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Figure 4 from: Baković N, Matoničkin Kepčija R, Siemensma FJ (2022) Transitional and small aquatic cave habitats diversification based on protist assemblages in the Veternica cave (Medvednica Mt., Croatia). Subterranean Biology 42: 43-60. https://doi.org/10.3897/subtbiol.42.78037
Figure 4 A, BRaphidocystis marginataA LM micrograph of a living cell B REM micrograph of plate-scales and spine-scales C, DAcanthocystis myriospinaC LM micrograph of a living cell D REM micrograph of plate-scales. Scale bars: 20 µm (A, C); 2 µm (B, D); LM, light microscopy; REM, raster electron microscopy.
Figure 1 from: Yi M-R, Hsu K-C, Gu S, He X-B, Luo Z-S, Lin H-D, Yan Y-R (2022) Complete mitogenomes of four Trichiurus species: A taxonomic review of the T. lepturus species complex. ZooKeys 1084: 1-26. https://doi.org/10.3897/zookeys.1084.71576
Figure 1 A Eighteen sampling localities of the genus the Trichiurus along the Chinese coast and the species composition after our surveys. Refer to Suppl. material 1: Table S1 for the abbreviations of localities. B The maximum-likelihood (ML) tree of these four Trichiurus species along the coast based on the COI gene. The numbers at the nodes are bootstrap values of the ML and NJ (neighbor-joining) analyses. The sampling size (n) indicated in parentheses C The photographs of four Trichiurus species used in the mitogenomes analyses.
Figure 3 from: Yi M-R, Hsu K-C, Gu S, He X-B, Luo Z-S, Lin H-D, Yan Y-R (2022) Complete mitogenomes of four Trichiurus species: A taxonomic review of the T. lepturus species complex. ZooKeys 1084: 1-26. https://doi.org/10.3897/zookeys.1084.71576
Figure 3 The maximum-likelihood (ML) tree of the Trichiuridae based on the sequences of mitogenome (excluding d-loop). The numbers at the nodes are bootstrap values of the ML and NJ (neighbor-joining) analyses.
Supplementary material 1 from: Yi M-R, Hsu K-C, Gu S, He X-B, Luo Z-S, Lin H-D, Yan Y-R (2022) Complete mitogenomes of four Trichiurus species: A taxonomic review of the T. lepturus species complex. ZooKeys 1084: 1-26. https://doi.org/10.3897/zookeys.1084.71576
Table S1–S4, Figure S1, S2
Figure 5 from: Yi M-R, Hsu K-C, Gu S, He X-B, Luo Z-S, Lin H-D, Yan Y-R (2022) Complete mitogenomes of four Trichiurus species: A taxonomic review of the T. lepturus species complex. ZooKeys 1084: 1-26. https://doi.org/10.3897/zookeys.1084.71576
Figure 5 The simple regression and the boxplot analysis in T. japonicus (blue), T. lepturus (orange) and T. nanhaiensis (grey) A Total length [D(i,n)] and Preanal length [D(i,m)] B Caudal length [D(m,n)] and Body depth at anus [D(e,f)] C Head depth [D(d,o)] and Orbital length [D(j,k)] and D Head length [D(i,l)] and Head depth [D(d,o)]. The landmarks are illustrated in Fig. 2.
Figure 4 from: Yi M-R, Hsu K-C, Gu S, He X-B, Luo Z-S, Lin H-D, Yan Y-R (2022) Complete mitogenomes of four Trichiurus species: A taxonomic review of the T. lepturus species complex. ZooKeys 1084: 1-26. https://doi.org/10.3897/zookeys.1084.71576
Figure 4 The maximum-likelihood (ML) tree of six Trichiurus species in the world based on the COI gene. The numbers at the nodes are bootstrap values of the ML and NJ (neighbor-joining) analyses.
Figure 9 from: Yi M-R, Hsu K-C, Gu S, He X-B, Luo Z-S, Lin H-D, Yan Y-R (2022) Complete mitogenomes of four Trichiurus species: A taxonomic review of the T. lepturus species complex. ZooKeys 1084: 1-26. https://doi.org/10.3897/zookeys.1084.71576
Figure 9 Frequencies of different amino acids in the mitogenomes of the five Trichiurus species; the stop codon is not included.
Figure 10 from: Yi M-R, Hsu K-C, Gu S, He X-B, Luo Z-S, Lin H-D, Yan Y-R (2022) Complete mitogenomes of four Trichiurus species: A taxonomic review of the T. lepturus species complex. ZooKeys 1084: 1-26. https://doi.org/10.3897/zookeys.1084.71576
Figure 10 . The mean partwise interspecific (gray) and intergeneric (black) p-distance in each gene.
Figure 8 from: Yi M-R, Hsu K-C, Gu S, He X-B, Luo Z-S, Lin H-D, Yan Y-R (2022) Complete mitogenomes of four Trichiurus species: A taxonomic review of the T. lepturus species complex. ZooKeys 1084: 1-26. https://doi.org/10.3897/zookeys.1084.71576
Figure 8 Relative synonymous codon usage (RSCU) of the mitogenomes of the five Trichiurus species; the stop codon is not included. T. japonicus (TJ), T. lepturus (TL), T. nanhaiensis (TN), T. gangeticus (TG) and T. brevis (TB).
Figure 7 from: Yi M-R, Hsu K-C, Gu S, He X-B, Luo Z-S, Lin H-D, Yan Y-R (2022) Complete mitogenomes of four Trichiurus species: A taxonomic review of the T. lepturus species complex. ZooKeys 1084: 1-26. https://doi.org/10.3897/zookeys.1084.71576
Figure 7 A Mean evolutionary rates for each protein coding gene in mitogenomes of five Trichiurus species B Evolutionary rates of ND6 gene of five Trichiurus species. C Evolutionary rates of Ka/Ks in ATP8 gene of five Trichiurus species. Indicated the rates of non-synonymous substitutions to the rate of synonymous substitutions (ka/ks). T. japonicus (TJ), T. lepturus (TL), T. nanhaiensis (TN), T. gangeticus (TG) and T. brevis (TB).
Figure 2 from: Yi M-R, Hsu K-C, Gu S, He X-B, Luo Z-S, Lin H-D, Yan Y-R (2022) Complete mitogenomes of four Trichiurus species: A taxonomic review of the T. lepturus species complex. ZooKeys 1084: 1-26. https://doi.org/10.3897/zookeys.1084.71576
Figure 2 Positions of 14 (a–n) landmarks used to contrast the morphological differences between Trichiurus species.
Supplementary material 1 from: DeRoy EM, Crookes S, Matheson K, Scott R, McKenzie CH, Alexander ME, Dick JTA, MacIsaac HJ (2022) Predatory ability and abundance forecast the ecological impacts of two aquatic invasive species. NeoBiota 71: 91-112. https://doi.org/10.3897/neobiota.71.75711
Table S1
Supplementary material 1 from: Odorico D, Nicosia E, Datizua C, Langa C, Raiva R, Souane J, Nhalungo S, Banze A, Caetano B, Nhauando V, Ragú H, Machunguene Jr M, Caminho J, Mutemba L, Matusse E, Osborne J, Wursten B, Burrows J, Cianciullo S, Malatesta L, Attorre F (2022) An updated checklist of Mozambique's vascular plants. PhytoKeys 189: 61-80. https://doi.org/10.3897/phytokeys.189.75321
The updated checklist of Mozambique's vascular plants
Figure 6 from: Odorico D, Nicosia E, Datizua C, Langa C, Raiva R, Souane J, Nhalungo S, Banze A, Caetano B, Nhauando V, Ragú H, Machunguene Jr M, Caminho J, Mutemba L, Matusse E, Osborne J, Wursten B, Burrows J, Cianciullo S, Malatesta L, Attorre F (2022) An updated checklist of Mozambique's vascular plants. PhytoKeys 189: 61-80. https://doi.org/10.3897/phytokeys.189.75321
Figure 6 Extinction risk of Mozambique's vascular plants. A assessed taxa B IUCN category for the evaluated taxa.
Figure 3 from: Odorico D, Nicosia E, Datizua C, Langa C, Raiva R, Souane J, Nhalungo S, Banze A, Caetano B, Nhauando V, Ragú H, Machunguene Jr M, Caminho J, Mutemba L, Matusse E, Osborne J, Wursten B, Burrows J, Cianciullo S, Malatesta L, Attorre F (2022) An updated checklist of Mozambique's vascular plants. PhytoKeys 189: 61-80. https://doi.org/10.3897/phytokeys.189.75321
Figure 3 Floristic patterns for Mozambique's vascular plants. A frequency of plant groups B geographic origin of taxa.
Figure 5 from: Zheng Y-N, Cai X-R, Ma L-B (2022) Taxonomy of Landrevus species group of Velarifictorus Randell, 1964 (Orthoptera, Gryllidae, Gryllinae) with one new species and morphological diversity of Velarifictorus flavifrons Chopard, 1966. ZooKeys 1084: 101-117. https://doi.org/10.3897/zookeys.1084.77096
Figure 5 Calling song of Velarifictorus landrevusA oscillogram of chirp (amplitude versus time) B oscillogram of pulse (amplitude versus time) C spectrogram (frequency versus time).
Figure 8 from: Zheng Y-N, Cai X-R, Ma L-B (2022) Taxonomy of Landrevus species group of Velarifictorus Randell, 1964 (Orthoptera, Gryllidae, Gryllinae) with one new species and morphological diversity of Velarifictorus flavifrons Chopard, 1966. ZooKeys 1084: 101-117. https://doi.org/10.3897/zookeys.1084.77096
Figure 8 Front view of heads of VelarifictorusA, DV. zhengi sp. nov. B, EV. landrevusC, FV. flavifronsA–C male D–F female.
Figure 9 from: Zheng Y-N, Cai X-R, Ma L-B (2022) Taxonomy of Landrevus species group of Velarifictorus Randell, 1964 (Orthoptera, Gryllidae, Gryllinae) with one new species and morphological diversity of Velarifictorus flavifrons Chopard, 1966. ZooKeys 1084: 101-117. https://doi.org/10.3897/zookeys.1084.77096
Figure 9 Dorsal view of heads and pronotum of VelarifictorusA, DV. zhengi sp. nov. B, EV. landrevusC, FV. flavifronsA–C male D–F female.
Figure 4 from: Zheng Y-N, Cai X-R, Ma L-B (2022) Taxonomy of Landrevus species group of Velarifictorus Randell, 1964 (Orthoptera, Gryllidae, Gryllinae) with one new species and morphological diversity of Velarifictorus flavifrons Chopard, 1966. ZooKeys 1084: 101-117. https://doi.org/10.3897/zookeys.1084.77096
Figure 4 Calling song of Velarifictorus zhengi sp. nov. A oscillogram of chirp (amplitude versus time) B oscillogram of pulse (amplitude versus time) C spectrogram (frequency versus time).
Figure 14 from: Zheng Y-N, Cai X-R, Ma L-B (2022) Taxonomy of Landrevus species group of Velarifictorus Randell, 1964 (Orthoptera, Gryllidae, Gryllinae) with one new species and morphological diversity of Velarifictorus flavifrons Chopard, 1966. ZooKeys 1084: 101-117. https://doi.org/10.3897/zookeys.1084.77096
Figure 14 Ovipositor of VelarifictorusA, BV. zhengi sp. nov. C, DV. landrevusE, FV. flavifronsA, C, E inside of ovipositor B, D, F outside of ovipositor.
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
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.