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Figure 14 from: Sukhorukov AP, Sennikov AN, Nilova MV, Mazei Y, Kushunina M, Marchioretto MS, Hanáček P (2019) Evolutionary relationships and taxonomy of Microtea (Microteaceae), a basal lineage in the core Caryophyllales. PhytoKeys 115: 1-50. https://doi.org/10.3897/phytokeys.115.29041

Figure 14 Neotype of Galeniacelosioides (BR0000005575398).

Figure 16 from: Sukhorukov AP, Sennikov AN, Nilova MV, Mazei Y, Kushunina M, Marchioretto MS, Hanáček P (2019) Evolutionary relationships and taxonomy of Microtea (Microteaceae), a basal lineage in the core Caryophyllales. PhytoKeys 115: 1-50. https://doi.org/10.3897/phytokeys.115.29041

Figure 16 Distribution map of Microteapapillosa.

Figure 23 from: Sukhorukov AP, Sennikov AN, Nilova MV, Mazei Y, Kushunina M, Marchioretto MS, Hanáček P (2019) Evolutionary relationships and taxonomy of Microtea (Microteaceae), a basal lineage in the core Caryophyllales. PhytoKeys 115: 1-50. https://doi.org/10.3897/phytokeys.115.29041

Figure 23 Distribution map of Microteamaypurensis in its native range.

Figure 13 from: Sukhorukov AP, Sennikov AN, Nilova MV, Mazei Y, Kushunina M, Marchioretto MS, Hanáček P (2019) Evolutionary relationships and taxonomy of Microtea (Microteaceae), a basal lineage in the core Caryophyllales. PhytoKeys 115: 1-50. https://doi.org/10.3897/phytokeys.115.29041

Figure 13 Records of Microteadebilis as an alien plant in Africa.

Figure 24 from: Sukhorukov AP, Sennikov AN, Nilova MV, Mazei Y, Kushunina M, Marchioretto MS, Hanáček P (2019) Evolutionary relationships and taxonomy of Microtea (Microteaceae), a basal lineage in the core Caryophyllales. PhytoKeys 115: 1-50. https://doi.org/10.3897/phytokeys.115.29041

Figure 24 The record of Microteamaypurensis as an alien plant in Indonesia.

Figure 12 from: Sukhorukov AP, Sennikov AN, Nilova MV, Mazei Y, Kushunina M, Marchioretto MS, Hanáček P (2019) Evolutionary relationships and taxonomy of Microtea (Microteaceae), a basal lineage in the core Caryophyllales. PhytoKeys 115: 1-50. https://doi.org/10.3897/phytokeys.115.29041

Figure 12 Distribution map of Microteadebilis in its native range.

Figure 20 from: Sukhorukov AP, Sennikov AN, Nilova MV, Mazei Y, Kushunina M, Marchioretto MS, Hanáček P (2019) Evolutionary relationships and taxonomy of Microtea (Microteaceae), a basal lineage in the core Caryophyllales. PhytoKeys 115: 1-50. https://doi.org/10.3897/phytokeys.115.29041

Figure 20 Distribution map of Microteaportoricensis.

Figure 19 from: Sukhorukov AP, Sennikov AN, Nilova MV, Mazei Y, Kushunina M, Marchioretto MS, Hanáček P (2019) Evolutionary relationships and taxonomy of Microtea (Microteaceae), a basal lineage in the core Caryophyllales. PhytoKeys 115: 1-50. https://doi.org/10.3897/phytokeys.115.29041

Figure 19 Distribution map of Microteasulcicaulis (circles) and M.bahiensis (star).

opennotspecifiedJun 2012View details →

Fig. 1 in Evolutionary and taxonomic relationships of Acacia s.l. (Leguminosae: Mimosoideae)

Fig. 1. Topologies of the Bayesian trees without branch lengths. The three boxes indicate the three subgenera of Acacia s.l. Shaded groupings indicate segregate and suggested segregate groupings. Bold lines indicate Bayesian posterior probability above 95%. African Vachellia and Senegalia are indicated in white text. Bootstrap values are given above nodes and bootstrap values below 80% are in italic.

Fig. 5 in Evolutionary relationships of wing venation and wing size and shape in Aphidiinae (Hymenoptera: Braconidae)

Fig. 5 Phylogenetic hypothesis for the subfamily Aphidiinae based on the mtCOI gene and character states of wing venation allocated based on Parsimony ancestral state reconstruction method: left – unordered; right –

Fig. 2 in Evolutionary relationships of wing venation and wing size and shape in Aphidiinae (Hymenoptera: Braconidae)

Fig. 2 Nomenclature of Aphidiinae wing venation following Wharton et al. (1997). CU cubitus, M media, R radius, RS radial sector, m-cu transverse medio-cubital vein, r transverse radial vein, r + m transverse radio-medial vein; cells: I marginal, II 1st submarginal, III 2nd submarginal, IV 3rd submarginal, V basal, VI 1st discal, VII 2nd discal, VIII subbasal, IX 1st subdiscal, X 2nd subdiscal, XI anal

Fig. 6 in Evolutionary relationships of wing venation and wing size and shape in Aphidiinae (Hymenoptera: Braconidae)

Fig. 6 Distribution of species in the morphospace defined by three PC axes. Phylogeny is mapped over graph. a Mapped distribution of the species means in phylomorphospace. Ellipses of the symbols represent

Fig. 3 in Evolutionary relationships of wing venation and wing size and shape in Aphidiinae (Hymenoptera: Braconidae)

Fig. 3 Set of landmarks positioned on the forewing of a Ephedrus plagiator, species with fully developed venation, and forewing of b Binodoxys angelicae, species with a reduced wing venation. First five landmarks (landmarks 1 to 5) describe the proximal part of the wing; landmarks 5, 6 and 7 describe the stigma, 7 and 8 mark the length of metacarpus, 6 and 9 mark the radial vein and together from 6 to 11 represent the distal area of the wing

opennotspecifiedFeb 2011View details →

Fig. 3 in Flowering phenology of co-occurring Asteraceae: a matter of climate, ecological interactions, plant attributes or of evolutionary relationships among species?

Fig. 3 Flowering phenology of 43 Asteraceae species in Chaco Serrano forests of La SerranitaLos Aromos separated in three groups: (A) 'massive blooming', (B) 'sparse blooming', (C) 'intermediate' species (see Results Section). Numbers indicate the species detailed in Table 1; lines represent their flowering times; ♦ = flowering midpoint (week in center of recorded flowering period)

opennotspecifiedFeb 2015View details →

FIG. 3 in Evolutionary Relationships of the Deep-Sea Pearleyes (Aulopiformes: Scopelarchidae) and a New Genus of Pearleye from Antarctic Waters

FIG. 3. Evolutionary relationships of the pearleyes (Scopelarchidae) based on total evidence (eight gene fragments and 16 anatomical and early-life-history characters) from maximum likelihood topology estimation. Asterisks indicate taxa that do not have DNA data. Bold numbers by nodes indicate bootstrap values. Numbers near circles on branches indicate unambiguous synapomorphies, with the first number corresponding to one of the 16 anatomical and early-life-history characters (see text for details), with the second number indicating character state. White circles represent unreversed characters, while black circles represent homoplastic characters. Colors on branches and distribution map correspond to the regions of the oceans where each species has been predominantly collected (note that many species have more restricted ranges within these zones). Circles at nodes indicate results from parsimony ancestral character reconstruction of regions (green: boreal and subarctic waters of North Pacific, orange: centraltropical waters, blue: Antarctic waters).

opennotspecifiedFeb 2015View details →

FIG. 1 in Evolutionary Relationships of the Deep-Sea Pearleyes (Aulopiformes: Scopelarchidae) and a New Genus of Pearleye from Antarctic Waters

FIG. 1. Lagiacrusichthys macropinnis, from meso-bathypelagic Antarctic waters (MCZ 125832). A small dorsal fin (5–6 rays), indicated by the arrow, and a long anal fin (35–39 rays) are differentially diagnostic features of the genus Lagiacrusichthys. Scale bars equal 1 cm.