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Figure 6 in A Puzzle No More: The Identity of Spirobranchus tetraceros (Schmarda, 1861) (Annelida, Serpulidae) is Revealed
Figure 6. Scanning electron microscopic micrographs of S. schmardai sp. nov. paratype W.42393. (A) lateral view of the anterior part; (B) collar chaetae bundle with special Spirobranchus-type chaetae; (C) thoracic chaetae; (D) thoracic uncini; (E) anterior abdominal uncini; (F) anterior abdominal chaetae.
Figure 2 in A Puzzle No More: The Identity of Spirobranchus tetraceros (Schmarda, 1861) (Annelida, Serpulidae) is Revealed
Figure 2. Bayesian majority rule consensus phylogram of the concatenated (18S + cyt b) sequence data set with congruent nodes indicated for maximum likelihood analysis. Numbers above branches are posterior probabilities obtained from the Bayesian analysis; numbers below branches are bootstrap values from ML analysis. Posterior probabilities>0.76 and bootstrap values>69 are shown.
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 1 in Identity of planidium larvae (Hymenoptera: Chalcidoidea) previously recorded on Antillean scorpions
Figure 1: Ventral aspect of the planidium found on Centruroides anchorellus (Scorpiones: Buthidae) (after Armas, 2003, fig. 1).
Fig. 2 in Nasopulmonary mites (Halarachnidae) of coastal Californian pinnipeds: Identity, prevalence, and molecular characterization
Fig. 2. Spatial distribution of marine mammal stranding sites included in the nasopulmonary mite prevalence dataset. The scale is fixed to allow comparison across hosts. Comparison southern sea otter map produced from dataset in Pesapane et al. (2018).
Fig. 1 in Nasopulmonary mites (Halarachnidae) of coastal Californian pinnipeds: Identity, prevalence, and molecular characterization
Fig. 1. Scanning electron micrographs of nasopulmonary mites (Halarachnidae) from marine mammals in California showing the different shapes of opisthosoma (posterior end of the body) and defining dorsal shield (Sh) characteristics, indicated by an arrow. (A) Adult Orthohalarachne attenuata from a northern fur seal, (B) adult O. attenuata from a California sea lion, (C) adult Halarachne miroungae from a northern elephant seal, (D) adult H. halichoeri from a harbor seal, and (E) adult H. halichoeri from a southern sea otter from Pesapane et al. (2018) for comparison.
Fig. 1 in First step towards understanding the specific identity of fish muscle parasites of the genus Sarcotaces (Copepoda: Philichthyidae)-New species and first molecular ID in the genus
Fig. 1. Photographs documenting copepod (Sarcotaces izawai sp. nov.) infection of fish (Mora moro); (A) Parasite-induced black-stained void in the body of host fish, (B) parasite gall in the muscles of host fish, (C) The same with myomeres removed, (D) Composite microphotograph of the male parasite, lateral view. Scale bars: A–C = 30 mm, D = 0.5 mm. Photos A–C: by Karolina Po´łtorak.
Fig. 4 in First step towards understanding the specific identity of fish muscle parasites of the genus Sarcotaces (Copepoda: Philichthyidae)-New species and first molecular ID in the genus
Fig. 4. SEM micrographs of Sarcotaces izawai sp. nov.; male; (A) Cephalon, dorsal, (B) Cephalothorax, ventral, (C) Cephalon, anterior view, (D) Antennule, dorsal, (E) Antennule, ventral, (F) Antenna, ventral.
Fig. 3 in First step towards understanding the specific identity of fish muscle parasites of the genus Sarcotaces (Copepoda: Philichthyidae)-New species and first molecular ID in the genus
Fig. 3. Line drawings of Sarcotaces izawai sp. nov.; male; (A–E) Caudal rami of other male specimens, ventral; (F) Antennule, ventral; (G) Antenna, ventral; (H) Mandible (Mdb), and maxillae (Mx), ventral; above—protuberances of supramandibular ridge; left mandible omitted), (I) First leg (right side), ventral, (J) Second leg (left side), ventral; Scale bars: A–E = 0.1 mm, F–J = 0.01 mm.
Fig. 5 in First step towards understanding the specific identity of fish muscle parasites of the genus Sarcotaces (Copepoda: Philichthyidae)-New species and first molecular ID in the genus
Fig. 5. SEM micrographs of Sarcotaces izawai sp. nov.; male; (A) Antenna, mandible and maxillule, ventral, (B) Mandibular claw and maxillule, ventral, (C) Maxillae, ventral, (D) Exopod of first thoracopod (left side), (E) Caudal rami of other male specimens, ventral, (F) Caudal ramus of another male specimens, ventral.
Fig. 2 in First step towards understanding the specific identity of fish muscle parasites of the genus Sarcotaces (Copepoda: Philichthyidae)-New species and first molecular ID in the genus
Fig. 2. Line drawings of Sarcotaces izawai sp. nov.; (A) Female (allotype), habitus, semi-ventral view; small black silhouettes on the right represent the males at the same scale (the highest number found in a single gall), (B) Male (holotype), habitus, ventral, (C, D, E) Other males, habitus, ventral, (F, G) Caudal rami of other male specimens; Abbreviations: M = mouth area, T IV–T VII = thoracic somites, A I–A IV = abdominal somites; Scale bars: A = 10 mm, B–E = 0.5 mm, F–G = 0.1 mm.
FIGURE 2. Dromilites belli n in Revision of Dromilites bucklandii (Crustacea, Decapoda, Brachyura): Type material revealing its real identity, a junior synonym, and a new species
FIGURE 2. Dromilites belli n. sp. type series from the Ypresian of London Clay (Copenhagen Fields, London, United Kingdom). 1. Holotype NHMUK PI OR 59089 (Wetherell coll.) coated with ammonium chloride (female individual): 1a. carapace in dorsal view, 1b. carapace in frontal view, 1c. carapace in ventral view, 1d. carapace in left-lateral view; 2. Paratype NHMUK PI OR 59091 (Wetherell coll.) coated with ammonium chloride (male individual): 2a. carapace in dorsal view, 2b. carapace in frontal view, 2c. carapace in ventral view, 2d. carapace in left-lateral view. Scale bars equal 10 mm. Photographs: Philip Hurst, Natural History Museum, London.
FIGURE 1. Dromilites bucklandii H. Milne Edwards, 1937. 1. Lectotype MNHN.F.B21561 in Revision of Dromilites bucklandii (Crustacea, Decapoda, Brachyura): Type material revealing its real identity, a junior synonym, and a new species
FIGURE 1. Dromilites bucklandii H. Milne Edwards, 1937. 1. Lectotype MNHN.F.B21561: (London Clay, Isle of Sheppey, Kent, United Kingdom): 1a. carapace in dorsal view, 1b. carapace in frontal view, 1c. carapace coated with ammonium chloride in dorsal view, 2. Holotype NHMUK PI IC 34026 (London Clay, Highgate, London, UK; Spencer coll.) of Dromilites simplex, nov. syn. of D. bucklandii: 2a. colored dorsal view, 2b. black and white dorsal view. Scale bars equal 10 mm. Photographs: Lilian Cazes (1) and Barry van Bakel (2).
FIGURE 3. Dromilites belli n in Revision of Dromilites bucklandii (Crustacea, Decapoda, Brachyura): Type material revealing its real identity, a junior synonym, and a new species
FIGURE 3. Dromilites belli n. sp. type series from the Ypresian London Clay (Division B1, Kent, United Kingdom). 1. Paratype MAB.k 3583 (Seasalter, foreshore exposure) coated with ammonium chloride: 1a. carapace in dorsal view, 1b. carapace in frontal view; 2. Paratype MAB.k 3584 (Seasalter, foreshore exposure): claws; 3. Paratype MAB.k 3585 (Seasalter, foreshore exposure) (female individual): abdomen in ventral view; 4. Paratype MAB.k 3587 (Seasalter, foreshore exposure) (female individual): abdomen in ventral view; 5. Paratype MAB.k 3586 (Tankerton, foreshore exposure) (male individual): abdomen in ventral view. Scale bars equal 1cm. Photographs. Lilian Cazes (1) and Barry van Bakel (2-5).
FIGURE 6 in DNA extracted from museum specimens of the 19 century provides a taxonomic resolution on the identity of the characid fish Psalidodon jequitinhonhae (Ostariophysi: Characiformes)
FIGURE 6 | Psalidodon jequitinhonhae. Two live specimens from Fanado River, tributary of Araçuaí River, Barragem das Almas, Minas Novas Municipality, Minas Gerais State, Brazil, Jequitinhonha River basin, 17°14'16.1"S 42°35'25.9"W. MZUEL 16425, not measured. Photo: José L. O. Birindelli.
FIGURE 5 in DNA extracted from museum specimens of the 19 century provides a taxonomic resolution on the identity of the characid fish Psalidodon jequitinhonhae (Ostariophysi: Characiformes)
FIGURE 5 | Psalidodon jequitinhonhae, LBP 8311, 55.9 mm SL. To the left: lateral view of maxillary, premaxillary and dentary teeth. To the right: medial view of premaxillary and dentary teeth.
FIGURE 4 in DNA extracted from museum specimens of the 19 century provides a taxonomic resolution on the identity of the characid fish Psalidodon jequitinhonhae (Ostariophysi: Characiformes)
FIGURE 4 | Psalidodon jequitinhonhae. Specimens from Jequitinhonha River, Itaobim Municipality, Minas Gerais State, Brazil, 16°30'36"S 41°20'02"W. LBP 8311, male, 57.7 mm SL, female, 57.4 mm SL.
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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.