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234 results for “molecular characterisation”
Figure 1 from: Lazarova SS, Elshishka M, Radoslavov G, Lozanova L, Hristov P, Mladenov A, Zheng J, Fanelli E, De Luca F, Peneva VK (2019) Molecular and morphological characterisation of Longidorus polyae sp. n. and L. pisi Edward, Misra & Singh, 1964 (Dorylaimida, Longidoridae) from Bulgaria. ZooKeys 830: 75-98. https://doi.org/10.3897/zookeys.830.32188
Figure 1 Longidoruspolyae sp. n. A, B anterior region C posterior region D, J variations in tail shape E vagina F anterior genital branch G lateral pieces H, I female and male pharyngeal bulb K variations in female and male habitus shapes. Female: all except C, G and I. Scale bars: 25 μm (A–E, J, G); 50 μm (F); 1 mm (K).
Figure 10 from: Lazarova SS, Elshishka M, Radoslavov G, Lozanova L, Hristov P, Mladenov A, Zheng J, Fanelli E, De Luca F, Peneva VK (2019) Molecular and morphological characterisation of Longidorus polyae sp. n. and L. pisi Edward, Misra & Singh, 1964 (Dorylaimida, Longidoridae) from Bulgaria. ZooKeys 830: 75-98. https://doi.org/10.3897/zookeys.830.32188
Figure 10 Phylogenetic tree using 18S rRNA gene inferred from a Bayesian analysis with GTR+I+G model. Numbers represent the Bayesian posterior probabilities.
Figure 2 from: Sługocki Ł, Rymaszewska A, Kirczuk L (2019) Insights into the morphology and molecular characterisation of glacial relict Eurytemora lacustris (Poppe, 1887) (Crustacea, Copepoda, Calanoida, Temoridae). ZooKeys 864: 15-33. https://doi.org/10.3897/zookeys.864.34259
Figure 2 Feeding appendages of EurytemoralacustrisA mandible B maxilla C maxilliped D maxillule. Scale bars: 20 µm.
Figure 4 from: Sługocki Ł, Rymaszewska A, Kirczuk L (2019) Insights into the morphology and molecular characterisation of glacial relict Eurytemora lacustris (Poppe, 1887) (Crustacea, Copepoda, Calanoida, Temoridae). ZooKeys 864: 15-33. https://doi.org/10.3897/zookeys.864.34259
Figure 4 Variability of number of setae on second segment of endopod on second pair of male leg of Eurytemoralacustris. Scale bar: 20 µm.
Figure 3 from: Sługocki Ł, Rymaszewska A, Kirczuk L (2019) Insights into the morphology and molecular characterisation of glacial relict Eurytemora lacustris (Poppe, 1887) (Crustacea, Copepoda, Calanoida, Temoridae). ZooKeys 864: 15-33. https://doi.org/10.3897/zookeys.864.34259
Figure 3 Legs of EurytemoralacustrisA first pair B second pair C third pair D fourth pair. Scale bars: 20 µm.
Figure 6 from: Sługocki Ł, Rymaszewska A, Kirczuk L (2019) Insights into the morphology and molecular characterisation of glacial relict Eurytemora lacustris (Poppe, 1887) (Crustacea, Copepoda, Calanoida, Temoridae). ZooKeys 864: 15-33. https://doi.org/10.3897/zookeys.864.34259
Figure 6 Evolutionary relationship of taxa based on mCOI sequences. The phylogenetic tree was inferred using the Minimum Evolution method (MEGA 10.0.5, Kumar et al. 2018). The evolutionary distances were computed using the Tamura 3-parameter method [3] and are in the units of the number of base substitutions per site. Sequences deposited at GenBank from Sukhikh et al. (2013, 2018), Vasquez et al. (2016), and Alekseev and Sukhikh (unpublished).
Figure 5 from: Sługocki Ł, Rymaszewska A, Kirczuk L (2019) Insights into the morphology and molecular characterisation of glacial relict Eurytemora lacustris (Poppe, 1887) (Crustacea, Copepoda, Calanoida, Temoridae). ZooKeys 864: 15-33. https://doi.org/10.3897/zookeys.864.34259
Figure 5 Fifth pair of legs of related Eurytemora species AE.affinisBE.veloxCE.lacustris. Abbreviations: AS – apical seta, DS – distal segment, LS – lateral spine, LB – left basipod, RB – right basipod. Arrows indicate important characteristics of fifth pair of legs.
Figure 1 from: Sługocki Ł, Rymaszewska A, Kirczuk L (2019) Insights into the morphology and molecular characterisation of glacial relict Eurytemora lacustris (Poppe, 1887) (Crustacea, Copepoda, Calanoida, Temoridae). ZooKeys 864: 15-33. https://doi.org/10.3897/zookeys.864.34259
Figure 1 Distribution map of Eurytemoralacustris. Dark grey colour indicates present distribution of E.lacustris. Light grey colour demonstrates countries in which occurrence of this species is uncertain. Black dots indicate records in 21st century, asterisk indicates a new record of E.lacustris in Lake Cieszęcino (Poland). The map does not include recent records in Volga basins (Popov 2011) and North America (Dussart and Defaye 2002).
Fig. 5 in Morphological and molecular characterisation of two closely related species: Myxobolus tihanyensis n. sp. and Myxobolus sandrae Reuss, 1906
Fig. 5. Bayesian inference phylogenetic tree based on dataset of 42 aligned myxosporean 18 S rDNA sequences. The GenBank accession numbers are shown next to the species names. Chloromyxum auratum was used as an outgroup. Posterior probabilities (PP)/maximum likelihood bootstrap (BS) values are shown above the nodes. Weakly supported nodes (PP <0.95 and BS <70%) are represented with dashes or blanks. Scale bar = 0.2 substitutions per site. Note: The fish host species names of Myxobolus tihanyensis n. sp. and Myxobolus sandrae are indicated under their drawings. The complete data of all sequences used in this analysis are listed in the Supplementary Table S1.
Figure 9 from: Lazarova S, Peneva V, Kumari S (2016) Morphological and molecular characterisation, and phylogenetic position of X. browni sp. n., X. penevi sp. n. and two known species of Xiphinema americanum-group (Nematoda, Longidoridae). ZooKeys 574: 1-42. https://doi.org/10.3897/zookeys.574.8037
Figure 9 - Cox1 amino acid sequence alignment of Xiphinema browni sp. n. and the closest species Xiphinema parasimile, Xiphinema simile and Xiphinema pachtaicum.
Figure 7 from: Lazarova S, Peneva V, Kumari S (2016) Morphological and molecular characterisation, and phylogenetic position of X. browni sp. n., X. penevi sp. n. and two known species of Xiphinema americanum-group (Nematoda, Longidoridae). ZooKeys 574: 1-42. https://doi.org/10.3897/zookeys.574.8037
Figure 7 - Xiphinema browni sp. n. Kurdĕjov. Juveniles and female: A–E Anterior ends of first- to fourth-stage juveniles and female F–J Tails of first to fourth juvenile stages and female (G1 and G2 – second-stage juvenile). Scale bar: 30μm.
Figure 6 from: Lazarova S, Peneva V, Kumari S (2016) Morphological and molecular characterisation, and phylogenetic position of X. browni sp. n., X. penevi sp. n. and two known species of Xiphinema americanum-group (Nematoda, Longidoridae). ZooKeys 574: 1-42. https://doi.org/10.3897/zookeys.574.8037
Figure 6 - Xiphinema browni sp. n., Kurdĕjov. Juveniles and female: A–E Anterior ends of first- to fourth-stage juveniles and female F–J Tails of first- to fourth- juvenile stages and female. Scale bar: 25 μm
Figure 4 from: Lazarova S, Peneva V, Kumari S (2016) Morphological and molecular characterisation, and phylogenetic position of X. browni sp. n., X. penevi sp. n. and two known species of Xiphinema americanum-group (Nematoda, Longidoridae). ZooKeys 574: 1-42. https://doi.org/10.3897/zookeys.574.8037
Figure 4 - Xiphinema browni sp. n. Female: A–D Genital system (B uterus full with sperm) E–G Labial region (E Amphid F Female G Male) H Ovary with endosymbionts I, K–N Variations in vagina J Lateral field A, B, H, I, J Kurdĕjov C, G Sokolnice D, K, M Mohyla míru E, F, L, N Moča. Scale bars: 30 μm (A–D, H–J); 12 μm (E–G, K–N).
Figure 3 from: Lazarova S, Peneva V, Kumari S (2016) Morphological and molecular characterisation, and phylogenetic position of X. browni sp. n., X. penevi sp. n. and two known species of Xiphinema americanum-group (Nematoda, Longidoridae). ZooKeys 574: 1-42. https://doi.org/10.3897/zookeys.574.8037
Figure 3 - Xiphinema browni sp. n. A–C Entire body (A, C females B male); Female: D–F Anterior ends G–I Pharyngeal bulbus J–M Tail shape variation A, F, I, M Mohyla míru B, E, H, L Sokolnice C, D, G, J, K Kurdĕjov (type population). Scale bars: (A–C) 400 μm; (D–M) 30 μm.
Figure 8 from: Lazarova S, Peneva V, Kumari S (2016) Morphological and molecular characterisation, and phylogenetic position of X. browni sp. n., X. penevi sp. n. and two known species of Xiphinema americanum-group (Nematoda, Longidoridae). ZooKeys 574: 1-42. https://doi.org/10.3897/zookeys.574.8037
Figure 8 - Scatter plot of odontostyle (■) and replacement odontostyle (□) against body length of Xiphinema browni sp. n. juveniles and females from Kurdĕjov population.
Figure 24 from: Lazarova S, Peneva V, Kumari S (2016) Morphological and molecular characterisation, and phylogenetic position of X. browni sp. n., X. penevi sp. n. and two known species of Xiphinema americanum-group (Nematoda, Longidoridae). ZooKeys 574: 1-42. https://doi.org/10.3897/zookeys.574.8037
Figure 24 - Sequence alignment of D2 28S rDNA region of Xiphinema parasimile from Bulgaria (KU250156) and Serbia (AM490214 and AM490217).
Figure 23 from: Lazarova S, Peneva V, Kumari S (2016) Morphological and molecular characterisation, and phylogenetic position of X. browni sp. n., X. penevi sp. n. and two known species of Xiphinema americanum-group (Nematoda, Longidoridae). ZooKeys 574: 1-42. https://doi.org/10.3897/zookeys.574.8037
Figure 23 - Scatter plot of odontostyle (■) and replacement odontostyle (□) against body length of Xiphinema penevi sp. n. juveniles and females from Morocco.
Figure 21 from: Lazarova S, Peneva V, Kumari S (2016) Morphological and molecular characterisation, and phylogenetic position of X. browni sp. n., X. penevi sp. n. and two known species of Xiphinema americanum-group (Nematoda, Longidoridae). ZooKeys 574: 1-42. https://doi.org/10.3897/zookeys.574.8037
Figure 21 - Xiphinema penevi sp. n. Juveniles: A–E Anterior ends of first- to fourth-stage juveniles and female F–J Tails of first to fourth juvenile stages and female (F1 and F2 tail of first stage juveniles). Scale bar: 25 μm.
Figure 22 from: Lazarova S, Peneva V, Kumari S (2016) Morphological and molecular characterisation, and phylogenetic position of X. browni sp. n., X. penevi sp. n. and two known species of Xiphinema americanum-group (Nematoda, Longidoridae). ZooKeys 574: 1-42. https://doi.org/10.3897/zookeys.574.8037
Figure 22 - Xiphinema penevi sp. n. Juveniles and female: A–D Neck region of first- to fourth-stage juveniles E Anterior end of female F–J Tails of first to fourth juvenile stages and female. Scale bar: 30μm.
Figure 20 from: Lazarova S, Peneva V, Kumari S (2016) Morphological and molecular characterisation, and phylogenetic position of X. browni sp. n., X. penevi sp. n. and two known species of Xiphinema americanum-group (Nematoda, Longidoridae). ZooKeys 574: 1-42. https://doi.org/10.3897/zookeys.574.8037
Figure 20 - Xiphinema penevi sp. n. Female. Variations in: A–D Anterior ends (B-holotype) F, J–L Vagina region G–I Tail shapes. Scale bars: 30 μm (A, B, F–I); 12 μm (C, D, J–L).
ScienceDex guides
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These curated guides explain access requirements, typical timelines, costs, and reuse considerations for widely used research datasets.
Allen Brain Atlas
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Annotated Behaviour and Observability Dataset (ABODe)
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DANDI Archive for NWB datasets
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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.