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Fig. 3 in Paleotropical Diversification Dominates the Evolution of the Hyperdiverse Ant Tribe Crematogastrini (Hymenoptera: Formicidae)

Fig. 3. The evolution of biogeography (A) and nesting preference (B) in Crematogastrini. Ancestral reconstructions based on a modified chronogram from the 50-best concatenated-partitioned analysis in BEAST2, from which all but one representative species per genus, as well as the outgroups, have been pruned from the tree. (A) Biogeographic reconstructions with BioGeoBEARS under the DEC model. N = Nearctic, T = Neotropical, P = Palearctic, E = Afrotropical, M = Malagasy, O = Indomalayan, and A = Australasian. (B) Nesting preference reconstructed under the ER model with rayDISC in corHMM. Black = arboreal nesting; white = ground nesting. See SuppTable 3 (online only) for geographic distributions and trait data for each genus.

Fig. 4 in Paleotropical Diversification Dominates the Evolution of the Hyperdiverse Ant Tribe Crematogastrini (Hymenoptera: Formicidae)

Fig. 4. Diversification of Crematogastrini. We performed BAMM analyses on the chronogram resulting from the 50-best concatenated-partitioned BEAST2 analysis using clade-specific sampling probabilities to account for incomplete sampling based either on species estimates only or including species and subspecies. Panels show (A) mean phylorate plots based on species only; (B) mean phylorate plots based on species and subspecies; (C) best shift configuration based on species only; (D) best shift configuration based on species and subspecies. SuppTable 5 (online only) lists diversity estimates per genus including and excluding subspecies.

Fig. 2 in Paleotropical Diversification Dominates the Evolution of the Hyperdiverse Ant Tribe Crematogastrini (Hymenoptera: Formicidae)

Fig. 2. Cladogram estimated for Crematogastrini, by ASTRAL-II species-tree analysis. We reconstructed a species tree from 1,763 UCE gene trees based on weighted statistical binning (Bayzid et al. 2015) and 883 supergenes. Only local posterior probabilities (LPP)> 0.7 are shown. Note that ASTRAL-II support values are branch support values that measure the support for a quadripartition, not a bipartition.The 10 major genus-groups are indicated; clade names in red highlight conflicts regarding the composition of these clades with respect to Fig. 1.

Fig. 1 in Paleotropical Diversification Dominates the Evolution of the Hyperdiverse Ant Tribe Crematogastrini (Hymenoptera: Formicidae)

Fig. 1. Phylogeny of Crematogastrini, estimated by concatenated ML analysis.We performed best-tree and bootstrap searches (N = 100) in RAxML v8.2.7. Both panels show the best ML tree resulting from analyses of a concatenated data matrix divided per UCE locus into 1,763 partitions. (A) Phylogram showing branch lengths and emphasizing generic relationships. (B) Cladogram with BS values indicated: white squares represent 100% BS; red squares indicate the support for that node.The 10 major genus-groups are indicated; the compositions of the two genus-groups highlighted in red conflict with those resulting from the ASTRAL-II analysis presented in Fig. 2.

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FIGURE 3 in A new Mylia Gray (Myliaceae, Hepaticae) species from North Vietnam extends the range of the genus to the Paleotropics

FIGURE 3 Mylia vietnamica Bakalin et Vilnet: 1—plant habit in dry condition (glistening stem is visible), 2—fissured leaf cuticle, 3—cells in the midleaf, 4—leaf margin, 5—underleaf; from Holotype (V-3-36-16, VBGI). Mylia taylorii (Hook.) Gray: 6, 7—leaf margin, 8—midleaf cells; from Khabarovsk Territory (Kh-18-22-16, VBGI). Scales: a—100 μm, for 2–8; b—2 mm, for 1.

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FIGURE 2 in A new Mylia Gray (Myliaceae, Hepaticae) species from North Vietnam extends the range of the genus to the Paleotropics

FIGURE 2 Mylia vietnamica Bakalin et Vilnet: 1, 2—plant habit, 3—stem cross section (fragment), 4–8—leaves. Scales: a—2 mm, for 1,2, 4–8; b—100 μm, for 3. All from Holotype (V-3-36-16, VBGI).

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FIGURE 1 in A new Mylia Gray (Myliaceae, Hepaticae) species from North Vietnam extends the range of the genus to the Paleotropics

FIGURE 1 Phylogram obtained in a maximum likelihood calculation for the genus Mylia based on the combined dataset of ITS1-2 nrDNA and trnL-F cpDNA nucleotide sequences. Bootstrap support values more than 50% (0.50) and length of cut branches are indicated.

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Data from: Paleotropical diversification dominates the evolution of the hyperdiverse ant tribe Crematogastrini (Hymenoptera: Formicidae)

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Figure 1 from: Kistenich S, Rikkinen JK, Thüs H, Vairappan CS, Wolseley PA, Timdal E (2018) Three new species of Krogia (Ramalinaceae, lichenised Ascomycota) from the Paleotropics. MycoKeys 40: 69-88. https://doi.org/10.3897/mycokeys.40.26025

Figure 1 Hypothesis of the phylogenetic relationships and placement of the 15 Krogia accessions. It shows the extended majority-rule consensus tree resulting from the Bayesian MCMC analysis with Bayesian PP ≥ 0.7 (above branch) and/or Garli maximum likelihood BS ≥ 50 (below branch) and branch lengths. Strongly supported branches (PP ≥ 0.95 and BS ≥ 95) are marked in bold; branches with PP ≥ 0.95 and BS ≥ 70 are marked in bold grey; branches only supported by PP ≥ 0.7 are marked with an asterisk above the branch. Bacidiarosella, B.rubella and B.sipmanii were used as outgroup. Scale bar indicates 0.05 changes per site.

Figure 4 from: Kistenich S, Rikkinen JK, Thüs H, Vairappan CS, Wolseley PA, Timdal E (2018) Three new species of Krogia (Ramalinaceae, lichenised Ascomycota) from the Paleotropics. MycoKeys 40: 69-88. https://doi.org/10.3897/mycokeys.40.26025

Figure 4 KrogiamacrophyllaA field photograph of JR36047B field photograph of holotype C herbarium photograph of holotype. Scale bar: 1 mm. Photo: J. Rikkinen (A, B), E. Timdal (C).

Figure 3 from: Kistenich S, Rikkinen JK, Thüs H, Vairappan CS, Wolseley PA, Timdal E (2018) Three new species of Krogia (Ramalinaceae, lichenised Ascomycota) from the Paleotropics. MycoKeys 40: 69-88. https://doi.org/10.3897/mycokeys.40.26025

Figure 3 Krogiaisidiata.A field photograph of JR35688B field photograph of JR35034C herbarium photograph of holotype. Scale bar: 1 mm. Photo: J. Rikkinen (A, B), E. Timdal (C).

Figure 5 from: Kistenich S, Rikkinen JK, Thüs H, Vairappan CS, Wolseley PA, Timdal E (2018) Three new species of Krogia (Ramalinaceae, lichenised Ascomycota) from the Paleotropics. MycoKeys 40: 69-88. https://doi.org/10.3897/mycokeys.40.26025

Figure 5 Habitat images from New Caledonia A Mont Humboldt Nature Reserve, site of K.macrophylla, with AraucariahumboldtensisB Blue River Provincial Park, site of K.isidiata and K.macrophyllaC Mont Mou Nature Reserve, holotype locality of K.macrophylla. Photo: J. Rikkinen.

Figure 2 from: Kistenich S, Rikkinen JK, Thüs H, Vairappan CS, Wolseley PA, Timdal E (2018) Three new species of Krogia (Ramalinaceae, lichenised Ascomycota) from the Paleotropics. MycoKeys 40: 69-88. https://doi.org/10.3897/mycokeys.40.26025

Figure 2 Krogiaborneensis. A Field photograph of the holotype B habitat at type locality C herbarium photograph of holotype. Scale bar: 1 mm. Photo: H. Thüs (A, B), E. Timdal (C).