| T00166890 |
Bartsia |
2016 |
A Phylogenomic Approach Based on PCR Target Enrichment and High Throughput Sequencing: Resolving the Diversity within the South American Species of Bartsia L. (Orobanchaceae) |
PLOS ONE |
RAxML bipartitions.Amplicon.np 39.R1 R2.nex.dna.fasta.aln one line.aln clean 02.phy |
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| T00175528 |
root |
2016 |
An early <scp>C</scp>ambrian chelicerate from the <scp>E</scp>mu <scp>B</scp>ay <scp>S</scp>hale, <scp>S</scp>outh <scp>A</scp>ustralia |
Palaeontology |
Wisangocaris REVISED MP MajRule |
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| T00119302 |
Passeriformes |
2016 |
Ancient mitochondrial genomes clarify the evolutionary history of New Zealand’s enigmatic acanthisittid wrens |
Molecular Phylogenetics and Evolution |
BEAST no3rdCodonPositions CretaceousMaximum KuiornisConstraint |
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| T00138355 |
root |
2016 |
Ancient mitochondrial DNA reveals convergent evolution of giant short-faced bears (Tremarctinae) in North and South America |
Biology Letters |
BEAST MaximumCladeCredibilityTree |
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| T00178429 |
root |
2016 |
A Large and Phylogenetically Diverse Class of Type 1 Opsins Lacking a Canonical Retinal Binding Site |
PLOS ONE |
SI Dataset 2 Haloarchaeal opsins tree |
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| T00160751 |
Ephedra |
2016 |
A high frequency of allopolyploid speciation in the gymnospermous genus <i><scp>E</scp>phedra</i> and its possible association with some biological and ecological features |
Molecular Ecology |
Haplotype.phy phyml tree |
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| T00159864 |
Anolis |
2015 |
Widespread parallel population adaptation to climate variation across a radiation: implications for adaptation to climate change |
Molecular Ecology |
marm BT BEAST |
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| T00174428 |
Asterales |
2015 |
Using phylogenomics to resolve mega‐families: An example from Compositae |
Journal of Systematics and Evolution |
clusters3964 lowcopy |
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| T00164450 |
Gesneriaceae |
2015 |
Untangling the influence of phylogeny, soil and climate on leaf element concentrations in a biodiversity hotspot |
Functional Ecology |
didymocarpoideae tree |
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| T00161287 |
Sebacinales |
2015 |
Two widespread green <i>Neottia</i> species (<scp>O</scp>rchidaceae) show mycorrhizal preference for <scp>S</scp>ebacinales in various habitats and ontogenetic stages |
Molecular Ecology |
Neottia 18S+ITS+trnL(UAA)intron |
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| T00143317 |
Lactobacillales |
2015 |
Three‐phase succession of autochthonous lactic acid bacteria to reach a stable ecosystem within 7 days of natural bamboo shoot fermentation as revealed by different molecular approaches |
Molecular Ecology |
Tree File for Fig. S2 |
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| T00164809 |
Tamalia |
2015 |
The origin and genetic differentiation of the socially parasitic aphid <i>Tamalia inquilinus</i> |
Molecular Ecology |
RAxML bestTree.Groel |
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| T00158135 |
Moraceae |
2015 |
The incidence and pattern of copollinator diversification in dioecious and monoecious figs |
Evolution |
COI Figure S1 |
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| T00152588 |
Holocentridae |
2015 |
The impact of shifts in marine biodiversity hotspots on patterns of range evolution: Evidence from the Holocentridae (squirrelfishes and soldierfishes) |
Evolution |
resampled withfossils.con |
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| T00171798 |
Thylamys |
2015 |
The impact of <scp>Q</scp>uaternary climate oscillations on divergence times and historical population sizes in <i><scp>T</scp>hylamys</i> opossums from the <scp>A</scp>ndes |
Molecular Ecology |
BEAST 26 Genes |
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