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Figures 10–15 in Bees of the genera Dufourea and Dieunomia of Michigan (Hymenoptera: Apoidea: Halictidae), with a key to the Dufourea of eastern North America
Figures 10–15. Males of Dufourea novaeangliae (Robertson) (10–12) and D. monardae (Viereck) (13–15). 10, 13. Propodea. 11, 14. Metatrochanters. 12, 15. Metasomal sterna six. Modified from Dumesh & Sheffield (2012).
Fig. 15 in Reproductive biology, embryonic development and matrotrophy in the phylactolaemate bryozoan Plumatella casmiana
Fig. 15 Longitudinal sections of brooded larvae of Plumatella casmiana. a. The embryo sac is conspicuous. The larval mantle is ciliated (arrowhead) and in earlier stages restricted to the anterior pole of the larva. Halfway along the longitudinal axis the mantle forms a deep groove (arrows). Two almost differentiated buds are present in the larva. b
Fig. 15 in New records of 24 ciliate species (Protozoa, Ciliophora) collected in South Korea
Fig. 15. Mesodinium pulex in vivo (A) and after protargol impregnation (B, C). A. Typical individual. B. Two macronuclear nodules. C. Somatic ciliature. Scale bars = 30 μm (A); 10 μm (B, C).
Fig. 15 in A report of 14 unrecorded bacterial species in Korea isolated in 2017
Fig. 15. Neighbor-joining phylogenetic tree based on 16S rRNA gene sequences shows the relationship between the strains isolated in this study and their relatives of the genus Bacillus. Bootstrap values (>70%) are shown above nodes for the neighbor-joining methods. Bar: 0.0050 substitutions per nucleotide position, respectively.
Fig. 15 in Unrecorded species of Korean invertebrates discovered through the project of 'Discovery of Korean Indigenous Species' III
Fig. 15. Robertgurneyella spinulosa (Sars, 1911), adult female: A. anal somite and caudal rami; B. antenna (top) and mandible (bottom); C. first swimming legs; D. second and third swimming legs; E. fourth swimming leg; F. fifth leg. Scales bars = 100 μm.
Fig. 2. A in A report on 15 unrecorded bacterial species of Korea isolated in 2016, belonging to the class Betaproteobacteria
Fig. 2. A neighbor-joining phylogenetic tree based on 16S rRNA gene sequences shows the relationship between the strains isolated in this study and their relatives of the genus Paraburkholderia. Bootstrap values (>70%) are shown above nodes for the neighbor-joining methods. Bar: 0.005 substitutions per nucleotide position.
Fig. 1 in A report on 15 unrecorded bacterial species of Korea isolated in 2016, belonging to the class Betaproteobacteria
Fig. 1. Transmission electron micrographs or scanning electron micrographs of cells of the strains isolated in this study. The cells were cultured at their optimal growth conditions. Strains: 1, POA39; 2, 2PKSH112; 3, D8-11; 4, 7227; 5, 8312; 6, 6191; 7, HMF4664; 8, HMF4541; 9, HMF4544; 10, SH4; 11, MMS16-CNU072; 12, MMS16-CNU135; 13, MMS16-CNU376; 14, MMS16-CNU436; 15, MMS16-CNU462.
Fig. 4. A in A report on 15 unrecorded bacterial species of Korea isolated in 2016, belonging to the class Betaproteobacteria
Fig. 4. A neighbor-joining phylogenetic tree based on 16S rRNA gene sequences shows the relationship between the strains isolated in this study and their relatives of the family Neisseriaceae, Oxalobacteraceae and Ralstonia_f. Bootstrap values (>70%) are shown above nodes for the neighbor-joining methods. Bar: 0.01 substitutions per nucleotide position.
Fig. 12 in Notes of 15 unrecorded macrofungi in Korea
Fig. 12. The phylogenetic tree of Scytinostroma acystidiatum (KUC20121019-32 and KUC20190620-28). The tree was constructed based on ITS gene datasets of the genus Scytinostroma. Confertobasidium olivaceoalbum was used as an outgroup. The newly generated sequence is shown in blue and bold. Bootstrap support values more than 70 are shown.
Fig. 3 in Notes of 15 unrecorded macrofungi in Korea
Fig. 3. The phylogenetic tree of Agaricus thiersii (KUC20180907- 19). The tree was constructed based on ITS gene datasets of the genus Agaricus subgenus Spissicaules. Agaricus bellanniae was used as an outgroup. The newly generated sequence is shown in blue and bold. Bootstrap support values more than 70 are shown.
Fig. 2 in Notes of 15 unrecorded macrofungi in Korea
Fig. 2. Micro-morphological characteristics of fifteen unrecorded macrofungi in Korea. A. Agaricus thiersii; B. Baorangia alexandri; C. Boletellus putuoensis; D. Entoloma bulakhae; E. Entoloma pygmaeopapillatum; F. Entoloma subtenuicystidiatum; G. Gerronema kuruvense; H. Hyphoderma nudicephalum; I. Hyphoderma tenue; J. Macrolepiota subcitrophylla; K. Mycena jingyinga; L. Mycena yuezhuoi; M. Ophiocordyceps vespulae; N. Scytinostroma acystidiatum; O. Steccherinum straminellum (scale bars = 10 μm).
Fig. 11 in Notes of 15 unrecorded macrofungi in Korea
Fig. 11. The phylogenetic tree of Ophiocordyceps vespulae (KUC20220825-06). The tree was constructed based on ITS gene datasets of the genus Ophiocordyceps. Ophiocordyceps sinensis was used as an outgroup. The newly generated sequence is shown in blue and bold. Bootstrap support values more than 70 are shown.
Fig. 6 in Notes of 15 unrecorded macrofungi in Korea
Fig. 6. The phylogenetic tree of Entoloma bulakhae (SFC20150903-26 and SFC20150903-31), E. pygmaeopapillatum (SFC20190822-20), and E. subtenuicystidiatum (SFC20140624-04). The tree was constructed based on ITS gene datasets of the genus Entolma. Clitopilus hirneolus was used as an outgroup. The newly generated sequence is shown in blue and bold. Bootstrap support values more than 70 are shown.
Fig. 5 in Notes of 15 unrecorded macrofungi in Korea
Fig. 5. The phylogenetic tree of Boletellus putuoensis (KUC20180907-19). The tree was constructed based on ITS gene datasets of the genus Boletellus. Aureoboletus venustus was used as an outgroup. The newly generated sequence is shown in blue and bold. Bootstrap support values more than 70 are shown.
Fig. 1 in Notes of 15 unrecorded macrofungi in Korea
Fig. 1. Macro-morphological characteristics of fifteen unrecorded macrofungi in Korea. A. Agaricus thiersii; B. Baorangia alexandri; C. Boletellus putuoensis; D. Entoloma bulakhae; E. Entoloma pygmaeopapillatum; F. Entoloma subtenuicystidiatum; G. Gerronema kuruvense; H. Hyphoderma nudicephalum; I. Hyphoderma tenue; J. Macrolepiota subcitrophylla; K. Mycena jingyinga; L. Mycena yuezhuoi; M. Ophiocordyceps vespulae; N. Scytinostroma acystidiatum; O. Steccherinum straminellum (scale bar = 10 mm for A-D, G-J, M-O; 5 mm for E, F, L; and 2.5 mm for K).
Fig. 13 in Notes of 15 unrecorded macrofungi in Korea
Fig. 13. The phylogenetic tree of Steccherinum straminellum (KUC201811101-53). The tree was constructed based on ITS and LSU gene datasets of the genus Steccherinum. Loweomyces fractipes was used as an outgroup. The newly generated sequence is shown in blue and bold. Bootstrap support values more than 70 are shown.
Fig. 10 in Notes of 15 unrecorded macrofungi in Korea
Fig. 10. The phylogenetic tree of Mycena jingyinga (KUC20220626-09, KUC20220626-13, and KUC20220626-14) and My. yuezhuoi (KUC20190731-37 and KUC20191011-27A). The tree was constructed based on ITS gene datasets of the genus Mycena. Xeromphalina campanella was used as an outgroup. The newly generated sequence is shown in blue and bold. Bootstrap support values more than 70 are shown.
Figures 12–15 in Review of the family Digamasellidae (Acari: Mesostigmata) in Iran with three new records and a key to species
Figures 12–15. Oligodentatus tridentatus Shcherbak & Bregetova (female) – 12. Coxa–tibia of leg I; 13. Coxa–tibia of leg II; 14. Coxa–tibia of leg III; 15. Coxa–tibia of leg IV.
BRAIN Journal-Brain-Like Artificial Intelligence for Automation-Figure 15. Input Sources of an Affective Neuro-Symbol Representing an Emotion
<p>Based on the descriptions given above and the concept of neuro-symbolic information<br> processing outlined in Section 4.2, so-called “affective neuro-symbols” were defined for the<br> affective situation assessment architecture (see Figure 15). These affective neuro-symbols can<br> principally receive information from four different sources: (1) body states, (2) objects and events<br> perceived in the environment (external perception), (3) from other emotions and (4) cognitive<br> (reasoning) processes. An input from one of these sources can in certain circumstances already be<br> sufficient to activate an affective neuro-symbol. Different sources can either have an exhibitory or<br> inhibitory effect on the activation of an affective neuro-symbol.</p>
Fig. 15 in Bees of the genus Lasioglossum (Hymenoptera: Halictidae) from Greater Puerto Rico, West Indies
Fig. 15. Lasioglossum ferrerii (Baker, 1906), ♀. A. Face. B. Lateral habitus. C. Dorsal habitus. Scale bars = 1 mm.
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.