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FIGURE 5 in Disentangling the diversity and taxonomy of Hymenophyllaceae (Hymenophyllales, Polypodiidae) in the Mascarene archipelago, with ecological implications
FIGURE 5. Distribution of Hymenophyllaceae species richness in relation to elevations, here on the windward side of La Réunion and on Mauritius (data are reported in Appendices 1 & 2). The range of each taxon is assumed to correspond to the range between the minimum and the maximum elevation at which they have been observed, even if the taxon has not been observed in all intermediate localities between such limits.
FIGURE 14. A in Disentangling the diversity and taxonomy of Hymenophyllaceae (Hymenophyllales, Polypodiidae) in the Mascarene archipelago, with ecological implications
FIGURE 14. A. Hymenophyllum fumarioides Bory ex. Willd, as epiphyte (La Réunion, 'Mare Longue'). B. H. fumarioides, detail of curled/crisped segments and sori with toothed margins. C. H. peltatum (Poir.) Desv., as epiphyte (La Réunion, 'Pitons Mare à Boue'). D. H. peltatum, detail of toothed/serrulate laminar margins. E. H. sibthorpioides (Bory ex Willd.) Mett. ex Kuhn, as epiphytic (La Réunion, 'Vallée Heureuse'). F. H. sibthorpioides, fertile frond and sori with toothed margins (photographs. A, E: C. Chaussidon; B, F: L. Bauret; C: J.-Y. Dubuisson; D: J.-M. Tamon).
FIGURE 4. Mauritian ecosystems. A in Disentangling the diversity and taxonomy of Hymenophyllaceae (Hymenophyllales, Polypodiidae) in the Mascarene archipelago, with ecological implications
FIGURE 4. Mauritian ecosystems. A. Lowland Sapotaceae rainforest, here invaded by the exotic Malagasy traveller's trees Ravenala madagascariensis (Strelitziaceae) ('Vallée d'Osterlog' forest, ~260 m). B. 'Pétrin' locality showing particular habitat with thickets of the endemic Erica brachyphylla (Ericaceae) (~670 m) (photographs by J.-Y. Dubuisson).
FIGURE 11 in Disentangling the diversity and taxonomy of Hymenophyllaceae (Hymenophyllales, Polypodiidae) in the Mascarene archipelago, with ecological implications
FIGURE 11. Crepidomanes trinerve (Baker) Dubuisson & Ebihara. A. As lithophyte in a wet ravine of the western side of La Réunion ('Les Canots'; photograph by J.-M. Tamon). B. Habit (from Comores, F. Rakotondrainibe 6651, P00310478; modified from Dubuisson et al. 2013).
FIGURE 3. Particular Mascarenan ecosystems. A in Disentangling the diversity and taxonomy of Hymenophyllaceae (Hymenophyllales, Polypodiidae) in the Mascarene archipelago, with ecological implications
FIGURE 3. Particular Mascarenan ecosystems. A. Hyperhumid montane 'Avoune' vegetation dominated by the endemic Erica reunionensis (Ericaceae), with most trunks and branches fully covered by epiphytes (liverworts, mosses, peat mosses, lycopods and ferns, especially here Hymenophyllum capillare and H. inaequale, and orchids) (La Réunion, 'Pitons Mare à Boue', ~1,600 m). B. Montane 'Tamarinaie' dominated by endemic Acacia heterophylla (Fabaceae), showing as for 'Avoune' tree-trunks and branches fully covered by epiphytes, including here H. inaequale (La Réunion, 'Bélouve', ~1,520 m). C. Remnant of leeward lowland semi-dry forest (La Réunion, 'Ilet Solitude', ~550 m). D. Typical wet ravines that host lithophytic Hymenophyllaceae on the wet and shaded rocks close to streams and waterfalls. (photographs. A: J.-Y. Dubuisson; B–C: J.-M. Tamon; D: A. Mercier).
FIGURE 8. A in Disentangling the diversity and taxonomy of Hymenophyllaceae (Hymenophyllales, Polypodiidae) in the Mascarene archipelago, with ecological implications
FIGURE 8. A. Crepidomanes bipunctatum (Poir.) Copel., as epiphyte on a tree-trunk (Mauritius, 'Bar le Duc'). B. C. bipunctatum, detail of segments with false veins parallel to the margins (fv). C. C. bipunctatum, sori (s) with triangular lips. D. C. bonapartei (C.Chr.) J.P.Roux, as lithophyte on wet rock (La Réunion, 'Grand Etang'). E. C. bonapartei, detail of subsessile or short-stipitate fronds and one sorus (photographs. A: J.-Y. Dubuisson; B–C: L. Bauret; D–E: E. Grangaud).
FIGURE 2. Wet Mascarenan ecosystems. A in Disentangling the diversity and taxonomy of Hymenophyllaceae (Hymenophyllales, Polypodiidae) in the Mascarene archipelago, with ecological implications
FIGURE 2. Wet Mascarenan ecosystems. A. Lowland windward rainforest dominated by Sapotaceae trees, showing the understory with numerous low epiphytic and terrestrial free-sporing plants (liverworts, mosses, ferns, lycopods and spikemosses) and a few herbaceous angiosperms (especially orchids) (La Réunion, 'Mare Longue' forest, ~450 m). B. Montane rainforest dominated by Dombeyoideae (Malvaceae) trees and Alsophila spp. tree-ferns (Cyatheaceae) as emergents from the canopy (La Réunion, 'Cassé de Takamaka, Bébour', 1,100–1,200 m). C. Montane ericoid thickets (La Réunion, 'Enclos du Piton de la Fournaise', ~2,200 m). (Photographs. A, C: C. Chaussidon; B: J.-M. Tamon).
FIGURE 10. A in Disentangling the diversity and taxonomy of Hymenophyllaceae (Hymenophyllales, Polypodiidae) in the Mascarene archipelago, with ecological implications
FIGURE 10. A. Crepidomanes inopinatum (Pic.Serm.) J.P.Roux var. inopinatum, as lithophyte (La Réunion, 'Petite Plaine'). B. C. inopinatum var. tamonii Y.Robert & Dubuisson, habit (Y. Robert 913, P02433924). C. C. minutum (Blume) K.Iwats. var. minutum, as epiphyte (La Réunion, 'Bébour'). D. C. minutum var. minutum, frond with long terete wingless stipe. E. C. minutum var. minutum, showing stipe proliferation, scale = 1 cm (from Madagascar, F. Rakotondrainibe 3698, P00085267). F. C. minutum var. mascarenense Pynee & Dubuisson, as epiphyte (La Réunion, 'Grand Etang'). G. C. minutum var. mascarenense, detail of fronds with short stipes. (photographs. A: J.-Y. Dubuisson; C–D: C. Chaussidon; F–G: E. Grangaud).
FIGURE 13 in Disentangling the diversity and taxonomy of Hymenophyllaceae (Hymenophyllales, Polypodiidae) in the Mascarene archipelago, with ecological implications
FIGURE 13. Didymoglossum cuspidatum (Willd.) Ebihara & Dubuisson. A. Typical sub-circular, and lanceolate to deltoid sterile forms as usually observed (La Réunion, 'Mare Longue'). B. Linear sterile forms (La Réunion, 'Grand Etang'). C. Ovate to lanceolate fertile fronds with apical sori (La Réunion, 'Forêt de Bon Accueil, Les Makes'). D. Narrowly lanceolate fertile frond with apical sori (La Réunion, 'Grand Etang'). E. Small sub-circular/ovate fertile frond with a single sorus, showing sub-marginal false vein (mfv) and false veins parallel to true veins (fv) (photographs. A–D: J.-Y. Dubuisson; E: L. Bauret).
FIGURE 17. A in Disentangling the diversity and taxonomy of Hymenophyllaceae (Hymenophyllales, Polypodiidae) in the Mascarene archipelago, with ecological implications
FIGURE 17. A. Hymenophyllum balfourii Baker, holotype (La Réunion, I.B. Balfour s.n., K000435603). B. H. inaequale (Poir.) Desv., as epiphyte, narrowly lanceolate form (La Réunion, 'Mare Longue'). C. H. inaequale, widely lanceolate to ovate form (La Réunion, 'Forêt de Bon Accueil, Les Makes'). D. H. inaequale, detail of glabrous segments and sori (photographs. B. L. Bauret; C–D: J.-Y. Dubuisson).
FIGURE 1 in Disentangling the diversity and taxonomy of Hymenophyllaceae (Hymenophyllales, Polypodiidae) in the Mascarene archipelago, with ecological implications
FIGURE 1. Location of the Mascarene Archipelago (or Mascarenes) in the western Indian Ocean (from Pynee et al. 2012).
FIGURE 16. A in Disentangling the diversity and taxonomy of Hymenophyllaceae (Hymenophyllales, Polypodiidae) in the Mascarene archipelago, with ecological implications
FIGURE 16. A. Hymenophyllum hirsutum (L.) Sw., as epiphyte (La Réunion, 'Grand Etang'). B. H. hirsutum, detail of a frond showing the hairy winged stipe. C. H. hirsutum, detail of bilabiate hairy sori. D. H. hygrometricum (Poir.) Desv., as epiphyte (La Réunion, 'Bébour'). E. H. hygrometricum, wet fronds become greener as shown here (photographs. A: J.-Y. Dubuisson; B–C: L. Bauret; D–E: C. Chaussidon).
FIGURE 20 in Disentangling the diversity and taxonomy of Hymenophyllaceae (Hymenophyllales, Polypodiidae) in the Mascarene archipelago, with ecological implications
FIGURE 20. Elevational distribution on each Hymenophyllaceae taxon on the windward (red plots) and leeward (blue plots) sides of La Réunion, and correspondence with thermal zones or ranges according to Cadet (1980) and provided here for the windward side, with ranges of annual average temperatures. The dotted horizontal lines correspond to the limits of leeward ecosystems. The plots indicate the average elevation. Crepidomanes trinerve is here lacking because it was only observed at a single locality on the leeward side ('Les Canots' at ~800 m). The range of each taxon, as illustrated by the vertical lines, is assumed to correspond to the range between the minimum and the maximum elevation at which they have been observed, even if the taxon has not been observed in all the intermediate localities between such limits.
FIGURE 2. Bayesian majority rule consensus tree inferred from the plastid DNA trnL-F in Evolutionary history of the tribe Astereae in the Flora Iranica area: Systematic implications
FIGURE 2. Bayesian majority rule consensus tree inferred from the plastid DNA trnL-F dataset. Numbers abovebranches are posterior probability (PP) and likelihood as well as parsimony bootstrap (BS) values, respectively. Values>50 % are shown.
FIGURE 1 in Evolutionary history of the tribe Astereae in the Flora Iranica area: Systematic implications
FIGURE 1. Bayesian majority rule consensus tree inferred from the combined nuclear DNA (ITS+ETS) data. Numbers above branches are posterior probability (PP) and likelihood as well as parsimony bootstrap (BS) values, respectively. Values>50 % are shown.
FIGURE 3 in Evolutionary history of the tribe Astereae in the Flora Iranica area: Systematic implications
FIGURE 3. Bayesian majority rule consensus tree inferred from the combined nrDNA+cpDNA dataset. Numbers abovebranches are posterior probability (PP) and likelihood as well as parsimony bootstrap (BS) values, respectively. Values>50 % are shown.
FIGURE 4 in Evolutionary history of the tribe Astereae in the Flora Iranica area: Systematic implications
FIGURE 4. Beast maximum clade credibility chronogram based on the Bayesian analysis of the combined nrDNA dataset. The 95% highest posterior density intervals (blue bars) are depicted. The numbers written above the nodes corresponding to the mean divergence time estimate shown in Table 3.
FIGURE 6 in A phylogenetic framework for the Hylocereeae (Cactaceae) and implications for the circumscription of the genera
FIGURE 6. Inversion in the matK gene. A) Four independent substitutions will be assumed if the inversion is overlooked in the alignment. B) The inverted motif corresponds to the terminal loop of a hairpin and can easily switch from one state to another. If aligned in different columns, two independent substitution events will be assumed. C) The inverted motif reverse-complemented prior to phylogenetic analysis represents the most accurate homology assessment. D) The motif re-inverted prior to phylogenetic analysis. E) Only one amino acid is substituted by the inversion.
FIGURE 7. Kimnachia ramulosa f in A phylogenetic framework for the Hylocereeae (Cactaceae) and implications for the circumscription of the genera
FIGURE 7. Kimnachia ramulosa f. ramulosa (left) and f. angustissima (right) (photo by W. Barthlott, Lotus-Salvinia.de). The specimen of f. angustissima pictured here originates from the collections of Marnier-Lapostolle at Lés Cedrés, and was very likely a clonotype from the plant Weber had described as Rhipsalis angustissima. A specimen is preserved at the Herbarium Berolinense (B-810013745, in spirit).
FIGURE 2A in A phylogenetic framework for the Hylocereeae (Cactaceae) and implications for the circumscription of the genera
FIGURE 2A. Majority-rule consensus tree from Bayesian inference. Values above branches are Posterior Probabilities (left) and Bootstrap support values from Maximum Likelihood (10.000 replicates) calculated with RAxML GUI using the "ML + thorough bootstrap" option, values below branches are Jackknife support values (10.000) calculated in PAUP. (-- denotes ML BS support below 50, n.f.: node not found). Taxon names in the cladogram reflect hitherto accepted names (Bauer 2003a, Hunt 2006), with the exception of new names in Disocactus published by Cruz et al. (2016). The new/updated generic concepts presented here are annotated with brackets.
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Allen Brain Atlas
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