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Figure 7. A in Demosponges of the genus Hymedesmia (Poecilosclerida: Hymedesmidae) from Rathlin Island, Northern Ireland, with a description of six new species
Figure 7. A, Hymedesmia (Hymedesmia) peachii Bowerbank, 1882. A, large acanthostyle; B, small acanthostyle; C, ends of ectosomal spicule; D, small chelae; E, large chelae. Scale bars: 10 Mm. B, Hymedesmia(Hymedesmia) peachii, surface.
Figure 4. A in Demosponges of the genus Hymedesmia (Poecilosclerida: Hymedesmidae) from Rathlin Island, Northern Ireland, with a description of six new species
Figure 4. A, Hymedesmia (Hymedesmia) cratera. sp. nov. A, large acanthostyle; B, base of large acanthostyle; C, small acanthostyle; D, ends of ectosomal spicule; E, chelae. Scale bars: 10 Mm. B, Hymedesmia (Hymedesmia) cratera. sp. nov., surface.
Figure 3. A in Demosponges of the genus Hymedesmia (Poecilosclerida: Hymedesmidae) from Rathlin Island, Northern Ireland, with a description of six new species
Figure 3. A, Hymedesmia (Hymedesmia) umbelliformis sp. nov. A, large acanthostyle; B, small acanthostyle; C, ends of ectosomal spicule; D, chelae. Scale bars: 10 Mm. B, Hymedesmia (Hymedesmia) umbelliformis sp. nov., surface.
Figure 1 in Demosponges of the genus Hymedesmia (Poecilosclerida: Hymedesmidae) from Rathlin Island, Northern Ireland, with a description of six new species
Figure 1. Sampling sites referred to in the text: 1, Damicornis Bay; 2, White Cliffs; 3, Loch Garry; 4, south-east of Doon Point; 5, north-east of Doon Point; 6, Duncan's Bo; 7, Ruecallan; 8, West of Derginan Point. The line around Rathlin Island depicts the 30-m depth contour.
Figure 10 in A new species of crown-antlered deer Stephanocemas (Artiodactyla, Cervidae) from the middle Miocene of Qaidam Basin, northern Tibetan Plateau, China, and a preliminary evaluation of its phylogeny
Figure 10. Species ranges, phyletic relationship, and zoogeographical positions of the Paradicrocerus–Stephanocemas clade. Most of the species ranges are approximate. Phyletic relationship is based on one of the shortest trees in our cladistic analysis, and some indeterminate taxa not included in the cladogram are inserted here based on our estimates of their relationships. The antlers are scaled to their approximate relative size, and dashed lines are mostly our own reconstructions of missing tines.
Figure 9 in A new species of crown-antlered deer Stephanocemas (Artiodactyla, Cervidae) from the middle Miocene of Qaidam Basin, northern Tibetan Plateau, China, and a preliminary evaluation of its phylogeny
Figure 9. Strict consensus of four shortest trees (tree length = 12) of the Paradicrocerus–Stephanocemas clade found by the branch and bound option of the PAUP program on a ten taxa ¥ nine characters data matrix (Table 1).
Figure 8. IVPP V15726 in A new species of crown-antlered deer Stephanocemas (Artiodactyla, Cervidae) from the middle Miocene of Qaidam Basin, northern Tibetan Plateau, China, and a preliminary evaluation of its phylogeny
Figure 8. IVPP V15726, Stephanocemas sp. from IVPP locality CD0406. A, dorsal, and B, ventral views of antler fragment. Scale is for both views.
Figure 6. IVPP V15724 in A new species of crown-antlered deer Stephanocemas (Artiodactyla, Cervidae) from the middle Miocene of Qaidam Basin, northern Tibetan Plateau, China, and a preliminary evaluation of its phylogeny
Figure 6. IVPP V15724, referred specimen of Stephanocemas palmatus sp. nov. A, dorsal, B, ventral, and C, medial views of posterior palm portion of a juvenile antler.
Figure 7. IVPP V15725 in A new species of crown-antlered deer Stephanocemas (Artiodactyla, Cervidae) from the middle Miocene of Qaidam Basin, northern Tibetan Plateau, China, and a preliminary evaluation of its phylogeny
Figure 7. IVPP V15725, Stephanocemas sp. from IVPP locality CD9818. A, stereophoto of dorsal view, B, lateral view, and C, ventral view of partial antler.
Figure 10. A in Demosponges of the genus Hymedesmia (Poecilosclerida: Hymedesmidae) from Rathlin Island, Northern Ireland, with a description of six new species
Figure 10. A, Hymedesmia (Stylopus) hibernica Stephens, 1916. A, large acanthostyle; B, small acanthostyle; C, ends of ectosomal spicule. Scale bars: 10 Mm. B, Hymedesmia (Stylopus) hibernica, surface.
Figure 11. A in Demosponges of the genus Hymedesmia (Poecilosclerida: Hymedesmidae) from Rathlin Island, Northern Ireland, with a description of six new species
Figure 11. A, Hymedesmia (Stylopus) primitiva Lundbeck, 1910. A, acanthostyle; B, ectosomal spicule. Scale bars: 10 Mm. B, Hymedesmia (Stylopus) primitiva, surface.
Figure 5. IVPP V15723 in A new species of crown-antlered deer Stephanocemas (Artiodactyla, Cervidae) from the middle Miocene of Qaidam Basin, northern Tibetan Plateau, China, and a preliminary evaluation of its phylogeny
Figure 5. IVPP V15723, referred specimen of Stephanocemas palmatus sp. nov. A, dorsal, and B, ventral views of palm portion of antler.
Figure 4. IVPP V15722 in A new species of crown-antlered deer Stephanocemas (Artiodactyla, Cervidae) from the middle Miocene of Qaidam Basin, northern Tibetan Plateau, China, and a preliminary evaluation of its phylogeny
Figure 4. IVPP V15722, left antler without pedicel, holotype of Stephanocemas palmatus sp. nov. from Qaidam Basin, northern Tibetan Plateau. A, medial, and B, ventral views. Left is posterior and right is anterior.
Figure 3 in A new species of crown-antlered deer Stephanocemas (Artiodactyla, Cervidae) from the middle Miocene of Qaidam Basin, northern Tibetan Plateau, China, and a preliminary evaluation of its phylogeny
Figure 3. Stereophoto of dorsal view of IVPP V15722, left antler without pedicel, holotype of Stephanocemas palmatus sp. nov. from Qaidam Basin, northern Tibetan Plateau. Top is posterior and bottom is anterior.
Figure 2 in A new species of crown-antlered deer Stephanocemas (Artiodactyla, Cervidae) from the middle Miocene of Qaidam Basin, northern Tibetan Plateau, China, and a preliminary evaluation of its phylogeny
Figure 2. Satellite image of the Barun Yawula anticline, with key fossil localities and their relative stratigraphical positions indicated. The east–west trending fold is asymmetrical with the south limb dipping more steeply than the north limb. A prominent resistant bed (a dark–light band combination, indicated by black dashed lines) within the rusty green sandstones layers helps to trace stratigraphical relationships between localities in eastern and western ends of the anticline, although multiple faults (with offsets ranging from 50 to 500 m), particularly those in the eastern end, complicate correlations. White lines are the measured section.
Shortgrass prairie (Colorado, USA) and northern mixedgrass prairie (Wyoming, USA) species traits
<p>These data support Mueller et al. 2023, entitled "Coordination of leaf, root, and seed traits shows the importance of whole plant economics in two semiarid grasslands."</p> <p>Uncertainty persists within trait-based ecology, partly because few studies assess multiple axes of functional variation and their effect on plant performance. For 55 species from two semiarid grasslands, we quantified: i) covariation between economic traits of leaves and absorptive roots, ii) covariation among economic traits, plant height, leaf size, and seed mass, and iii) relationships between these traits and species' abundance. Pairs of analogous leaf and root traits were at least weakly positively correlated (e.g., SLA and SRL). Two pairs of such traits, N content and DMC of leaves and roots, were at least moderately correlated (r>0.5) whether species were grouped by site, taxonomic group and growth form, or life history. Root diameter was positively correlated with seed mass for all groups of species except annuals and monocots. Species with higher LDMC tended to be more abundant (r=0.63). Annuals with larger seeds were more abundant (r=0.69). Compared to global-scale syntheses with many observations from mesic ecosystems, we observed stronger correlations between analogous leaf and root traits, weaker correlations between SLA and leaf N, and stronger correlations between SRL and root N. In dry grasslands, plant persistence may require coordination of above- and belowground traits, and dense tissues may facilitate dominance.</p>
Figure 1 in Taxonomic review of the "posteli-species group" of goatfishes (genus Parupeneus, Mullidae), with description of a new species from the northern Red Sea
Figure 1. – Relationships among eight morphometric characters including SL and total number of gill rakers in the five posteli-group species and three populations of Parupeneus posteli.
Figure 3. – A-E in Taxonomic review of the "posteli-species group" of goatfishes (genus Parupeneus, Mullidae), with description of a new species from the northern Red Sea
Figure 3. – A-E: Parupeneus posteli; A: SAIAB 83959, 88 mm SL, Baissac Bank, southern Mascarene Plateau (O. Alvheim and D. Tweddle); B: SAIAB 83959, 90 mm SL, same locality details (O. Alvheim and D. Tweddle); C: SAIAB 83898, 105 mm SL, Soudan Bank, southern Mascarene Plateau (O. Alvheim and D. Tweddle); D: large-sized fish (SL unknown), Réunion, Mascarene Islands (P. Guézé); E: MNHN 1965-0056, HT, 150 mm SL, same locality details (MNHN); F: Parupeneus sinai n. sp., MNHN 1967-0557, HT, 83 mm SL, northern Red Sea, right side shown, image reversed (F. Uiblein). Scale bars = 20 mm.
Figure 2. – A in Taxonomic review of the "posteli-species group" of goatfishes (genus Parupeneus, Mullidae), with description of a new species from the northern Red Sea
Figure 2. – A: Parupeneus chrysonemus BPBM 34775, 129 mm SL, Midway Atoll, Hawaiian Islands (J.E. Randall); B: P. chrysonemus BPBM 39141, 140 mm SL, Oahu, Hawaiian Islands (J.E. Randall); C: P. louise, large-sized fish (SL unknown), Rurutu, Austral Islands, French Polynesia (A. Stein); D: P. moffiti, HT, 230 mm SL, Guam, Mariana Islands (R.F. Myers). Scale bars = 20 mm.
Figure 2 in SYNOPSIS OF BEGONIA (BEGONIACEAE) FROM THE NORTHERN ARM OF SULAWESI AND SANGIHE ISLAND, INDONESIA, INCLUDING THREE NEW SPECIES
Figure 2. Distribution maps of Begonia species occurring on the northern arm of Sulawesi. Distribution points are from georeferenced collections from major herbarium collections (B, BO, E, K, KRB, L, SING), the Begonia Resource Centre (Hughes et al., 2015–) and the Sulawesi Begonia Data Portal (Thomas et al., 2013, continuously updated).
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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)
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.