Multi-Phase US Spread and Habitat Switching of a Post-Columbian Invasive, Sorghum halepense.
Johnsongrass (Sorghum halepense) is a striking example of a post-Columbian founder event. This natural experiment within ecological time-scales provides a unique opportunity for understanding patterns of continent-wide genetic diversity following range expansion. Microsatellite markers were used for...
Ausführliche Beschreibung
Autor*in: |
U Uzay Sezen [verfasserIn] Jacob N Barney [verfasserIn] Daniel Z Atwater [verfasserIn] Gary A Pederson [verfasserIn] Jeffrey F Pederson [verfasserIn] J Mike Chandler [verfasserIn] T Stan Cox [verfasserIn] Sheila Cox [verfasserIn] Peter Dotray [verfasserIn] David Kopec [verfasserIn] Steven E Smith [verfasserIn] Jill Schroeder [verfasserIn] Steven D Wright [verfasserIn] Yuannian Jiao [verfasserIn] Wenqian Kong [verfasserIn] Valorie Goff [verfasserIn] Susan Auckland [verfasserIn] Lisa K Rainville [verfasserIn] Gary J Pierce [verfasserIn] Cornelia Lemke [verfasserIn] Rosana Compton [verfasserIn] Christine Phillips [verfasserIn] Alexandra Kerr [verfasserIn] Matthew Mettler [verfasserIn] Andrew H Paterson [verfasserIn] |
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E-Artikel |
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Sprache: |
Englisch |
Erschienen: |
2016 |
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Übergeordnetes Werk: |
In: PLoS ONE - Public Library of Science (PLoS), 2007, 11(2016), 10, p e0164584 |
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Übergeordnetes Werk: |
volume:11 ; year:2016 ; number:10, p e0164584 |
Links: |
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DOI / URN: |
10.1371/journal.pone.0164584 |
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Katalog-ID: |
DOAJ043554369 |
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520 | |a Johnsongrass (Sorghum halepense) is a striking example of a post-Columbian founder event. This natural experiment within ecological time-scales provides a unique opportunity for understanding patterns of continent-wide genetic diversity following range expansion. Microsatellite markers were used for population genetic analyses including leaf-optimized Neighbor-Joining tree, pairwise FST, mismatch analysis, principle coordinate analysis, Tajima's D, Fu's F and Bayesian clusterings of population structure. Evidence indicates two geographically distant introductions of divergent genotypes, which spread across much of the US in <200 years. Based on geophylogeny, gene flow patterns can be inferred to have involved five phases. Centers of genetic diversity have shifted from two introduction sites separated by ~2000 miles toward the middle of the range, consistent with admixture between genotypes from the respective introductions. Genotyping provides evidence for a 'habitat switch' from agricultural to non-agricultural systems and may contribute to both Johnsongrass ubiquity and aggressiveness. Despite lower and more structured diversity at the invasion front, Johnsongrass continues to advance northward into cooler and drier habitats. Association genetic approaches may permit identification of alleles contributing to the habitat switch or other traits important to weed/invasive management and/or crop improvement. | ||
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10.1371/journal.pone.0164584 doi (DE-627)DOAJ043554369 (DE-599)DOAJ5ce3bee0405a477d880727ae54b796f8 DE-627 ger DE-627 rakwb eng U Uzay Sezen verfasserin aut Multi-Phase US Spread and Habitat Switching of a Post-Columbian Invasive, Sorghum halepense. 2016 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier Johnsongrass (Sorghum halepense) is a striking example of a post-Columbian founder event. This natural experiment within ecological time-scales provides a unique opportunity for understanding patterns of continent-wide genetic diversity following range expansion. Microsatellite markers were used for population genetic analyses including leaf-optimized Neighbor-Joining tree, pairwise FST, mismatch analysis, principle coordinate analysis, Tajima's D, Fu's F and Bayesian clusterings of population structure. Evidence indicates two geographically distant introductions of divergent genotypes, which spread across much of the US in <200 years. Based on geophylogeny, gene flow patterns can be inferred to have involved five phases. Centers of genetic diversity have shifted from two introduction sites separated by ~2000 miles toward the middle of the range, consistent with admixture between genotypes from the respective introductions. Genotyping provides evidence for a 'habitat switch' from agricultural to non-agricultural systems and may contribute to both Johnsongrass ubiquity and aggressiveness. Despite lower and more structured diversity at the invasion front, Johnsongrass continues to advance northward into cooler and drier habitats. Association genetic approaches may permit identification of alleles contributing to the habitat switch or other traits important to weed/invasive management and/or crop improvement. Medicine R Science Q Jacob N Barney verfasserin aut Daniel Z Atwater verfasserin aut Gary A Pederson verfasserin aut Jeffrey F Pederson verfasserin aut J Mike Chandler verfasserin aut T Stan Cox verfasserin aut Sheila Cox verfasserin aut Peter Dotray verfasserin aut David Kopec verfasserin aut Steven E Smith verfasserin aut Jill Schroeder verfasserin aut Steven D Wright verfasserin aut Yuannian Jiao verfasserin aut Wenqian Kong verfasserin aut Valorie Goff verfasserin aut Susan Auckland verfasserin aut Lisa K Rainville verfasserin aut Gary J Pierce verfasserin aut Cornelia Lemke verfasserin aut Rosana Compton verfasserin aut Christine Phillips verfasserin aut Alexandra Kerr verfasserin aut Matthew Mettler verfasserin aut Andrew H Paterson verfasserin aut In PLoS ONE Public Library of Science (PLoS), 2007 11(2016), 10, p e0164584 (DE-627)523574592 (DE-600)2267670-3 19326203 nnns volume:11 year:2016 number:10, p e0164584 https://doi.org/10.1371/journal.pone.0164584 kostenfrei https://doaj.org/article/5ce3bee0405a477d880727ae54b796f8 kostenfrei http://europepmc.org/articles/PMC5068735?pdf=render kostenfrei https://doaj.org/toc/1932-6203 Journal toc kostenfrei GBV_USEFLAG_A SYSFLAG_A GBV_DOAJ SSG-OLC-PHA GBV_ILN_11 GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_31 GBV_ILN_34 GBV_ILN_39 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_63 GBV_ILN_65 GBV_ILN_69 GBV_ILN_70 GBV_ILN_73 GBV_ILN_74 GBV_ILN_95 GBV_ILN_105 GBV_ILN_110 GBV_ILN_151 GBV_ILN_161 GBV_ILN_170 GBV_ILN_171 GBV_ILN_206 GBV_ILN_213 GBV_ILN_224 GBV_ILN_230 GBV_ILN_235 GBV_ILN_285 GBV_ILN_293 GBV_ILN_370 GBV_ILN_602 GBV_ILN_702 GBV_ILN_2001 GBV_ILN_2003 GBV_ILN_2005 GBV_ILN_2006 GBV_ILN_2008 GBV_ILN_2009 GBV_ILN_2010 GBV_ILN_2011 GBV_ILN_2014 GBV_ILN_2015 GBV_ILN_2020 GBV_ILN_2021 GBV_ILN_2025 GBV_ILN_2031 GBV_ILN_2038 GBV_ILN_2044 GBV_ILN_2048 GBV_ILN_2050 GBV_ILN_2055 GBV_ILN_2056 GBV_ILN_2057 GBV_ILN_2061 GBV_ILN_2111 GBV_ILN_2113 GBV_ILN_2190 GBV_ILN_2522 GBV_ILN_4012 GBV_ILN_4037 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4126 GBV_ILN_4249 GBV_ILN_4305 GBV_ILN_4306 GBV_ILN_4307 GBV_ILN_4313 GBV_ILN_4322 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4325 GBV_ILN_4335 GBV_ILN_4338 GBV_ILN_4367 GBV_ILN_4700 AR 11 2016 10, p e0164584 |
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10.1371/journal.pone.0164584 doi (DE-627)DOAJ043554369 (DE-599)DOAJ5ce3bee0405a477d880727ae54b796f8 DE-627 ger DE-627 rakwb eng U Uzay Sezen verfasserin aut Multi-Phase US Spread and Habitat Switching of a Post-Columbian Invasive, Sorghum halepense. 2016 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier Johnsongrass (Sorghum halepense) is a striking example of a post-Columbian founder event. This natural experiment within ecological time-scales provides a unique opportunity for understanding patterns of continent-wide genetic diversity following range expansion. Microsatellite markers were used for population genetic analyses including leaf-optimized Neighbor-Joining tree, pairwise FST, mismatch analysis, principle coordinate analysis, Tajima's D, Fu's F and Bayesian clusterings of population structure. Evidence indicates two geographically distant introductions of divergent genotypes, which spread across much of the US in <200 years. Based on geophylogeny, gene flow patterns can be inferred to have involved five phases. Centers of genetic diversity have shifted from two introduction sites separated by ~2000 miles toward the middle of the range, consistent with admixture between genotypes from the respective introductions. Genotyping provides evidence for a 'habitat switch' from agricultural to non-agricultural systems and may contribute to both Johnsongrass ubiquity and aggressiveness. Despite lower and more structured diversity at the invasion front, Johnsongrass continues to advance northward into cooler and drier habitats. Association genetic approaches may permit identification of alleles contributing to the habitat switch or other traits important to weed/invasive management and/or crop improvement. Medicine R Science Q Jacob N Barney verfasserin aut Daniel Z Atwater verfasserin aut Gary A Pederson verfasserin aut Jeffrey F Pederson verfasserin aut J Mike Chandler verfasserin aut T Stan Cox verfasserin aut Sheila Cox verfasserin aut Peter Dotray verfasserin aut David Kopec verfasserin aut Steven E Smith verfasserin aut Jill Schroeder verfasserin aut Steven D Wright verfasserin aut Yuannian Jiao verfasserin aut Wenqian Kong verfasserin aut Valorie Goff verfasserin aut Susan Auckland verfasserin aut Lisa K Rainville verfasserin aut Gary J Pierce verfasserin aut Cornelia Lemke verfasserin aut Rosana Compton verfasserin aut Christine Phillips verfasserin aut Alexandra Kerr verfasserin aut Matthew Mettler verfasserin aut Andrew H Paterson verfasserin aut In PLoS ONE Public Library of Science (PLoS), 2007 11(2016), 10, p e0164584 (DE-627)523574592 (DE-600)2267670-3 19326203 nnns volume:11 year:2016 number:10, p e0164584 https://doi.org/10.1371/journal.pone.0164584 kostenfrei https://doaj.org/article/5ce3bee0405a477d880727ae54b796f8 kostenfrei http://europepmc.org/articles/PMC5068735?pdf=render kostenfrei https://doaj.org/toc/1932-6203 Journal toc kostenfrei GBV_USEFLAG_A SYSFLAG_A GBV_DOAJ SSG-OLC-PHA GBV_ILN_11 GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_31 GBV_ILN_34 GBV_ILN_39 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_63 GBV_ILN_65 GBV_ILN_69 GBV_ILN_70 GBV_ILN_73 GBV_ILN_74 GBV_ILN_95 GBV_ILN_105 GBV_ILN_110 GBV_ILN_151 GBV_ILN_161 GBV_ILN_170 GBV_ILN_171 GBV_ILN_206 GBV_ILN_213 GBV_ILN_224 GBV_ILN_230 GBV_ILN_235 GBV_ILN_285 GBV_ILN_293 GBV_ILN_370 GBV_ILN_602 GBV_ILN_702 GBV_ILN_2001 GBV_ILN_2003 GBV_ILN_2005 GBV_ILN_2006 GBV_ILN_2008 GBV_ILN_2009 GBV_ILN_2010 GBV_ILN_2011 GBV_ILN_2014 GBV_ILN_2015 GBV_ILN_2020 GBV_ILN_2021 GBV_ILN_2025 GBV_ILN_2031 GBV_ILN_2038 GBV_ILN_2044 GBV_ILN_2048 GBV_ILN_2050 GBV_ILN_2055 GBV_ILN_2056 GBV_ILN_2057 GBV_ILN_2061 GBV_ILN_2111 GBV_ILN_2113 GBV_ILN_2190 GBV_ILN_2522 GBV_ILN_4012 GBV_ILN_4037 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4126 GBV_ILN_4249 GBV_ILN_4305 GBV_ILN_4306 GBV_ILN_4307 GBV_ILN_4313 GBV_ILN_4322 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4325 GBV_ILN_4335 GBV_ILN_4338 GBV_ILN_4367 GBV_ILN_4700 AR 11 2016 10, p e0164584 |
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10.1371/journal.pone.0164584 doi (DE-627)DOAJ043554369 (DE-599)DOAJ5ce3bee0405a477d880727ae54b796f8 DE-627 ger DE-627 rakwb eng U Uzay Sezen verfasserin aut Multi-Phase US Spread and Habitat Switching of a Post-Columbian Invasive, Sorghum halepense. 2016 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier Johnsongrass (Sorghum halepense) is a striking example of a post-Columbian founder event. This natural experiment within ecological time-scales provides a unique opportunity for understanding patterns of continent-wide genetic diversity following range expansion. Microsatellite markers were used for population genetic analyses including leaf-optimized Neighbor-Joining tree, pairwise FST, mismatch analysis, principle coordinate analysis, Tajima's D, Fu's F and Bayesian clusterings of population structure. Evidence indicates two geographically distant introductions of divergent genotypes, which spread across much of the US in <200 years. Based on geophylogeny, gene flow patterns can be inferred to have involved five phases. Centers of genetic diversity have shifted from two introduction sites separated by ~2000 miles toward the middle of the range, consistent with admixture between genotypes from the respective introductions. Genotyping provides evidence for a 'habitat switch' from agricultural to non-agricultural systems and may contribute to both Johnsongrass ubiquity and aggressiveness. Despite lower and more structured diversity at the invasion front, Johnsongrass continues to advance northward into cooler and drier habitats. Association genetic approaches may permit identification of alleles contributing to the habitat switch or other traits important to weed/invasive management and/or crop improvement. Medicine R Science Q Jacob N Barney verfasserin aut Daniel Z Atwater verfasserin aut Gary A Pederson verfasserin aut Jeffrey F Pederson verfasserin aut J Mike Chandler verfasserin aut T Stan Cox verfasserin aut Sheila Cox verfasserin aut Peter Dotray verfasserin aut David Kopec verfasserin aut Steven E Smith verfasserin aut Jill Schroeder verfasserin aut Steven D Wright verfasserin aut Yuannian Jiao verfasserin aut Wenqian Kong verfasserin aut Valorie Goff verfasserin aut Susan Auckland verfasserin aut Lisa K Rainville verfasserin aut Gary J Pierce verfasserin aut Cornelia Lemke verfasserin aut Rosana Compton verfasserin aut Christine Phillips verfasserin aut Alexandra Kerr verfasserin aut Matthew Mettler verfasserin aut Andrew H Paterson verfasserin aut In PLoS ONE Public Library of Science (PLoS), 2007 11(2016), 10, p e0164584 (DE-627)523574592 (DE-600)2267670-3 19326203 nnns volume:11 year:2016 number:10, p e0164584 https://doi.org/10.1371/journal.pone.0164584 kostenfrei https://doaj.org/article/5ce3bee0405a477d880727ae54b796f8 kostenfrei http://europepmc.org/articles/PMC5068735?pdf=render kostenfrei https://doaj.org/toc/1932-6203 Journal toc kostenfrei GBV_USEFLAG_A SYSFLAG_A GBV_DOAJ SSG-OLC-PHA GBV_ILN_11 GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_31 GBV_ILN_34 GBV_ILN_39 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_63 GBV_ILN_65 GBV_ILN_69 GBV_ILN_70 GBV_ILN_73 GBV_ILN_74 GBV_ILN_95 GBV_ILN_105 GBV_ILN_110 GBV_ILN_151 GBV_ILN_161 GBV_ILN_170 GBV_ILN_171 GBV_ILN_206 GBV_ILN_213 GBV_ILN_224 GBV_ILN_230 GBV_ILN_235 GBV_ILN_285 GBV_ILN_293 GBV_ILN_370 GBV_ILN_602 GBV_ILN_702 GBV_ILN_2001 GBV_ILN_2003 GBV_ILN_2005 GBV_ILN_2006 GBV_ILN_2008 GBV_ILN_2009 GBV_ILN_2010 GBV_ILN_2011 GBV_ILN_2014 GBV_ILN_2015 GBV_ILN_2020 GBV_ILN_2021 GBV_ILN_2025 GBV_ILN_2031 GBV_ILN_2038 GBV_ILN_2044 GBV_ILN_2048 GBV_ILN_2050 GBV_ILN_2055 GBV_ILN_2056 GBV_ILN_2057 GBV_ILN_2061 GBV_ILN_2111 GBV_ILN_2113 GBV_ILN_2190 GBV_ILN_2522 GBV_ILN_4012 GBV_ILN_4037 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4126 GBV_ILN_4249 GBV_ILN_4305 GBV_ILN_4306 GBV_ILN_4307 GBV_ILN_4313 GBV_ILN_4322 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4325 GBV_ILN_4335 GBV_ILN_4338 GBV_ILN_4367 GBV_ILN_4700 AR 11 2016 10, p e0164584 |
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10.1371/journal.pone.0164584 doi (DE-627)DOAJ043554369 (DE-599)DOAJ5ce3bee0405a477d880727ae54b796f8 DE-627 ger DE-627 rakwb eng U Uzay Sezen verfasserin aut Multi-Phase US Spread and Habitat Switching of a Post-Columbian Invasive, Sorghum halepense. 2016 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier Johnsongrass (Sorghum halepense) is a striking example of a post-Columbian founder event. This natural experiment within ecological time-scales provides a unique opportunity for understanding patterns of continent-wide genetic diversity following range expansion. Microsatellite markers were used for population genetic analyses including leaf-optimized Neighbor-Joining tree, pairwise FST, mismatch analysis, principle coordinate analysis, Tajima's D, Fu's F and Bayesian clusterings of population structure. Evidence indicates two geographically distant introductions of divergent genotypes, which spread across much of the US in <200 years. Based on geophylogeny, gene flow patterns can be inferred to have involved five phases. Centers of genetic diversity have shifted from two introduction sites separated by ~2000 miles toward the middle of the range, consistent with admixture between genotypes from the respective introductions. Genotyping provides evidence for a 'habitat switch' from agricultural to non-agricultural systems and may contribute to both Johnsongrass ubiquity and aggressiveness. Despite lower and more structured diversity at the invasion front, Johnsongrass continues to advance northward into cooler and drier habitats. Association genetic approaches may permit identification of alleles contributing to the habitat switch or other traits important to weed/invasive management and/or crop improvement. Medicine R Science Q Jacob N Barney verfasserin aut Daniel Z Atwater verfasserin aut Gary A Pederson verfasserin aut Jeffrey F Pederson verfasserin aut J Mike Chandler verfasserin aut T Stan Cox verfasserin aut Sheila Cox verfasserin aut Peter Dotray verfasserin aut David Kopec verfasserin aut Steven E Smith verfasserin aut Jill Schroeder verfasserin aut Steven D Wright verfasserin aut Yuannian Jiao verfasserin aut Wenqian Kong verfasserin aut Valorie Goff verfasserin aut Susan Auckland verfasserin aut Lisa K Rainville verfasserin aut Gary J Pierce verfasserin aut Cornelia Lemke verfasserin aut Rosana Compton verfasserin aut Christine Phillips verfasserin aut Alexandra Kerr verfasserin aut Matthew Mettler verfasserin aut Andrew H Paterson verfasserin aut In PLoS ONE Public Library of Science (PLoS), 2007 11(2016), 10, p e0164584 (DE-627)523574592 (DE-600)2267670-3 19326203 nnns volume:11 year:2016 number:10, p e0164584 https://doi.org/10.1371/journal.pone.0164584 kostenfrei https://doaj.org/article/5ce3bee0405a477d880727ae54b796f8 kostenfrei http://europepmc.org/articles/PMC5068735?pdf=render kostenfrei https://doaj.org/toc/1932-6203 Journal toc kostenfrei GBV_USEFLAG_A SYSFLAG_A GBV_DOAJ SSG-OLC-PHA GBV_ILN_11 GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_31 GBV_ILN_34 GBV_ILN_39 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_63 GBV_ILN_65 GBV_ILN_69 GBV_ILN_70 GBV_ILN_73 GBV_ILN_74 GBV_ILN_95 GBV_ILN_105 GBV_ILN_110 GBV_ILN_151 GBV_ILN_161 GBV_ILN_170 GBV_ILN_171 GBV_ILN_206 GBV_ILN_213 GBV_ILN_224 GBV_ILN_230 GBV_ILN_235 GBV_ILN_285 GBV_ILN_293 GBV_ILN_370 GBV_ILN_602 GBV_ILN_702 GBV_ILN_2001 GBV_ILN_2003 GBV_ILN_2005 GBV_ILN_2006 GBV_ILN_2008 GBV_ILN_2009 GBV_ILN_2010 GBV_ILN_2011 GBV_ILN_2014 GBV_ILN_2015 GBV_ILN_2020 GBV_ILN_2021 GBV_ILN_2025 GBV_ILN_2031 GBV_ILN_2038 GBV_ILN_2044 GBV_ILN_2048 GBV_ILN_2050 GBV_ILN_2055 GBV_ILN_2056 GBV_ILN_2057 GBV_ILN_2061 GBV_ILN_2111 GBV_ILN_2113 GBV_ILN_2190 GBV_ILN_2522 GBV_ILN_4012 GBV_ILN_4037 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4126 GBV_ILN_4249 GBV_ILN_4305 GBV_ILN_4306 GBV_ILN_4307 GBV_ILN_4313 GBV_ILN_4322 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4325 GBV_ILN_4335 GBV_ILN_4338 GBV_ILN_4367 GBV_ILN_4700 AR 11 2016 10, p e0164584 |
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10.1371/journal.pone.0164584 doi (DE-627)DOAJ043554369 (DE-599)DOAJ5ce3bee0405a477d880727ae54b796f8 DE-627 ger DE-627 rakwb eng U Uzay Sezen verfasserin aut Multi-Phase US Spread and Habitat Switching of a Post-Columbian Invasive, Sorghum halepense. 2016 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier Johnsongrass (Sorghum halepense) is a striking example of a post-Columbian founder event. This natural experiment within ecological time-scales provides a unique opportunity for understanding patterns of continent-wide genetic diversity following range expansion. Microsatellite markers were used for population genetic analyses including leaf-optimized Neighbor-Joining tree, pairwise FST, mismatch analysis, principle coordinate analysis, Tajima's D, Fu's F and Bayesian clusterings of population structure. Evidence indicates two geographically distant introductions of divergent genotypes, which spread across much of the US in <200 years. Based on geophylogeny, gene flow patterns can be inferred to have involved five phases. Centers of genetic diversity have shifted from two introduction sites separated by ~2000 miles toward the middle of the range, consistent with admixture between genotypes from the respective introductions. Genotyping provides evidence for a 'habitat switch' from agricultural to non-agricultural systems and may contribute to both Johnsongrass ubiquity and aggressiveness. Despite lower and more structured diversity at the invasion front, Johnsongrass continues to advance northward into cooler and drier habitats. Association genetic approaches may permit identification of alleles contributing to the habitat switch or other traits important to weed/invasive management and/or crop improvement. Medicine R Science Q Jacob N Barney verfasserin aut Daniel Z Atwater verfasserin aut Gary A Pederson verfasserin aut Jeffrey F Pederson verfasserin aut J Mike Chandler verfasserin aut T Stan Cox verfasserin aut Sheila Cox verfasserin aut Peter Dotray verfasserin aut David Kopec verfasserin aut Steven E Smith verfasserin aut Jill Schroeder verfasserin aut Steven D Wright verfasserin aut Yuannian Jiao verfasserin aut Wenqian Kong verfasserin aut Valorie Goff verfasserin aut Susan Auckland verfasserin aut Lisa K Rainville verfasserin aut Gary J Pierce verfasserin aut Cornelia Lemke verfasserin aut Rosana Compton verfasserin aut Christine Phillips verfasserin aut Alexandra Kerr verfasserin aut Matthew Mettler verfasserin aut Andrew H Paterson verfasserin aut In PLoS ONE Public Library of Science (PLoS), 2007 11(2016), 10, p e0164584 (DE-627)523574592 (DE-600)2267670-3 19326203 nnns volume:11 year:2016 number:10, p e0164584 https://doi.org/10.1371/journal.pone.0164584 kostenfrei https://doaj.org/article/5ce3bee0405a477d880727ae54b796f8 kostenfrei http://europepmc.org/articles/PMC5068735?pdf=render kostenfrei https://doaj.org/toc/1932-6203 Journal toc kostenfrei GBV_USEFLAG_A SYSFLAG_A GBV_DOAJ SSG-OLC-PHA GBV_ILN_11 GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_31 GBV_ILN_34 GBV_ILN_39 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_63 GBV_ILN_65 GBV_ILN_69 GBV_ILN_70 GBV_ILN_73 GBV_ILN_74 GBV_ILN_95 GBV_ILN_105 GBV_ILN_110 GBV_ILN_151 GBV_ILN_161 GBV_ILN_170 GBV_ILN_171 GBV_ILN_206 GBV_ILN_213 GBV_ILN_224 GBV_ILN_230 GBV_ILN_235 GBV_ILN_285 GBV_ILN_293 GBV_ILN_370 GBV_ILN_602 GBV_ILN_702 GBV_ILN_2001 GBV_ILN_2003 GBV_ILN_2005 GBV_ILN_2006 GBV_ILN_2008 GBV_ILN_2009 GBV_ILN_2010 GBV_ILN_2011 GBV_ILN_2014 GBV_ILN_2015 GBV_ILN_2020 GBV_ILN_2021 GBV_ILN_2025 GBV_ILN_2031 GBV_ILN_2038 GBV_ILN_2044 GBV_ILN_2048 GBV_ILN_2050 GBV_ILN_2055 GBV_ILN_2056 GBV_ILN_2057 GBV_ILN_2061 GBV_ILN_2111 GBV_ILN_2113 GBV_ILN_2190 GBV_ILN_2522 GBV_ILN_4012 GBV_ILN_4037 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4126 GBV_ILN_4249 GBV_ILN_4305 GBV_ILN_4306 GBV_ILN_4307 GBV_ILN_4313 GBV_ILN_4322 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4325 GBV_ILN_4335 GBV_ILN_4338 GBV_ILN_4367 GBV_ILN_4700 AR 11 2016 10, p e0164584 |
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U Uzay Sezen @@aut@@ Jacob N Barney @@aut@@ Daniel Z Atwater @@aut@@ Gary A Pederson @@aut@@ Jeffrey F Pederson @@aut@@ J Mike Chandler @@aut@@ T Stan Cox @@aut@@ Sheila Cox @@aut@@ Peter Dotray @@aut@@ David Kopec @@aut@@ Steven E Smith @@aut@@ Jill Schroeder @@aut@@ Steven D Wright @@aut@@ Yuannian Jiao @@aut@@ Wenqian Kong @@aut@@ Valorie Goff @@aut@@ Susan Auckland @@aut@@ Lisa K Rainville @@aut@@ Gary J Pierce @@aut@@ Cornelia Lemke @@aut@@ Rosana Compton @@aut@@ Christine Phillips @@aut@@ Alexandra Kerr @@aut@@ Matthew Mettler @@aut@@ Andrew H Paterson @@aut@@ |
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Multi-Phase US Spread and Habitat Switching of a Post-Columbian Invasive, Sorghum halepense. |
abstract |
Johnsongrass (Sorghum halepense) is a striking example of a post-Columbian founder event. This natural experiment within ecological time-scales provides a unique opportunity for understanding patterns of continent-wide genetic diversity following range expansion. Microsatellite markers were used for population genetic analyses including leaf-optimized Neighbor-Joining tree, pairwise FST, mismatch analysis, principle coordinate analysis, Tajima's D, Fu's F and Bayesian clusterings of population structure. Evidence indicates two geographically distant introductions of divergent genotypes, which spread across much of the US in <200 years. Based on geophylogeny, gene flow patterns can be inferred to have involved five phases. Centers of genetic diversity have shifted from two introduction sites separated by ~2000 miles toward the middle of the range, consistent with admixture between genotypes from the respective introductions. Genotyping provides evidence for a 'habitat switch' from agricultural to non-agricultural systems and may contribute to both Johnsongrass ubiquity and aggressiveness. Despite lower and more structured diversity at the invasion front, Johnsongrass continues to advance northward into cooler and drier habitats. Association genetic approaches may permit identification of alleles contributing to the habitat switch or other traits important to weed/invasive management and/or crop improvement. |
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Johnsongrass (Sorghum halepense) is a striking example of a post-Columbian founder event. This natural experiment within ecological time-scales provides a unique opportunity for understanding patterns of continent-wide genetic diversity following range expansion. Microsatellite markers were used for population genetic analyses including leaf-optimized Neighbor-Joining tree, pairwise FST, mismatch analysis, principle coordinate analysis, Tajima's D, Fu's F and Bayesian clusterings of population structure. Evidence indicates two geographically distant introductions of divergent genotypes, which spread across much of the US in <200 years. Based on geophylogeny, gene flow patterns can be inferred to have involved five phases. Centers of genetic diversity have shifted from two introduction sites separated by ~2000 miles toward the middle of the range, consistent with admixture between genotypes from the respective introductions. Genotyping provides evidence for a 'habitat switch' from agricultural to non-agricultural systems and may contribute to both Johnsongrass ubiquity and aggressiveness. Despite lower and more structured diversity at the invasion front, Johnsongrass continues to advance northward into cooler and drier habitats. Association genetic approaches may permit identification of alleles contributing to the habitat switch or other traits important to weed/invasive management and/or crop improvement. |
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Johnsongrass (Sorghum halepense) is a striking example of a post-Columbian founder event. This natural experiment within ecological time-scales provides a unique opportunity for understanding patterns of continent-wide genetic diversity following range expansion. Microsatellite markers were used for population genetic analyses including leaf-optimized Neighbor-Joining tree, pairwise FST, mismatch analysis, principle coordinate analysis, Tajima's D, Fu's F and Bayesian clusterings of population structure. Evidence indicates two geographically distant introductions of divergent genotypes, which spread across much of the US in <200 years. Based on geophylogeny, gene flow patterns can be inferred to have involved five phases. Centers of genetic diversity have shifted from two introduction sites separated by ~2000 miles toward the middle of the range, consistent with admixture between genotypes from the respective introductions. Genotyping provides evidence for a 'habitat switch' from agricultural to non-agricultural systems and may contribute to both Johnsongrass ubiquity and aggressiveness. Despite lower and more structured diversity at the invasion front, Johnsongrass continues to advance northward into cooler and drier habitats. Association genetic approaches may permit identification of alleles contributing to the habitat switch or other traits important to weed/invasive management and/or crop improvement. |
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Multi-Phase US Spread and Habitat Switching of a Post-Columbian Invasive, Sorghum halepense. |
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