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Figs. 18–20 in Taxonomy, distribution and biology of selected European Dinax, Strongylogaster and Taxonus species (Hymenoptera: Symphyta)
Figs. 18–20, Taxonus Hartig, 1837, last instar larvae: 18 – Taxonus agrorum Fallén, 1808: a – bare larva (lateral view); b – bare larva (dorsal view); c – pruinose larva (lateral view). 19 – T. sticticus (Klug, 1817): a – laterodorsal view; b – dorsal view. 20 – T. alboscutellatus Niezabitowski, 1899: a – dorsal view (plain form); b – laterodorsal view (plain form); c – dorsal view (patterned form). Scale: 10 mm.
Figs. 2–7. Strongylogaster Dahlbom, 1835 in Taxonomy, distribution and biology of selected European Dinax, Strongylogaster and Taxonus species (Hymenoptera: Symphyta)
Figs. 2–7. Strongylogaster Dahlbom, 1835, adults: 2 – S. macula (Klug, 1817); 3 – S. baikalensis Naito, 1990; 4 – S. mixta (Klug, 1817); 5 – S. filicis (Klug, 1817); 6 – S. multifasciata (Geoffroy, 1785); 7 – S. xanthocera (Stephens, 1835). Scale: 10 mm.
Fig. 1 in Taxonomy, distribution and biology of selected European Dinax, Strongylogaster and Taxonus species (Hymenoptera: Symphyta)
Fig. 1. Dinax ermak (Zhelochovtsev, 1968): a – female (dorsal view); b – male (dorsal view); c – female (lateral view); d – last instar larva (dorsal view); e – last instar larva (laterodorsal view); f – eonymph (dorsal view); g – eonymph (laterodorsal view). Scale: 5 mm.
Figs.15–17. Taxonus Hartig, 1837 in Taxonomy, distribution and biology of selected European Dinax, Strongylogaster and Taxonus species (Hymenoptera: Symphyta)
Figs.15–17. Taxonus Hartig, 1837, adults: 15 – T. agrorum Fallén, 1808; 16 – T. sticticus (Klug, 1817); 17 – T. alboscutellatus Niezabitowski, 1899. Scale: 10 mm.
Figs. 13–14. Strongylogaster Dahlbom, 1835 in Taxonomy, distribution and biology of selected European Dinax, Strongylogaster and Taxonus species (Hymenoptera: Symphyta)
Figs. 13–14. Strongylogaster Dahlbom, 1835, penis valve, lateral view: 13 – S. baikalensis Naito, 1990; 14 – S. macula (Klug, 1817). Scale: 0.5 mm.
Fig. 1 in Home range size and microhabitat selection by a tropical partridge species in moist evergreen forest
Fig. 1. Analysis of green-legged partridges' group range based on radio locations using the characteristic hull polygon (CHP) and minimum convex polygon (MCP; 100%, 95% and 50%) methods. F refers to females, and M refers to males.
Fig. 2 in Home range, habitat use and roost-site selection by lowland female Siamese fireback Lophura diardi in northeastern Thailand
Fig. 2. The variation in home ranges and core areas of the eight female Siamese fireback in 2011 during different reproductive periods, estimated using 95% MCP and CHP Hot Spot methods. Locations shown were the food supplement sites (1 and 2) and nesting sites during the breeding season.
Fig. 3 in Home range, habitat use and roost-site selection by lowland female Siamese fireback Lophura diardi in northeastern Thailand
Fig. 3. The occurrence probability of Siamese fireback in relation to habitat variables. Shown are predicted values and 95% confidence limits for breeding (black solid lines) and non-breeding (gray dashed lines) periods.
Fig. 1 in Home range, habitat use and roost-site selection by lowland female Siamese fireback Lophura diardi in northeastern Thailand
Fig. 1. Location of Sakaerat Environmental Research Station (SERS), northeastern Thailand, including the locations of 60 available sites, two food supplementary sites, 14 nesting sites, and 52 roosting sites. Polygons shown are the home range boundaries of the eight radiotagged Siamese firebacks (group A–H).
Fig. 4 in Sub-Montane Habitat Selection By A Lowland Pheasant
Fig. 4. The comparison of percentage tree cover (height>5 meters) between used areas during the three periods of the year cycle and random areas for Female 1 and Female 2 (a), and the comparison of tree density (height 0.5-3 meters) between used areas during the three periods and random areas for Female 1 and Female 2 (b).
Fig. 1. a in Sub-Montane Habitat Selection By A Lowland Pheasant
Fig. 1. a, Ranging size during different periods of the year cycle of Siamese Fireback, Female 1 and Female 2, estimated using 95% minimum convex polygons (MCP); b, 95 % MCP home range size compared in different phases of the year cycle between the two female Siamese Firebacks.
Fig. 2. A in Sub-Montane Habitat Selection By A Lowland Pheasant
Fig. 2. A comparison of slope in areas used during different periods of the year cycle and randomly chosen areas for Female 1 (a) and Female 2 (b).
Fig. 3 in Nesting ecology and nest site selection of green-legged partridge
Fig. 3. Location of a green-legged partridge nest between the buttress of a large tree. The arrow shows the location of nest.
Fig. 1. Precipitation during 2009 and 2010 in Nesting ecology and nest site selection of green-legged partridge
Fig. 1. Precipitation during 2009 and 2010 and the nesting period for the same two years of green-legged partridge at Khao Yai National Park.
Fig. 2 in Nesting ecology and nest site selection of green-legged partridge
Fig. 2. Hourly variations (mean ± SD) in departure and return times of incubating female green-legged partridge (N = 6) at the Mo Singto Plot, Khao Yai National Park during 2009 and 2010.
Fig. 47. Relationships among selected Cretaceous and early Tertiary eutherians. A in New Data On The Skull And Dentition In The Mongolian Late Cretaceous Eutherian Mammal Zalambdalestes
Fig. 47. Relationships among selected Cretaceous and early Tertiary eutherians. A. The eutherian portion of the strict consensus of 144 equally most parsimonious trees produced by PAUP analysis of Rougier et al.'s matrix of 156 craniodental characters (Rougier et al., 1998: supplementary information; see also Wible et al., 2001). B. The eutherian portion of the strict consensus of 288 equally most parsimonious trees produced by PAUP analysis of the Rougier et al. matrix with our amendments to 21 character states for Zalambdalestes.
Figure S1 in Natural selection on various sites of ribosomal proteins: a cladistic view
Figure S1. Conserved sites of ribosomal protein 40S subunit labeling on crystal structure. The ribbons colored in red represent the synapomorphic s. str. sites of Eukaryota, the green ones represent the synapomorphic s. lat. sites of Eukaryota, and the blue ones represent the potential autapomorphic sites of clades lower than Eukaryota. The magenta ribbons represent the sites related to DBA, and the sites presented by sticks and balls are also synapomorphic sites. Because there are too many synapomorphic sites according to clades lower than Eukaryota in the RP, only the synapomorphic sites related to DBA are colored in this figure (shown in orange).
Figure S2 in Natural selection on various sites of ribosomal proteins: a cladistic view
Figure S2. Conserved sites of ribosomal protein 60S subunit labeling on crystal structure. The ribbons colored in red represent the synapomorphic s. str. sites of Eukaryota, the green ones represent the synapomorphic s. lat. sites of Eukaryota and the blue ones represent the potential autapomorphic sites of clades lower than Eukaryota. The magenta ribbons represent the sites related to DBA, and the sites shown by sticks and balls are also synapomorphic sites. Because there are too many synapomorphic sites according to clades lower than Eukaryota in the RP, only the synapomorphic sites related to DBA are colored in this figure (shown in orange).
Figure 1 in Natural selection on various sites of ribosomal proteins: a cladistic view
Figure 1. Summarized distribution of group-specific sites in the cladogram of eukaryotic diversification. The numerals shown above the line correspond to RPL, and the numerals shown below correspond to RPS. The Ecdysozoa-Neoptera and Chordata-Mammalia lineages are highlighted with blue and yellow, respectively. The amino acids with equivalent biochemical properties were not taken into account.
Figure 2 in Natural selection on various sites of ribosomal proteins: a cladistic view
Figure 2. Conserved sites in the tertiary structures of RPL11 (A) and RPS19 (B). The red ribbons represent the synapomorphic s. str. sites of Eukaryota, the green ones represent the synapomorphic sites s. lat. of Eukaryota, and the blue ones represent the potential autapomorphic sites of clades lower than Eukaryota. The ribbons with sticks and balls represent sites related to DBA. The synapomorphic sites related to DBA are shown in orange. The magenta ones represent the sites for which it is difficult to deduce the synapomorphy but appear to be related to DBA.
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.