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Fig. 1 in Population trends and conservation status of proboscis monkeys (Nasalis larvatus) in the face of habitat change in the Klias Peninsula, Sabah, Borneo, Malaysia
Fig. 1. Map showing the Klias Peninsula region in western Sabah, in the northern part of Borneo (inset), Malaysia, and the research sampling sites in riverine, mangrove, and mixed mangrove-riverine forests along rivers in Padang Teratak Bird Sanctuary, Padas Damit Forest Reserve, Menumbok Forest Reserve, Binsulok Forest Reserve, Klias Forest Reserve, Kg. Hindian Forest Reserve, and Nabahan Forest Reserve, where the river surveys of the sleeping sites of proboscis monkeys were conducted.
FIGURE 10 in Systematics and Taxonomy of Great Striped-Faced Bats of the Genus Vampyrodes Thomas, 1900 (Chiroptera: Phyllostomidae)
FIGURE 10. Posterior views of the occipital region in Vampyrodes caraccioli (A, USNM 405129) and V. major (B, FMNH 127114) illustrating taxonomic differences in the groove between the occipital condyle and the paracondylar process (arrow) and the position of the parietal foramina (pf). In V. caraccioli the groove between the occipital condyle and paracondylar process is weakly developed and the pf are well separated from the nuchal crest. In V. major, however the groove between the occipital condyle and the paracondylar process is well developed and the pf are closer to the nuchal crest.
FIGURE 8 in Systematics and Taxonomy of Great Striped-Faced Bats of the Genus Vampyrodes Thomas, 1900 (Chiroptera: Phyllostomidae)
FIGURE 8. Dorsal (A) and ventral (B) views of the skull of Vampyrodes caraccioli (USNM 405129; male) from Amazonas, Venezuela; the stylohyals were reconstructed from USNM 582872, a female from Cuzco, Peru. Dorsal (C) and ventral (D) views of the skull of V. major (FMNH 127114; male) from Veracruz, Mexico.
FIGURE 7 in Systematics and Taxonomy of Great Striped-Faced Bats of the Genus Vampyrodes Thomas, 1900 (Chiroptera: Phyllostomidae)
FIGURE 7. Labial view of the left P3–M1 illustrating presence and absence of perikymata. Top, Vampyrodes caraccioli (AMNH 230653) with distinct perikymata (arrow). Bottom, Platyrrhinus lineatus (AMNH 23771) without distinct perikyma.
FIGURE 6 in Systematics and Taxonomy of Great Striped-Faced Bats of the Genus Vampyrodes Thomas, 1900 (Chiroptera: Phyllostomidae)
FIGURE 6. Map showing collecting localities of Vampyrodes caraccioli (circles) and V. major (squares). Numbers refer to entries in the Gazetteer (appendix).
FIGURE 5 in Systematics and Taxonomy of Great Striped-Faced Bats of the Genus Vampyrodes Thomas, 1900 (Chiroptera: Phyllostomidae)
FIGURE 5. Principal components analysis (performed on cranial, dental and one external variables) showing dispersion of scores representing Vampyrodes caraccioli (circles) and V. major (triangles) along: (A) first and second axes (B) first and third axes. PC1 represents a size axis (with larger specimens appearing toward the right side of the plot) and PC2 portrays a difference in shape.
FIGURE 4. Combined cyt-b and D in Systematics and Taxonomy of Great Striped-Faced Bats of the Genus Vampyrodes Thomas, 1900 (Chiroptera: Phyllostomidae)
FIGURE 4. Combined cyt-b and D-loop maximum likelihood phylogram for both species of Vampyrodes. Support statistics from a parsimony bootstrap analysis, a maximum likelihood bootstrap analysis, and a Bayesian analysis are indicated at each resolved node. For the parsimony and maximum likehood analyses (MP and ML, respectively), white indicates bootstrap frequencies ≤50%, grey indicates bootstrap frequencies between 50% and 75%, and black indicates bootstrap frequencies ≥75%. For the Bayesian analysis (BPP), white indicates posterior probabilities <0.95, whereas black indicates posterior probabilities ≥0.95. For each terminal, an alphanumeric identifier and the country of origin (from table 1). Numbers in parentheses refer to localities mapped in figure 6 and listed in the Gazetteer (appendix).
FIGURE 3 in Systematics and Taxonomy of Great Striped-Faced Bats of the Genus Vampyrodes Thomas, 1900 (Chiroptera: Phyllostomidae)
FIGURE 3. Diagram of the cranium of an adult Vampyrodes caraccioli showing limits of cranial and dental measurements.
Text-fig. 2. (A) Orientation of Schizocrania filosa (HALL, 1847) on articulated shells of benthic brachiopod Rafinesquina sp. (A1–A3 – on dorsal valve of articulated shells, A4 – on ventral valve of articulated shell; forward growth direction is unclear in three specimens) from Upper Ordovician, Corryville Formation, Lawrenceburg, Indiana (after www.drydredgers.org/scizo.htm). (B) Orientation of Schizocrania multistriata (REED, 1905) shells on outer face of conulariid Metaconularia imperialis test (Dobrotivá Formation, Kařízek mine, Barrandian area; after Havlíček and Vaněk 1996); preserved conulariid shell in white, suggested outline of incomplete conulariid test in grey. Arrows indicate direction of forward growth of Schizocrania specimens. in Schizocrania (Brachiopoda, Discinoidea): Taxonomy, Occurrence, Ecology And History Of The Earliest Epizoan Lingulate Brachiopod
Text-fig. 2. (A) Orientation of Schizocrania filosa (HALL, 1847) on articulated shells of benthic brachiopod Rafinesquina sp. (A1–A3 – on dorsal valve of articulated shells, A4 – on ventral valve of articulated shell; forward growth direction is unclear in three specimens) from Upper Ordovician, Corryville Formation, Lawrenceburg, Indiana (after www.drydredgers.org/scizo.htm). (B) Orientation of Schizocrania multistriata (REED, 1905) shells on outer face of conulariid Metaconularia imperialis test (Dobrotivá Formation, Kařízek mine, Barrandian area; after Havlíček and Vaněk 1996); preserved conulariid shell in white, suggested outline of incomplete conulariid test in grey. Arrows indicate direction of forward growth of Schizocrania specimens.
Text-fig. 29. Scanning electron microscope (SEM) images of monocolpate pollen of Goczania punctata sp. nov.; Torres Vedras locality, Portugal. a–c) Holotype; anther fragment (a) with group of pollen grains showing the distal face (b, c) with clearly delimited colpus, the almost psilate tectum with occasional small perforations, and poorly differentiated microechinae on the proximal face (b). Specimen, TV44-S148024 (holotype). Scale bars 300 Μm (a), 6 Μm (b, c). in The Early Cretaceous Mesofossil Flora Of Torres Vedras (Ne Of Forte Da Forca), Portugal: A Palaeofloristic Analysis Of An Early Angiosperm Community
Text-fig. 29. Scanning electron microscope (SEM) images of monocolpate pollen of Goczania punctata sp. nov.; Torres Vedras locality, Portugal. a–c) Holotype; anther fragment (a) with group of pollen grains showing the distal face (b, c) with clearly delimited colpus, the almost psilate tectum with occasional small perforations, and poorly differentiated microechinae on the proximal face (b). Specimen, TV44-S148024 (holotype). Scale bars 300 Μm (a), 6 Μm (b, c).
Text-fig. 5. Scanning electron microscope (SEM) images of megaspores with possible affinities to Isoetales (a–d) and megaspores of uncertain affinity (e–i); Torres Vedras locality, Portugal. a) Paxillitriletes reticulatus megaspore in lateral view showing long appendages on the flanges of the laesurae and the reticulate-spiny distal surface; b) Dijkstraisporites sp. megaspore in oblique lateral view showing long, sometimes dichotomizing, appendages on the equatorial flanges and bordering the laesurae; c, d) Tenellisporites sp. megaspore in proximal view (c) showing equatorial flanges and laesurae with short, broad, flattened and unbranched appendages; note numerous, spiny microspores adhering to the proximal face of the megaspore (d); e) Megaspore type sp. 2 in lateral view showing apical gula and ornamentation of scattered spines; f, g) Megaspore type sp. 3 in lateral (f) and proximal (g) view showing broad, often dichotomously branched appendages covering the megaspore surface; h, i) aff. Flabellisporites sp. megaspores in proximal (h) and lateral (i) view showing long, narrow appendages covering the megaspore surface. Specimens, TV39-S174619 (a), TV38-S170220 (b), TV38-S170221 (c, d), TV44-S174574 (e), TV44-S174575 (f), TV44-S174577 (g), TV38-S170223 (h), TV38-S170222 (i). Scale bars 100 Μm (a–c, e–i), 25 Μm (d). in The Early Cretaceous Mesofossil Flora Of Torres Vedras (Ne Of Forte Da Forca), Portugal: A Palaeofloristic Analysis Of An Early Angiosperm Community
Text-fig. 5. Scanning electron microscope (SEM) images of megaspores with possible affinities to Isoetales (a–d) and megaspores of uncertain affinity (e–i); Torres Vedras locality, Portugal. a) Paxillitriletes reticulatus megaspore in lateral view showing long appendages on the flanges of the laesurae and the reticulate-spiny distal surface; b) Dijkstraisporites sp. megaspore in oblique lateral view showing long, sometimes dichotomizing, appendages on the equatorial flanges and bordering the laesurae; c, d) Tenellisporites sp. megaspore in proximal view (c) showing equatorial flanges and laesurae with short, broad, flattened and unbranched appendages; note numerous, spiny microspores adhering to the proximal face of the megaspore (d); e) Megaspore type sp. 2 in lateral view showing apical gula and ornamentation of scattered spines; f, g) Megaspore type sp. 3 in lateral (f) and proximal (g) view showing broad, often dichotomously branched appendages covering the megaspore surface; h, i) aff. Flabellisporites sp. megaspores in proximal (h) and lateral (i) view showing long, narrow appendages covering the megaspore surface. Specimens, TV39-S174619 (a), TV38-S170220 (b), TV38-S170221 (c, d), TV44-S174574 (e), TV44-S174575 (f), TV44-S174577 (g), TV38-S170223 (h), TV38-S170222 (i). Scale bars 100 Μm (a–c, e–i), 25 Μm (d).
Assessing Orchestration Load in Teacher-Facing Dashboards - Figure 2
<p>Figure of the results of the second session in the paper Assessing Orchestration Load in Teacher-Facing Dashboards.</p>
Assessing Orchestration Load in Teacher-Facing Dashboards - Figure 1
<p>Figure of the results of the first session in the paper Assessing Orchestration Load in Teacher-Facing Dashboards.</p>
Assessing Orchestration Load in Teacher-Facing Dashboards - Figure 4
<p>Figure of the results of the fourth session in the paper Assessing Orchestration Load in Teacher-Facing Dashboards.</p>
Assessing Orchestration Load in Teacher-Facing Dashboards - Figure 3
<p>Figure of the results of the third session in the paper Assessing Orchestration Load in Teacher-Facing Dashboards.</p>
Structural models of ProPEc in inward-facing and outward-facing conformations
<p>This deposit contains relevant data to supplement the study titled as "Structural determinants and functional significance of dimerization for osmosensing transporter ProP in <em>Escherichia coli</em>" to be published by Ozturk et al. (2022). </p> <p>ProPEc_XylEEc_all_alignments.rtf is the list of pairwise alignments of <em>E.coli</em> ProP and XylE generated by different alignment tools</p> <p>propec-inward-facing-homology-model-based-on-4qiq.pdb is the inward-facing structural model of ProP<em>Ec</em>.</p> <p>propec-outward-facing-homology-model-based-on-4gc0.pdb is the outward-facing structural model of ProP<em>Ec</em>.</p>
DATASETS FOR: A keystone avian predator faces elevated energy expenditure in a warming Arctic
<p> Here, we provide two datasets from a study in which we used triaxial accelerometers (Axy 4, Technosmart, 3g) to collect detailed behavioral records from little auks (<em>Alle alle</em>) at Ukaleqarteq (UK), East Greenland (70°44′N, 21°35′W) and Hornsund (HS) (77°00′N, 15°33′E; Svalbard archipelago), during the chick rearing period. We used this data to compile time activity budgets, from which we estimated daily energy expenditure (DEE). Data spans five years (2017-2021) at UK and two years at HS (2020, 2021). We assessed whether variation in DEE was affected by variability in climate change-sensitive environmental variables that affect availability of the little auk’s resource base of cold water zooplankton, that is sea surface temperature (SST) and sea ice coverage (SIC). SIC was only used for UK, since there was no appreciable sea ice at HS, which experiences higher average SST than UK. We also obtained small ~0.2-0.5 ml blood samples from the brachial veins of focal individuals to measure contamination from a potent chemical contaminant, mercury (Hg). We assessed the hypothesis that DEE is forced upward by challenging foraging conditions, but may be limited at some point due to energetic thresholds. We also assessed whether Hg contamination levels modified patterns of energy expenditure.</p> <p> In addition, to further examine the relationship that emerged between DEE and SST, we compiled a dataset of 12 site-year observations of average DEE of breeding little auks using data from Gabrielsen et al. (1991) (n = 13), Grémillet et al. (2012) (n = 70) and the present study. This dataset spanned 35 years (1986-2021) and 3 sites (UK, HS, and Kongsfjorden, KF). KF is another breeding colony of little auks on Svalbard that experiences even warmer SST than HS.</p>
Face processing in the infant brain after pandemic lockdown
<p>The role of visual experience in the development of face processing has long been debated. We present a new angle on this question through a serendipitous study that cannot easily be repeated. Infants viewed short blocks of faces during fMRI in a repetition suppression task. The same identity was presented multiple times in half of the blocks (Repeat condition) and different identities were presented once each in the other half (Novel condition). In adults, the fusiform face area (FFA) tends to show greater neural activity for Novel vs. Repeat blocks in such designs, suggesting that it can distinguish same vs. different face identities. As part of an ongoing study, we collected data before the COVID-19 pandemic and after an initial local lockdown was lifted. The resulting sample of 12 infants (9–24 months) was divided equally into pre-and post-lockdown groups with matching ages and data quantity/quality. The groups had strikingly different FFA responses: pre-lockdown infants showed repetition suppression (Novel > Repeat), whereas post-lockdown infants showed the opposite (Repeat > Novel), often referred to as repetition enhancement. These findings provide speculative evidence that altered visual experience during the lockdown, or other correlated environmental changes, may have affected face processing in the infant brain.</p>
Text-fig. 19. Synchrotron radiation X-ray tomographic microscopy (SRXTM, a–c) of Aristospermum huberi and scanning electron microscope (SEM, d, e) images of Choffaticarpus compactus; Catefica locality, Portugal. a) Volume rendering of strongly flattened, triangular seed with pointed micropylar region; note thin-walled cells of outer integument preserved along the margins of the seed and pitted surface of the crystalliferous inner cells of outer integument where the outer cells are abraded and the narrow, lateral funicle/raphe; b) Volume rendering of seed showing surface of inner integument (endotesta) with cells showing clear imprints of crystals (arrows); c) Longitudinal section (orthoslice yz0241) of seed showing crystalliferous cells of endotesta (white arrows) and the two fiber layers of the tegmen that are perpendicular to each other (inner integument, ii-f, black arrows); d) Fragment of multiparted, apocarpous fruiting structure showing several helically-arranged, laterally flattened, fruitlets; e) Fruitlet in lateral view showing the prominent ventral face with its lateral groove, short attachment scar, and sunken regions of the fruit wall that indicate the probable presence of oil cells. Specimens, Catefica 49-S266049 (a–c), Catefica 49-S172558 (d), Catefica 49-S118675 (e). Scale bars = 300 Μm (a, c–e), 100 Μm (b). in The Early Cretaceous Mesofossil Flora Of Catefica, Portugal: Angiosperms
Text-fig. 19. Synchrotron radiation X-ray tomographic microscopy (SRXTM, a–c) of Aristospermum huberi and scanning electron microscope (SEM, d, e) images of Choffaticarpus compactus; Catefica locality, Portugal. a) Volume rendering of strongly flattened, triangular seed with pointed micropylar region; note thin-walled cells of outer integument preserved along the margins of the seed and pitted surface of the crystalliferous inner cells of outer integument where the outer cells are abraded and the narrow, lateral funicle/raphe; b) Volume rendering of seed showing surface of inner integument (endotesta) with cells showing clear imprints of crystals (arrows); c) Longitudinal section (orthoslice yz0241) of seed showing crystalliferous cells of endotesta (white arrows) and the two fiber layers of the tegmen that are perpendicular to each other (inner integument, ii-f, black arrows); d) Fragment of multiparted, apocarpous fruiting structure showing several helically-arranged, laterally flattened, fruitlets; e) Fruitlet in lateral view showing the prominent ventral face with its lateral groove, short attachment scar, and sunken regions of the fruit wall that indicate the probable presence of oil cells. Specimens, Catefica 49-S266049 (a–c), Catefica 49-S172558 (d), Catefica 49-S118675 (e). Scale bars = 300 Μm (a, c–e), 100 Μm (b).
Fig. 118. Face. A. Lasioglossum puteulanum Gibbs, 2009 in Revision of the Nearctic species of the Lasioglossum (Dialictus) gemmatum species complex (Hymenoptera: Halictidae)
Fig. 118. Face. A. Lasioglossum puteulanum Gibbs, 2009, ♂, slightly longer. B. L. tegulare (Robertson, 1890), ♂, slightly shorter. 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.