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Figure 2 in Description of 17 new species of Semisulcospiridae (Gastropoda: Cerithioidea) from southern China based on morphological and molecular evidence
Figure 2. Opercula of Semisulcospiridae species from China. Hua suifuensis (A); H. yiliangensis sp. nov. (B); H. rayeae sp. nov. (C); H. yunong sp. nov. (D); H. heimao sp. nov. (E); H. jiuxiangensis sp. nov. (F); H. penicillata sp. nov. (G); H. wudangensis sp. nov. (H); H. pyriformis sp. nov. (I); H. censongyangi sp. nov. (J); H. jundazhaoi sp. nov. (K); H. jiahaojingi sp. nov. (L); H. mileensis sp. nov. (M); Semisulcospira fasciata sp. nov. (N); S. guilinensis sp. nov. (O); S. tigra sp. nov. (P); S. sangpuensis sp. nov. (Q); K. zhiyuanfui sp. nov. (R). Scale bar = 3 mm.
Figure 1 in Description of 17 new species of Semisulcospiridae (Gastropoda: Cerithioidea) from southern China based on morphological and molecular evidence
Figure 1. Hua suifuensis (A) Holotype, NNUH20241501; H. yiliangensis sp. nov. (B) Holotype, NNUH20241301; H. rayeae sp. nov. (C) Holotype, NNUH20241701; H. yunong sp. nov. (D) Holotype, NNUH20241801; H. heimao sp. nov. (E) Holotype, NNUH20241601; H. jiuxiangensis sp. nov. (F) Holotype, NNUH20241901; H. penicillata sp. nov. (G) Holotype, NNUH20240201; H. wudangensis sp. nov. (H) Holotype, NNUH20240301; H. pyriformis sp. nov. (I) Holotype, NNUH20240401; H. censongyangi sp. nov. (J) Holotype, NNUH20240501; H. jundazhaoi sp. nov. (K) Holotype, NNUH20240601; H. jiahaojingi sp. nov. (L) Holotype, NNUH20240701; H. mileensis sp. nov. (M) Holotype, NNUH20240901; Semisulcospira fasciata sp. nov. (N) Holotype, NNUH20240901; S. guilinensis sp. nov. (O) Holotype, NNUH20240101; S. tigra sp. nov. (P) Holotype, NNUH20241001; S. sangpuensis sp. nov. (Q) Holotype, NNUH20240801; K. zhiyuanfui sp. nov. (R) Holotype, NNUH20240801. Scale bar = 10 mm.
Figure 3 in Description of 17 new species of Semisulcospiridae (Gastropoda: Cerithioidea) from southern China based on morphological and molecular evidence
Figure 3. Radulae of Semisulcospiridae species from China. Hua suifuensis (A); H. yiliangensis sp. nov. (B); H. rayeae sp. nov. (C); H. yunong sp. nov. (D); H. heimao sp. nov. (E); H. jiuxiangensis sp. nov. (F); H. penicillata sp. nov. (G); H. wudangensis sp. nov. (H); H. pyriformis sp. nov. (I); H. censongyangi sp. nov. (J); H. jundazhaoi sp. nov. (K); H. jiahaojingi sp. nov. (L); H. mileensis sp. nov. (M); Semisulcospira fasciata sp. nov. (N); S. guilinensis sp. nov. (O); S. tigra sp. nov. (P); S. sangpuensis sp. nov. (Q); K. zhiyuanfui sp. nov. (R).
Fig. 6 in New Species Of Ilyoplax (Brachyura: Ocypodidae: Dotillinae) From The Philippines And Indonesia: Behavioral, Molecular, And Morphological Evidence
Fig. 6. Neighbor-joining tree for three morphologically similar species of Ilyoplax based on 864 base pairs of mtDNA coding for the 16S rRNA, with Ilyoplax dentata and Ilyoplax serrata as outgroups. Numbers are bootstrap values obtained after replicates.
Fig. 3 in New Species Of Ilyoplax (Brachyura: Ocypodidae: Dotillinae) From The Philippines And Indonesia: Behavioral, Molecular, And Morphological Evidence
Fig. 3 Comparison of the form of the first male pleopod, shape of carapace and shape of the lobe near outer side of the infraorbital border among I. orientalis, I. tansuiensis, and Ilyoplax pacifica, new species. A, magnification of apex of first pleopod: Ilyoplax pacifica, new species, paratype male (OMNH-Ar 7105); I. tansuiensis, male (5.2 mm c.b.) (OMNH-Ar 7111), Tanshui, Taiwan, coll. K. Wada, (27 Mar.1996); I. orientalis, male (5.2 mm c.b.) (OMNH-Ar 7109), Ranong, Thailand, coll. K. Wada, (6 Dec.1982). B, side margin of male carapace: Ilyoplax pacifica, new species, paratype male (OMNH-Ar 7105); I. orientalis, male (OMNH-Ar 7109); I. tansuiensis, male (OMNH-Ar 7111). C, dorsal view of characteristic lobe of the infraorbital border: Ilyoplax pacifica, new species, paratype male (OMNH-Ar 7105); I. orientalis, male (OMNH- Ar 7109); I. tansuiensis, male (OMNH- Ar 7111).
Fig. 2 in New Species Of Ilyoplax (Brachyura: Ocypodidae: Dotillinae) From The Philippines And Indonesia: Behavioral, Molecular, And Morphological Evidence
Fig. 2 Ilyoplax pacifica, new species: A, suborbital margin; B, male abdomen; C, male first pleopod; D, E, magnifications of apex of first pleopod; F, left chela; G, female abdomen. A, C-F, holotype male; B, paratype male (OMNH-Ar 7105); G, paratype ovig. female (OMNHAr 7106).
Fig. 4 in Resolution of the identity of three species of Diplostomum (Digenea: Diplostomidae) parasitising freshwater fishes in South Africa, combining molecular and morphological evidence
Fig. 4. Metacercariae of Diplostomum spp. from eye lenses of different fish hosts; (a) Diplostomum sp. from Tilipia sparrmanii, live, ventral view (b) Diplostomum sp. from Tilipia sparrmanii, fixed, ventral view (c) Diplostomum sp. from Tilipia sparrmanii, live, sunken pseudosuckers (arrowhead) (hologenophore, GenBank MN813526, MN813534 and MN808616) (d) Diplostomum sp. 14 sensu Locke et al. (2015) from Synodontis zambezensis, live, ventral view (hologenophore, GenBank MN813541) (e) Diplostomum sp. 14 sensu Locke et al. (2015) from Oreochromis mossambicus, fixed, ventral view, small excretory granules (arrowhead) (hologenophore, GenBank MN813531, MN813539 and MN808621) (f) Diplostomum sp. 14 sensu Locke et al. (2015) from Synodontis zambezensis, fixed, ventral view, large excretory granules (arrowhead) (hologenophore, GenBank MN813541) (g) Diplostomum sp. 16 sensu Locke et al. (2015) from Pseudocrenilabrus philander, fixed, ventral view, everted pseudosuckers (arrowhead) (hologenophore, GenBank MN813532, MN813547 and MN808627) (h) Diplostomum sp. 16 sensu Locke et al. (2015) from Pseudocrenilabrus philander, fixed, ventral view, inverted pseudosuckers (arrowhead) (hologenophore, GenBank MN813533, MN813548 and MN808628) (i) Diplostomum sp. 16 sensu Locke et al. (2015) from Pseudocrenilabrus philander, live metacercariae inside of fish lens. Scale bars: a–h = 100 μm; i = 700 μm.
Fig. 3 in Resolution of the identity of three species of Diplostomum (Digenea: Diplostomidae) parasitising freshwater fishes in South Africa, combining molecular and morphological evidence
Fig. 3. Bayesian inference (BI) and maximum likelihood (ML) phylogram reconstructed using cox1 sequences for species of Diplostomum. Nodal support from BI and ML analyses indicated as BI/ML; only values> 0.90 (BI) and> 70 (ML) are displayed. Scale-bar indicates the expected number of substitution per site. Sequences generated in this study are in bold and indicated by blue rectangles. Codes with isolate information for newly generated sequences are provided in Table 3. Sequences derived from Africa are highlighted in blue, from Asia in purple, from Europe in orange, from North America in green (according to the map) and sequences reported from more than one continent are highlighted in black. Black arrows on the map demonstrate distribution of Diplostomum spathaceum and 'D. mergi Lineage 2' in both, Asia and Europe, and Diplostomum sp. 14 and Diplostomum sp. 16 in both, Africa and Asia. (For interpretation of the references to colour in this figure legend, the reader is referred to the Web version of this article.)
Fig. 2 in Resolution of the identity of three species of Diplostomum (Digenea: Diplostomidae) parasitising freshwater fishes in South Africa, combining molecular and morphological evidence
Fig. 2. Bayesian inference (BI) and maximum likelihood (ML) phylograms reconstructed using (a) partial 28S rDNA sequences (b) ITS1-5.8S-ITS2 sequences for species of Diplostomum. Nodal support from BI and ML analyses indicated as BI/ML; only values> 0.90 (BI) and> 70 (ML) are displayed. Scale-bar indicates the expected number of substitution per site. Sequences generated in this study are in bold and indicated by blue rectangles. Codes with isolate information for newly generated sequences are provided in Table 3. (For interpretation of the references to colour in this figure legend, the reader is referred to the Web version of this article.)
Fig. 1 in Resolution of the identity of three species of Diplostomum (Digenea: Diplostomidae) parasitising freshwater fishes in South Africa, combining molecular and morphological evidence
Fig. 1. Map illustrating the sampling localities on (a) River Riet in Mokala National Park (b) River Phongolo (Site 1, Site 2 and Nyamithi Lake) and the River Usuthu (Shokwe Pan) in Ndumo Game Reserve and (c) River Mooi (Boskop Dam) in Boskop Dam Nature Reserve, South Africa. The illustration was compiled in ArcGIS 10.6 (Available from https://support.esri.com/en/downloads).
Figure 2 in Dina serbica, a new species of leeches (Annelida: Hirudinea: Erpobdellidae) from Serbia, based on morphological and molecular evidence
Figure 2. Results of ASAP analysis for COI sequences. (A) Distribution of pairwise differences, (B) Ranked pairwise differences.
Figure 6 in Dina serbica, a new species of leeches (Annelida: Hirudinea: Erpobdellidae) from Serbia, based on morphological and molecular evidence
Figure 6. Photographs of the type localities of selected Dina species. A – a first-order stream in the Tara river canyon, Montenegro (locus typicus of D. minuoculata). B – rheopsammocrene spring along the road to Kamena Gora, Serbia (locus typicus of D. serbica sp. nov.). C – rheocrene spring Toplla, Dečani, Kosovo* (locus typicus of D. prokletijaca). D – spring at Štavna, Komovi Mt., Montenegro (locus typicus of D. montana). Photos by V. Pešić (A, D), L. Pešić (B), V. Berlajolli (C).
Figure 2 in Hygrobates calabricus, a new species of water mite (Acariformes, Hydrachnidia, Hygrobatidae) from Italy, based on morphological and molecular evidence
Figure 2. Hygrobates calabricus sp. nov., holotype ♂, Giganti de la Sila, Italy: A – gnathosoma, coxal and genital field; B – genital field; C – palp, medial view (P-1 lacking); D – palp, lateral view (P-1 lacking); E – chelicera; F – IV- L-5 and -6 (inset: proximo and –medioventral setae of IV-L-6). Scale bars = 100 µm.
Figure 1 in Dina serbica, a new species of leeches (Annelida: Hirudinea: Erpobdellidae) from Serbia, based on morphological and molecular evidence
Figure 1. Neighbour-Joining tree of the Dina spp., obtained from 75 nucleotide COI sequences. The results of species delimitation by ASAP procedure are indicated by vertical bars.
Figure 5 in Dina serbica, a new species of leeches (Annelida: Hirudinea: Erpobdellidae) from Serbia, based on morphological and molecular evidence
Figure 5. Map of studied area with marked type localities of Dina serbica sp. nov. (1), D. minuoculata (2), D. montana (3) and D. prokletijaca (4). Inset: Live specimen and coccon of D. serbica sp. nov. from the type locality (Kamena Gora, Serbia).
Figure 3 in Dina serbica, a new species of leeches (Annelida: Hirudinea: Erpobdellidae) from Serbia, based on morphological and molecular evidence
Figure 3. Dina serbica sp. nov. A – mouth opening, paratype; B – lateral view, paratype; C – colour of the dorsal surface, holotype; E-D – genital atrium, ventral view, paratype.
Fig. 2. Pancola ailurus n in Morphological and molecular evidence reveals a new species of chewing louse Pancola ailurus n. sp. (Phthiraptera: Trichodectidae) from the endangered Chinese red panda Ailurus styani
Fig. 2. Pancola ailurus n. sp. (A) Male Pancola ailurus n. sp., habitus (dorsal morphology to the left of the midline, ventral morphology to the right) (B) Female Pancola ailurus n. sp., habitus (dorsal morphology to the left of the midline, ventral morphology to the right) (C) Meso-metasternal plate of Pancola ailurus n. sp. (D) Male genitalia (E) Female genitalia.
Fig. 3 in Morphological and molecular evidence reveals a new species of chewing louse Pancola ailurus n. sp. (Phthiraptera: Trichodectidae) from the endangered Chinese red panda Ailurus styani
Fig. 3. Phylogenetic trees based on the partial mitochondrial (cox1 and 12S rRNA) sequences of Trichodectidae and Bovicoliidae species using Maximum Likelihood (ML). The bootstrap frequencies (Bf) were shown on each node.
Fig. 4 in Morphological and molecular evidence reveals a new species of chewing louse Pancola ailurus n. sp. (Phthiraptera: Trichodectidae) from the endangered Chinese red panda Ailurus styani
Fig. 4. Divergence time and Bayesian analysis based on the partial cox1 sequence of Trichodectidae and Bovicoliidae species using Beast v.1.10.4 with Liposcelis bostrichophila as the outgroup.
Fig. 1 in Morphological and molecular evidence reveals a new species of chewing louse Pancola ailurus n. sp. (Phthiraptera: Trichodectidae) from the endangered Chinese red panda Ailurus styani
Fig. 1. Chinese red panda Ailurus styani and the lice collected from its surface. (A) the Chinese red panda from Chengdu Research Base of Giant Panda Breeding, Chengdu County, Sichuan Province, China (N30.743◦, E104.150◦) (B) the abdomen of male Pancola ailurus (C) the back of male P. ailurus (D) the back of female P. ailurus (E) the abdomen of female P. ailurus.
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.