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17 results for “cytb”

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zenodo40/100

Fig. 9 in Cryptic Speciation And Characteristics Of The Transition Bias Following An Example Of The Cytb Gene In Palearctic Mammals

Fig. 9. Variation of summarized tv/ts-index in micro- (1) and macromammals (2) depending on nucleotide substitution level. Thick lines illustrate exponential approximation.

opencc-by-4.0Mar 2024View details →
zenodo40/100

Fig. 8 in Cryptic Speciation And Characteristics Of The Transition Bias Following An Example Of The Cytb Gene In Palearctic Mammals

Fig. 8. Variation of transition (upper lines) and transversion (lower lines) frequencies accordingly to substitution frequencies level. Think lines are empirical data for each subfamily/family, thick ones — polynomial approximations of averaged data.

opencc-by-4.0Mar 2024View details →
zenodo40/100

Fig. 2 in Cryptic Speciation And Characteristics Of The Transition Bias Following An Example Of The Cytb Gene In Palearctic Mammals

Fig. 2. Average frequencies of nucleotide substitutions frequencies (sub) and its standard errors of the three taxonomical levels in micromammals (black) and macromammals (gray).

opencc-by-4.0Mar 2024View details →
zenodo40/100

T a b l e 1 in Cryptic Speciation And Characteristics Of The Transition Bias Following An Example Of The Cytb Gene In Palearctic Mammals

T a b l e 1. Average (M), sample deviations (SD) of nucleotide substitution, ts/tv and F indexes of different taxonomical levels within 15 Palearctic mammal families/subfamilies

opencc-by-4.0Mar 2024View details →
zenodo40/100

figure 5 Lineage through time plot within G. subgutturosa with cytb. The 95 in Unraveling goitered gazelle (Gazella subgutturosa) diversification: insights from phylogeography and species distribution modeling

figure 5 Lineage through time plot within G. subgutturosa with cytb. The 95% highest posterior density interval is shown in blue.

opencc-by-4.0Mar 2024View details →
zenodo40/100

figure 2 The dated phylogenetic trees using the cytb gene for G. subgutturosa. Blue bars show 95 in Unraveling goitered gazelle (Gazella subgutturosa) diversification: insights from phylogeography and species distribution modeling

figure 2 The dated phylogenetic trees using the cytb gene for G. subgutturosa. Blue bars show 95% highest posterior density intervals of the estimated node ages; numbers next to the nodes are mean node ages (Mya). The red and green lines show new haplotypes from this study.

opencc-by-4.0Mar 2024View details →
dryad36/100

COI and Cytb data of Lagocephalus spadiceus in eight populations

<p>The Late Pleistocene-Holocene climate fluctuations have had a major impact on phylogeographic structure and historical dynamics of marine fishes in the marginal seas of the western Pacific Ocean. <em>Lagocephalus spadiceus </em>is a high-nutritional and economic-value species in the Southeast China Sea. The study was to assess the population genetic diversity and demography of <em>L. spadiceus</em> in the South China Sea (SCS). A sample of 300 specimens from eight geographic locations along the coast of mainland China and Hainan Island were obtained for this study. The mitochondrial cytochrome oxidase <em>I </em>(<em>COI</em>) and cytochrome <em>b</em> (Cyt <em>b</em>) gene datasets had high haplotype diversity but low nucleotide diversity. The genetic structure and phylogenetic analyses indicated that there was no significant population structure among the eight geographic locations. The low genetic diversity of <em>L. spadiceus</em> was associated with population expansion in the Late Pleistocene-Holocene period. This was supported by star haplotype networks, neutrality tests, unimodal mismatch distributions and Bayesian skyline plots. These findings have important reference value for the protection of genetic resources. Furthermore, the study illuminates the complex relationship between Pleistocene-Holocene temperature variability and phylogeography.</p>

opencc-zeroMar 2024View details →
dryad36/100

Cytb gene sequences of Fejervarya species from Lesser Sunda, Indonesia and other Asian countries

<p>Cyt b gene sequences of Fejervarya species were done and later submitted to DDBJ. Then, we received accession number which are used in our manuscript "Postmating isolation and evolutionary relationships among Fejervarya species from Lesser Sunda, Indonesia and other Asian countries revealed by crossing experiments and mtDNA Cytb sequences analyses". These are genuine data. There is no conflict of interest of these data.</p>

opencc-zeroOct 2022View details →
dryad36/100

COI and Cytb data of Lagocephalus spadiceus in eight populations

Open the record for dataset details and reuse information.

publicMar 2024View details →
dryad36/100

Cytb gene sequences of Fejervarya species from Lesser Sunda, Indonesia and other Asian countries

Open the record for dataset details and reuse information.

publicOct 2022View details →
zenodo32/100

III Average nucleotide distances (%) based on the Kimura 2-parameter (K2P) model between Aselliscus spp., and associated outgroups based on complete mitochondrial Cytb (1,140 bp, below the diagonal) and COI (657 bp, above the diagonal) gene sequences in Description of a new species of the genus Aselliscus (Chiroptera, Hipposideridae) from Vietnam

III Average nucleotide distances (%) based on the Kimura 2-parameter (K2P) model between Aselliscus spp., and associated outgroups based on complete mitochondrial Cytb (1,140 bp, below the diagonal) and COI (657 bp, above the diagonal) gene sequences

opennotspecifiedNov 2015View details →
zenodo32/100

FIGURE 1. Maximum likelihood tree for cytb and ITS2 in Contributions to Disholcaspis Dalla Torre And Kieffer (Hymenoptera: Cynipidae: Cynipini)

FIGURE 1. Maximum likelihood tree for cytb and ITS2, for known species of Disholcaspis and unidentified specimens. Names starting with "D_" represent specimens from Nicholls et al. (2017). Names starting with USNM are newly collected; those in blue (only) can be assigned to previously-described species based on phylogenetic placement, genetic distances, and host plant data. Bootstrap values above 50% are shown to the left of the nodes.

opennotspecifiedOct 2020View details →
zenodo32/100

FIGURE 4. Combined haplotype networks from CytB data for Laminatubus paulbrooksi n in Laminatubus (Serpulidae, Annelida) from eastern Pacific hydrothermal vents and methane seeps, with description of two new species

FIGURE 4. Combined haplotype networks from CytB data for Laminatubus paulbrooksi n. sp. (top) from Pacific Costa Rica margin and Gulf of California (Mexico) localities and L. joycebrooksae n. sp. (bottom) from Costa Rica. There was little variability among the L. joycebrooksae n. sp. sequences and a distinct break to L. paulbrooksi n. sp. This corresponds to a minimum 6.4% uncorrected distance. Laminatubus paulbrooksi n. sp. showed marked intraspecific variability with distinct breaks among the three main sites; Costa Rica (9°N), Pescadero (23°N) and Guaymas Basin (27°N). * indicates the holotypes for L. paulbrooksi n. sp. and L. joycebrooksae n. sp. respectively.

opennotspecifiedJan 2021View details →
dryad32/100

Cytb + ND2 Prinia gracilis complex

<p>Prinias (Cisticolidae: Prinia) are resident warblers of open areas across Africa and Asia and include many polytypic species whose species limits have not been seriously reevaluated recently. Based on an integrative taxonomic analysis of morphology, song, and mitochondrial DNA (mtDNA), we suggest that 2 species should be recognized in the Graceful Prinia (<em>Prinia gracilis</em>) complex. In addition, our morphological analyses show the existence of a well-marked undescribed form in southeastern Somalia, which we name herein as a new subspecies. <em>Prinia gracilis</em> is a small, drab, long-tailed species with streaking above and plain pale underparts that has been suggested to fall into 2 groups: the southwestern nominate group (from Egypt to Oman) and the northeastern <em>lepida </em>group (from Turkey through India). However, the characters presented to justify this grouping are variable and show a mosaic pattern, and whether genetic and vocal differences exist is unknown. We found consistent between-group song differences, with the nominate group giving consistently longer inter-phrase intervals, whereas the members of the <em>lepida </em>group sing an essentially continuous reel. An mtDNA tree suggests a deep split between the nominate and <em>lepida </em>groups, with a coalescence time between these clades of ~ 2.2 million years ago. Vocal and mtDNA analyses provided evidence that the northeastern Arabian Peninsula taxon <em>carpenteri </em>belongs to the <em>lepida </em>group. We found that, of all the morphological characters proposed, only proportions and tail barring and spotting relatively consistently distinguish the 2 groups. However, these characters strongly suggest that the eastern Arabian Peninsula is populated by taxa of both the <em>gracilis </em>and <em>lepida </em>groups, in different areas, but we lack genetic and bioacoustic data to corroborate this. Although further study is needed in potential contact zones, we suggest that 2 species should be recognized in the <em>P. gracilis</em> complex, and we propose the retention of the English name Graceful Prinia for <em>P. gracilis </em>sensu stricto, while we suggest that <em>P. lepida</em> be known as Delicate Prinia.</p>

opencc-zeroMar 2022View details →
zenodo32/100

mtKO_nucleoids dataset 05 - CYTB KO

<p>This is one of five&nbsp;imaging datasets to compare mtDNA mutant cell lines with isogenic wild-type cell lines by mtFociCounter.</p> <p>Images are&nbsp;<strong>Spinning Disk Confocal&nbsp;</strong>Images of unsorted 3t3 NIH mouse fibroblasts stably expressing&nbsp;<strong>mitochondrially</strong>targeted dsRed, immunofluorescence against dsDNA (mitochondrial&nbsp;<strong>nucleoids</strong>) and AlexaFluor 647, and&nbsp;stained&nbsp;<strong>nuclei</strong>with Hoechst.<br> Samples&nbsp;from the same day are 13mm coverslips processed in parallel (seeding of cells, fixation, immunofluorescence, microscopy)&nbsp;and mounted on the same glass slide (#1 on left, #2 centre, #3 right).</p> <p>This dataset&nbsp;contains data from&nbsp;<strong>WT</strong>&nbsp;cells and&nbsp;<strong>CYTB loss of function</strong>&nbsp;mutations from the following acquisition dates:<br> 20221217<br> 20221220<br> 20221221</p> <p>For further details, please do not hesitate to contact the author, timorey AT hotmail DOT com.<br> A preprint with experimental details and analysis will be available soon.</p>

opencc-by-4.0Feb 2023View details →
dryad32/100

Cytb + ND2 Prinia gracilis complex

Open the record for dataset details and reuse information.

publicMar 2022View details →
zenodo20/100

List of specimens, species codes, localities (NI, Northern Iberia; CI, Central Iberia; SI, Southern Iberia; AU, Austria; BL, Bulgaria; CR, Croatia; CZ, Czech Republic; DK, Denmark; FR, France; GE, Germany; GR, Greece; HN, Hungary; SD, Sweden; SW, Switzerland; TK, Turkey), haplotypes codes for species and GenBank accession numbers of the samples used for an overall molecular screening of bat cryptic diversity in Iberia using a mtDNA cytb fragment in The Iberian contribution to cryptic diversity in European bats

List of specimens, species codes, localities (NI, Northern Iberia; CI, Central Iberia; SI, Southern Iberia; AU, Austria; BL, Bulgaria; CR, Croatia; CZ, Czech Republic; DK, Denmark; FR, France; GE, Germany; GR, Greece; HN, Hungary; SD, Sweden; SW, Switzerland; TK, Turkey), haplotypes codes for species and GenBank accession numbers of the samples used for an overall molecular screening of bat cryptic diversity in Iberia using a mtDNA cytb fragment

opennotspecifiedNov 2006View details →

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