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867 results for “Malagasy species”
Supplementary material 1 from: Yoshimura M, Fisher B (2014) A revision of the ant genus Mystrium in the Malagasy region with description of six new species and remarks on Amblyopone and Stigmatomma (Hymenoptera, Formicidae, Amblyoponinae). ZooKeys 394: 1-99. https://doi.org/10.3897/zookeys.394.6446
A data sheet for all specimens of Mystrium examined: Explanation note: Comprehensive data for all Mystrium specimens examined including information of specimens ID, species name, sex and caste, collection data, and depository.
FIGURES 1A–F in A review of the Malagasy species of the genus Trigonochilus Brenske (Coleoptera Scarabaeidae: Rutelinae: Adoretini) with description of a new species
FIGURES 1A–F. Trigonochilus oedipus (Fairmaire, 1903) (A–C), T. macrotarsus Montreuil & Frolov, new species (D–F) and locality map (G). A, male, dorsal view; B, aedeagus, lateral and dorsal view; C, female, dorsal view; D, male, holotype, dorsal view; E, aedeagus, lateral and dosal view; F, female, paratype, dorsal view; G, locality map (black circle – T. oedipus, white circle – T. macrotarsus). Scale bar = 1.0 mm.
FIGURE 5 in Discussion on the taxonomy of African fern Abrodictyum rigidum (Sw.) Ebihara & Dubuisson and description of two new Abrodictyum C.Presl species (Hymenophyllaceae, Polypodiidae) for the Afro-Malagasy region
FIGURE 5. Bayesian phylogeny inferred from rbcL sequences showing relationships within genus Abrodictyum (noted A). Support values on nodes are posterior probabilities. The species/populations studied and compared here are shown in coloured boxes (the colours used here are arbitrary). T = trichomanoids. Clades noted α and β are commented in text.
FIGURE 1 in Discussion on the taxonomy of African fern Abrodictyum rigidum (Sw.) Ebihara & Dubuisson and description of two new Abrodictyum C.Presl species (Hymenophyllaceae, Polypodiidae) for the Afro-Malagasy region
FIGURE 1. Comparison of three Abrodictyum species in situ, which show a similar gross morphology but are clearly molecularly distinct according to Bauret et al. (2015). A. A. rigidum (Sw.) Ebihara & Dubuisson, Guadeloupe (photograph by J.-Y. Dubuisson); B. Abrodictyum sp1 (= A. pseudorigidum Bauret & Dubuisson, sp. nov.), Madagascar (photograph by L. Bauret); C. Abrodictyum sp2 (= A. franceae Bauret & Dubuisson, sp. nov.), Madagascar (photograph by L. Bauret); D. Abrodictyum sp2 (= A. franceae sp. nov.), the fronds are often more or less curled in the wild as shown here (photograph by L. Bauret).
FIGURE 4 in Discussion on the taxonomy of African fern Abrodictyum rigidum (Sw.) Ebihara & Dubuisson and description of two new Abrodictyum C.Presl species (Hymenophyllaceae, Polypodiidae) for the Afro-Malagasy region
FIGURE 4. Multivariate analyses. PCA (above) and CDA (below) results for selected trait ratios. The PCA shows the contribution of each trait to overall morphological variation; the CDA shows the distribution of the four taxa in morphological 2-D trait space.
FIGURE 7 in Discussion on the taxonomy of African fern Abrodictyum rigidum (Sw.) Ebihara & Dubuisson and description of two new Abrodictyum C.Presl species (Hymenophyllaceae, Polypodiidae) for the Afro-Malagasy region
FIGURE 7. Abrodictyum franceae Bauret & Dubuisson, sp. nov. (G. Rouhan et al. 267, holotype P00749196). A. Habitus; B. Detail of a pinna with sori; C. Detail of indusium; D. Detail of laminar cells, the arrow shows the margin.
FIGURE 6 in Discussion on the taxonomy of African fern Abrodictyum rigidum (Sw.) Ebihara & Dubuisson and description of two new Abrodictyum C.Presl species (Hymenophyllaceae, Polypodiidae) for the Afro-Malagasy region
FIGURE 6. Abrodictyum pseudorigidum Bauret & Dubuisson, sp. nov. (F. Rakotondrainibe 2708, holotype P00059914). A. Habitus; B. Detail of a pinna, the arrows show some of the sori; C. Detail of a terminal pinnule with a basal sorus; D. Detail of indusium; E. Detail of laminar cells, the arrow shows the margin.
FIGURE 2 in Discussion on the taxonomy of African fern Abrodictyum rigidum (Sw.) Ebihara & Dubuisson and description of two new Abrodictyum C.Presl species (Hymenophyllaceae, Polypodiidae) for the Afro-Malagasy region
FIGURE 2. Proportional synthetic and schematic representations, at the same scale, of the frond gross morphology of the studied taxa and populations taking into account length and width mean values (see Table 2).
FIGURE 3 in Discussion on the taxonomy of African fern Abrodictyum rigidum (Sw.) Ebihara & Dubuisson and description of two new Abrodictyum C.Presl species (Hymenophyllaceae, Polypodiidae) for the Afro-Malagasy region
FIGURE 3. Multivariate analyses. PCA (above) and CDA (below) results for selected quantitative traits. The PCA shows the contribution of each trait to overall morphological variation; the CDA shows the distribution of the four taxa in morphological 2-D trait space.
FIGURE 1 in Molecular systematics of Malagasy poison frogs in the Mantella betsileo and M. laevigata species groups
FIGURE 1. Localities of the collected samples included in the molecular analyses of the Mantella betsileo and Mantella laevigata groups.
FIGURE 2. Phylogram from a Maximum Parsimony analysis, representing a 50 in Molecular systematics of Malagasy poison frogs in the Mantella betsileo and M. laevigata species groups
FIGURE 2. Phylogram from a Maximum Parsimony analysis, representing a 50% majority-rule consensus tree of 65700 equally most parsimonious trees. Mantella bernhardi was defined as outgroup. Specimens with identical haplotypes were merged; numbers in brackets after names of taxa give the number of specimens with the same haplotype. Numbers at nodes are bootstrap values in percent from a Maximum Parsimony bootstrap analysis with 250 replicates. Asterisks denote posterior probabilities from a partitioned Bayesian analysis: (*)>90%; *>95%; **>99%.
FIGURE 21. Maximum parsimony 16S rRNA phylogram for the Boophis albipunctatus group. From 485 total characters, 391 were constant and 72 in Integrative taxonomy of Malagasy treefrogs: combination of molecular genetics, bioacoustics and comparative morphology reveals twelve additional species of Boophis 2383
FIGURE 21. Maximum parsimony 16S rRNA phylogram for the Boophis albipunctatus group. From 485 total characters, 391 were constant and 72 parsimony informative. MP searches retained 26 trees of which a strict consensus is shown. Consensus support values higher than 50, from 2000 bootstrap replicates, are shown; an asterisk indicates Bayesian posterior probabilities equal or higher than 95%. Species newly described herein are in bold.
FIGURE 27 in Integrative taxonomy of Malagasy treefrogs: combination of molecular genetics, bioacoustics and comparative morphology reveals twelve additional species of Boophis 2383
FIGURE 27. Spectrogram and waveform of call type 1 of Boophis luciae sp. nov. from Andasibe (recorded on 1 February 1995, air temperature 22°C).
FIGURE 19 in Integrative taxonomy of Malagasy treefrogs: combination of molecular genetics, bioacoustics and comparative morphology reveals twelve additional species of Boophis 2383
FIGURE 19. (A) Male holotype of Boophis sandrae sp. nov. (ZMA 20133) from Ranomafana; (B) female paratype of Boophis sandrae sp. nov. (ZSM 236/2006) from Ambatolahy.
FIGURE 10 in Integrative taxonomy of Malagasy treefrogs: combination of molecular genetics, bioacoustics and comparative morphology reveals twelve additional species of Boophis 2383
FIGURE 10. Male holotype of Boophis entingae sp. nov. (ZSM 2083/2007): (A) dorsolateral view; (B) ventral view; (C) detail showing colouration of posterior surfaces of thigh.
FIGURE 8 in Integrative taxonomy of Malagasy treefrogs: combination of molecular genetics, bioacoustics and comparative morphology reveals twelve additional species of Boophis 2383
FIGURE 8. Male of Boophis brachychir (ZSM 2157/2007) from Forêt d'Ambre Special Reserve: (A) dorsolateral view; (B) ventral view.
FIGURE 5 in Integrative taxonomy of Malagasy treefrogs: combination of molecular genetics, bioacoustics and comparative morphology reveals twelve additional species of Boophis 2383
FIGURE 5. Spectrograms and waveforms of advertisement calls of: (A) Boophis andrangoloaka from Ambohitantely Special Reserve (recorded on 18 January 2005, air temperature app. 18°C); (B) Boophis rhodoscelis from Ranomafanakely, Ranomafana National Park (recorded on 28 January 2004, air temperature app. 21°C).
FIGURE 9 in Integrative taxonomy of Malagasy treefrogs: combination of molecular genetics, bioacoustics and comparative morphology reveals twelve additional species of Boophis 2383
FIGURE 9. Spectrogram, corresponding waveform and expanded waveform of the advertisement call of Boophis brachychir from Manongarivo Special Reserve (recorded on 1 February 2003, air temperature 24.5°C).
FIGURE 7. Maximum parsimony 16S in Integrative taxonomy of Malagasy treefrogs: combination of molecular genetics, bioacoustics and comparative morphology reveals twelve additional species of Boophis 2383
FIGURE 7. Maximum parsimony 16S rRNA phylogram of species of the Boophis goudoti group. From 510 total characters, 340 were constant and 130 parsimony informative. MP searches retained 3681 trees of which a strict consensus is shown. Consensus support values higher than 50, from 2000 bootstrap replicates, are shown; an asterisk indicates Bayesian posterior probabilities equal or higher than 95%. Species newly described or resurrected herein are in bold.
FIGURE 25 in Integrative taxonomy of Malagasy treefrogs: combination of molecular genetics, bioacoustics and comparative morphology reveals twelve additional species of Boophis 2383
FIGURE 25. Comparative waveform sections (each 2000 ms duration) of advertisement calls of species in the Boophis albipunctatus group: (A) Boophis schuboeae (Ranomafana National Park, 23°C); (B) Boophis haingana sp. nov. (Andohahela National Park, low altitude, 23.2°C); (C) Boophis haingana sp. nov. (Andohahela National Park, 1600 m a.s.l., 17.6°C); (D) Boophis ankaratra (Manjakatompo, 18°C); (E) Boophis miadana sp. nov. (Andohahela National Park, 1550 m a.s.l., 17.6°C).
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International Brain Laboratory public data
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OpenNeuro
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