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8 results for “Rhodopsalta”
Figure 7. cox1 in Phylogeography of the endemic red-tailed cicadas of New Zealand (Hemiptera: Cicadidae: Rhodopsalta), and molecular, morphological and bioacoustical confirmation of the existence of Hudson's Rhodopsalta microdora
Figure 7. cox1 chronogram from the *BEAST multispecies coalescent analysis, showing divergence times for intraspecific haplotype clades as bars indicating the 95% highest posterior density intervals. Taxa with asterisks were missing cox1, and their positions within the species clades are determined by the EF1α gene tree.
Figure 8 in Phylogeography of the endemic red-tailed cicadas of New Zealand (Hemiptera: Cicadidae: Rhodopsalta), and molecular, morphological and bioacoustical confirmation of the existence of Hudson's Rhodopsalta microdora
Figure 8. Lectotype of Tettigonia cruentata Fabricius, 1775, type species of genus Rhodopsalta Dugdale, 1972, with attached labels shown. Scale bars: 1 cm. Photographs by B. Price.
Figure 6 in Phylogeography of the endemic red-tailed cicadas of New Zealand (Hemiptera: Cicadidae: Rhodopsalta), and molecular, morphological and bioacoustical confirmation of the existence of Hudson's Rhodopsalta microdora
Figure 6. Primary geographical subclades found for the sequenced specimens, mapped for each Rhodopsalta species.
Figure 5 in Phylogeography of the endemic red-tailed cicadas of New Zealand (Hemiptera: Cicadidae: Rhodopsalta), and molecular, morphological and bioacoustical confirmation of the existence of Hudson's Rhodopsalta microdora
Figure 5. Single-gene Bayesian phylogenetic trees based on mitochondrial cox1 (1486 bp; A) and nuclear EF1α (798 bp; B) using CIPRES v.3.3. Branch support values represent Bayesian posterior probabilities and RAXML bootstrap percentages from 1000 non-parametric pseudoreplicates. The number of parsimony informative sites is 239 for cox1 and 61 for EF1α.
Figure 4 in Phylogeography of the endemic red-tailed cicadas of New Zealand (Hemiptera: Cicadidae: Rhodopsalta), and molecular, morphological and bioacoustical confirmation of the existence of Hudson's Rhodopsalta microdora
Figure 4. Bayesian phylogenetic tree based on 2284 bp of concatenated genes (5′ and 3′ cox1 and EF1α). Six partition subsets were used (by gene and codon position for each gene, respectively). Branch support values represent Bayesian posterior probabilities and RAXML bootstrap percentages from 1000 non-parametric pseudoreplicates. The number of parsimony-informative sites is 300. Grey boxes show mean divergence time estimates and 95% confidence intervals from the *BEAST analysis.
Figure 3 in Phylogeography of the endemic red-tailed cicadas of New Zealand (Hemiptera: Cicadidae: Rhodopsalta), and molecular, morphological and bioacoustical confirmation of the existence of Hudson's Rhodopsalta microdora
Figure 3. Waveforms illustrating song phenotypes of the three Rhodopsalta species. All fully developed Rhodopsalta songs consist of repeated phrases, the first one of which is indicated by a bracket in graphs A–F. Stars indicate the observed or inferred (Rhodopsalta microdora) positions of wing-flick responses produced by sexually receptive females.
Figure 1 in Phylogeography of the endemic red-tailed cicadas of New Zealand (Hemiptera: Cicadidae: Rhodopsalta), and molecular, morphological and bioacoustical confirmation of the existence of Hudson's Rhodopsalta microdora
Figure 1. Palaeogeographical maps depicting topographical change in the North Island of New Zealand throughout the Pliocene and Pleistocene epochs. Maps were modified and reprinted from Ellis et al. (2015), with permission.
Figure 2 in Phylogeography of the endemic red-tailed cicadas of New Zealand (Hemiptera: Cicadidae: Rhodopsalta), and molecular, morphological and bioacoustical confirmation of the existence of Hudson's Rhodopsalta microdora
Figure 2. Maps of Simon-lab field records of the three Rhodopsalta species.
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