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409 results for “Molecular Genetics”
Figure 6 in Molecular-genetic-based contribution to the taxonomy of the Acanthocyclops robustus group
Figure 6. Acanthocyclops americanus (Marsh) female neotype (A–C) and male allotype (4) from the terra typica, Madison, Wisconsin, USA. (A) Female Leg 5; (B) female antennal basipod frontal side; (C) female antennal basipod caudal side; (D) male Leg 4. Note: Scale bar 50 µm.
Figure 8 in Molecular-genetic-based contribution to the taxonomy of the Acanthocyclops robustus group
Figure 8. Pairwise COI sequence divergence within the americanus–robustus–vernalis complex. Genetic distance (Kimura 2-parameter) is compared between and within the three clades depicted in the tree of Figure 7. Note: Columns indicate mean values and bars indicate range (min.–max.).
Figure 7 in Molecular-genetic-based contribution to the taxonomy of the Acanthocyclops robustus group
Figure 7. Phylogenetic relationships based on maximum-likelihood analysis of mitochondrial COI sequences. Numbers beside nodes indicate bootstrap support values>70%. Individuals are identified by locality and the haplotype name is added if there more than one haplotype in the same locality. Notes: Haplotype names a1-a10 correpond to COIa1-COIa10 and vernalis 1–5 to COIv1-COIv5 from Table 1 and Figure 9; a map showing the geographical position of sampled areas and the number of localities in each area is shown in the top left part of the figure.
Figure 4 in Molecular-genetic-based contribution to the taxonomy of the Acanthocyclops robustus group
Figure 4. Acanthocyclops americanus (Marsh) female neotype from the terra typica, Madison, Wisconsin, USA. (A) Antennule; (B) antenna; (C) mandible; (D) maxillule; (E) maxilla; (F) maxilliped. Note: Scale bar = 50 µm.
Figure 5 in Molecular-genetic-based contribution to the taxonomy of the Acanthocyclops robustus group
Figure 5. Acanthocyclops americanus (Marsh) female neotype from the terra typica, Madison, Wisconsin, USA. (A–D) Swimming legs 1–4, in order. Note: Scale bar = 50 µm.
Figure 3 in Molecular-genetic-based contribution to the taxonomy of the Acanthocyclops robustus group
Figure 3. Acanthocyclops americanus (Marsh) from the terra typica, Madison, Wisconsin, USA. (A–B) Female neotype; (C) male allotype. Notes: Scale bar = 200 µm; neotype and allotype are from same samples used for molecular genetics, registered in Table 1, as are those in Figures 4–6).
Figure 2 in Molecular-genetic-based contribution to the taxonomy of the Acanthocyclops robustus group
Figure 2. Acanthocyclops robustus (Sars) female (A–F) and male (G–H) from the type locality, Lake Maridalsvann Oslo, Norway. (A) Leg 5 and genital segment in ventral view; (B) furca; (C) antennal basipod frontal side (D) antennal basipod caudal side; (E) Leg 4; (G) Leg4 distal segment of endopod; (H) Leg 4 endopod and exopod. Notes: All from the same samples used for molecular genetics, registered in Table 1.
Figure 1 in Molecular-genetic-based contribution to the taxonomy of the Acanthocyclops robustus group
Figure 1. Acanthocyclops vernalis (Fisher) female (A–D) and male (E) from the type locality, Peterhof, St Petersburg, Russia. (A) Abdomen ventral view; (B) antennal basipod frontal side; (C) antennal basipod caudal side; (D) Leg 4 with coxa and intercoxal sclerite; (E) furca, and Legs 5 and 6. Notes: D and E are from the same samples used for molecular genetics, registered in Table 1.
Figure 9 in Molecular-genetic-based contribution to the taxonomy of the Acanthocyclops robustus group
Figure 9. Phylogenetic relationships based on maximum-likelihood analysis of mitochondrial 12S rRNA sequences. Numbers beside nodes indicate bootstrap support values>70%. Individuals for which nucleotide sequences are determined in this work are shown in bold; they are identified by locality and the corresponding COI haplotype name registered in Table 1 and shown abbreviated in Figure 7. The set of added existing 12S sequences for comparative purposes are identified by country, locality (when coincident with our sequences), GenBank accession number and assigned taxonomcal nomenclature; they are all taken from Bláha et al. (2010).
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).
FIGURE 22 in Integrative taxonomy of Malagasy treefrogs: combination of molecular genetics, bioacoustics and comparative morphology reveals twelve additional species of Boophis 2383
FIGURE 22. Male holotype of Boophis miadana sp. nov. (ZSM 5107/2005) from Andohahela, 1550 m a.s.l.: (A) dorsolateral view; (B) ventral view.
FIGURE 23 in Integrative taxonomy of Malagasy treefrogs: combination of molecular genetics, bioacoustics and comparative morphology reveals twelve additional species of Boophis 2383
FIGURE 23. Male holotype of Boophis haingana sp. nov. (ZSM 5109/2005) from Andohahela: (A) dorsolateral view; (B) ventral view.
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International Brain Laboratory public data
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OpenNeuro
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