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Data for the publication "Ozone concentration versus Temperature: Atmospheric aging of soot particles"
<p>The repository contains the data for the paper:</p> <p>Friebel, F and Mensah, A. A. Ozone concentration versus Temperature: Atmospheric aging of soot particles, <em>Langmuir </em> <strong>2019</strong>, 35, 45, 14437–14450 <a href="https://doi.org/10.1021/acs.langmuir.9b02372">https://doi.org/10.1021/acs.langmuir.9b02372</a></p>
Data for Age and socioeconomic status in relation to risk of maternal anemia among the Ariaal of northern Kenya
<p>Data used for a paper entitled, "Age and socioeconomic status in relation to risk of maternal anemia among the Ariaal agropastoralists of northern Kenya"</p>
Racionální užití léků ve stáří (rational use of drugs in geriaric age- EU COST Action IS1402 and EUROAGEISM H2020 project)
<p>During the EU COST Action IS1402 video presentations, the information on ageism in medication use, ageist approaches at regulatory level, at the level of service provision and in rationality of drug prescribing in older adults have been emphasized, as well as main aims of FIP7 project in the EUROAGEISM H2020 (FIP project is entitled "Inappropriate prescribing and availability of medication safety and medication management services in older patients in Europe and other countries"). Video presentation is in national language- Czech. </p>
Fig. 2 in Unusual Age Structure Of The Winter Aggregation Of Nyctalus Noctula (Mammalia, Chiroptera) In Kyiv
Fig. 2. Age of common noctule bats in the examined sample: A — total sample, n = 113, the model of the logarithmic regression is indicated with the line; B — females, n = 31; C — males, n = 77.
Fig. 1 in The Study Of Age-Related Variability Of Pigmentation Patterns Of The Shells Of Dreissena Polymorpha (Bivalvia, Dreissenidae) From Different Parts Of It'S Range
Fig. 1. Change of pattern types on zebra mussel shell. The present shell has four age zones (0+, 1+, 2+, 3+). The pattern sequence is С–АС–А–А.
Figure 6 in Age, growth, and reproductive biology of Atlantic bonito (Sarda sarda Bloch, 1793) from the Turkish coasts of the Black Sea and the Sea of Marmara
Figure 6. Micrographs from gonad cross-sections of immature stage (a), nonspawning mature stage (b), spawning stage (c), and postovulatory stage (d).
Figure 1 in Age, growth, and reproductive biology of Atlantic bonito (Sarda sarda Bloch, 1793) from the Turkish coasts of the Black Sea and the Sea of Marmara
Figure 1. Length–frequency distribution for females, males, unidentified specimens, and all samples of S. sarda (n = 212).
Figure 1 in The body size, age structure, and growth of Bosc's fringe-toed lizard, Acanthodactylus boskianus (Daudin, 1802)
Figure 1. Cross-sections (18 µm thick) at the diaphysis level of a phalange of juvenile (A) and male (B) Acanthodactylus boskianus. A) Four-year-old juvenile, 45.14 mm body length. Four LAGs were observed in the periosteal bone. B) Eight-yearold male, 79.86 mm body length. Eight LAGs were observed in the periosteal bone (arrow heads). Endosteal resorption and endosteal bone were present. Periphery (black arrow) was not regarded as a LAG (m.c. = marrow cavity, r.l. = reversal line, e.r. = endosteal resorption, e.b. = endosteal bone).
Figure 4 in Age-dependent variations in the venom proteins of Vipera kaznakovi Nikolsky, 1909 and Vipera ammodytes (Linnaeus, 1758) (Ophidia: Viperidae)
Figure 4. Gel photograph showing the electrophoretic separation of the venom protein sample obtained from the 55-cm-long Vipera kaznakovi specimen, together with its densitometric tracing curve. For further explanation, see caption of Figure 2.
Figure 1 in Age-dependent variations in the venom proteins of Vipera kaznakovi Nikolsky, 1909 and Vipera ammodytes (Linnaeus, 1758) (Ophidia: Viperidae)
Figure 1. Polyacrylamide gel electrophoresis of venoms of V. kaznakovi of different lengths. A. 16.5 cm, B. 30 cm, C. 55 cm (S: Start, junction between the stacking and separation gels).
Figure 3 in Age-dependent variations in the venom proteins of Vipera kaznakovi Nikolsky, 1909 and Vipera ammodytes (Linnaeus, 1758) (Ophidia: Viperidae)
Figure 3. Gel photograph showing the electrophoretic separation of the venom protein sample obtained from the 30-cm-long Vipera kaznakovi specimen, together with its densitometric tracing curve. For further explanation, see caption of Figure 2.
Figure 8 in Age-dependent variations in the venom proteins of Vipera kaznakovi Nikolsky, 1909 and Vipera ammodytes (Linnaeus, 1758) (Ophidia: Viperidae)
Figure 8. Gel photograph showing the electrophoretic separation of the venom protein sample obtained from the 51.5-cm-long Vipera ammodytes specimen, together with its densitometric tracing curve. For further explanation, see caption of Figure 2.
Figure 5 in Age-dependent variations in the venom proteins of Vipera kaznakovi Nikolsky, 1909 and Vipera ammodytes (Linnaeus, 1758) (Ophidia: Viperidae)
Figure 5. Polyacrylamide gel electrophoresis of venoms of V. ammodytes of different lengths. A. 28.5 cm, B. 36.7 cm, C. 51.5 cm (S: Start, junction between the stacking and separation gels).
Figure 2 in Age structure and body size of the Strauch's racerunner, Eremias strauchi strauchi Kessler, 1878
Figure 2. Age frequency distributions for males and females of an Eremias strauchi strauchi sample population.
Figure 5 in Age and growth of swordfish (Xiphias gladius L.) in the Aegean Sea
Figure 5. Von Bertalanffy growth curve fitted by length-at-age for swordfish, Xiphias gladius, in the Aegean Sea.
Fig. 1 in Helminths in common eiders (Somateria mollissima): Sex, age, and migration have differential effects on parasite loads
Fig. 1. Distributions of breeding and wintering populations of S. m. borealis, S. m. dresseri, and S. m. sedentaria in North America and Greenland. Populations of S. m. borealis are wintering in two areas in the pictured region; one in Southwest Greenland and one in East Canada (Newfoundland and Labrador). Individuals wintering in Southwest Greenland migrate to breed in West Greenland or Arctic Canada, whereas individuals wintering in East Canada have breeding areas in Arctic Canada (illustrated by the different direction of the red diagonal lines). For S. m. dresseri the breeding and wintering ranges overlap in one area that covers Newfoundland and Labrador as well as the northeastern part of the US, as shown by the grey horizontal lines. The subspecies S. m. sedentaria has its year-round residence in the Hudson Bay area as shown by the blue vertical lines. Dark stars mark the sampling locations of eiders in this study, whereas the white star marks the sampling location of eiders by Tourangeau et al. (2018). (For interpretation of the references to colour in this figure legend, the reader is referred to the Web version of this article.)
Fig. 3 in Helminths in common eiders (Somateria mollissima): Sex, age, and migration have differential effects on parasite loads
Fig. 3. Prevalences of the cestodes Lateriporus sp. (A) and Microsomacanthus spp. (B), and the acanthocephalan Profilicollis sp. (C) in common eiders. Abbreviations: bor, CD = S. m. borealis, Cape Dorset; bor, GRLD = S. m. borealis, Greenland; bor, NFLD = S. m. borealis, Newfoundland; dre, NFLD = S. m. dresseri, Newfoundland; sed, BI = S. m. sedentaria [data published in Tourangeau et al. (2018)]. n-m = non-migratory, po-m = post-migratory, prm = pre-migratory. Letters describe significant differences between groups: if two groups share a letter, there is no significant difference in their prevalences.
Fig. 2 in Helminths in common eiders (Somateria mollissima): Sex, age, and migration have differential effects on parasite loads
Fig. 2. Examples of gastrointestinal parasites retrieved from common eiders in this study. (A) The trematode Notocotylus sp., (B) the cestode Lateriporus sp., (C) the acanthocephalan, Profilicollis sp. (D) microphallid trematodes, and (E) Microsomacanthus spp. cestodes.
Fig. 5 in Helminths in common eiders (Somateria mollissima): Sex, age, and migration have differential effects on parasite loads
Fig. 5. Cumulative percentages of birds infected with (A) Microsomacanthus spp., (B) Microphallus spp. and (C) Gymnophallus spp. from five different locations. Legend denotes the five infection levels: 0, 1s, 10s, 100s, and 1000s of parasite individuals within a single host. Abbreviations: bor, GRLD = S. m. borealis, Greenland; bor, NFLD = S. m. borealis, Newfoundland; dre, NFLD = S. m. dresseri, Newfoundland; bor, CD = S. m. borealis, Cape Dorset; sed, BI = S. m. sedentaria, Belcher Islands [data published in (Tourangeau et al., 2018)]. nm = non-migratory, po-m = post-migratory, pr-m = pre-migratory.
Figure 5 in Diurnal activity pattern of age-sex groups of a small and fragmented population of Blackbuck (Antilope cervicapra L.) in Western Haryana, India
Figure 5. Behavioural activities recorded for sub adult male vs. total time spent during different season(s).
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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.