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FIGURES 6–9 in Two new species of Phyllodistomum Braun, 1899 (Digenea: Gorgoderidae), from freshwater fishes (Cyprinodontiformes: Goodeidae: Goodeinae) in central Mexico: An integrative taxonomy approach using morphology, ultrastructure and molecular phylogenetics
FIGURES 6–9. Scanning electron microscopy of a specimen of Phyllodistomum cribbi n. sp. 6. Adult, ventral view. 7. Oral sucker, showing 4 pairs of papillae. 8. Ventral sucker, showing 3 pairs of papillae. 9. Ventral surface of hindbody exhibiting papillae on the tegument.
FIGURES 2–5 in Two new species of Phyllodistomum Braun, 1899 (Digenea: Gorgoderidae), from freshwater fishes (Cyprinodontiformes: Goodeidae: Goodeinae) in central Mexico: An integrative taxonomy approach using morphology, ultrastructure and molecular phylogenetics
FIGURES 2–5. Line drawings of the holotype of P. cribbi n. sp. and P. wallacei n. sp., and detail of the male reproductive system of both species 2. Phyllodistomum cribbi n. sp. from Zoogoneticus quitzeoensis, ventral view. 3. Detail of the cirrus sac of P. cribbi n. sp. 4. Phyllodistomum wallacei n. sp. from Ilyodon furcidens, ventral view. 5. Detail of the cirrus sac of P. wallacei n. sp. Symbols: os = oral sucker, gp = genital pore, c = cecum, vs = ventral sucker, vg = vitelline gland, o = ovary, t = testis, e = eggs.
FIGURE 1. Hydrological systems and collection sites for Phyllodistomum cribbi n in Two new species of Phyllodistomum Braun, 1899 (Digenea: Gorgoderidae), from freshwater fishes (Cyprinodontiformes: Goodeidae: Goodeinae) in central Mexico: An integrative taxonomy approach using morphology, ultrastructure and molecular phylogenetics
FIGURE 1. Hydrological systems and collection sites for Phyllodistomum cribbi n. sp. (square) and P. wallacei n. sp. (circles) in central Mexico. Full green circles and square correspond to localities where specimens were collected for molecular phylogenetic analyses; full grey circle and square indicate specimens identified either as Dendrorchis sp. or Phyllodistomum sp. from previous studies. These records were not included in the phylogenetic analyses in this study.
Supplementary material 1 from: Grismer LL, Aowphol A, Yodthong S, Ampai N, Termprayoon K, Aksornneam A, Rujirawan A (2022) Integrative taxonomy delimits and diagnoses cryptic arboreal species of the Cyrtodactylus brevipalmatus group (Squamata, Gekkonidae) with descriptions of four new species from Thailand. ZooKeys 1129: 109-162. https://doi.org/10.3897/zookeys.1129.90535
Data frame for the multiple factor analysis of the putative species of the Cyrtodactylus brevipalmatus group
Integrative taxonomy of two thrush complexes (Aves: Turdidae) reveals introgression across sister species
<p>The classification of some <i>Turdus</i> species, such as the Naumann's and dusky thrush complexes and the red-throated and black-throated thrush complexes, is controversial. Herein, we used molecular data and morphological characters to review the taxonomy of these thrush complexes and analyze the genetic differentiation between them. Herein, we examined the genetic characteristics of 13 microsatellite loci in all individuals and total of 129 alleles were detected. In parallel, we have a further judgment on their classification status by measuring 5 morphological features (tail length, wing length, toe length, claw length and instep length).</p>
Figure 4 in Integrative taxonomy of eared nightjars (Aves: Lyncornis) underscores the complementarity of morphology, vocalizations and DNA evidence
Figure 4. Sonograms of territorial songs of Lyncornis. A, Lyncornis macrotis bourdilloni, Kerala, India, B. King. B, Lyncornis macrotis cerviniceps, Thailand, J. C. Roché (BLSA 42510). C, Lyncornis macrotis jacobsoni, Simeulue Island, F. Verbelen. D, Lyncornis temminckii, Johore, Malaysia, T. C. White (BLSA 6414). E, L. temminckii, Way Kambas, Sumatra, A. B. van den Berg (ML 70527). F, Lyncornis macrotis macrotis, Mindanao, A. Greensmith (BLSA 34287). G, Lyncornis macrotis macropterus, Tangkoko Batuangus, Sulawesi, G. Sangster (GS 1841).
Figure 8 in Integrative taxonomy of eared nightjars (Aves: Lyncornis) underscores the complementarity of morphology, vocalizations and DNA evidence
Figure 8. Integrative taxonomy of Lyncornis nightjars, illustrating contrasting sensitivities of datasets and the failure of each dataset to recover all five species.
Figure 3 in Integrative taxonomy of eared nightjars (Aves: Lyncornis) underscores the complementarity of morphology, vocalizations and DNA evidence
Figure 3. Maximum likelihood tree of cytochrome b sequences of the genus Lyncornis and various outgroups. Bootstrap proportions (> 70%) and posterior probabilities (> 0.8) are indicated above and below branches, respectively.
Figure 1 in Integrative taxonomy of eared nightjars (Aves: Lyncornis) underscores the complementarity of morphology, vocalizations and DNA evidence
Figure 1. Map showing range of currently recognized taxa in the Lyncornis macrotis complex. Taxonomy follows Cleere (1998).
Figure 7 in Integrative taxonomy of eared nightjars (Aves: Lyncornis) underscores the complementarity of morphology, vocalizations and DNA evidence
Figure 7. Upper tail of four taxa in the Lyncornis macrotis complex, illustrating differences in pattern and coloration. Note the marked differences in pattern and coloration between L. m. cerviniceps and L. m. jacobsoni. G. Sangster/©Naturalis Biodiversity Center, Leiden.
Figure 2 in Integrative taxonomy of eared nightjars (Aves: Lyncornis) underscores the complementarity of morphology, vocalizations and DNA evidence
Figure 2. Measurement of acoustic variables. For definitions of acoustic variables, see 'Measurements of acoustic characters'.
Figure 7 in Integrative taxonomic analysis of new collections from the central Angolan highlands resolves the taxonomy of African pipistrelloid bats on a continental scale
Figure 7. Lateral photograph of the alcohol-preserved head and anterior portion of the forearm and thumb of the holotype of N. hlandzeni, DM 8423 (left) and close-up photographs of the thumb and proximal forearm of the holotype, DM 8423 (centre) and paratype, DM 8422 (right) showing a distinct white marking at the base to the thumb. The thumb (encircled) is slightly longer than that of a typical pipistrelloid bat.
Figure 6 in Integrative taxonomic analysis of new collections from the central Angolan highlands resolves the taxonomy of African pipistrelloid bats on a continental scale
Figure 6. Dorsal, ventral, lateral cranial and lateral mandibular views of DM 8423 (holotype) and DM 8422 (paratype) of N. hlandzeni sp. nov. Scale bar represents 1 mm.
Figure 5 in Integrative taxonomic analysis of new collections from the central Angolan highlands resolves the taxonomy of African pipistrelloid bats on a continental scale
Figure 5. Photographs and drawings of bacula of N. hlandzeni sp. nov. from Eswatini (DM 8423, 8422), KwaZulu-Natal Province, South Africa (DM 2269, 8787, 5353, 5358), together with N. anchietae from Botswana (TM 48489), Angola (FWC 7521), and Zambia (NHM 70.2632; from Hill & Harrison, 1987). In the top row, D=dorsal, L=lateral and V=ventral view. Images in the lower row are of the ventral view, except for the far right image which is of the lateral view. Abbreviations of museums as follows: DM = Durban Natural Science Museum; TM = Ditsong National Museum of Natural History; NHM = The Natural History Museum, London. FWC indicates the field number of Fenton (Woody) Cotterill. The vertical scale bar on the bottom right indicates 1 mm.
Figure 4 in Integrative taxonomic analysis of new collections from the central Angolan highlands resolves the taxonomy of African pipistrelloid bats on a continental scale
Figure 4. PCA of 12 log-transformed cranial and dental length variables (a) and plots of forearm length and mass (b) and forearm and condylobasal skull length (c) in Angolan small vespertilionid bats with anterior premolar absent (open squares: N. zuluensis; dots: L. capensis). Species identification based on DNA barcoding of the cytb, CO1 and 12S genes.
Figure 3 in Integrative taxonomic analysis of new collections from the central Angolan highlands resolves the taxonomy of African pipistrelloid bats on a continental scale
Figure 3. PCA of components 1 and 2 (a) and components 1 and 3 (b) from 12 log-transformed cranial and dental variables in DNA barcoded Angolan small vespertilionid bats with anterior upper premolar present, in comparison with positively identified samples from South Africa and Eswatini. Species identification based on DNA barcoding of the cytb, CO1 and 12S genes for P. rusticus (open squares) and N. anchietae (dots) from Angola and on either sequences or baculum photographs for N. hlandzeni (open circles) from South Africa and Eswatini and P. hesperidus (crosses) from Eswatini and South Africa.
Figure 1. Maps showing A, 19 in Integrative taxonomic analysis of new collections from the central Angolan highlands resolves the taxonomy of African pipistrelloid bats on a continental scale
Figure 1. Maps showing A, 19 localities in southern Africa of all pipistrelloid bat specimens examined by this study (numbers correspond with locality numbers given in Supporting Information, Table S1; duplicate numbers represent closely spaced GPS points classified as the same locality) and B, seven localities of six species of pipistrelloid bats collected in central Angola by the National Geographic Okavango Wilderness project (in the area demarcated by the dashed lines) between 2016 and 2019. Species identifications based on CO1, 12S RNA and cytb genes. Shaded regions represent elevations of 1200 m a.s.l. and greater. The star represents the holotype locality of N. anchietae in the western Angolan highlands.
FIGURE 10 in Revising the taxonomy of Darevskia valentini (Boettger, 1892) and Darevskia rudis (Bedriaga, 1886) (Squamata, Lacertidae): a Morpho-Phylogenetic integrated study in a complex Anatolian scenario
FIGURE 10. Parsimony networks corresponding to Cyt-b (A) and MC1R (B) represent reconstruction of the studied group. Numbers within parentheses represent a mutational step, black circles missing haplotypes, and colored circles haplotypes. The circle area is proportional to the number of individuals. The new nomenclature proposed in the text is used.
FIGURE 9 in Revising the taxonomy of Darevskia valentini (Boettger, 1892) and Darevskia rudis (Bedriaga, 1886) (Squamata, Lacertidae): a Morpho-Phylogenetic integrated study in a complex Anatolian scenario
FIGURE 9. Maximum Likelihood (ML) tree (left) and collapsed one for the same tree (right) are given. Numbers on branches indicate the bootstrap and posterior probability (pp) values (ML/BI). Each species delimitation result is shown, and a vertical bar represents each cluster obtained from the analysis. Red circles indicate the internal nodes of each OTUs. The new nomenclature proposed in the text is used.
FIGURE 4 in Revising the taxonomy of Darevskia valentini (Boettger, 1892) and Darevskia rudis (Bedriaga, 1886) (Squamata, Lacertidae): a Morpho-Phylogenetic integrated study in a complex Anatolian scenario
FIGURE 4. UPGMA tree derived from the matrix of distances (Table 1) among MALE samples, showing three great groups: a basal one, well different, with D. bithynica (inc. ssp. tristis), and two more closer groups that include the former rudis and valentini-complexes. See the text for an explanation of the results. The tree, derived from the calculation of ultrametric distances calculated in UPGMA, reflects very well the relationships in respect to the original distanced matrix (see Table 1). Its Cophenetic Correlation Index, r = 0.95, shows that the obtained dendrogram has a very good fit (r> 0.9; Rohlf 2000).
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Allen Brain Atlas
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OpenNeuro
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