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FIGURE 9 in A new species of Corydoras (Siluriformes: Callichthyidae) from the rio Madre de Dios basin, Peruvian Amazon, with comments on Corydoras aeneus identity
FIGURE 9 | Uncatalogued aquarium specimens of Corydoras maclurei (not measured) showing variations of the color pattern in life: specimens can variably present greyish orange (A) or reddish orange (B) ground color of body. In C, the detail of a conspicuously reddish orange dorsal fin. Anterior portion of first dorsolateral body plate typically with orange (D) or yellow (E) bright patch. Photographs (D) and (E) by Ian Fuller.
FIGURE 8 in A new species of Corydoras (Siluriformes: Callichthyidae) from the rio Madre de Dios basin, Peruvian Amazon, with comments on Corydoras aeneus identity
FIGURE 8 | Uncatalogued aquarium specimen of Corydoras maclurei (A) showing its typical color pattern in life (lateral view), collected in its type-locality (B), a small stream tributary to the rio Araza, rio Madre de Dios basin, rio Madeira basin in Peru.
FIGURE 7 in A new species of Corydoras (Siluriformes: Callichthyidae) from the rio Madre de Dios basin, Peruvian Amazon, with comments on Corydoras aeneus identity
FIGURE 7 | Pelvic girdle and caudal skeleton in c&s paratypes of Corydoras maclurei (CITL 430). A. Anterior internal process of basipterygium slightly laterally expanded, and anterior external process not expanded posteriorly (38.2 mm SL); B. Anterior internal process of basipterygium conspicuously laterally expanded, and anterior external process slightly expanded posteriorly (47.8 mm SL); C. General morphology of caudal skeleton, showing the small cartilage (yellow arrow) between upper principal and procurrent caudal-fin rays (38.2 mm SL). Abbreviations: bp: basipterygium, ccc: compound caudal centrum, cfr: caudal-fin principal rays, dpcr: dorsal procurrent rays, epu: epural, has: haemal spine, hyp 1–5: hypurals 1 to 5, nes: neural spine, pae: anterior external process, pai: anterior internal process, par: parhypural, pi: dorsal ischiac process, pu 2–4: preural centra 2 to 4, un: uroneural. Red arrows in A and B indicate the dorsal lamina on anterior internal process of basipterygium. Scale bars = 1 mm.
FIGURE 6 in A new species of Corydoras (Siluriformes: Callichthyidae) from the rio Madre de Dios basin, Peruvian Amazon, with comments on Corydoras aeneus identity
FIGURE 6 | Lateral view of (A) the dorsal-fin spine (38.2 mm SL) and dorsal view of (B) the right pectoral-fin spine (47.8 mm SL), showing the serration patterns in c&s paratypes of Corydoras maclurei (CITL 430). Scale bars = 1 mm.
FIGURE 2 in A new species of Corydoras (Siluriformes: Callichthyidae) from the rio Madre de Dios basin, Peruvian Amazon, with comments on Corydoras aeneus identity
FIGURE 2 | Head osteological pattern in c&s paratypes of Corydoras maclurei, showing (A) general morphology in lateral view (CITL 430, 47.8 mm SL), with (B) the detail of the lateral ethmoid morphology (CITL 430, 38.2 mm SL). Abbreviations: f: frontal, fdbp: first dorsolateral body plate, io1–2: infraorbital 1 and 2, iop: interopercle, le: lateral ethmoid, n: nasal, me: mesethmoid, op: opercle, pes: pteroticextrascapular, pop: preopercle, prh: posterodorsal ridge of hyomandibula, pso: parieto-supraoccipital, sph: sphenotic. Scale bar = 1 mm.
FIGURE 1 in A new species of Corydoras (Siluriformes: Callichthyidae) from the rio Madre de Dios basin, Peruvian Amazon, with comments on Corydoras aeneus identity
FIGURE 1 | Corydoras maclurei, holotype, MUSM 70671, 37.0 mm SL, Camanti District, Quispicanchi Province, Cusco Region, Peru, small stream tributary to the rio Araza, a bigger affluent of the rio Inambari, itself a tributary to the rio Madre de Dios, rio Madeira basin.
FIGURE 5 in A new species of Corydoras (Siluriformes: Callichthyidae) from the rio Madre de Dios basin, Peruvian Amazon, with comments on Corydoras aeneus identity
FIGURE 5 | Infraorbital series in lateral (A) and dorsal (B) views, and (C) suspensorium plus operculum in lateral view of a c&s paratype of Corydoras maclurei (CITL 430, 38.2 mm SL). Abbreviations: aa: anguloarticular, d: dentary, hym: hyomandibula, io1–2: infraorbital 1 and 2, iop: interopercle, mp: metapterygoid, op: opercle, pop: preopercle, prh: posterodorsal ridge of hyomandibula, q: quadrate. Black arrow indicates the roughly triangular process on middle portion of posterior margin of infraorbital 2, and red arrows indicate inner laminar expansion of both infraorbitals. Scale bar = 1 mm.
FIGURE 4 in A new species of Corydoras (Siluriformes: Callichthyidae) from the rio Madre de Dios basin, Peruvian Amazon, with comments on Corydoras aeneus identity
FIGURE 4 | Predorsal region of trunk in c&s paratypes of Corydoras maclurei, showing the variation in the distance between the posterior process of the parieto-supraoccipital and the nuchal plate, which ranges from (A) clearly separated from each other (CITL 430, 45.6 mm SL) to (B) separated but nearly contacting (CITL 430, 38.2 mm SL). Abbreviations: fdbp: first dorsolateral body plate, np: nuchal plate, pso: parieto-supraoccipital, spn: spinelet. Dotted lines indicate the limits of the tip of the posterior process of the parieto-supraoccipital and anterior tip of the nuchal plate. Red arrows indicate the small platelets between parieto-supraoccipital and nuchal plate. Scale bar = 1 mm.
Fig. 2. Canonical discriminant functional analyses showing 3 in Life history traits of three cryptic species Asia I, Asia II-1 and Asia II-7 of Bemisia tabaci (Hemiptera: Aleyrodidae) reconfirm their genetic identities
Fig. 2. Canonical discriminant functional analyses showing 3 genetic groups of Bemisia tabaci species complex.
Fig. 1 in Life history traits of three cryptic species Asia I, Asia II-1 and Asia II-7 of Bemisia tabaci (Hemiptera: Aleyrodidae) reconfirm their genetic identities
Fig. 1. Component analysis (PCA) showing the clustering of genetic groups of Bemisia tabaci species complex.
Linked collectors and determiners for: A new species of Polietina (Diptera: Muscidae) from South America, with an updated phylogeny of the genus and a review of species' identity in GenBank.
Natural history specimen data linked to collectors and determiners held within, "A new species of Polietina (Diptera: Muscidae) from South America, with an updated phylogeny of the genus and a review of species' identity in GenBank". Claims or attributions were made on Bionomia by volunteer Scribes, <a href="http://bionomia.net/dataset/a30b0cfb-72ef-49cf-b982-d1a7f7be5027">https://bionomia.net/dataset/a30b0cfb-72ef-49cf-b982-d1a7f7be5027</a> using specimen data from the dataset aggregated by the Global Biodiversity Information Facility, <a href="https://gbif.org/dataset/a30b0cfb-72ef-49cf-b982-d1a7f7be5027">https://gbif.org/dataset/a30b0cfb-72ef-49cf-b982-d1a7f7be5027</a>. Formatted as a Frictionless Data package.
Data from: Rhizosphere bacterial community composition depends on plant species identity and soil legacy effects
<p>This record contains supplementary information for the article "Rhizosphere bacterial community composition depends on plant diversity legacy in soil and plant species identity".</p> <p><strong>Supplemental Table S1.</strong> The table contains the annotation for all the samples sequenced and analyzed.</p> <p><strong>Supplemental Table S2. </strong>The table contains all primer sequences used in the study.</p> <p><strong>Supplemental Table S3.</strong> The zip-file contains a table with the taxonomic annotation of the operational taxonomic units (OTUs) identified in the study.</p> <p><strong>Supplemental Table S4. </strong> The zip-file contains a table with sequence counts of the operational taxonomic units (OTUs) identified in the study.</p> <p><strong>Supplemental Table S5. </strong>The workbook contains a sheet with the number of operational taxonomic units (OTUs) exhibiting differential abundance in any of the contrasts tested in this study. Note that “down/up” indicates whether the OTU was less (“down”) or more (“up”) abundant in the first group of the contrast. For example, given the contrast “PH_mix_vs_mon_”, “down” corresponds to higher abundance in the pots from the monoculture plant history. Conversely, “up” refers to higher abundance in the pots from the mixed culture plant history. In addition, the workbook contains one sheet per contrast with the logBaseMean (log2 of the average normalized abundance across all samples), the logFC (log2 of the fold-change), the <em>P</em>-value, and the adjusted <em>P</em>-value (FDR). Only OTUs with a <em>P</em>-value <= 0.05 or an adjusted <em>P</em>-value (FDR) <= 0.1 are given.</p> <p><strong>Supplemental Table S6. </strong>The table contains the number of bacterial OTUs annotated with a given bacterial phylum.</p> <p><strong>Supplemental Table S7. </strong>The table contains all phyla tested for enrichment/depletion in the set of OTUs with an increased abundance in monoculture and mixed culture soils respectively. “Total counts (all OTUs)” corresponds to the total number of all OTUs annotated with a given phyla (reference set). “Observed” corresponds to the number of OTUs annotated with a given phyla in the set OTUs with increased abundance in monoculture/mixed culture soils (test set). "Expected" gives the number of OTUs which would be expected to be annotated with a given phyla if the test set were randomly sampled from the reference set.</p> <p><strong>Supplemental File S1.</strong> The zip-file contains a fasta file with the 10'205 OTU sequences identified in the study.</p> <p> </p> <p> </p>
Text-fig. 3. Rhinoppioides quadrituberculatus MIKO gen. et sp. nov. Above: assumed fragments of legs as seen in body cavity of holotype (Aa – in dorsal view, Ab – in ventral view) and paratype (B, only dorsal view available). Below: speculative reconstruction of legs, assumed segments leg IV in above rows (numbers 1, 3, 5, 7, 12, 13, 14), assumed segments of leg I below (numbers 6, 9, 10). Rest of the segments assumed to belong to legs II and III. Only trochanters III (nr. 8) and IV (nr. 7, 12) undoubtedly belonging to the new species. Bars indicating 50 µm, numbers indicate identity of segments. in Oribatid Mite Fossils From Quaternary And Pre-Quaternary Sediments In Slovenian Caves I.Two New Genera And Two New Species Of The Family Oppiidae From The Early Pleistocene
Text-fig. 3. Rhinoppioides quadrituberculatus MIKO gen. et sp. nov. Above: assumed fragments of legs as seen in body cavity of holotype (Aa – in dorsal view, Ab – in ventral view) and paratype (B, only dorsal view available). Below: speculative reconstruction of legs, assumed segments leg IV in above rows (numbers 1, 3, 5, 7, 12, 13, 14), assumed segments of leg I below (numbers 6, 9, 10). Rest of the segments assumed to belong to legs II and III. Only trochanters III (nr. 8) and IV (nr. 7, 12) undoubtedly belonging to the new species. Bars indicating 50 µm, numbers indicate identity of segments.
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).
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.
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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.