<HashMap><database>biostudies-literature</database><scores/><additional><submitter>de Faria SM</submitter><funding>Swiss National Science Foundation</funding><funding>Conselho Nacional de Desenvolvimento Científico e Tecnológico</funding><funding>Fundação de Amparo à Pesquisa do Estado da Bahia</funding><funding>Foreign, Commonwealth and Development Office</funding><funding>Bill and Melinda Gates Foundation</funding><pagination>2365-2377</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC9541511</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>235(6)</volume><pubmed_abstract>Nitrogen-fixing symbiosis is globally important in ecosystem functioning and agriculture, yet the evolutionary history of nodulation remains the focus of considerable debate. Recent evidence suggesting a single origin of nodulation followed by massive parallel evolutionary losses raises questions about why a few lineages in the N&lt;sub>2&lt;/sub> -fixing clade retained nodulation and diversified as stable nodulators, while most did not. Within legumes, nodulation is restricted to the two most diverse subfamilies, Papilionoideae and Caesalpinioideae, which show stable retention of nodulation across their core clades. We characterize two nodule anatomy types across 128 species in 56 of the 152 genera of the legume subfamily Caesalpinioideae: fixation thread nodules (FTs), where nitrogen-fixing ba</pubmed_abstract><journal>The New phytologist</journal><pubmed_title>The innovation of the symbiosome has enhanced the evolutionary stability of nitrogen fixation in legumes.</pubmed_title><pmcid>PMC9541511</pmcid><funding_grant_id>OPP11772165</funding_grant_id><funding_grant_id>310003A_156140</funding_grant_id><funding_grant_id>APP0037/2016</funding_grant_id><funding_grant_id>312125/2020‐8</funding_grant_id><funding_grant_id>156140</funding_grant_id><funding_grant_id>31003A_182453/1</funding_grant_id><pubmed_authors>Hughes CE</pubmed_authors><pubmed_authors>Tak N</pubmed_authors><pubmed_authors>Songwattana P</pubmed_authors><pubmed_authors>de Faria SM</pubmed_authors><pubmed_authors>de Lima HC</pubmed_authors><pubmed_authors>Ringelberg JJ</pubmed_authors><pubmed_authors>Cardoso D</pubmed_authors><pubmed_authors>Teaumroong N</pubmed_authors><pubmed_authors>Ardley J</pubmed_authors><pubmed_authors>Gehlot HS</pubmed_authors><pubmed_authors>Ametsitsi GKD</pubmed_authors><pubmed_authors>Zartman CE</pubmed_authors><pubmed_authors>Koenen EJM</pubmed_authors><pubmed_authors>Maluk M</pubmed_authors><pubmed_authors>James EK</pubmed_authors><pubmed_authors>Wright KM</pubmed_authors><pubmed_authors>Akomatey J</pubmed_authors><pubmed_authors>Prin Y</pubmed_authors><pubmed_authors>Gross E</pubmed_authors><pubmed_authors>Sprent JI</pubmed_authors></additional><is_claimable>false</is_claimable><name>The innovation of the symbiosome has enhanced the evolutionary stability of nitrogen fixation in legumes.</name><description>Nitrogen-fixing symbiosis is globally important in ecosystem functioning and agriculture, yet the evolutionary history of nodulation remains the focus of considerable debate. Recent evidence suggesting a single origin of nodulation followed by massive parallel evolutionary losses raises questions about why a few lineages in the N&lt;sub>2&lt;/sub> -fixing clade retained nodulation and diversified as stable nodulators, while most did not. Within legumes, nodulation is restricted to the two most diverse subfamilies, Papilionoideae and Caesalpinioideae, which show stable retention of nodulation across their core clades. We characterize two nodule anatomy types across 128 species in 56 of the 152 genera of the legume subfamily Caesalpinioideae: fixation thread nodules (FTs), where nitrogen-fixing ba</description><dates><release>2022-01-01T00:00:00Z</release><publication>2022 Sep</publication><modification>2025-04-04T20:03:41.948Z</modification><creation>2025-04-04T20:03:41.948Z</creation></dates><accession>S-EPMC9541511</accession><cross_references><pubmed>35901264</pubmed><doi>10.1111/nph.18321</doi></cross_references></HashMap>