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Fig. 2 in Fig. 2 in Positive association between PTN polymorphisms and schizophrenia in Northeast Chinese Han population.
Fig. 2. Biogeographic affinities and distributional areas of Oileus species. a) UPGMA cluster analysis performed with proportion of biogeographic provinces of distribution area for each species, b) Size of potential distribution area; wing morphology is illustrated for each species. O. bifidus (O. bif), O. heros (O. her), O. nonstriatus (O. non), O. rimator (O. rim), O. sargi (O. sar). Blue lines indicate species restricted to the west of the Tehuantepec Isthmus. Red lines indicates species restricted to the east of the Tehuantepec Isthmus. Black lines indicate species distributed on both sides of the Tehuantepec Isthmus.
Fig. 4. SEM photos showing the jaws and radula. A in Positive association between PTN polymorphisms and schizophrenia in Northeast Chinese Han population.
Fig. 4. SEM photos showing the jaws and radula. A, Overview of a jaw; B, Jaw element; C, Central teeth presented on the radula; D, Close-up image of the denticles. Scale bars: A = 500 µm; B = 20 µm; C = 500 µm; D = 20 µm.
Fig. 6 in Fig. 2 in Positive association between PTN polymorphisms and schizophrenia in Northeast Chinese Han population.
Fig. 6. Morphology of Oileus gasparilomi Cano & Schuster. a) head and pronotum, b) aedeagus ventral view, c) aedeagus lateral view, d) hind wing, e–g: stridulatory spines of plectrum, e) apical zone (Z1), f) medial zone (Z2), g) posterior zone (Z3). Scale bar (black lines) 1 mm.
Fig. 4 in Fig. 1 in Positive association between PTN polymorphisms and schizophrenia in Northeast Chinese Han population.
Fig. 4. Relative percentage availability of the three habitat types (bare rock, crevice and oyster) and resting habitat locations of the limpets at levels where they were most abundant at each shore (n = 58 individuals for S. guamensis at Sunset beach and n = 100 individuals in all others).
Fig. 1 in Fig. 2 in Positive association between PTN polymorphisms and schizophrenia in Northeast Chinese Han population.
Fig. 1. Species distribution models (SDM) and occurrences for Oileus species. a) SDM for Oileus bifidus, b) SDM for Oileus heros, c) SDM for Oileus nonstriatus, d) SDM for Oileus rimator, e) SDM for Oileus sargi, f) Occurrences for Oileus gasparilomi and Oileus bezai sp. nov. Polygon color changes with biogeographic provinces. Points correspond to species occurrences.
Fig. 4 in Positive association between PTN polymorphisms and schizophrenia in Northeast Chinese Han population.
Fig. 4. Top panel (A): Bayesian inference based on concatenated COI and 16S sequences. Bayesian posterior probabilities (top) and bootstrap support values (bottom) are provided next to each node. The scale bar indicates substitutions per site according to the applied models of sequence evolution. Letters after the species name indicate the geographical location of the sequences used in our analyses (GR: Greece; MC: Northern Macedonia; SP: Spain). Bottom panel (B): Map of the distribution of Diaphanosoma spp. in water bodies in the Balkan Peninsula based on recent morphological and molecular studies (Alexiou et al. 2021; Korovchinsky 2022; Korovchinsky and Petkovski 2014; this study). Each species is designated by one color in the phylogeny and the map to aid interpretation.
Fig. 1 in Fig. 1 in Positive association between PTN polymorphisms and schizophrenia in Northeast Chinese Han population.
Fig. 1. Map of the study sites. (A) map of Thailand; (B) Lanta Island which is located on the west coast of Thailand; (C) the two shores at Phra-ae and Sunset beach (Google Maps 2016).
Fig. 4 in Positive association between PTN polymorphisms and schizophrenia in Northeast Chinese Han population.
Fig. 4. Sarcophaga (Mehria) lorosa Hall specimens reared from egg sacs of Metepeira galatheae (Thorell). A, C, E, G, H: Lateral habitus, dorsal habitus, head in frontal view, terminalia in posterior view, and terminalia in lateral view of male, respectively; B, D, F: Lateral habitus, dorsal habitus, and head in frontal view of female, respectively.
Fig. 3 in Positive association between PTN polymorphisms and schizophrenia in Northeast Chinese Han population.
Fig. 3. Holotype male of Sarcophaga lorosa Hall (NHMUK) and holotype male of Arachnidomyia travassosi Tibana and Mello (CNC), respectively. A, B: Lateral habitus and labels; C, D: Dorsal habitus; E, F: Head in frontal view.
Fig. 1 in Positive association between PTN polymorphisms and schizophrenia in Northeast Chinese Han population.
Fig. 1. Record of Sarcophaga (Mehria) lorosa Hall (Diptera: Sarcophagidae) in Metepeira galatheae (Thorell) (Araneae: Araneidae). A–C, Female, male, and egg sac of M. galatheae, respectively; D, Puparium of S. (M.) lorosa.
Fig. 5 in Fig. 2 in Positive association between PTN polymorphisms and schizophrenia in Northeast Chinese Han population.
Fig. 5. Morphology of Oileus rimator (Truqui). a) head and pronotum, b) aedeagus ventral view, c) aedeagus lateral view, d) hind wing, e–g: stridulatory spines of plectrum, e) apical zone (Z1), f) medial zone (Z2), g) posterior zone (Z3). Scale bar (black lines) 1 mm.
Fig. 2 in Positive association between PTN polymorphisms and schizophrenia in Northeast Chinese Han population.
Fig. 2. Measurements of Diaphanosoma populations in the Balkan Peninsula (Lakes Ohrid, Prespa, and Dojran). Measurements of specimens from Lake Ohrid were retrieved from Korovchinsky (2022) from specimens collected in this study, while measurements from Lake Prespa and Lake Dojran were retrieved from Korovchinsky and Petkovski (2014).
Fig. 4 in Positive association between PTN polymorphisms and schizophrenia in Northeast Chinese Han population.
Fig. 4. Ordination diagram of redundancy analysis (RDA) with 17 of the most common bird species recorded on Tenerife Island explained by the point-count locations in relation to distance from the road. Abbreviations of species names include the first one letter of the genus and the first three letters of species scientific names.
Fig. 2. A in Positive association between PTN polymorphisms and schizophrenia in Northeast Chinese Han population.
Fig. 2. A, Distribution map of Sarcophaga (Mehria) lorosa Hall, highlighting the type localities of the junior synonyms Arachnidomyia travassosi Tibana and Mello, syn. nov., and Weyrauchimyia ruficauda Lopes and Tibana, syn. nov.; B, Study areas in the Atacama region, Chile, during a desert bloom. Map created with SimpleMappr (https://www.simplemappr.net/).
Fig. 5 in Positive association between PTN polymorphisms and schizophrenia in Northeast Chinese Han population.
Fig. 5. Phylogenetic tree of the concatenated COI/16S/H3 sequence dataset constructed using the maximum likelihood method. Bootstrap values> 50 are shown in the nodes.
Fig. 2 in Positive association between PTN polymorphisms and schizophrenia in Northeast Chinese Han population.
Fig. 2. Composition and frequency of the most common (> 10 individuals) birds on the island of Tenerife. Abbreviations of species names include the first one letter of the genus and the first three letters of species scientific names.
Fig. 9 in Fig. 2 in Positive association between PTN polymorphisms and schizophrenia in Northeast Chinese Han population.
Fig. 9. Morphology of Oileus bifidus (Zang). a) head and pronotum, b) aedeagus ventral view, c) aedeagus lateral view, d) hind wing, e–g: stridulatory spines of plectrum, e) apical zone (Z1), f) medial zone (Z2), g) posterior zone (Z3). Scale bar (black lines) 1 mm.
Fig. 5 in Positive association between PTN polymorphisms and schizophrenia in Northeast Chinese Han population.
Fig. 5. Analysis of the niche width (BCom) of bacteria (a) and nematodes (b) (at the genus level) in each treatment based on correlation and optimal multiple regression model, Mantel test of community diversity and niche breadth of soil bacteria and nematodes (c), and RDA analysis of soil bacterial-feeding nematode and bacterial genera (d).
Fig. 3 in Positive association between PTN polymorphisms and schizophrenia in Northeast Chinese Han population.
Fig. 3. Redundancy analysis of the top 15 bacteria (a) and nematodes (b) (at the genus level) with soil physicochemical properties. The colored dots represent relative abundance. The bars represent the total proportion of explained variations in the physicochemical properties by key bacteria and nematodes. AP, Available phosphorus; AK, Available potassium; NH +-N, Ammoniacal nitrogen; NO --N, Nitrate nitrogen; MBC, Microbial biomass 4 3 carbon.
Fig. 4 in Fig. 2 in Positive association between PTN polymorphisms and schizophrenia in Northeast Chinese Han population.
Fig. 4. Morphology of Oileus sargi (Kaup). a) head and pronotum, b) aedeagus ventral view, c) aedeagus lateral view, d) hind wing, e–g: stridulatory spines of plectrum, e) apical zone (Z1), f) medial zone (Z2), g) posterior zone (Z3). Scale bar (black lines) 1 mm.
ScienceDex guides
Understand access before you commit
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.