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Estimated Timeline for the Evolution of Symbiotic Nitrogen Fixing Paraburkholderia
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Outgoing claims: the papers this work cites, builds on, or argues with.
inferredcites →https://doi.org/10.1007/bf02111283openalex-snapshot
Evolution in bacteria: Evidence for a universal substitution rate in cellular genomes
inferredcites →https://doi.org/10.1007/s00203-020-01843-wopenalex-snapshot
Paraburkholderia atlantica sp. nov. and Paraburkholderia franconis sp. nov., two new nitrogen-fixing nodulating species isolated from Atlantic forest soils in Brazil
inferredcites →https://doi.org/10.1007/s00248-011-9929-1openalex-snapshot
Common Features of Environmental and Potentially Beneficial Plant-Associated Burkholderia
inferredcites →https://doi.org/10.1007/s00248-014-0427-0openalex-snapshot
Burkholderia sp. Induces Functional Nodules on the South African Invasive Legume Dipogon lignosus (Phaseoleae) in New Zealand Soils
inferredcites →https://doi.org/10.1007/s00253-016-7520-xopenalex-snapshot
Burkholderia: an update on taxonomy and biotechnological potential as antibiotic producers
inferredcites →https://doi.org/10.1007/s10482-019-01269-5openalex-snapshot
Paraburkholderia strydomiana sp. nov. and Paraburkholderia steynii sp. nov.: rhizobial symbionts of the fynbos legume Hypocalyptus sophoroides
inferredcites →https://doi.org/10.1007/s11104-017-3521-5openalex-snapshot
Soil characteristics determine the rhizobia in association with different species of Mimosa in central Brazil
inferredcites →https://doi.org/10.1007/s11274-013-1400-7openalex-snapshot
Diversity and symbiotic effectiveness of beta-rhizobia isolated from sub-tropical legumes of a Brazilian Araucaria Forest
inferredcites →https://doi.org/10.1007/s12275-018-8014-6openalex-snapshot
UBCG: Up-to-date bacterial core gene set and pipeline for phylogenomic tree reconstruction
inferredcites →https://doi.org/10.1016/0098-3004(76)90096-0openalex-snapshot
A continental drift ‘flip book’
inferredcites →https://doi.org/10.1016/j.crpv.2013.07.003openalex-snapshot
A practical guide to molecular dating
inferredcites →https://doi.org/10.1016/j.micres.2021.126788openalex-snapshot
Phylogenomics reveals the evolution of root nodulating alpha- and beta-Proteobacteria (rhizobia)
inferredcites →https://doi.org/10.1016/j.sajb.2018.02.406openalex-snapshot
Horizontal gene transfer among rhizobia of the Core Cape Subregion of southern Africa
inferredcites →https://doi.org/10.1016/j.soilbio.2013.01.009openalex-snapshot
Novel Burkholderia bacteria isolated from Lebeckia ambigua – A perennial suffrutescent legume of the fynbos
inferredcites →https://doi.org/10.1016/j.syapm.2004.09.002openalex-snapshot
Prevalence of Burkholderia sp. nodule symbionts on four mimosoid legumes from Barro Colorado Island, Panama
inferredcites →https://doi.org/10.1016/j.syapm.2008.02.004openalex-snapshot
An effect of 16S rRNA intercistronic variability on coevolutionary analysis in symbiotic bacteria: Molecular phylogeny of Arsenophonus triatominarum
inferredcites →https://doi.org/10.1016/j.syapm.2015.09.003openalex-snapshot
Burkholderia kirstenboschensis sp. nov. nodulates papilionoid legumes indigenous to South Africa
inferredcites →https://doi.org/10.1016/j.syapm.2017.12.003openalex-snapshot
Brazilian species of Calliandra Benth. (tribe Ingeae) are nodulated by diverse strains of Paraburkholderia
inferredcites →https://doi.org/10.1016/j.syapm.2020.126151openalex-snapshot
Phylogeny of symbiotic genes reveals symbiovars within legume-nodulating Paraburkholderia species
inferredcites →https://doi.org/10.1016/j.tplants.2018.10.005openalex-snapshot
A Resurrected Scenario: Single Gain and Massive Loss of Nitrogen-Fixing Nodulation
inferredcites →https://doi.org/10.1016/j.tree.2011.08.009openalex-snapshot
Long-distance dispersal: a framework for hypothesis testing
inferredcites →https://doi.org/10.1016/j.ympev.2008.01.037openalex-snapshot
Origin and diversification of the Greater Cape flora: Ancient species repository, hot-bed of recent radiation, or both?
inferredcites →https://doi.org/10.1016/j.ympev.2010.04.024openalex-snapshot
FASconCAT: Convenient handling of data matrices
inferredcites →https://doi.org/10.1016/s0016-7037(02)00950-xopenalex-snapshot
Volcanic gases, black smokers, and the great oxidation event
inferredcites →https://doi.org/10.1016/s0022-2836(05)80360-2openalex-snapshot
Basic Local Alignment Search Tool
inferredcites →https://doi.org/10.1017/s1473550415000579openalex-snapshot
Cyanobacterial evolution during the Precambrian
inferredcites →https://doi.org/10.1038/nature13591openalex-snapshot
Pre-Columbian mycobacterial genomes reveal seals as a source of New World human tuberculosis
inferredcites →https://doi.org/10.1038/nbt.4229openalex-snapshot
A standardized bacterial taxonomy based on genome phylogeny substantially revises the tree of life
inferredcites →https://doi.org/10.1038/nmeth.4285openalex-snapshot
ModelFinder: fast model selection for accurate phylogenetic estimates
inferredcites →https://doi.org/10.1038/nrg.2015.8openalex-snapshot
Bayesian molecular clock dating of species divergences in the genomics era
inferredcites →https://doi.org/10.1038/s41467-021-24396-yopenalex-snapshot
Timing the evolution of antioxidant enzymes in cyanobacteria
inferredcites →https://doi.org/10.1038/s41587-020-0501-8openalex-snapshot
A complete domain-to-species taxonomy for Bacteria and Archaea
inferredcites →https://doi.org/10.1071/bt00023openalex-snapshot
The breakup history of Gondwana and its impact on pre-Cenozoic floristic provincialism
inferredcites →https://doi.org/10.1078/07232020260517634openalex-snapshot
Burkholderia tuberum sp. nov. and Burkholderia phymatum sp. nov., Nodulate the Roots of Tropical Legumes
inferredcites →https://doi.org/10.1080/07352689.2014.897899openalex-snapshot
Bacterial Associations with Legumes
inferredcites →https://doi.org/10.1080/10635150390235520openalex-snapshot
A Simple, Fast, and Accurate Algorithm to Estimate Large Phylogenies by Maximum Likelihood
inferredcites →https://doi.org/10.1080/10635150802429642openalex-snapshot
A Rapid Bootstrap Algorithm for the RAxML Web Servers
inferredcites →https://doi.org/10.1093/aob/mcm227openalex-snapshot
Nodulation of Cyclopia spp. (Leguminosae, Papilionoideae) by Burkholderia tuberum
inferredcites →https://doi.org/10.1093/bioinformatics/btr088openalex-snapshot
ProtTest 3: fast selection of best-fit models of protein evolution
inferredcites →https://doi.org/10.1093/bioinformatics/btu033openalex-snapshot
RAxML version 8: a tool for phylogenetic analysis and post-analysis of large phylogenies
inferredcites →https://doi.org/10.1093/bioinformatics/bty633openalex-snapshot
ape 5.0: an environment for modern phylogenetics and evolutionary analyses in R
inferredcites →https://doi.org/10.1093/molbev/msac174openalex-snapshot
TimeTree 5: An Expanded Resource for Species Divergence Times
inferredcites →https://doi.org/10.1093/molbev/msn247openalex-snapshot
A Major Clade of Prokaryotes with Ancient Adaptations to Life on Land
inferredcites →https://doi.org/10.1093/molbev/msu300openalex-snapshot
IQ-TREE: A Fast and Effective Stochastic Algorithm for Estimating Maximum-Likelihood Phylogenies
inferredcites →https://doi.org/10.1093/molbev/msv037openalex-snapshot
Tree of Life Reveals Clock-Like Speciation and Diversification
inferredcites →https://doi.org/10.1093/molbev/msw245openalex-snapshot
The Timetree of Prokaryotes: New Insights into Their Evolution and Speciation
inferredcites →https://doi.org/10.1093/molbev/msx116openalex-snapshot
TimeTree: A Resource for Timelines, Timetrees, and Divergence Times
inferredcites →https://doi.org/10.1093/molbev/msx281openalex-snapshot
UFBoot2: Improving the Ultrafast Bootstrap Approximation
inferredcites →https://doi.org/10.1093/nar/gkab301openalex-snapshot
Interactive Tree Of Life (iTOL) v5: an online tool for phylogenetic tree display and annotation
inferredcites →https://doi.org/10.1093/nar/gkf436openalex-snapshot
MAFFT: a novel method for rapid multiple sequence alignment based on fast Fourier transform
inferredcites →https://doi.org/10.1093/oso/9780199535033.001.0001openalex-snapshot
The Timetree of Life
inferredcites →https://doi.org/10.1093/oxfordjournals.molbev.a003974openalex-snapshot
Estimating Absolute Rates of Molecular Evolution and Divergence Times: A Penalized Likelihood Approach
inferredcites →https://doi.org/10.1093/oxfordjournals.molbev.a026311openalex-snapshot
The Glutamine Synthetases of Rhizobia: Phylogenetics and Evolutionary Implications
inferredcites →https://doi.org/10.1093/sysbio/syaa041openalex-snapshot
The Origin of the Legumes is a Complex Paleopolyploid Phylogenomic Tangle Closely Associated with the Cretaceous–Paleogene (K–Pg) Mass Extinction Event
inferredcites →https://doi.org/10.1093/sysbio/syq010openalex-snapshot
New Algorithms and Methods to Estimate Maximum-Likelihood Phylogenies: Assessing the Performance of PhyML 3.0
inferredcites →https://doi.org/10.1093/sysbio/syr087openalex-snapshot
Calibrated Tree Priors for Relaxed Phylogenetics and Divergence Time Estimation
inferredcites →https://doi.org/10.1094/mpmi-05-16-0091-ropenalex-snapshot
Symbiotic Burkholderia Species Show Diverse Arrangements of nif/fix and nod Genes and Lack Typical High-Affinity Cytochrome cbb3 Oxidase Genes
inferredcites →https://doi.org/10.1094/mpmi-06-11-0172openalex-snapshot
Legume-Nodulating Betaproteobacteria: Diversity, Host Range, and Future Prospects
inferredcites →https://doi.org/10.1097/00001888-193907000-00030openalex-snapshot
Bergey's Manual of Determinative Bacteriology
inferredcites →https://doi.org/10.1098/rspb.2010.1035openalex-snapshot
Estimating the age of fire in the Cape flora of South Africa from an orchid phylogeny
inferredcites →https://doi.org/10.1098/rstb.2006.1834openalex-snapshot
Fossil evidence of Archaean life
inferredcites →https://doi.org/10.1098/rstb.2006.1835openalex-snapshot
A fresh look at the fossil evidence for early Archaean cellular life
inferredcites →https://doi.org/10.1099/ijs.0.037408-0openalex-snapshot
Burkholderia symbiotica sp. nov., isolated from root nodules of Mimosa spp. native to north-east Brazil
inferredcites →https://doi.org/10.1099/ijs.0.039859-0openalex-snapshot
Burkholderia diazotrophica sp. nov., isolated from root nodules of Mimosa spp.
inferredcites →https://doi.org/10.1099/ijs.0.048777-0openalex-snapshot
Burkholderia sprentiae sp. nov., isolated from Lebeckia ambigua root nodules
inferredcites →https://doi.org/10.1099/ijs.0.058602-0openalex-snapshot
Burkholderia dilworthii sp. nov., isolated from Lebeckia ambigua root nodules
inferredcites →https://doi.org/10.1099/ijs.0.64325-0openalex-snapshot
Burkholderia mimosarum sp. nov., isolated from root nodules of Mimosa spp. from Taiwan and South America
inferredcites →https://doi.org/10.1099/ijs.0.64873-0openalex-snapshot
Burkholderia nodosa sp. nov., isolated from root nodules of the woody Brazilian legumes Mimosa bimucronata and Mimosa scabrella
inferredcites →https://doi.org/10.1099/ijsem.0.000639openalex-snapshot
Burkholderia dipogonis sp. nov., isolated from root nodules of Dipogon lignosus in New Zealand and Western Australia
inferredcites →https://doi.org/10.1099/ijsem.0.001065openalex-snapshot
Transfer of eleven species of the genus Burkholderia to the genus Paraburkholderia and proposal of Caballeronia gen. nov. to accommodate twelve species of the genera Burkholderia and Paraburkholderia
inferredcites →https://doi.org/10.1099/ijsem.0.001648openalex-snapshot
Paraburkholderia piptadeniae sp. nov. and Paraburkholderia ribeironis sp. nov., two root-nodulating symbiotic species of Piptadenia gonoacantha in Brazil
inferredcites →https://doi.org/10.1099/ijsem.0.003932openalex-snapshot
Pararobbsia silviterrae gen. nov., sp. nov., isolated from forest soil and reclassification of Burkholderia alpina as Pararobbsia alpina comb. nov.
inferredcites →https://doi.org/10.1099/ijsem.0.004332openalex-snapshot
List of Prokaryotic names with Standing in Nomenclature (LPSN) moves to the DSMZ
inferredcites →https://doi.org/10.1111/1462-2920.12286openalex-snapshot
The geographical patterns of symbiont diversity in the invasive legume M imosa pudica can be explained by the competitiveness of its symbionts and by the host genotype
inferredcites →https://doi.org/10.1111/gfs.12522openalex-snapshot
The history and distribution of nodulating Paraburkholderia, a potential inoculum for Fynbos forage species
inferredcites →https://doi.org/10.1111/j.1348-0421.1992.tb02129.xopenalex-snapshot
Proposal of Burkholderia gen. nov. and Transfer of Seven Species of the Genus Pseudomonas Homology Group II to the New Genus, with the Type Species Burkholderia cepacia (Palleroni and Holmes 1981) comb. nov.
inferredcites →https://doi.org/10.1111/j.1365-294x.2009.04458.xopenalex-snapshot
Burkholderia species are ancient symbionts of legumes
inferredcites →https://doi.org/10.1111/j.1461-0248.2009.01360.xopenalex-snapshot
Global patterns in belowground communities
inferredcites →https://doi.org/10.1111/j.1462-2920.2007.01461.xopenalex-snapshot
Life in Darwin's dust: intercontinental transport and survival of microbes in the nineteenth century
inferredcites →https://doi.org/10.1111/j.1462-2920.2008.01799.xopenalex-snapshot
Burkholderia spp. are the most competitive symbionts of Mimosa , particularly under N‐limited conditions
inferredcites →https://doi.org/10.1111/j.1469-8137.2005.01533.xopenalex-snapshot
β‐Rhizobia from Mimosa pigra , a newly discovered invasive plant in Taiwan
inferredcites →https://doi.org/10.1111/j.1469-8137.2006.01894.xopenalex-snapshot
Burkholderia phymatum is a highly effective nitrogen‐fixing symbiont of Mimosa spp. and fixes nitrogen ex planta
inferredcites →https://doi.org/10.1111/j.1469-8137.2010.03267.xopenalex-snapshot
Nodulation and nitrogen fixation by Mimosa spp. in the Cerrado and Caatinga biomes of Brazil
inferredcites →https://doi.org/10.1111/j.1472-4669.2009.00220.xopenalex-snapshot
Timing of morphological and ecological innovations in the cyanobacteria – a key to understanding the rise in atmospheric oxygen
inferredcites →https://doi.org/10.1111/j.1574-6941.2011.01235.xopenalex-snapshot
Genetic diversity of Mimosa pudica rhizobial symbionts in soils of French Guiana: investigating the origin and diversity of Burkholderia phymatum and other beta-rhizobia
inferredcites →https://doi.org/10.1111/j.1574-6976.2000.tb00547.xopenalex-snapshot
The phylogeny of proteobacteria: relationships to other eubacterial phyla and eukaryotes
inferredcites →https://doi.org/10.1111/jipb.12065openalex-snapshot
Out of Africa: Miocene Dispersal, Vicariance, and Extinction within Hyacinthaceae Subfamily Urgineoideae
inferredcites →https://doi.org/10.1111/nph.13573openalex-snapshot
Endemic M imosa species from M exico prefer alphaproteobacterial rhizobial symbionts
inferredcites →https://doi.org/10.1111/nph.15011openalex-snapshot
Constraining uncertainty in the timescale of angiosperm evolution and the veracity of a Cretaceous Terrestrial Revolution
inferredcites →https://doi.org/10.1128/aem.00591-16openalex-snapshot
Biogeographical Patterns of Legume-Nodulating Burkholderia spp.: from African Fynbos to Continental Scales
inferredcites →https://doi.org/10.1128/aem.04142-15openalex-snapshot
Novel Cupriavidus Strains Isolated from Root Nodules of Native Uruguayan Mimosa Species
inferredcites →https://doi.org/10.1128/aem.72.2.1198-1206.2006openalex-snapshot
Coexistence of Burkholderia , Cupriavidus , and Rhizobium sp. Nodule Bacteria on two Mimosa spp. in Costa Rica
inferredcites →https://doi.org/10.1128/jb.01756-12openalex-snapshot
Genome Sequences of Burkholderia sp. Strains CCGE1002 and H160, Isolated from Legume Nodules in Mexico and Brazil
inferredcites →https://doi.org/10.1128/jb.01821-12openalex-snapshot
Complete Genome Sequence of Burkholderia phenoliruptrix BR3459a (CLA1), a Heat-Tolerant, Nitrogen-Fixing Symbiont of Mimosa flocculosa
inferredcites →https://doi.org/10.1128/jb.182.20.5641-5652.2000openalex-snapshot
Keys to Symbiotic Harmony
inferredcites →https://doi.org/10.1128/microbiolspec.mtbp-0014-2016openalex-snapshot
Transmission in the Origins of Bacterial Diversity, From Ecotypes to Phyla
inferredcites →https://doi.org/10.1130/g47988.1openalex-snapshot
The role of megacontinents in the supercontinent cycle
inferredcites →https://doi.org/10.1186/1471-2148-12-17openalex-snapshot
Evolution of the intercontinental disjunctions in six continents in the Ampelopsis clade of the grape family (Vitaceae)
inferredcites →https://doi.org/10.1186/1471-2148-4-44openalex-snapshot
A genomic timescale of prokaryote evolution: insights into the origin of methanogenesis, phototrophy, and the colonization of land
inferredcites →https://doi.org/10.1371/annotation/cff22061-44d5-4301-b853-41702d160203openalex-snapshot
Correction: The Role of Selection in Shaping Diversity of Natural M. tuberculosis Populations
inferredcites →https://doi.org/10.1371/journal.pbio.0040088openalex-snapshot
Relaxed Phylogenetics and Dating with Confidence
inferredcites →https://doi.org/10.1371/journal.pcbi.1006650openalex-snapshot
BEAST 2.5: An advanced software platform for Bayesian evolutionary analysis
inferredcites →https://doi.org/10.1371/journal.pone.0068406openalex-snapshot
South African Papilionoid Legumes Are Nodulated by Diverse Burkholderia with Unique Nodulation and Nitrogen-Fixation Loci
inferredcites →https://doi.org/10.1371/journal.ppat.1003543openalex-snapshot
The Role of Selection in Shaping Diversity of Natural M. tuberculosis Populations
inferredcites →https://doi.org/10.1371/journal.ppat.1008067openalex-snapshot
The molecular clock of Mycobacterium tuberculosis
inferredcites →https://doi.org/10.14601/phytopathol_mediterr-14998u1.29openalex-snapshot
BIOEDIT: A USER-FRIENDLY BIOLOGICAL SEQUENCE ALIGNMENT EDITOR AND ANALYSIS PROGRAM FOR WINDOWS 95/98/ NT
inferredcites →https://doi.org/10.2139/ssrn.4860743openalex-snapshot
Mimosa Species Endemic to Acidic Soils in Central Brazil are Nodulated by a High Diversity of Paraburkholderia Genotypes, But Widespread Species are Nodulated by Paraburkholderia, Cupriavidus or Rhizobium Depending on Soil Characteristics
inferredcites →https://doi.org/10.2175/106143098x123525openalex-snapshot
The effect of environmental factors on bacterial populations and community dynamics in high rate oxidation ponds
inferredcites →https://doi.org/10.2307/2260320openalex-snapshot
Variations in Soil Phosphorus in the Fynbos Biome, South Africa
inferredcites →https://doi.org/10.2475/07.2009.03openalex-snapshot
Phanerozoic atmospheric oxygen: New results using the GEOCARBSULF model
inferredcites →https://doi.org/10.3389/fevo.2022.723286openalex-snapshot
The Origins and Historical Assembly of the Brazilian Caatinga Seasonally Dry Tropical Forests
inferredcites →https://doi.org/10.3389/fgene.2020.00526openalex-snapshot
Rates and Rocks: Strengths and Weaknesses of Molecular Dating Methods
inferredcites →https://doi.org/10.3389/fmicb.2022.855859openalex-snapshot
Ecological and Evolutionary Implications of Microbial Dispersal
inferredcites →https://doi.org/10.3390/nitrogen4010010openalex-snapshot
Nitrogen-Fixing Symbiotic Paraburkholderia Species: Current Knowledge and Future Perspectives
inferredcites →https://doi.org/10.4137/ebo.s39070openalex-snapshot
Estimating Divergence Times and Substitution Rates in Rhizobia
inferredcites →https://doi.org/10.7326/0003-4819-102-1-151_3openalex-snapshot
Bergey's Manual of Systematic Bacteriology.
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