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13,397 results for “sp. nov.”
Figure 3 in Vladimiretskia nathani gen. et sp. nov. (Diptera, Cecidomyiidae: Porricondylinae, Asynaptini, Vladimiretskiana subtr. nov.) from Eocene Rovno amber with description of their eggs
Figure 3. Vladimiretskia nathani Fedotova et Perkovsky sp. nov. (holotype, female, Rovno amber, SIZK W-73, drawings): a – wing; b – 13–16th flagellomeres; c – 6–7th flagellomeres; d – palpi; e – fore tarsus; f – 1st fore tarsomere; g –5th mesotarsomere dorsally; h – 5th fore tarsomere laterally; i – apex part of head with eye, scape, pedicel and 1-3rd flagellomeres; j – IX abdominal segment and cerci (ovipositor). Scales = 0.1 mm (d, f); 0.2 mm (e); 0.25 mm (a).
Figure 2 in Vladimiretskia nathani gen. et sp. nov. (Diptera, Cecidomyiidae: Porricondylinae, Asynaptini, Vladimiretskiana subtr. nov.) from Eocene Rovno amber with description of their eggs
Figure 2. Vladimiretskia nathani Fedotova et Perkovsky sp. nov. (holotype, female, Rovno amber, SIZK W-73, photomicrographs): a – head, palpi, antennae proximally, thorax, halter, fore coxa and trochanter; b – head, palpi and antennae frontally; c – fore tibia distally and 1st tarsomere with lateral spiniform projection; d – left wing and halters; e – 5th mesotarsomere with tarsal claw dorsally; f – 5th fore tarsomere with claw laterally; g – 6-16th flagellomeres. Scales =1.0 mm (d); 0.5 mm (b); 0.2 mm (a, c, e, f, g).
Figure 1 in Vladimiretskia nathani gen. et sp. nov. (Diptera, Cecidomyiidae: Porricondylinae, Asynaptini, Vladimiretskiana subtr. nov.) from Eocene Rovno amber with description of their eggs
Figure 1. Vladimiretskia nathani Fedotova et Perkovsky sp. nov. (holotype, female, Rovno amber, SIZK W-73, photomicrographs): a, d, f – eggs; b – general view, laterally and eggs; c – palpi; e – part of abdomen; g – ovipositor; h – 6 and 7 flagellomeres; 1–7 -аrrangement of eggs by numbers. Scales = 1.3 mm (b); 0.1 mm (a, dh); 0.2 mm (c).
Figure 1 in Hepatics from Rovno amber (Ukraine). 12. Jubula polessica sp. nov.
Figure 1. Jubula polessica sp. n., photo and drawing. A, C – general view of the inclusion, two parts of the same shoot, ventral aspect; B – graphic reconstruction of the shoot, ventral aspect.
Figure 2 in Ambulyx labuanensis sp. nov. from Flores Island, Indonesia (Lepidoptera: Sphingidae)
Figure 2. Male genitalia of Ambulyx spp.: A) A. moorei Moore, 1858, Vietnam; B) A. labuanensis sp. nov., Flores Island, Indonesia (holotype). Photos: Elizaveta A. Spitsyna.
Figure 1 in Ambulyx labuanensis sp. nov. from Flores Island, Indonesia (Lepidoptera: Sphingidae)
Figure 1. Ambulyx spp.: A-B) A. moorei Moore, 1858, Vietnam; C-F) A. labuanensis sp. nov., Flores Island, Indonesia: C-D) holotype male; E-F) paratype female. Photos: Elizaveta A. Spitsyna.
Fig. 5 in Description of Sarcocystis scandentiborneensis sp. nov. from treeshrews (Tupaia minor, T. tana) in northern Borneo with annotations on the utility of COI and 18S rDNA sequences for species delineation
Fig. 5. Phylogenetic tree based on analysis of mitochondrial COI sequences of the Sarcocystidae including the new Sarcocystis sp. examined in this study (black symbols). Other taxa of the Apicomplexa served as root. Evolutionary history was inferred by the Maximum Likelihood (ML) method based on the TamuraNei model, whereby 619 positions were included in the final data set. All positions with less than 95% site coverage were eliminated; that is, fewer than 5% alignment gaps, missing data, and ambiguous bases were allowed at any position. Bootstrap percentages (1000 iterations) are shown next to branches. COI sequences E357-13 and E120-13 (not shown in the tree) are available at GenBank (MN732561 and MN732562, respectively).
Fig. 2 in Description of Sarcocystis scandentiborneensis sp. nov. from treeshrews (Tupaia minor, T. tana) in northern Borneo with annotations on the utility of COI and 18S rDNA sequences for species delineation
Fig. 2. Ultrastructure of S. scandentiborneensis sp. nov. Note, due to ethanol-fixation some ultrastructural details are poorly resolved (e.g. membranes). A) Longitudinal section through the same sample as in Fig. 1C, showing a gross view of the sarcocyst and its villous protrusions (VP) that are sectioned in different orientations. The inset shows a cross section through various VP that reveals the arrangement of microtubules in their inner core; while in this case 16 microtubules are visible (asterisks), sections through more apical portions of the VP showed lower numbers. B) Longitudinal section through the fingerlike VPs that appear to be anchored in the ground substance (arrow) by microtubules (asterisks) that extend into each protrusion; note the electron-dense, U-shaped structure at each tip of the protrusions (arrowheads) and the apparently serrated surface of the VP (flat arrowheads). The inset shows a higher magnification of the apical part of a single VP with the typical U-shaped apex (asterisk), which appears to be connected with the host cell through an electronlucent contact zone (white arrowheads); interestingly, the protrusion appears fenestrated (also visible in the main image) possessing thorn-like structures (black arrows; the white arrow indicates a crosssectional view) that could be responsible for the serration visible at lower magnification. CZ, cystozoites; HC, host cell; VP, villous protrusion.
Fig. 1 in Description of Sarcocystis scandentiborneensis sp. nov. from treeshrews (Tupaia minor, T. tana) in northern Borneo with annotations on the utility of COI and 18S rDNA sequences for species delineation
Fig. 1. Light microscopy of Sarcocystis scandentiborneensis sp. nov. A and B, Haematoxylin & Eosinstained histological sections of striated musculature; C and D, Richardson's dye-stained 1.0 μm thin sections of sarcocysts. A) Tissue section of laryngeal muscle with various sarcocysts in cross section (asterisks), indicating a relatively high density of cysts in this part of musculature. B) Longitudinal section through a sarcocyst, showing a cigar-shaped appearance; however, isolated native sarcocysts, which were not available, may look different. C) Part of a longitudinal section through the tip of a sarcocyst, note the very thin ground substance (arrows) and the fine septae extending into the interior of the cyst (arrowheads); cystozoites (CZ) were loosely scattered within chambers while metrocytes were rarely seen, indicating maturity of the cyst; bars indicate the variable thickness of the cyst wall: the wall was thinner in regions where the villous protrusions were bent (right bar); note that the intense staining at the interface between host cell (HC) and parasite is part of the host cell. D) Cross-section through a sarcocyst showing cystozoites and the cyst wall (bar) including its thin ground substance (arrows).
Fig. 4 in Description of Sarcocystis scandentiborneensis sp. nov. from treeshrews (Tupaia minor, T. tana) in northern Borneo with annotations on the utility of COI and 18S rDNA sequences for species delineation
Fig. 4. Mapping (to the Toxoplasma gondii reference molecule M97703) of frequencies (%) of base pair changes observed in sequence comparisons of nu clear 18S rDNA within the new Sarcocystis sp. from treeshrews (intraspecific variation: isolates E364–13 versus E357–13) and between the new species and Sarcocystis zuoi and/or S. clethrionomyelaphis (interspecific variation: E364–13 versus S. zuoi/clethrionomyelaphis). Results were combined for the two latter species to simplify the graph. Here, 87.2% of 2118 alignment positions showed moderate to high levels of consistency, while sections of ambiguous alignment did not relate to the species under investigation. Due to gaps in the alignment, not all of the observed nt changes could be mapped to a homologous position of the reference molecule (i.e., 7 out of 24 bp changes in intraspecific comparison; 33 out of 74 bp changes in interspecific comparison), in which case the position of each nt relative to the helix was inferred from neighboring nt for which such position was known. Gaps were mainly due to insertions in helices V2, V4, and V9 rendering E357-13/E364-13 longer than the sequence of T. gondii. The percentage of parsimony-informative (pi) bp changes per helix is shown for helices V1, V2, V4, V7, and V9 above each column. Also shown is the ratio of transitions versus transversions (Ti/Tv) for selected helices.
Figure 1 in Neumania bhutana sp. nov. a new water mite from Bhutan (Acari, Hydrachnidia: Unionicolidae)
Figure 1. Neumania bhutana sp. nov., male holotype, Haa River, Bhutan: A = idiosoma, dorsal view; B = idiosoma, ventral view; C-D palp. Scale bars = 100 μm.
Figure 6 in Dina crnogorensis sp. nov. (Annelida, Hirudinea: Erpobdellidae) - a new leech species from Montenegro
Figure 6. Photograph of the type locality of Dina crnogorensis sp. nov.: spring at Trešnjevik, Komovi Mt., Montenegro. Photo by V. Pešić
Figure 5 in Dina crnogorensis sp. nov. (Annelida, Hirudinea: Erpobdellidae) - a new leech species from Montenegro
Figure 5. Schematic diagrams of reproduktive system (A-D) and genital atrium (E-H; photographs and drawings, respectively) of selected Dina spp. A, E — Dina crnogorensis sp. nov., holotype; B, F — Dina minuoculata, paratype; C, G — Dina serbica, paratype; D, H — Dina orientalis, holotype. Abbreviations: a — genital atrium, b — ovarian sacks, c — vas deferens, d — testisacs.
Figure 3. Colour, dorsal view. A in Dina crnogorensis sp. nov. (Annelida, Hirudinea: Erpobdellidae) - a new leech species from Montenegro
Figure 3. Colour, dorsal view. A — Dina crnogorensis sp. nov. (holotype); B — Dina minuoculata (left paratype, right holotype); C — Dina serbica (holotype); D — Dina orientalis (paratype).
Figure 2 in Dina crnogorensis sp. nov. (Annelida, Hirudinea: Erpobdellidae) - a new leech species from Montenegro
Figure 2. Results of ASAP analysis for COI sequences. (A) Distribution of pairwise differences, (B) Ranked pairwise differences.
Figures 4–10 in Papillocepheus banari sp. nov. (Acari, Oribatida, Otocepheidae) from Malawi
Figures 4–10. Papillocepheus banari sp. nov., adult: 4—subcapitulum, ventral view; 5—palp, right, antiaxial view; 6—chelicera, right, antiaxial view; 7—leg I, right, antiaxial view; 8—leg II (tarsus omitted), right, antiaxial view; 9— leg III (tarsus omitted), left, antiaxial view; 10—leg IV, left, antiaxial view. Scale bars 50 μm (4, 6–10), 20 μm (5).
Figure 4 in A new species Unionicola (Dimockatax stat. rev.) haungthayawensis sp. nov. (Trombidiformes: Unionicolidae) from the freshwater mussel Lamellidens generosus (Gould, 1847) in Myanmar
Figure 4. Morphological details of Unionicola (Dimockatax stat. rev.) haungthayawensis sp. nov. The holotype male RMBH Hyd 363: (A, B) pedipalps (P-1–5); (C) first walking leg (I-L-1–6); (D) claw of first walking leg; (E) fourth walking leg (IV-L-1–6); (F) genital field. The paratype female RMBH Hyd 363_1: (G) genital field; (H) first walking leg (I-L1–6); (I) claw of first walking leg; (J) fourth walking leg (IV-L-1–6); (K, L) pedipalp (P-1–5). Scale bars = 100 µm. (Graphics: Yulia E. Chapurina).
Figure 2 in A new species Unionicola (Dimockatax stat. rev.) haungthayawensis sp. nov. (Trombidiformes: Unionicolidae) from the freshwater mussel Lamellidens generosus (Gould, 1847) in Myanmar
Figure 2. Unionicola (Dimockatax stat. rev.) haungthayawensis sp. nov. Light microscopy pictures of male and female and details of morphology: (A, B) general view; (C, F) tarsal claw and fragment of IV-L-6; (D, G) tarsus of pedipalp (P-5); (E) spinous flaps of genital plates. Specimens: (A) paratype female RMBH Hyd 363_1; (C, D, E) paratype female RMBH Hyd 621_1; (B, F, G) holotype male RMBH Hyd 363. Scale bars = 200µm (A-B) and 50µm (C-E). (Photos: Yulia E. Chapurina).
Figure 1 in A new species Unionicola (Dimockatax stat. rev.) haungthayawensis sp. nov. (Trombidiformes: Unionicolidae) from the freshwater mussel Lamellidens generosus (Gould, 1847) in Myanmar
Figure 1. Maximum likelihood phylogeny of Unionicola based on the dataset COI gene fragment. Numbers near nodes are bootstrap support (BS) values of IQ-TREE. Scale bar indicates the branch lengths. The red color indicates Unionicola (Dimockatax stat. rev.) haungthayawensis sp. nov. sequences from Myanmar.
Figure 1 in Planuncus laguerrei sp. nov. from Peru (Lepidoptera: Erebidae: Arctiinae)
Figure 1. Holotype male of Planuncus laguerrei sp. nov. and type locality: A) upperside; B) underside. Scale bar = 5 mm; C) male genitalia and aedeagus. Scale bar = 1 mm; D) Type locality of P. laguerrei sp. nov. near Satipo, Peru.
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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)
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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.