Concordant Signal of Genetic Variation Across Marker Densities in the Desert Annual Chylismia brevipes Is Linked With Timing of Winter Precipitation
ABSTRACT Climate change coupled with large‐scale surface disturbances necessitate active restoration strategies to promote resilient and genetically diverse native plant communities. However, scarcity of native plant materials hinders restoration efforts, leading practitioners to choose from potenti...
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Climate change coupled with large‐scale surface disturbances necessitate active restoration strategies to promote resilient and genetically diverse native plant communities. However, scarcity of native plant materials hinders restoration efforts, leading practitioners to choose from potentially viable but nonlocal seed sources. Genome scans for genetic variation linked with selective environmental gradients have become a useful tool in such efforts, allowing rapid delineation of seed transfer zones along with predictions of genomic vulnerability to climate change. When properly applied, genome scans can reduce the risk of maladaptation due to mismatches between seed source and planting site. However, results are rarely replicated among complimentary data sources. Here, we compared RAD‐seq datasets with 819 and 2699 SNPs (in 625 and 356 individuals, respectively) from the Mojave Desert winter annual Chylismia brevipes. Overall, we found that the datasets consistently characterized both neutral population structure and genetic–environmental associations. Ancestry analyses indicated consistent spatial genetic structuring into four regional populations. We also detected a marked signal of isolation by resistance (IBR), wherein spatial genetic structure was better explained by habitat resistance than by geographic distance. Potentially adaptive loci identified from genome scans were associated with the same environmental gradients—fall precipitation, winter minimum temperature, and precipitation timing—regardless of dataset. Paired with our finding that habitat resistance best explained genetic divergence, our results suggest that isolation of populations within environmentally similar habitats—and subsequent local adaption along gradients parallel to these habitats—drive genome‐wide divergence in this species. Moreover, strong genetic associations with winter precipitation timing, along with forecasted shifts in precipitation regime due to midcentury climate change, could impact future population dynamics, habitat distribution, and genetic connectivity for C. brevipes populations within the Mojave Desert. |
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Climate change coupled with large‐scale surface disturbances necessitate active restoration strategies to promote resilient and genetically diverse native plant communities. However, scarcity of native plant materials hinders restoration efforts, leading practitioners to choose from potentially viable but nonlocal seed sources. Genome scans for genetic variation linked with selective environmental gradients have become a useful tool in such efforts, allowing rapid delineation of seed transfer zones along with predictions of genomic vulnerability to climate change. When properly applied, genome scans can reduce the risk of maladaptation due to mismatches between seed source and planting site. However, results are rarely replicated among complimentary data sources. Here, we compared RAD‐seq datasets with 819 and 2699 SNPs (in 625 and 356 individuals, respectively) from the Mojave Desert winter annual Chylismia brevipes. Overall, we found that the datasets consistently characterized both neutral population structure and genetic–environmental associations. Ancestry analyses indicated consistent spatial genetic structuring into four regional populations. We also detected a marked signal of isolation by resistance (IBR), wherein spatial genetic structure was better explained by habitat resistance than by geographic distance. Potentially adaptive loci identified from genome scans were associated with the same environmental gradients—fall precipitation, winter minimum temperature, and precipitation timing—regardless of dataset. Paired with our finding that habitat resistance best explained genetic divergence, our results suggest that isolation of populations within environmentally similar habitats—and subsequent local adaption along gradients parallel to these habitats—drive genome‐wide divergence in this species. Moreover, strong genetic associations with winter precipitation timing, along with forecasted shifts in precipitation regime due to midcentury climate change, could impact future population dynamics, habitat distribution, and genetic connectivity for C. brevipes populations within the Mojave Desert.</description><identifier>ISSN: 1752-4571</identifier><identifier>EISSN: 1752-4571</identifier><identifier>DOI: 10.1111/eva.70046</identifier><identifier>PMID: 39691745</identifier><language>eng</language><publisher>England: John Wiley & Sons, Inc</publisher><subject>Adaptation ; Climate change ; Climate prediction ; Datasets ; Deserts ; Divergence ; Endangered & extinct species ; Environmental restoration ; Genetic analysis ; Genetic diversity ; Genetic structure ; genome scan ; Genomes ; Geographical distribution ; Habitats ; isolation by environment ; Nonnative species ; Original ; Plant communities ; Population dynamics ; Population genetics ; Population structure ; Precipitation ; restoration ; seed sourcing ; Seeds ; Single-nucleotide polymorphism ; Temperature ; Winter</subject><ispartof>Evolutionary applications, 2024-12, Vol.17 (12), p.e70046-n/a</ispartof><rights>Published 2024. This article is a U.S. Government work and is in the public domain in the USA. published by John Wiley & Sons Ltd.</rights><rights>Published 2024. This article is a U.S. Government work and is in the public domain in the USA. Evolutionary Applications published by John Wiley & Sons Ltd.</rights><rights>2024. This work is published under http://creativecommons.org/licenses/by/4.0/ (the "License"). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><cites>FETCH-LOGICAL-c4006-46fab781ad58202254ffce7a51b5420262890b7431089c2ac5495058049fcf163</cites><orcidid>0000-0003-0330-9815</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC11649585/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC11649585/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,314,723,776,780,860,881,1411,2095,11542,27903,27904,45553,45554,46031,46455,53770,53772</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/39691745$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Shryock, Daniel F.</creatorcontrib><creatorcontrib>Lê, Nila</creatorcontrib><creatorcontrib>DeFalco, Lesley A.</creatorcontrib><creatorcontrib>Esque, Todd C.</creatorcontrib><title>Concordant Signal of Genetic Variation Across Marker Densities in the Desert Annual Chylismia brevipes Is Linked With Timing of Winter Precipitation</title><title>Evolutionary applications</title><addtitle>Evol Appl</addtitle><description>ABSTRACT
Climate change coupled with large‐scale surface disturbances necessitate active restoration strategies to promote resilient and genetically diverse native plant communities. However, scarcity of native plant materials hinders restoration efforts, leading practitioners to choose from potentially viable but nonlocal seed sources. Genome scans for genetic variation linked with selective environmental gradients have become a useful tool in such efforts, allowing rapid delineation of seed transfer zones along with predictions of genomic vulnerability to climate change. When properly applied, genome scans can reduce the risk of maladaptation due to mismatches between seed source and planting site. However, results are rarely replicated among complimentary data sources. Here, we compared RAD‐seq datasets with 819 and 2699 SNPs (in 625 and 356 individuals, respectively) from the Mojave Desert winter annual Chylismia brevipes. Overall, we found that the datasets consistently characterized both neutral population structure and genetic–environmental associations. Ancestry analyses indicated consistent spatial genetic structuring into four regional populations. We also detected a marked signal of isolation by resistance (IBR), wherein spatial genetic structure was better explained by habitat resistance than by geographic distance. Potentially adaptive loci identified from genome scans were associated with the same environmental gradients—fall precipitation, winter minimum temperature, and precipitation timing—regardless of dataset. Paired with our finding that habitat resistance best explained genetic divergence, our results suggest that isolation of populations within environmentally similar habitats—and subsequent local adaption along gradients parallel to these habitats—drive genome‐wide divergence in this species. Moreover, strong genetic associations with winter precipitation timing, along with forecasted shifts in precipitation regime due to midcentury climate change, could impact future population dynamics, habitat distribution, and genetic connectivity for C. brevipes populations within the Mojave Desert.</description><subject>Adaptation</subject><subject>Climate change</subject><subject>Climate prediction</subject><subject>Datasets</subject><subject>Deserts</subject><subject>Divergence</subject><subject>Endangered & extinct species</subject><subject>Environmental restoration</subject><subject>Genetic analysis</subject><subject>Genetic diversity</subject><subject>Genetic structure</subject><subject>genome scan</subject><subject>Genomes</subject><subject>Geographical distribution</subject><subject>Habitats</subject><subject>isolation by environment</subject><subject>Nonnative species</subject><subject>Original</subject><subject>Plant communities</subject><subject>Population dynamics</subject><subject>Population genetics</subject><subject>Population structure</subject><subject>Precipitation</subject><subject>restoration</subject><subject>seed sourcing</subject><subject>Seeds</subject><subject>Single-nucleotide polymorphism</subject><subject>Temperature</subject><subject>Winter</subject><issn>1752-4571</issn><issn>1752-4571</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2024</creationdate><recordtype>article</recordtype><sourceid>24P</sourceid><sourceid>WIN</sourceid><sourceid>ABUWG</sourceid><sourceid>AFKRA</sourceid><sourceid>AZQEC</sourceid><sourceid>BENPR</sourceid><sourceid>CCPQU</sourceid><sourceid>DWQXO</sourceid><sourceid>GNUQQ</sourceid><sourceid>DOA</sourceid><recordid>eNp1ks1uEzEQgFcIRH_gwAsgS1zgkNbetffnhKJQSqQgkCjt0fJ6Z5NJd-1ge1PlPXhgnGypWiR8sTX-9M3YM0nyhtEzFtc5bNVZQSnPnyXHrBDphIuCPX90PkpOvF9TmtM8S18mR1mVV6zg4jj5PbNGW9coE8gPXBrVEduSSzAQUJNr5VAFtIZMtbPek6_K3YIjn8B4DAieoCFhBTHgwQUyNWaIhtlq16HvUZHawRY3kZt7skBzCw25wbAiV9ijWe5T3aAJ0fjdgcYNhkO2V8mLVnUeXt_vp8nPzxdXsy-TxbfL-Wy6mGge3zLheavqomSqEWVK01TwttVQKMFqwWMgT8uK1gXPGC0rnSoteCWoKCmvWt2yPDtN5qO3sWotNw575XbSKpSHgHVLqVz8hw4kp0LThqZQUc3brFC6oKJpy1KXdQZCRNfH0bUZ6h4aDSY41T2RPr0xuJJLu5WM5bGscm94f29w9tcAPsgevYauUwbs4GXGeB7rz1gZ0Xf_oGs7uNi8A1WJIhdZFakPI3XonYP2oRpG5X5wZBwceRicyL59XP4D-XdSInA-AnfYwe7_JnlxPR2VfwAr5807</recordid><startdate>202412</startdate><enddate>202412</enddate><creator>Shryock, Daniel F.</creator><creator>Lê, Nila</creator><creator>DeFalco, Lesley A.</creator><creator>Esque, Todd C.</creator><general>John Wiley & Sons, Inc</general><general>John Wiley and Sons Inc</general><general>Wiley</general><scope>24P</scope><scope>WIN</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>8FD</scope><scope>8FE</scope><scope>8FH</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BBNVY</scope><scope>BENPR</scope><scope>BHPHI</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FR3</scope><scope>GNUQQ</scope><scope>HCIFZ</scope><scope>LK8</scope><scope>M7P</scope><scope>P64</scope><scope>PIMPY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>RC3</scope><scope>7X8</scope><scope>5PM</scope><scope>DOA</scope><orcidid>https://orcid.org/0000-0003-0330-9815</orcidid></search><sort><creationdate>202412</creationdate><title>Concordant Signal of Genetic Variation Across Marker Densities in the Desert Annual Chylismia brevipes Is Linked With Timing of Winter Precipitation</title><author>Shryock, Daniel F. ; Lê, Nila ; DeFalco, Lesley A. ; Esque, Todd C.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c4006-46fab781ad58202254ffce7a51b5420262890b7431089c2ac5495058049fcf163</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2024</creationdate><topic>Adaptation</topic><topic>Climate change</topic><topic>Climate prediction</topic><topic>Datasets</topic><topic>Deserts</topic><topic>Divergence</topic><topic>Endangered & extinct species</topic><topic>Environmental restoration</topic><topic>Genetic analysis</topic><topic>Genetic diversity</topic><topic>Genetic structure</topic><topic>genome scan</topic><topic>Genomes</topic><topic>Geographical distribution</topic><topic>Habitats</topic><topic>isolation by environment</topic><topic>Nonnative species</topic><topic>Original</topic><topic>Plant communities</topic><topic>Population dynamics</topic><topic>Population genetics</topic><topic>Population structure</topic><topic>Precipitation</topic><topic>restoration</topic><topic>seed sourcing</topic><topic>Seeds</topic><topic>Single-nucleotide polymorphism</topic><topic>Temperature</topic><topic>Winter</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Shryock, Daniel F.</creatorcontrib><creatorcontrib>Lê, Nila</creatorcontrib><creatorcontrib>DeFalco, Lesley A.</creatorcontrib><creatorcontrib>Esque, Todd C.</creatorcontrib><collection>Wiley Online Library Open Access</collection><collection>Wiley Free Content</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Technology Research Database</collection><collection>ProQuest SciTech Collection</collection><collection>ProQuest Natural Science Collection</collection><collection>ProQuest Central (Alumni Edition)</collection><collection>ProQuest Central UK/Ireland</collection><collection>ProQuest Central Essentials</collection><collection>Biological Science Collection</collection><collection>ProQuest Central</collection><collection>Natural Science Collection</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central Korea</collection><collection>Engineering Research Database</collection><collection>ProQuest Central Student</collection><collection>SciTech Premium Collection</collection><collection>ProQuest Biological Science Collection</collection><collection>Biological Science Database</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>Publicly Available Content Database</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central China</collection><collection>Genetics Abstracts</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><collection>DOAJ Directory of Open Access Journals</collection><jtitle>Evolutionary applications</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Shryock, Daniel F.</au><au>Lê, Nila</au><au>DeFalco, Lesley A.</au><au>Esque, Todd C.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Concordant Signal of Genetic Variation Across Marker Densities in the Desert Annual Chylismia brevipes Is Linked With Timing of Winter Precipitation</atitle><jtitle>Evolutionary applications</jtitle><addtitle>Evol Appl</addtitle><date>2024-12</date><risdate>2024</risdate><volume>17</volume><issue>12</issue><spage>e70046</spage><epage>n/a</epage><pages>e70046-n/a</pages><issn>1752-4571</issn><eissn>1752-4571</eissn><abstract>ABSTRACT
Climate change coupled with large‐scale surface disturbances necessitate active restoration strategies to promote resilient and genetically diverse native plant communities. However, scarcity of native plant materials hinders restoration efforts, leading practitioners to choose from potentially viable but nonlocal seed sources. Genome scans for genetic variation linked with selective environmental gradients have become a useful tool in such efforts, allowing rapid delineation of seed transfer zones along with predictions of genomic vulnerability to climate change. When properly applied, genome scans can reduce the risk of maladaptation due to mismatches between seed source and planting site. However, results are rarely replicated among complimentary data sources. Here, we compared RAD‐seq datasets with 819 and 2699 SNPs (in 625 and 356 individuals, respectively) from the Mojave Desert winter annual Chylismia brevipes. Overall, we found that the datasets consistently characterized both neutral population structure and genetic–environmental associations. Ancestry analyses indicated consistent spatial genetic structuring into four regional populations. We also detected a marked signal of isolation by resistance (IBR), wherein spatial genetic structure was better explained by habitat resistance than by geographic distance. Potentially adaptive loci identified from genome scans were associated with the same environmental gradients—fall precipitation, winter minimum temperature, and precipitation timing—regardless of dataset. Paired with our finding that habitat resistance best explained genetic divergence, our results suggest that isolation of populations within environmentally similar habitats—and subsequent local adaption along gradients parallel to these habitats—drive genome‐wide divergence in this species. Moreover, strong genetic associations with winter precipitation timing, along with forecasted shifts in precipitation regime due to midcentury climate change, could impact future population dynamics, habitat distribution, and genetic connectivity for C. brevipes populations within the Mojave Desert.</abstract><cop>England</cop><pub>John Wiley & Sons, Inc</pub><pmid>39691745</pmid><doi>10.1111/eva.70046</doi><tpages>18</tpages><orcidid>https://orcid.org/0000-0003-0330-9815</orcidid><oa>free_for_read</oa></addata></record> |
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subjects | Adaptation Climate change Climate prediction Datasets Deserts Divergence Endangered & extinct species Environmental restoration Genetic analysis Genetic diversity Genetic structure genome scan Genomes Geographical distribution Habitats isolation by environment Nonnative species Original Plant communities Population dynamics Population genetics Population structure Precipitation restoration seed sourcing Seeds Single-nucleotide polymorphism Temperature Winter |
title | Concordant Signal of Genetic Variation Across Marker Densities in the Desert Annual Chylismia brevipes Is Linked With Timing of Winter Precipitation |
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