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Fig. 2 in Epizoic Anthoathecate Species (Cnidaria, Hydrozoa) Growing on Eroded Shells of Live Gastropods (Nassarius festivus) in Japan
Fig. 2. Nassarius festivus collected from Torinosu, Shirahama, Wakayama Pref., showing erosion of older shells. A–B. fresh shells; C–E. old eroded shells. Scale=5 mm.
Fig. 2 in Diet Composition Of Otters (Lutra Lutra L.) Living On Small Watercourses In Southwestern Hungary
Fig. 2. The diet pattern of otters living by streams and channels in the Dráva region. For locations (W1–5) see Fig. 1, n = number of spraint samples
Fig. 1 in Diet Composition Of Otters (Lutra Lutra L.) Living On Small Watercourses In Southwestern Hungary
Fig. 1. Locality of the small watercourses studied in the Drava region. 1 = Dombó-channel (W1, Gyékényes), 2 = Dombó-channel (W2, Berzence), 3 = Babócsai stream (W3, Babócsa), 4 = Barcs-Kom-
Fig. 3 in Diet Composition Of Otters (Lutra Lutra L.) Living On Small Watercourses In Southwestern Hungary
Fig. 3. Percentage biomass consumption (mean±SE) of fish prey in the diet of otters living by streams and channels, on the basis of fish weight (a) and guild (b). Fish guilds: RE – reophilic or flow preferring, EU – eurytopic or tolerant for rivers and stagnant waters and ST – stagnophilic or stagnant water
Fig 2 in Sexual Size Dimorphism In Free-Living Populations Of Mus Musculus: Are Male House Mice Bigger?
Fig 2. Variation in SSD during the first five weeks of postnatal development in five mice populations. SSD is expressed as Lowich-Gibbons ratios of mean body weight (see under Material and Methods)
Fig. 1 in Sexual Size Dimorphism In Free-Living Populations Of Mus Musculus: Are Male House Mice Bigger?
Fig. 1. Map of the studied localities: 1 = Czech Republic, 2 = The Balkans, 3 = Iran, 4 = Jordan, 5 = hybrids. See Material and Methods for coordinates of the localities
Figs 16–17 in Free-Living Nematodes From Two Dolomite Hills In Hungary, With Description Of Sclerolaimus Hungaricus Sp. N.
Figs 16–17. Sclerolaimus hungaricus sp. n.: 16 = female genital region, 17 = male genital region. (Scale bars 40 µm each)
Figs 12–15 in Free-Living Nematodes From Two Dolomite Hills In Hungary, With Description Of Sclerolaimus Hungaricus Sp. N.
Figs 12–15. Sclerolaimus hungaricus sp. n.: 12 = anterior end, 13 = female tail, 14–15 = male tail. (Scale bars 40 µm each)
Figs 5–10 in Free-Living Nematodes From Two Dolomite Hills In Hungary, With Description Of Sclerolaimus Hungaricus Sp. N.
Figs 5–10. Sclerolaimus hungaricus sp. n.: 5–6 = male tail, 7–11 = female tail. (Scale bars 20 µm each)
Figs 1–4 in Free-Living Nematodes From Two Dolomite Hills In Hungary, With Description Of Sclerolaimus Hungaricus Sp. N.
Figs 1–4. Sclerolaimus hungaricus sp. n.: 1 = anterior end, 2 = cardial region, 3 = vulval region, 4 = intestine–prerectal junction. (Scale bars 20 µm each)
Figures 98–106. Stricosus and Thalassiosira. Figs 98–103. Stricosus harrisonii. Figs 98, 99. Living cells showing plastids with pyrenoids. Figs 100, 101 in Marine benthic diatoms of Guam: new records, Dictyoneis apapae sp. nov., and updates to the checklist
Figures 98–106. Stricosus and Thalassiosira. Figs 98–103. Stricosus harrisonii. Figs 98, 99. Living cells showing plastids with pyrenoids. Figs 100, 101. Acid cleaned valves in LM and SEM. Fig. 102. External apex showing triangular hyaline area, two spines, rimoportula opening, and ocellulimbus with at least 7 rows of pores (contrast Fig. 62, Hyalosynedra). Fig. 103. Apex internal view showing symmetrical rimoportula (arrow). Figs 104–106. Thalassiosira nanolineata. Fig. 104. Valve in LM at two focal planes. Fig. 105, 106. External and internal aspects in SEM, showing central fultoportulae (F) and rimoportula (R) (arrows). Scale bars: Figs 98, 100, 101 = 20 µm, Fig 104 = 10 µm, Figs 99, 103, 105, 106 = 5 µm, Fig. 102 = 2 µm.
Long-lived magnetization in an atomic spin chain tuned to a diabolic point
<p>This is the OpenData Folder for the paper under the same name.</p>
Fig. 9 in Constraints on Phylogenetic Interrelationships among Four Free-living Litostomatean Lineages Inferred from 18S rRNA gene-ITS Region sequences and Secondary Structure of the ITS2 molecule
Fig. 9. Evolutionary hypothesis of interrelationships among the four free-living litostomatean lineages studied. This scenario was suggested on the basis of morphology and the consensus secondary structure of the ITS2 molecules. CK – circumoral kinety, DB – dorsal brush, OB – oral bulge, OO – oral bulge opening, P – proboscis, PE – perioral kinety, PR – preoral kineties, SK – somatic kineties.
Fig. 5 in Constraints on Phylogenetic Interrelationships among Four Free-living Litostomatean Lineages Inferred from 18S rRNA gene-ITS Region sequences and Secondary Structure of the ITS2 molecule
Fig. 5. Quartet likelihood-mapping showing distribution of phylogenetic signal in the 18S-A and the CON-1 alignment for three possible relationships among the four main free-living litostomatean lineages studied. The corners of the triangles show the percentage of fully resolved trees, i.e., phylogenetically informative signal. The rectangular areas show the percentage of trees that are in conflict. The central triangle shows the percentage of unresolved star-like trees, i.e., phylogenetically uninformative signal. Coding of free-living litostomatean lineages: H – Haptorida, P – Pleurostomatida, R – Rhynchostomatia, S – Spathidiida.
Fig. 4 in Constraints on Phylogenetic Interrelationships among Four Free-living Litostomatean Lineages Inferred from 18S rRNA gene-ITS Region sequences and Secondary Structure of the ITS2 molecule
Fig. 4. Super-network of 66 free-living litostomatean taxa constructed from 80 randomly selected post-burn-in trees from the Bayesian inference of the 18S-A–D, ITSR-C and ITSR-D as well as the CON-1 and CON-2 alignments. The super-network was constructed in the program SplitsTree, using the Z-closure option, tree size weighted mean, ten runs, and the refined heuristic technique. For details on taxa and characteristics of the alignments analyzed, see Supplementary Table S1 and S2.
Fig. 3 in Constraints on Phylogenetic Interrelationships among Four Free-living Litostomatean Lineages Inferred from 18S rRNA gene-ITS Region sequences and Secondary Structure of the ITS2 molecule
Fig. 3. Phylogeny based on the 18S rRNA gene and the ITS1-5.8S-ITS2 region of 56 free-living litostomatean taxa (alignment CON-1). Posterior probabilities for the Bayesian inference and bootstrap values for maximum likelihood were mapped onto the 50% majority rule ML tree. Dashes indicate posterior probabilities below 0.50 and ML bootstrap values below 50%. The scale bar indicates five substitutions per ten nucleotide positions. For details on taxa, evolutionary model used, and characteristics of the CON-1 alignment, see Supplementary Table S1 and S2.
Fig. 1 in Constraints on Phylogenetic Interrelationships among Four Free-living Litostomatean Lineages Inferred from 18S rRNA gene-ITS Region sequences and Secondary Structure of the ITS2 molecule
Fig. 1. Phylogeny based on the 18S rRNA gene of 64 free-living litostomatean taxa (alignment 18S-A). Posterior probabilities for Bayesian inference and bootstrap values for maximum likelihood were mapped onto the 50% majority rule Bayesian consensus tree. Dashes indicate ML bootstrap values below 50%. Sequences in bold were obtained during this study. The scale bar indicates two substitutions per one hundred nucleotide positions. For details on taxa, evolutionary model used, and characteristics of the 18S-A alignment, see Supplementary Table S1 and S2.
Fig. 8 in Constraints on Phylogenetic Interrelationships among Four Free-living Litostomatean Lineages Inferred from 18S rRNA gene-ITS Region sequences and Secondary Structure of the ITS2 molecule
Fig. 8. Structure logo of ITS2 helices II and III in various higher litostomatean taxa. The height of a base is proportional to its frequency in multiple sequence alignments.
Fig. 2 in Constraints on Phylogenetic Interrelationships among Four Free-living Litostomatean Lineages Inferred from 18S rRNA gene-ITS Region sequences and Secondary Structure of the ITS2 molecule
Fig. 2. Phylogeny based on the ITS1-5.8S-ITS2 region of 60 free-living litostomatean taxa (alignment ITSR-A). Posterior probabilities for Bayesian inference and bootstrap values for maximum likelihood were mapped onto the best ML tree. Dashes indicate posterior probabilities below 0.50 and ML bootstrap values below 50%. Sequences in bold were obtained during this study. The scale bar indicates nine substitutions per one hundred nucleotide positions. For details on taxa, evolutionary model used, and characteristics of the ITSR-A alignment, see Supplementary Table S1 and S2.
Fig. 7 in Constraints on Phylogenetic Interrelationships among Four Free-living Litostomatean Lineages Inferred from 18S rRNA gene-ITS Region sequences and Secondary Structure of the ITS2 molecule
Fig. 7. Consensus secondary structure of ITS2 helices II and III in various higher litostomatean taxa.
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.