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635 results for “Phylogenetics: comparative”
Phlorest phylogeny derived from Birchall et al. 2016 'A combined comparative and phylogenetic analysis of the Chapacuran language family'
<p>Cite the source of the dataset as:</p> <blockquote> <p>Birchall, Joshua, Michael Dunn, and Simon J. Greenhill. 2016. A combined comparative and phylogenetic analysis of the Chapacuran language family. International Journal of American Linguistics 82 (3): 255–84. doi: 10.1086/687383</p> </blockquote>
CLDF dataset derived from Birchall et al.'s "A Combined Comparative and Phylogenetic Analysis of the Chapacuran Language Family" from 2016
<p>Cite the source of the dataset as:</p> <blockquote> <p>Birchall J, Dunn M, & Greenhill SJ. 2016. A Combined Comparative and Phylogenetic Analysis of the Chapacuran Language Family. International Journal of American Linguistics 82(3). 255–284.</p> </blockquote>
Supplementary phylogenetic data for Rouïl et. al. 2020 "The protector within: Comparative genomics of APSE phages across aphids reveals rampant recombination and diverse toxin arsenals"
<p>Supplementary phylogenetic data for Rouïl <em>et. al.</em> 2020 "The protector within: Comparative genomics of APSE phages across aphids reveals rampant recombination and diverse toxin arsenals"</p> <p> </p> <p>The data set consists of the following sub-directories:</p> <p>1) "APSE_conserved_proteins_alns": Single-copy conserved genes codon sequences and alignments in FASTA format.</p> <p>2) "APSE_phylogeny": Files used for APSE phylogenetic and recombination analyses.</p> <p>3) "APSE_reannotations": GenBank-formatted files of the assemblies and re-annotations of APSE phages. Newly-sequenced phages deposited at the European nucleotide Archive are also included. ***New in this version***</p> <p>4) "APSE_toxin_lyzozyme": Files used for APSE toxin-cassette and lyzozyme-related gene phylogenies.</p> <p>5) "Arsenophonus_PHASTER": PHASTER phage annotation output files organised by organisim and contig/scaffold.</p> <p>6) "Hamiltonella_drafts": Newly-sequenced low-coverage draft <em>Hamiltonella</em> genomes in FASTA format.</p> <p>7) "Hamiltonella_phylogeny": files used for <em>Hamiltonella</em> phylogenetic analysis.</p> <p> </p> <p>See enclosed README.txt file for more details.</p> <p> </p> <p>* ver. 1.1.1: Updated annotations for APSE genomes including inteins missing in previous annotation files.</p>
Figs 274‒288. 274–279 ‒ male sternite 8 in Comparative genitalic morphology in ten genera of thread-legged bugs of the tribe Metapterini, and its phylogenetic importance (Hemiptera: Heteroptera: Reduviidae)
Figs 274‒288. 274–279 ‒ male sternite 8 (S8): 274–276 ‒ ventral view, 277‒279 ‒ lateral view; 280‒288 ‒ pygophore: 280‒282 ‒ dorsal view, 283‒285 ‒ lateral view, 286‒288 ‒ ventral view. 274, 277, 280, 283, 286 ‒ Bergemesa brachmanni (Berg, 1884); 275, 278, 281, 284, 287 ‒ Gardena faustina McAtee & Malloch, 1925; 276, 279, 282, 285, 288 ‒ Tagalis seminigra Champion, 1899. Scale bar: 0.5 mm
Figs 79‒88 in Comparative genitalic morphology in ten genera of thread-legged bugs of the tribe Metapterini, and its phylogenetic importance (Hemiptera: Heteroptera: Reduviidae)
Figs 79‒88. Pygophore in lateral view. 79–81 – Ghinallelia Wygodzinsky, 1966; 82–83 – Liaghinella Wygodzinsky, 1966; 84 – Onychomesa Wygodzinsky, 1966; 85–86 – Pseudometapterus Wygodzinsky, 1966; 87–88 – Schidium Bergroth, 1916. Scale bar: 0.5 mm. Abbreviations: mpp – medial posterior process of pygophore; pa – paramere; vpp – ventral protruding of the pygophore.
Figs 122‒131 in Comparative genitalic morphology in ten genera of thread-legged bugs of the tribe Metapterini, and its phylogenetic importance (Hemiptera: Heteroptera: Reduviidae)
Figs 122‒131. Phallus in dorsal view. 122–124 – Ghinallelia Wygodzinsky, 1966; 125–126 – Liaghinella Wygodzinsky, 1966; 127 – Onychomesa Wygodzinsky, 1966; 128–129 – Pseudometapterus Wygodzinsky, 1966; 130–131 – Schidium Bergroth, 1916. Scale bar: 0.5 mm. Abbreviations: dps – dorsal phallothecal sclerite; duc – ductifer.
FIGURE 15 in Molecular phylogenetic analysis and comparative morphology reveals the diversity and distribution of needle nematodes of the genus Longidorus (Dorylaimida: Longidoridae) from Spain
FIGURE 15 Light micrographs of Longidorus pini Andrés and Arias, 1988 paratypes from San Martín del Pimpollar, Avila province (A–F), and the population from Nava de Francia, Salamanca province (G–M). A–C, G–I, female anterior regions. D–F, J–K, female tails. L-M, male tail with detail of spicules. Abbreviations: a = anus; gr = guiding ring; sp = spicules; spl = ventromedian supplements. Scale bars = 20 μm
FIGURE 13 in Molecular phylogenetic analysis and comparative morphology reveals the diversity and distribution of needle nematodes of the genus Longidorus (Dorylaimida: Longidoridae) from Spain
FIGURE 13 Light micrographs of Longidorus cf. olegi Kankina & Metlitskaya, 1983. (A)–(B) female anterior region. (C)–(F) female lip regions. (G) detail of basal bulb. (H) vulval region. (I)–(L) female tails. (M) and (N), male tail with detail of spicules. (O)–(R) First-, second-, third-, and fourth-stage juvenile (J1–J4) tails, respectively. Abbreviations: a = anus; af = amphidial fovea; gr = guiding ring. Scale bars = 20 μm
FIGURE 14 in Molecular phylogenetic analysis and comparative morphology reveals the diversity and distribution of needle nematodes of the genus Longidorus (Dorylaimida: Longidoridae) from Spain
FIGURE 14 Relationship of body length to length of functional and replacement odontostyle (Ost and rOst, respectively) length in all developmental stages from first-stage juveniles (J1) to mature females of Longidorus cf. olegi Kankina & Metlitskaya, 1983
FIGURE 12 in Molecular phylogenetic analysis and comparative morphology reveals the diversity and distribution of needle nematodes of the genus Longidorus (Dorylaimida: Longidoridae) from Spain
FIGURE 12 Light micrographs of Longidorus nevesi Macara 1985. (A) female anterior region. (B) female lip region. (C) vulval region. (D) female tail. (E)–(F) male tail with detail of spicules. Abbreviations: a = anus; gr = guiding ring; spl = ventromedian supplements; V = vulva. Scale bars = 20 μm
Figure 11 in Molecular phylogenetic analysis and comparative morphology reveals the diversity and distribution of needle nematodes of the genus Longidorus (Dorylaimida: Longidoridae) from Spain
Figure 11 Light micrographs of Longidorus carpetanensis Arias et al., 1986 from Puebla de Sanabria, Zamora (A)–(F), and topotypes from Navalmoral, Avila (G)–(L). A–C, G and H, female anterior regions. D, I, female tails. E and F, J and L, male tail with detail of spicules. Abbreviations: a = anus; gr = guiding ring; spl = ventromedian supplements. Scale bars = 20 µm
FIGURE 9 in Molecular phylogenetic analysis and comparative morphology reveals the diversity and distribution of needle nematodes of the genus Longidorus (Dorylaimida: Longidoridae) from Spain
FIGURE 9 Light micrographs of Longidorus pacensis sp. nov. (A)–(G) Anterior regions. (H) Vulval region. (I)–(K) Female tails. (L) Detail of sperm cells. (M) and (N) Male tails. (O)–(R) First-, second-, third-, and fourth-stage juvenile (J1–J4) tails, respectively. Abbreviations: a = anus; af = amphidial fovea; gr = guiding ring; sp = spicules; spl = ventromedian supplements; v = vulva. Scale bars = 20 μm
FIGURE 10 in Molecular phylogenetic analysis and comparative morphology reveals the diversity and distribution of needle nematodes of the genus Longidorus (Dorylaimida: Longidoridae) from Spain
FIGURE 10 Light micrographs of Longidorus africanus Merny, 1966. (A) female anterior region. (B) female lip region. (C) vulval region. (D)–(E) female tails. Abbreviations: a = anus; gr = guiding ring; v = vulva. Scale bars = 20 μm
FIGURE 8 in Molecular phylogenetic analysis and comparative morphology reveals the diversity and distribution of needle nematodes of the genus Longidorus (Dorylaimida: Longidoridae) from Spain
FIGURE 8 Line drawings of Longidorus pacensis sp. nov. (A) Female neck region. (B) and (C) Female lip regions. (D) and (E) Female tails. (F) Male tail. (G) First-stage juvenile tail
FIGURE 7 in Molecular phylogenetic analysis and comparative morphology reveals the diversity and distribution of needle nematodes of the genus Longidorus (Dorylaimida: Longidoridae) from Spain
FIGURE 7 Relationship of body length to length of functional and replacement odontostyle (Ost and rOst, respectively) length in all developmental stages from first-stage juveniles (J1) to mature females of. (A) Longidorus iliturgiensis sp. nov. (B) Longidorus pacensis, sp. nov.
FIGURE 4 Phylogenetic relationships within the genus Longidorus. Bayesian 50 in Molecular phylogenetic analysis and comparative morphology reveals the diversity and distribution of needle nematodes of the genus Longidorus (Dorylaimida: Longidoridae) from Spain
FIGURE 4 Phylogenetic relationships within the genus Longidorus. Bayesian 50% majority rule consensus tree as inferred from cytochrome c oxidase subunit I (CoxI) mtDNA gene sequence alignment under the general time-reversible model of sequence evolution with correction for invariable sites and a gammashaped distribution (GTR + I + G). Posterior probabilities greater than 0.70 are given for appropriate clades. Newly obtained sequences in this study are shown in bold. Scale bar = expected changes per site.
FIGURE 6 in Molecular phylogenetic analysis and comparative morphology reveals the diversity and distribution of needle nematodes of the genus Longidorus (Dorylaimida: Longidoridae) from Spain
FIGURE 6 Light micrographs of Longidorus iliturgiensis, sp. nov. (A)–(D) Anterior regions. (E) Vulval region. (F)–(I) Female tails. (J)–(M) First-, second-, third-, and fourth-stage juvenile (J1–J4) tails, respectively. (N)–(O) Male tail. Abbreviations: a = anus; af = amphidial fovea; spl = ventromedian supplements; v = vulva. Scale bars (A)–(C), (E)–(O) = 20 μm; (D) = 10 μm
FIGURE 5 in Molecular phylogenetic analysis and comparative morphology reveals the diversity and distribution of needle nematodes of the genus Longidorus (Dorylaimida: Longidoridae) from Spain
FIGURE 5 Line drawings of Longidorus iliturgiensis, sp. nov. paratypes. (A) Female neck region. (B) and (C) Female lip regions. (D) and (E) Female tails. (F) Male tail. (G) First-stage juvenile tail
FIGURE 3 Phylogenetic relationships within the genus Longidorus. Bayesian 50 in Molecular phylogenetic analysis and comparative morphology reveals the diversity and distribution of needle nematodes of the genus Longidorus (Dorylaimida: Longidoridae) from Spain
FIGURE 3 Phylogenetic relationships within the genus Longidorus. Bayesian 50% majority rule consensus tree as inferred from 18S rRNA gene sequence alignment under a transitional model with invariable sites and a gamma correction (TIM 2 + I + G). Posterior probabilities greater Downloaded than 0.70 from are Brill given.comfor08/29/ appropriate 2023 05:44:51PM clades. Newly obtained sequences in this study are shown in bold. Scale bar = expected changesvia per site free. access
FIGURE 1 Phylogenetic relationships within the genus Longidorus. Bayesian 50 in Molecular phylogenetic analysis and comparative morphology reveals the diversity and distribution of needle nematodes of the genus Longidorus (Dorylaimida: Longidoridae) from Spain
FIGURE 1 Phylogenetic relationships within the genus Longidorus. Bayesian 50% majority rule consensus tree as inferred from D2 and D3 expansion domains of 28S rRNA sequence alignment under an SYM model with invariable sites and a gamma-shaped distribution (SYM + I + G). Posterior probabilities greater than 0.70 are given for appropriate clades. Newly obtained sequences in this study are shown in bold. Scale bar = expected changes per site. ** = Branches collapsed, indicating clustered Longidorus species. For a more specific detail of collapsed clades, see supplementary fig. S1.
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International Brain Laboratory public data
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OpenNeuro
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