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71 results for “DNA barcodes analysis”
FIGURES 44–46 in Exploring the diversity of Gracillariidae (Lepidoptera) in South Africa: host plants, distribution, and DNA barcoding analysis, with the description of nine new species
FIGURES 44–46. Male genitalia of South African Gracillariidae. Phodoryctis tephrosiella sp. nov.: 44, holotype, ventral view; 45, phallus with bulbus ejaculatorius; 46, segment VIII in ventral view (ae: aedeagus; pb: phallobase; be: bulbus ejaculatorius). (All scale bars 190 μm).
FIGURES 25−30 in Exploring the diversity of Gracillariidae (Lepidoptera) in South Africa: host plants, distribution, and DNA barcoding analysis, with the description of nine new species
FIGURES 25−30. Forewing pattern of South African Gracillariidae. 25, Leucocercops curatellifoliae sp. nov., Limpopo. 26, Phodoryctis tephrosiella sp. nov., Gauteng. 27, Telamoptilia cordati sp. nov., South Africa, Limpopo. 28, Telamoptilia sp., Madagascar. 29, Cameraria melhaniella sp. nov., Limpopo. 30, Phyllonorycter pseudogrewiella sp. nov., Limpopo.
FIGURES 13–18 in Exploring the diversity of Gracillariidae (Lepidoptera) in South Africa: host plants, distribution, and DNA barcoding analysis, with the description of nine new species
FIGURES 13–18. Adults of South African Gracillariidae. 13, Cryptolectica capnodecta, Limpopo, Hoedspruit, A. & I. Sharp leg. 14, C. terminalina, Limpopo, Hoedspruit, A. & I. Sharp leg. 15, Dialectica pyramidota, Limpopo, Hoedspruit, A. & I. Sharp leg. 16, Amblyptila cynanchi, Western Cape, Knysna, S. Mecenero leg. 17, Leucocercops dasmophora, Gauteng, Tshwane, A. & I. Sharp leg. 18, L. curatellifoliae sp. nov. Limpopo, Hoedspruit, A. & I. Sharp leg.
FIGURES 32–34 in Exploring the diversity of Gracillariidae (Lepidoptera) in South Africa: host plants, distribution, and DNA barcoding analysis, with the description of nine new species
FIGURES 32–34. Forewing pattern of the South African Phyllocnistinae. 32, Phyllocnistis magalismontani sp. nov., drawn by holotype; 33, P. allisonae sp. nov., holotype; 34, P. faureae, holotype.
FIGURE 31 in Exploring the diversity of Gracillariidae (Lepidoptera) in South Africa: host plants, distribution, and DNA barcoding analysis, with the description of nine new species
FIGURE 31. Forewing pattern of the Afrotropical Phyllocnistinae. A, Phyllocnistis pharetrucha; B, P. saligna; C, P. magalismontani sp. nov.; D, P. faureae sp. nov.; E, P. loxosticha; F, P. citrella; G, P. allisonae sp. nov..
FIGURES 1−6 in Exploring the diversity of Gracillariidae (Lepidoptera) in South Africa: host plants, distribution, and DNA barcoding analysis, with the description of nine new species
FIGURES 1−6. Adults of South African Gracillariidae. 1, Caloptilia sp., Limpopo, Lekgalameetse N. R., A. & I. Sharp leg. 2, Caloptilia rhusina, Western Cape, Robberg Nature Reserve, S. Mecenero leg. 3, Macarostola noellineae, Limpopo, Hoedspruit, A. & I. Sharp leg. 4, Caloptilia cataractias, Limpopo, Hoedspruit, leg. A. & I. Sharp. 5, Ectropina spirostachydis sp. nov., Limpopo, Hoedspruit, A. & I. Sharp leg. 6, Graphiocephala barbitias, Gauteng, Tshwane, A. Sharp leg.
FIGURES 7–12 in Exploring the diversity of Gracillariidae (Lepidoptera) in South Africa: host plants, distribution, and DNA barcoding analysis, with the description of nine new species
FIGURES 7–12. Adults of South African Gracillariidae. 7, Semnocera procellaris, Limpopo, Hoedspruit, A. & I. Sharp leg. 8, Conopomorphina ochnivora, Gauteng, Magaliesburg, A. & I. Sharp leg. 9, C. aptata, Limpopo, Hoedspruit, A. & I. Sharp leg. 10, Cuphodes melanostola, Limpopo, Hoedspruit, A. & I. Sharp leg. 11, Acrocercops syzygiena, Gauteng, Tshwane, A. Sharp leg. 12, A. combreticola, Gauteng, Tshwane, A. Sharp leg.
Isotope analysis combined with DNA barcoding provide new insights into the dietary niche of khulan in the Mongolian Gobi
<p><span>With increasing livestock numbers, competition and avoidance are increasingly shaping resource availability for wild ungulates. Shifts in the dietary niche of wild ungulates are likely and can be expected to negatively affect their fitness. The Mongolian Gobi constitutes the largest remaining refuge for several threatened ungulates, but unprecedentedly high livestock numbers are sparking growing concerns over rangeland health and impacts on threatened ungulates like the Asiatic wild ass (khulan).</span></p> <p><span>Previous stable isotope analysis of khulan tail hair from the Dzungarian Gobi suggested that they graze in summer but switch to a poorer mixed C3 grass / C4 shrub diet in winter, most likely in reaction to local herders and their livestock. Here we attempt to validate these findings with a different methodology, DNA metabarcoding. Further, we extend the scope of the original study to the South Gobi Region, where we expect higher proportions of low-quality browse in the khulan winter diet due to a higher human and livestock presence.</span></p> <p><span>Barcoding confirmed the assumptions behind the seasonal diet change observed in the Dzungarian Gobi isotope data, and new isotope analysis revealed a strong seasonal pattern and higher C4 plant intake in the South Gobi Region, in line with our expectations. However, DNA barcoding revealed C4 domination of winter diet was due to C4 grasses (rather than shrubs) for the South Gobi Region. Slight climatic differences result in regional shifts in the occurrence of C3 and C4 grasses and shrubs, which do not allow for an isotopic separation along the grazer-browser continuum over the entire Gobi. </span></p> <p><span>Our findings do not allow us to confirm human impacts upon dietary preferences in khulan as we lack seasonal samples from the South Gobi Region. However, these data provide novel insight into khulan diet, raise new questions about plant availability versus preference, and provide a cautionary tale about indirect analysis methods if used in isolation or extrapolated to the landscape level. Good concordance between relative read abundance of C4 genera from barcoding and proportion of C4 plants from isotope analysis adds to a growing body of evidence that barcoding is a promising quantitative tool to understand resource partitioning in ungulates.</span></p>
FIGURE 4. A in Pinellia hunanensis (Araceae), a new species supported by morphometric analysis and DNA barcoding
FIGURE 4. A classification tree of combined rbcL and matK data using neighbor-joining (NJ) and Bayesian of phylogenetic methods.
FIGURE 5 in Pinellia hunanensis (Araceae), a new species supported by morphometric analysis and DNA barcoding
FIGURE 5. Scatter plot of the first two axes from a detrended correspondence analysis (DCA) for 38 quantitative morphological variables (taxonomic characters) of 24 specimens (classification of 6 Pinellia species). The new species Pinellia hunanensis is circled, including its respective intraspecific variation.
FIGURE 2. Pinellia hunanensis—A in Pinellia hunanensis (Araceae), a new species supported by morphometric analysis and DNA barcoding
FIGURE 2. Pinellia hunanensis—A: habit; B: juvenile plant; C: leaf; D: inflorescence; E: spadix; F: infructescence; G: pistil; H: fruit; I: seed (Drawn after the holotype by Yitao Liu).
Data for morphometric analysis and DNA barcode sequence for the new fish species Polymixia hollisterae
<p>Two datasets are provided to support the journal article (https://doi.org/10.1643/i2020112) by T. C. Grande and M. V. H. Wilson naming the new Bermuda fish species <em>Polymixia hollisterae</em>. The first dataset is for 2-D multivariate morphometric comparisons of selected specimens and species of the fish genus <em>Polymixia</em>. The file is in TPS format, as a plain text file, for use in the application MorphoJ. The data are for 27 specimens with pixel coordinates for 34 landmarks digitized in ImageJ and used to generate Fig. 13 in the referenced publication. The second dataset, published here courtesy of Dr. R. Eytan, is a mitochondrial DNA barcode sequence in fasta format for the second paratype specimen, a small juvenile of the new species. The specimen is only the third one known of the new species and the only one not from Bermuda. It was collected in the north-central Gulf of Mexico and is now deposited in the Harvard University MCZ fish collection as catalog number MCZ 174218. The fasta file can be used as input to the barcode identification function at boldsystems.org, although its original identification in BOLD was incorrect.</p>
FIGURE. DnaSP DNA polymorphism analysis - Nucleotide variability (Pi) comparison between Strobilanthes lupulina and S. glandulata. The window length and step size were set to 600bp and 200bp respectively. The most varying regions and the commonly used barcoding regions are listed against the base-pair differences found. in Strobilanthes glandulata (Acanthaceae), a new species from Sri Lanka based on the morphological and molecular evidences
FIGURE. DnaSP DNA polymorphism analysis - Nucleotide variability (Pi) comparison between Strobilanthes lupulina and S. glandulata. The window length and step size were set to 600bp and 200bp respectively. The most varying regions and the commonly used barcoding regions are listed against the base-pair differences found.
Isotope analysis combined with DNA barcoding provide new insights into the dietary niche of khulan in the Mongolian Gobi
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Data from: Comparison of diets for largemouth and smallmouth bass in Eastern Lake Ontario using DNA barcoding and stable isotope analysis
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Data for morphometric analysis and DNA barcode sequence for the new fish species Polymixia hollisterae
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Data from: Species diversity can be overestimated by a fixed empirical threshold: insights from DNA barcoding of the genus Cletus (Hemiptera: Coreidae) and the meta-analysis of COI data from previous phylogeographical studies
The use of genetic distances to identify species within the framework of DNA barcoding has to some extent improved the development of biodiversity studies. However, using a fixed empirical threshold to delimit species may lead to overestimating species diversity. In this study, we use a new data set of COI sequences for 366 specimens within the genus of Cletus as well as conduct an analysis on the same genetic data for collected morphologically defined species from previous phylogeographical studies, to test whether high intraspecific genetic divergences are common with the premises of comprehensive sampling. The results indicate C. graminis Hsiao & Cheng 1964, is the same species with C. punctiger (Dallas, 1852) and should be synonymized and that the distributional record of C. pugnator (Fabricius, 1787) in China is correct. High intraspecific genetic differentiations (0%–4.35%) were found in C. punctiger. Furthermore, as to the mined data, the maximum intraspecific K2P distances of 186 species (48.44% of 384) exceed 3%, and 101 species (26.30%) can be divided into two or more clusters with a threshold of 3% in cluster analysis. If genetic distance is used to delimit species boundaries, the minimum interspecific K2P distance of the congeneric species should be considered rather than only using the fixed empirical value; otherwise, the species richness may be overestimated in some cases.
Figure 9 from: Syromyatnikov MY, Golub VB, Kokina AV, Soboleva VA, Popov VN (2017) DNA barcoding and morphological analysis for rapid identification of most economically important crop-infesting Sunn pests belonging to Eurygaster Laporte, 1833 (Hemiptera, Scutelleridae). ZooKeys 706: 51-71. https://doi.org/10.3897/zookeys.706.13888
Figure 9 - Restriction fragments of COI PCR products (restriction enzyme, species): 1 AhlI, E. maura or E. testudinaria 2 AhlI, E. integriceps 3 PsiI, E. maura or E. testudinaria 4 PsiI, E. integriceps 5 Bst2UI, E. maura or E. testudinaria 6 Bst2UI, E. integriceps; M, 100 bp DNA ladder.
Figure 8 from: Syromyatnikov MY, Golub VB, Kokina AV, Soboleva VA, Popov VN (2017) DNA barcoding and morphological analysis for rapid identification of most economically important crop-infesting Sunn pests belonging to Eurygaster Laporte, 1833 (Hemiptera, Scutelleridae). ZooKeys 706: 51-71. https://doi.org/10.3897/zookeys.706.13888
Figure 8 - Neighbor joining analysis of COI gene sequences from Eurygaster species. * - sequences obtained in this work.
Figure 5 from: Syromyatnikov MY, Golub VB, Kokina AV, Soboleva VA, Popov VN (2017) DNA barcoding and morphological analysis for rapid identification of most economically important crop-infesting Sunn pests belonging to Eurygaster Laporte, 1833 (Hemiptera, Scutelleridae). ZooKeys 706: 51-71. https://doi.org/10.3897/zookeys.706.13888
Figure 5 - Species of the genus Eurygaster Laporte, general view: A E. integriceps (Puton) B E. maura L. C E. testudinaria (Geoffroy) D E. dilaticollis Dohrn. Specimens A–C were collected in the Voronezh Region; specimen D was from the Teberda Nature Reserve, Caucasus.
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Allen Brain Atlas
Allen Brain Atlas is an Allen Institute collection of brain map atlases, datasets, APIs, and analysis tools covering mouse, human, and non-human primate brain resources.
Annotated Behaviour and Observability Dataset (ABODe)
ABODe is a University of Edinburgh DataShare dataset for behavior classification in group-housed mice using home-cage video, identities, bounding boxes, ground-plate positions, and annotator labels.
DANDI Archive for NWB datasets
DANDI is a BRAIN Initiative archive for publishing and sharing neurophysiology data, including electrophysiology, optophysiology, and behavioral data packaged as NWB and related standards.
International Brain Laboratory public data
The International Brain Laboratory public data releases expose standardized mouse decision-making experiments, including Neuropixels recordings, widefield calcium imaging, behavior, and session metadata accessed through the ONE API.
OpenNeuro
OpenNeuro is a free, open platform for sharing neuroimaging datasets, with public search, dataset pages, and download paths for web, S3, DataLad, and the OpenNeuro CLI.