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142 results for “paraphyly”

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Figure 6 in Paraphyly and low levels of genetic divergence in morphologically distinct taxa: revision of the Pseudoanthidium scapulare complex of carder bees (Apoidea: Megachilidae: Anthidiini)

Figure 6. Palaearctic distribution of A, Pseudoanthidium nanum; B, P. scapulare; C, P. stigmaticorne; D, P. tenellum.

opennotspecifiedSep 2021View details →
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Figure 4. Lectotype, Pseudoanthidium reptans. A in Paraphyly and low levels of genetic divergence in morphologically distinct taxa: revision of the Pseudoanthidium scapulare complex of carder bees (Apoidea: Megachilidae: Anthidiini)

Figure 4. Lectotype, Pseudoanthidium reptans. A, face; B, dorsal view; C, labels; D, ventral view; E, apex of metasoma, showing tips of gonostyli.

opennotspecifiedSep 2021View details →
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Figure 2 in Paraphyly and low levels of genetic divergence in morphologically distinct taxa: revision of the Pseudoanthidium scapulare complex of carder bees (Apoidea: Megachilidae: Anthidiini)

Figure 2. Best-scoring maximum likelihood tree based on analysis of COI data. Numbers shown at nodes are maximum likelihood bootstrap values based on 1000 bootstrap replicates in RAxML. Only bootstrap values greater than 50% are shown. Terminals are labelled with a DNA extraction code, species name, collection locality and either as male (m) or female (f). Barcodes were obtained using Sanger sequencing technology, except for those corresponding to specimens 1802 and 1805, which were obtained from non-UCE assemblies generated during UCE sequencing. A, Pseudoanthidium tenellum, Burgenland, Austria (m), photo Bernhard Jacobi; B, P. cribratum, Bukhara, Uzbekistan (f), photo Jessica Litman; C, P. canariense, Santa Cruz de Tenerife, Canary Islands, Spain (m), photo Jessica Litman; D, P. stigmaticorne, Crimea, Russia, photo Alexander V. Fateryga; E, P. scapulare, Portugal, photo Ian Cross; F, P. nanum, photo Entomologie/Botanik, ETH Zürich / Albert Krebs; G, P. palestinicum, photo Jessica Litman.

opennotspecifiedSep 2021View details →
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Figure 1. A in Paraphyly and low levels of genetic divergence in morphologically distinct taxa: revision of the Pseudoanthidium scapulare complex of carder bees (Apoidea: Megachilidae: Anthidiini)

Figure 1. A, nest of Pseudoanthidium stigmaticorne, in a capsule of Tulipa biflora Pall. (Lisya Bay, Crimea). Insert in lower right shows close-up of the same nest. Three males eventually emerged (photo Alexander V. Fateryga); B, Pseudoanthidium stigmaticorne nesting in a stem of Crambe maritima L. (Arabatskaya Strelka sand spit, Crimea). A pin is inserted to mark the nest (photo Sergey P. Ivanov).

opennotspecifiedSep 2021View details →
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Figure 3 in Paraphyly and low levels of genetic divergence in morphologically distinct taxa: revision of the Pseudoanthidium scapulare complex of carder bees (Apoidea: Megachilidae: Anthidiini)

Figure 3. Best-scoring maximum likelihood tree based on analyses of the (A) 75% UCE matrix and (B) 100% UCE matrix. Numbers shown at nodes are maximum likelihood bootstrap values based on 1000 bootstrap replicates in RAxML. Only bootstrap values greater than 50% are shown. Terminals are labelled with a DNA extraction code corresponding to the whole-body extraction performed for UCE sequencing, the DNA extraction code for the same specimen based on single leg extractions performed for barcode sequencing, the species name, collection locality and either as male (m) or female (f). Three specimens (1800, 1802 and 1805) were only sequenced following the UCE protocol and thus have only a UCE extraction code.

opennotspecifiedSep 2021View details →
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Figure 9 in Lost and found: Totton's Minyaspis faroni revived and molecular evidence of paraphyly of Oxynaspis and Minyaspis

Figure 9. Maximum likelihood phylogenetic tree of Oxynaspis and Minyaspis using Lepas as an outgroup based on concatenating the two mitochondrial genes 12s rDNA and cytochrome oxidase subunit I (COI).

opennotspecifiedOct 2022View details →
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Figure 8 in Lost and found: Totton's Minyaspis faroni revived and molecular evidence of paraphyly of Oxynaspis and Minyaspis

Figure 8. Minyaspis faroni. Lateral view of cirri. (a) Cirrus I. (b) Cirrus I, basal segment. (c) Cirrus II. (d) Cirrus III. (e) Cirrus IV. (f) Cirrus V. (g) Cirrus VI and penis.

opennotspecifiedOct 2022View details →
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Figure 7 in Lost and found: Totton's Minyaspis faroni revived and molecular evidence of paraphyly of Oxynaspis and Minyaspis

Figure 7. Minyaspis faroni. Mouth parts. (a) Labrum and palpus. (b) Tip of labrum. (c) Maxilla I. (d) Maxilla II. (e) Mandible.

opennotspecifiedOct 2022View details →
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Figure 5 in Lost and found: Totton's Minyaspis faroni revived and molecular evidence of paraphyly of Oxynaspis and Minyaspis

Figure 5. Minyaspis faroni. Isolated shell plate, tergum and scutum outside and inside view, carina side view.

opennotspecifiedOct 2022View details →
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Figure 4 in Lost and found: Totton's Minyaspis faroni revived and molecular evidence of paraphyly of Oxynaspis and Minyaspis

Figure 4. Minyaspis faroni. Whole specimen, isolated shell plate (from the same specimen) superimposed on surface of capitulum. Scale bar= 3mm.

opennotspecifiedOct 2022View details →
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Figure 6 in Lost and found: Totton's Minyaspis faroni revived and molecular evidence of paraphyly of Oxynaspis and Minyaspis

Figure 6. Minyaspis faroni. Soma lateral view. Labrum (L) and palpus (P) are indicated. C1–C6: cirri.

opennotspecifiedOct 2022View details →
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Figure 2. A in Lost and found: Totton's Minyaspis faroni revived and molecular evidence of paraphyly of Oxynaspis and Minyaspis

Figure 2. A colony of the antipatharians Antipathes cf. lentipinna, specimens of Minyaspis faroni attached to the basis of the colony.

opennotspecifiedOct 2022View details →
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Figure 3. A in Lost and found: Totton's Minyaspis faroni revived and molecular evidence of paraphyly of Oxynaspis and Minyaspis

Figure 3. A tridimensional model of the wreck origin location of the antipatharian indicated by an arrow. Source: https://sketchfab.com/3d-models/satil-shipwreck-00c31066177e4e8a b9ebdc9cd4b2b8e2. Matan Yuval, Marine Imaging Lab, Dept. of Marine Technologies, University of Haifa.

opennotspecifiedOct 2022View details →
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Fig. 16–18 in Species Paraphyly and Social Parasitism: Phylogenomics, Morphology, and Geography Clarify the Evolution of the Pseudomyrmex elongatulus Group (Hymenoptera:

Fig. 16–18. Pseudomyrmex elongatulus group, workers, full-face dorsal view of head (a) and lateral profile of body (b). 16, P. nimbus, holotype, Costa Rica (CASENT0863541); 17, P. salvini, syntype, Mexico (CASENT0902879); 18, P. veracruzensis, holotype, Mexico (CASENT0863542). Images from AntWeb (www. antweb.org); photographers Phil Ward (16, 18), Zach (Ziv) Lieberman (17).

opennotspecifiedJan 2022View details →
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Fig. 3 in Species Paraphyly and Social Parasitism: Phylogenomics, Morphology, and Geography Clarify the Evolution of the Pseudomyrmex elongatulus Group (Hymenoptera:

Fig. 3. Bivariate plots of measurements and indices concerned with eye size and petiole shape, in workers of P. apache (n = 17) and P. arcanus (n = 17). (a) PL/ LHT (petiole length/metatibia length) by HW (head width); (b) REL2 (eye length/head width) by PLI (petiole height/petiole length).

opennotspecifiedJan 2022View details →
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Fig. 19–26 in Species Paraphyly and Social Parasitism: Phylogenomics, Morphology, and Geography Clarify the Evolution of the Pseudomyrmex elongatulus Group (Hymenoptera:

Fig. 19–26. Pseudomyrmex elongatulus group: distribution maps. 19, P. apache; 20, P. arcanus (circles), P. fasciatus (triangles); 21, P. championi; 22, P. capillatus (triangles), P. cognatus (circles); 23, P. elongatulus (circles), probable introduced populations (stars); 24, P. comitator (square), P. ereptor (triangle), P. exoratus (circles); 25, P. salvini; 26, P. nimbus (circles), P. veracruzensis (triangle).

opennotspecifiedJan 2022View details →
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FIGURE 1 in Paraphyly of Chinese Amolops (Anura, Ranidae) and phylogenetic position of the rare Chinese frog, Amolops tormotus

FIGURE 1. Bayesian inference tree derived from partial DNA sequences of the mitochondrial genes 12S and 16S. Numbers above branches are bootstrap support for maximum parsimony (1000 replicates) / maximum likelihood (10 replicates) analyses (>50 retained), and numbers below branches indicate Bayesian posterior probabilities (>90% retained). Species new to this study are indicated in bold. Species groups of Chinese Amolops from Fei et al. (2005) are indicated.

opennotspecifiedJul 2007View details →
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FIGURE 17 in On the paraphyly of Homaloptera (Teleostei: Balitoridae) and description of a new genus of hillstream loaches from the Western Ghats of India

FIGURE 17. Type localities for species of Ghatsa. Asterisk represents the type species of the genus.

opennotspecifiedDec 2015View details →
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FIGURE 16 in On the paraphyly of Homaloptera (Teleostei: Balitoridae) and description of a new genus of hillstream loaches from the Western Ghats of India

FIGURE 16. Ghatsa montana, CAS-SU 39871 (holotype), 46.4 mm SL. (A) Dorsal, lateral, and ventral views, Puthutotam Estate, brook in Anamallai Hills, India; (B) radiograph. Photos by CAS, Ichthyology Section.

opennotspecifiedDec 2015View details →
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FIGURE 14 in On the paraphyly of Homaloptera (Teleostei: Balitoridae) and description of a new genus of hillstream loaches from the Western Ghats of India

FIGURE 14. Dorsal, lateral, and ventral views of preserved Pseudohomaloptera tatereganii, RMNH 7632 (holotype), 64.6 mm SL, Bo River, Upper Mahakam River basin, East Kalimantan, Borneo, Indonesia.

opennotspecifiedDec 2015View details →

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International Brain Laboratory public data

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