s largest rookery: assessing threats across the South AtlanticProc R Soc B2011278233823472120894910.1098/rspb.2010.2467
– reference: GuoSWThompsonEAPerforming the exact test of Hardy–Weinberg proportion for multiple allelesBiometrics199248361372163796610.2307/25322961:STN:280:DyaK38zksFGgsA%3D%3D
– reference: SambrookJFritschEFManiatisTMolecular cloning: a laboratory manual1989New YorkCold Spring Harbour Laboratory Press
– reference: Evans D, Ordonez C, Troeng S, Drews C (2007) Satellite tracking of leatherback turtles from Caribbean Central America reveals unexpected foraging grounds. In: Book of abstracts. Twenty-seventh annual symposium on sea turtle biology and conservation. NOAA, Miami, p 70–71
– reference: Taylor BL (1997) Defining ‘‘population’’ to meet management objectives for marine mammals. In: Dizon AE, Chivers SJ, Perrin WF (eds) Molecular genetics of marine mammals, special publication 3. Society for Marine Mammalogy, Lawrence, p 49–65
– reference: GirondotMFreteyJLeatherback turtles, Dermochelys coriacea, nesting in French Guiana, 1978–1995Chelonian Conserv Biol19962204208
– reference: WallaceBPDiMatteoADHurleyBJFinkbeinerEMBoltenABChaloupkaMYHutchinsonBJRegional management units for marine turtles: a novel framework for prioritizing conservation and research across multiple scalesPLoS One20105e154652125300710.1371/journal.pone.0015465
– reference: Dutton PH (1996) Methods for collection and preservation of samples for sea turtle genetic studies. In: Bowen BW, Witzell WN (eds) Proceedings of the international symposium on sea turtle conservation genetics. NOAA technical memorandum NMFS-SEFSC-396. NOAA, Miami, p 17–24
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– reference: TaylorBLDizonAEFirst policy then science: why a management unit based solely on genetic criteria cannot workMol Ecol19998S11S161070354810.1046/j.1365-294X.1999.00797.x1:STN:280:DC%2BD3c7mvVWqsQ%3D%3D
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– reference: WittMJBaertBBroderickACFormiaAFreteyJGibudiAMounguenguiGAMMoussoundaCNougessonoSParnellRJRoumetDSounguetG-PVerhageSZogoAGodleyBJAerial surveying of the world’s largest leatherback turtle rookery: a more effective methodology for large-scale monitoringBiol Conserv20091421719172710.1016/j.biocon.2009.03.009
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Snippet This study presents a comprehensive genetic analysis of stock structure for leatherback turtles ( Dermochelys coriacea ), combining 17 microsatellite loci and...
This study presents a comprehensive genetic analysis of stock structure for leatherback turtles (Dermochelys coriacea), combining 17 microsatellite loci and...
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StartPage 625
SubjectTerms Animal Genetics and Genomics
Biodiversity
Biomedical and Life Sciences
Brazil
Conservation Biology/Ecology
Dermochelys coriacea
Ecology
Endangered species
Evolutionary Biology
gene flow
Gene loci
Genetic markers
Haplotypes
Indian Ocean
Life Sciences
microsatellite repeats
Mitochondrial DNA
Nesting
nesting sites
Plant Genetics and Genomics
Population differentiation
Reptiles & amphibians
Research Article
Satellite DNA
surveys
Turtles
Western Africa
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Title Population stock structure of leatherback turtles (Dermochelyscoriacea) in the Atlantic revealed using mtDNA and microsatellite markers
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