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Image of sky region around Crab obtained by JEM-X1 instrument in the energy range 3-20 keV.
<p>https://www.astro.unige.ch/cdci/astrooda_?DEC=22.0145&E1_keV=3&E2_keV=20&RA=83.633083333333&T1=2003-03-15T23%3A27%3A40.0&T2=2019-03-16T00%3A03%3A15.0&T_format=isot&detection_threshold=20&instrument=jemx&jemx_num=1&osa_version=OSA10.2&product_type=jemx_image&query_status=new&query_type=Real&radius=5&src_name=Crab&use_scws=no</p> <p> </p>
Appendix Morphometric parameters of Chaetonotus (Chaetonotus) antrumus Kolicka sp. nov. Abbreviations: N = number of specimens or structures analysed; Range = the smallest and the largest structure measurement found among all specimens measured; SD = standard deviation. All measurements are given in micrometers (μm); all indicators are given as a percentage (%) and italicized. in A new species of freshwater Chaetonotidae (Gastrotricha, Chaetonotida) from Obodska Cave (Montenegro) based on morphological and molecular characters
Appendix Morphometric parameters of Chaetonotus (Chaetonotus) antrumus Kolicka sp. nov. Abbreviations: N = number of specimens or structures analysed; Range = the smallest and the largest structure measurement found among all specimens measured; SD = standard deviation. All measurements are given in micrometers (μm); all indicators are given as a percentage (%) and italicized.
Fig. 4 in New narrow-range endemic land snails from the sky islands of northern South Africa (Gastropoda: Streptaxidae and Urocyclidae)
Fig. 4. Ptilototheca soutpansbergensis gen. et sp. nov. A–D. Holotype, diameter 9.2 mm (NMSA V5567/ T4069). E. Protoconch showing sculpture of punctate spiral lines, Entabeni Forest (paratype, NMSA P0186/T4063). F. SEM of protoconch microsculpture, Thathe Vondo Forest (paratype, NMSA W2080/ T4064). Scale bars: E = 0.5 mm; F = 250 µm.
Fig. 13 in New narrow-range endemic land snails from the sky islands of northern South Africa (Gastropoda: Streptaxidae and Urocyclidae)
Fig. 13. Sheldonia wolkbergensis sp. nov., holotype, diameter 7.7 mm, height 5.2 mm (NMSA P0156/ T4074).
Fig. 1 in New narrow-range endemic land snails from the sky islands of northern South Africa (Gastropoda: Streptaxidae and Urocyclidae)
Fig. 1. Gulella davisae sp. nov. A–D. Holotype, height 6.1 mm, diameter 2.9 mm (NMSA P0418/ T4086). E. Juvenile specimen showing apertural dentition, diameter 2.7 mm (paratype, NMSA P0235/ T4091).
Fig. 3 in New narrow-range endemic land snails from the sky islands of northern South Africa (Gastropoda: Streptaxidae and Urocyclidae)
Fig. 3. Gulella hadroglossa sp. nov. A–E. Holotype, height 3.0 mm, diameter 1.5 mm (NMSA P0230/ T4084). F–G. Juvenile specimen showing apertural dentition, diameter 1.5 mm (paratype, NMSA P0417/T4085).
Fig. 10 in New narrow-range endemic land snails from the sky islands of northern South Africa (Gastropoda: Streptaxidae and Urocyclidae)
Fig. 10. Sheldonia monsmaripi sp. nov., living animals. A–B. Mariepskop Forest Reserve, mist-belt forest, shell diameter 11.6 mm (paratype, NMSA P0276/T4073). C–D. Mariepskop Forest Reserve, summit fynbos, shell diameter 16.3 mm (NMSA P0278).
Fig. 7 in New narrow-range endemic land snails from the sky islands of northern South Africa (Gastropoda: Streptaxidae and Urocyclidae)
Fig. 7. Ptilototheca soutpansbergensis gen. et sp. nov., genitalia. A. Entire genital system. B. Basal portion of penis opened to show penial verge and coarsely papillate preputial region. C. Flagellum and epiphallus. D. Spermatophore. A–C. Paratype, NMSA P0304/T4060. D. Paratype, NMSA W2259/T4067.
Fig. 6 in New narrow-range endemic land snails from the sky islands of northern South Africa (Gastropoda: Streptaxidae and Urocyclidae)
Fig. 6. Ptilototheca soutpansbergensis gen. et sp. nov., radula, holotype (NMSA V5567/T4069). A. Rachidian and left lateral teeth. B. Rachidian and innermost lateral teeth. C. Inner left marginal teeth. D. Outer left marginal teeth. Scale bars: A, C = 50 µm; B, D = 25 µm.
Fig. 15 in New narrow-range endemic land snails from the sky islands of northern South Africa (Gastropoda: Streptaxidae and Urocyclidae)
Fig. 15. Sheldonia wolkbergensis sp. nov., radula, holotype (NMSA P0156/T4074). A. Rachidian and lateral teeth. B. Rachidian and innermost lateral teeth. C. Inner marginal teeth. D. Outer marginal teeth. Scale bars: A–C = 50 µm; D = 25 µm.
Neutron powder diffraction data from solid nitrogen in the range 6K-70K
<p>Neutron powder diffraction patterns from nitrogen solidified in-situ. This data accompanies a submitted paper.</p>
Data from: Occupancy patterns and upper range limits of lowland Bornean birds along an elevational gradient
<p>Aim: The traditional view of species' distributions is that they are less abundant near the edges of their ranges and more abundant toward the center. Testing this pattern is difficult because of the complexity of distributions across wide geographical areas. An alternative strategy, however, is to measure species' distributional patterns along elevational gradients. We applied this strategy to examine whether lowland forest birds are indeed less common near their upper range limits on a Bornean mountain, and tested co-occurrence patterns among species for potential causes of attenuation, including signatures of habitat selection and competition at the periphery of their ranges.</p> <p>Location: Mt. Mulu, Borneo</p> <p>Taxon: Rain forest birds Methods: We surveyed lowland forest birds on Mt. Mulu (2,376 m), classified their elevation-occupancy distributions using Huisman – Olff – Fresco (HOF) models, and examined co-occurrence patterns of species pairs for signatures of shared habitat patches and interspecific competition.</p> <p>Results: For 39 of 50 common species, occupancy was highest at sea level then gradually declined near their upper range edges, in keeping with a 'rare periphery' hypothesis. With respect to habitat selection, lowland species do not appear to cluster together at sites of patchy similar habitat near their upper range limits; neither are most lowland species segregated from potential montane competitors where ranges overlap.</p> <p>Main conclusions: High relative abundance at sea level implies that species inhabit 'truncated niches' and are not currently near the limits of their fundamental niche, unless unknown critical response thresholds exist. However, indirect effects of increasing temperature predicted under climate change scenarios could still influence lower range limits of lowland species indirectly by altering habitat, precipitation regimes, and competitive interactions. The lack of non-random co-occurrence patterns implies that patchy habitat and simple pairwise species interactions are unlikely to be responsible for upper range limits in most species; diffuse competition across diverse rain forest bird communities could still play a role.</p>
Figure 2 in New Polypheretima and Pithemera (Oligochaeta: Megascolecidae) species from the Mt. Malindang Range, Mindanao Island, Philippines
Figure 2. Schematic drawings of the external anterio-ventral area of (A) Polypheretima mindanaoensis sp. nov., (B) Pithemera malindangensis sp. nov., (C) Pithemera duminagati sp. nov. and (D) Pithemera donvictorianoi sp. nov. Abbreviations: fp, female pore; cl, clitellum; mp, male pore; gm, genital markings. Scale bars: 5 mm.
Figure 1 in The hermit crab Sympagurus dimorphus (Anomura: Parapaguridae) at the edge of its range in the south-western Atlantic Ocean: population and morphometry features
Figure 1. Sympagurus dimorphus. Densities (number of individuals/100 m2) in the sampling areas from 2002 through 2006. Left column shows presence/absence data including all sampling sites, and right column shows densities on a relative scale.
Figure 1 in Home range and foraging habitat selection by breeding lesser kestrels (Falco naumanni) in Greece
Figure 1. Minimum convex polygon home ranges (outer: 100%, interior: 95% of locations) of male (A) and female (B) lesser kestrels during the breeding season in central Greece, 2008.
Figure 2. Summer core area delineation. The straight line with a in Demographic characteristics, seasonal range and habitat topography of Balkan chamois population in its southernmost limit of its distribution (Giona mountain, Greece)
Figure 2. Summer core area delineation. The straight line with a slope of –1 represents the random use of space within the population seasonal range. The curve that sags below the line of random use represents the clumped use of space. The summer core area can be defined at the point whose tangent has slope –1, e.g. 85%, that is, whose tangent is parallel to the line of random use. This is also the point of the curve that is furthest from the line of random use.
Figure 1 in Range and natural history of point-tailed palmcreepers (Aves: Furnariidae)
Figure 1. Range of point-tailed palmcreepers Berlepschia rikeri based on a wide review of the literature (dark circles), personally examined museum specimens (dark squares), online databases (dark triangles) and unpublished field records (white triangles). The dashed line indicates the range of this species according to Ridgely and Tudor (2009).
Automated vegetation cover estimation from close-range photogrammetric point clouds in mountain terrain for comparison of vegetation location properties - Dataset
<p>Vegetation cover data of the used plots, showing values for manually digitized, in-situ, and photogrammetric methods.</p>
Close range hyperspectral camera dataset with high temporal resolution of strawberry with eco-physiological data of one leaf
<p>This high temporal resolution dataset of a strawberry plant was captured in two experiments, each lasting 100h. On leaf was inserted into a leaf chamber of the LI-6400XT gas exchange system, capturing information on transpiration, photosynthesis and stomatal conductance. Environmental characteristics are also captured at canopy height. These experiments were conducted in a growth chamber at ILVO (Melle, Belgium) and only covered conditions that did not result in stress in the plant. As such, this dataset attempts to capture subtle dynamic variation in the plant.</p>
Molecular species delimitation of larks (Aves: Alaudidae), and integrative taxonomy of the genus Calandrella, with the description of a range-restricted African relic taxon
<p>This deposition contains the phylogenetic and species delimitation data for the manuscript "Molecular species delimitation of larks (Aves: Alaudidae), and integrative taxonomy of the genus <em>Calandrella</em>, with the description of a range-restricted African relic taxon" by Stervander <em>et al</em>. </p> <p>For details of samples/sequences/leaves, please refer to Appendix A of the above manuscript. </p> <p><strong>Phylogenetic analyses</strong></p> <ol> <li>Fasta sequence alignment of cytochrome b for the lark family and outgroups: Alaudidae_cytb_extended_200316.fa</li> <li>BEAST v. 2.6.1 input file: Alaudidae_cytb_HKYGI_BDrelLN_modOp2003_20M1K.xml</li> <li>BEAST v. 2.6.1 output log file: Alaudidae_cytb_HKYGI_BDrelLN_modOp_20M1K.log</li> <li>BEAST v. 2.6.1 output (raw) trees file: Alaudidae_cytb_HKYGI_BDrelLN_modOp_20M1K.trees</li> <li>TreeAnnotator maximum credibility clade tree based on BEAST v. 2.6.1 output, newick format: Alaudidae_cytb_HKYGI_BDrelLN_modOp_20M1K_c40Mbi5.mccmed.nwk</li> </ol> <p><strong>Species delimitation</strong></p> <ol> <li>Input tree, manipulated to remove negative branch lengths (replaced by 0) and tips/leafs that are single representatives of a species, based on current taxonomy (IOC v. 10.2), newick format: Alaudidae_cytb_HKYGI_BDrelLN_c40Mbi5_mccmed_nonNeg_multiSeq_ingroup_remDuplicate.nwk</li> <li>mPTP text output of the multi-rate species delimitation, containing command for run and species delimitation results: Alaudidae200316_cytb_HKYGI_BDrelLN_c40Mbi5_remDuplCaboweni201007_mccmed_delim_varRate_10M_minbrAUTO.1602073064.txt</li> <li>mPTP likelihood log of the multi-rate species delimitation: Alaudidae200316_cytb_HKYGI_BDrelLN_c40Mbi5_remDuplCaboweni201007_mccmed_delim_varRate_10M_minbrAUTO.out.txt</li> <li>mPTP output tree in SVG format, with support values for species delimitation: Alaudidae200316_cytb_HKYGI_BDrelLN_c40Mbi5_remDuplCaboweni201007_mccmed_delim_varRate_10M_minbrAUTO.1602073064.combined.svg</li> </ol>
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.