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82 results for “Caryophyllales”
Fig. 1 in Pollen characters and DNA sequence data converge on a monophyletic genus Iresine (Amaranthaceae, Caryophyllales) and help to elucidate its species diversity
Fig. 1. Morphological diversity of Iresine. A, Synflorescence of I. interrupta (Borsch & al. 3789); B, Pistillate flowers at maturity and C, Staminate flowers of I. interrupta (Borsch & al. 3789); D, Upright woody stem of Iresine type XXXIV (Borsch & al. 5390); E, Inflorescence and F, Woody stem of I. nigra (S. Zumaya & al. 77); G, Part of synflorescence with staminate (Borsch & al. 5385) and H, Pistillate flowers of I. ajuscana (Borsch & al. 5367). — Photos: T. Borsch.
FIGURE 3 in The family Nyctaginaceae (Caryophyllales) in Sonora, Mexico
FIGURE 3. Neotype of the name Senkenbergia coulteri (K000572646). © copyright of the Board of Trustees of the Royal Botanic Gardens, Kew. http://specimens.kew.org/herbarium/K000572646
FIGURE 4 in The family Nyctaginaceae (Caryophyllales) in Sonora, Mexico
FIGURE 4. Distribution of the Nyctaginaceae genera in the State of Sonora. A: genera Abronia, Allionia, Acleisanthes, Okenia, and Pisonia; B: genus Boerhavia; C: genus Mirabilis; D: genera Boldoa, Commicarpus, Cyphomeris, and Salpianthus.
FIGURE 2 in The family Nyctaginaceae (Caryophyllales) in Sonora, Mexico
FIGURE 2. Some Nyctaginaceae species occurring in Sonora (Mexico). A: Abronia maritima; B: Abronia villosa; C: Allionia incarnata; D: Boerhavia xanti; E: Boerhavia coccinea; F: Commicarpus scandens; G: Mirabilis coccinea; H: Mirabilis laevis; I: Pisonia capitata; J: Salpianthus macrodontus (photos by J. J. Sánchez-Escalante).
Data from: Dissecting molecular evolution in the highly diverse plant clade Caryophyllales using transcriptome sequencing
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Data from: From cacti to carnivores: improved phylotranscriptomic sampling and hierarchical homology inference provide further insight into the evolution of Caryophyllales
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Data from: Phylogeny and generic delimitation in Molluginaceae, new pigment data in Caryophyllales, and the new family Corbichoniaceae
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Data from: Keeping an eye on coloration: ecological correlates of the evolution of pitcher traits in the genus Nepenthes (Caryophyllales)
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Data from: Widespread paleopolyploidy, gene tree conflict, and recalcitrant relationships among the carnivorous Caryophyllales
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Fig. 8 in Pollen characters and DNA sequence data converge on a monophyletic genus Iresine (Amaranthaceae, Caryophyllales) and help to elucidate its species diversity
Fig. 8. Evolution of pollen morphology using the maximum clade credibility tree of the plastid analysis with a reduced sampling. Pie charts depict the ancestral states reconstructed for pollen form (character 1), aperture number (character 2), aperture diameter (character 3), shape and diameter of mesoporia (characters 4, 5), and pollen size (character 6). For character and state definitions see Appendix 2.
Fig. 10 in Pollen characters and DNA sequence data converge on a monophyletic genus Iresine (Amaranthaceae, Caryophyllales) and help to elucidate its species diversity
Fig. 10. Evolution of pollen morphology, continued from Fig. 9. Pie charts depict the ancestral states reconstructed for the ektexinous bodies on the aperture membrane including their number (character 13), density (character 14) and shape (character 15). Character 16 defines the reproductive system. Consistently hermaphroditic flowers (state 0) are ancestral and widespread in Amaranthaceae, while the Iresinoids are mostly dioecious (state 1) or sometimes gynodioecious (bisexual and pistillate flowers appear on the same plant; state 2).
Fig. 3 in Pollen characters and DNA sequence data converge on a monophyletic genus Iresine (Amaranthaceae, Caryophyllales) and help to elucidate its species diversity
Fig. 3. Phylogenetic relationships of Iresine and related Gomphrenoideae based on the analysis of nrITS sequence data and depicting the 50% majority-rule tree of the Bayesian analysis. Subclades A (with further subclades A1, A2 and A3) and B are largely congruent in composition to the plastid tree depicted in Fig. 2. Posterior probabilities are shown above branches, bootstrap values from parsimony (left, bold) and maximum likelihood analysis (right, italics) below branches. The annota- tion bars for the species concepts are placed for identical groups of individuals as in the plastid tree.
Fig. 9 in Pollen characters and DNA sequence data converge on a monophyletic genus Iresine (Amaranthaceae, Caryophyllales) and help to elucidate its species diversity
Fig. 9. Evolution of pollen morphology, continued from Fig. 8. Pie charts depict the ancestral states reconstructed for tectum characters including tectum completeness (character 7), diameter and frequency of tectum perforations (characters 8, 9), and placement, height and frequency of microspines (characters 10, 11, 12).
Fig. 2 in Pollen characters and DNA sequence data converge on a monophyletic genus Iresine (Amaranthaceae, Caryophyllales) and help to elucidate its species diversity
Fig. 2. Phylogenetic relation- ships of Iresine and related Gomphrenoideae based on a combined analysis of matK-trnK, rpl16 and trnLF sequence data depicting the 50% majority-rule tree of the Bayesian analysis. Posterior probabilities are shown above branches, bootstrap values from parsimony (left, bold) and maximum likelihood analysis (right, italics) below branches.
Figure 9 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 9 Cross-section of Microteaglochidiata fruit (Brazil, Bahia, Tucano Mun., 20 Feb 1992, A.M. de Carvalho & D.J.N. Hind 3841, PACA). A image of the cross-section B schematic representation. Abbreviations: P – pericarp; T – testa; TE – tegmen.
Figure 11 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 11 Microteadebilis: A general view of the plants (La Selva Biological Station, Costa Rica, 2001) B close-up of the inflorescence (La Selva Biological Station, Costa Rica, 2001). Photographs by Orlando Vargas Ramírez. See also https://sura.ots.ac.cr/florula4/find_sp3.php?key_species_code=LS001515.
Figure 6 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 6 Fruits and seeds of Microteasulcicaulis and M.bahiensis: A, B fruit of M.sulcicaulis, enclosed in the perianth (Paraguay, Caazapá Dept., Tavai, 7 Dec 1988, F. Mereles 2122, G) C, D seed of M.sulcicaulis (Paraguay, Caazapá Dept., Tavai, 7 Dec 1988, F. Mereles 2122, G) E, F fruit of M.bahiensis (Brazil, Bahia state, Salvador, Dunas de Itapuã, nr Hotel Stella Maris, N from Condomínio Alamedas da Praia, 8 Jun 1993, P. de Queiroz 3211, PACA) G, H seed of M.bahiensis (Brazil, Bahia state, Salvador, Dunas de Itapuã, nr Hotel Stella Maris, N from Condomínio Alamedas da Praia, 8 Jun 1993, P. de Queiroz 3211, PACA). Magnification: A, E – 30×, B, F – 100×, C, G – 50×, D, H – 300×.
Figure 8 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 8 Fruits and seeds of Microteamaypurensis and M.tenuifolia: A, B fruit of M.maypurensis, enclosed in the perianth (Bolivia, La Paz Dept., Beni river, Jul 1886, H.H. Rusby 1379, LE) C, D seed of M.maypurensis (Bolivia, La Paz Dept., Beni river, Jul 1886, H.H. Rusby 1379, LE) E, F fruit of M.tenuifolia enclosed in the perianth (Brazil, Minas Gerais, Serrra das Vertentes, Jun 1893, A. Glaziou 20437, B) G, H seed of M.tenuifolia (Brazil, Jacobina Mountains in Bahia, 1836, Blanchet 2588, P00798998). Magnification: A, E – 30×, B, F – 100×, C, G – 50×, D, H – 300×.
Figure 10 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 10 Classification of Microtea species by group average linkage algorithm of cluster analysis based on 13 characters. Black branches connect significantly (P < 0.05) different groups, red branches – insignificantly different groups.
Figure 1 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 1 The phylogenetic tree from maximum likelihood analysis of matK region sequences. The tree with the highest log likelihood (-2983.53) is shown. The analysis involved 18 nucleotide sequences. Codon positions included were 1st+2nd+3rd+Noncoding. There were a total of 828 positions in the final dataset.
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