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Figure 2 in Economic injury level of date spider mite, Oligonychus afrasiaticus (Acari: Tetranychidae) on six commercial date cultivars
Figure 2. Regression between mite-day as an independent variable and fruits injury rate as a dependent variable in the different date cultivars studied in 2018.
Figure 8 in Egyptian Funerary Boat Model in the Australian Museum: Dating and Analysis
Figure 8. Section of canopy with red and black vertical lines; in places the black over-paint (earlier) red lines. Photo by Stuart Humphreys (Australian Museum), adapted by S. Florek.
Figure 7 in Egyptian Funerary Boat Model in the Australian Museum: Dating and Analysis
Figure 7. Boat model port (left side)—mummy is facing the wrong way. Photo from 1970s, Australian Museum.
Figure 6 in Egyptian Funerary Boat Model in the Australian Museum: Dating and Analysis
Figure 6. Figures on board, showing separately attached arms, belt around the waist (figure on the right), dark hair
Figure 4 in Egyptian Funerary Boat Model in the Australian Museum: Dating and Analysis
Figure 4. Back of ram's head showing two bases of broken horns, one in the left—solid timber, the right one with hole for pegging horn extension. Photo by Heather Bleechmore.
Figure 11 in Egyptian Funerary Boat Model in the Australian Museum: Dating and Analysis
Figure 11. Scanning electron micrograph of a tangential longitudinal section of Ziziphus spina-christi (sidr) wood. Electron micrograph by C. R. Cartwright, The British Museum.
Figure 1 in Egyptian Funerary Boat Model in the Australian Museum: Dating and Analysis
Figure 1. Funerary boat model (E60381), portboard (left side)—mummy is facing the wrong way. Photo by Stuart Humphreys (Australian Museum, Sydney). See also Plate 1.
Figure 3. X in Egyptian Funerary Boat Model in the Australian Museum: Dating and Analysis
Figure 3. X-ray showing two holes drilled in ram's head, horizontal for pegging horn protrusion and vertical for inserting head insignia. Image by Paula Dredge, adapted by S. Florek.
UAV observations of the NDVI, snow depth and melt out date, retreived ar the Izas Experimental Catchment in 2020 and 2021
<p>This dataset includes very high spatial resolution observations at 1 m spatial resolution observations of the snow depth, the NDVI and the melt-out date (DOY of year) acquired with an Unmanned Aerial Vehicle at a sub-alpine site in the Pyrenees, the Izas Experimental Catchment. During two snow seasons (2019-2020 and 2020-2021), 14 NDVI and 17 snow depth distributions were acquired over 48ha. From the snow depth observations the melt-out dates have been derived. Also information on the main topographic variables (elevation, aspect and slope) is included, with same spatial resolution, in this dataset.</p>
Stable isotopes and radiocarbon dating results on Late Pleistocene red deer and horse from the Serinyà caves (Girona, Catalonia, Spain)
<p>Table 1: Minimum (Min), maximum (Max), mean and standard-deviations (SD) of <em>δ</em><sup>13</sup>C<sub>carb</sub> and <em>δ</em><sup>18</sup>O<sub>carb</sub> values per horse and red deer tooth. Numbers in bold indicate isotopic values corresponding to peaks (summer) or troughs (winter) detected from clear sinusoidal patterns in <em>δ</em><sup>18</sup>O<sub>carb</sub> values. Numbers in bold correspond to minimum and maximum values in teeth revealing a sinusoidal pattern. LM3 and UM3 stand for lower third molar and upper third molar, respectively. LM2 stands for lower second molar. R is for the right side, L is for the left side. N: number of analyses.</p> <p>Table 2: Minimum, maximum, mean and standard-deviations of <em>δ</em><sup>13</sup>C<sub>coll</sub>, <em>δ</em><sup>15</sup>N<sub>coll</sub> for horse and red deer per technocomplex phases. na stands for not applicable. N: number of samples.</p> <p>Table A.1: Detailed isotopic results (<em>δ</em><sup>13</sup>C<sub>carb</sub> and <em>δ</em><sup>18</sup>O<sub>carb</sub>) for horse teeth with incremental sampling. Underlined numbers correspond to outlier data. Brackets are added around isotopic values that are not considered for further interpretation. R stands for the right side, L is for the left side.</p> <p>Table A.2: Detailed isotopic results (<em>δ</em><sup>13</sup>C<sub>carb</sub> and <em>δ</em><sup>18</sup>O<sub>carb</sub>) for red deer teeth with incremental sampling. Underlined numbers correspond to outlier data. Brackets are added around isotopic values that are not considered reliable for further interpretation. R is for the right side, L is for the left side.</p> <p>Table A.3: Results of elemental analysis on bone or dentine (N<sub>bone or dentine</sub>) and collagen (C<sub>coll</sub>, N<sub>coll</sub>, C:N<sub>coll</sub>) and of isotopic analysis on collagen (<em>δ</em><sup>13</sup>C<sub>coll</sub>, <em>δ</em><sup>15</sup>N<sub>coll</sub>) from horse (<em>Equus ferus</em>), red deer (<em>Cervus elaphus</em>) at the Serinyà caves. Underlined numbers correspond to outlier data. Brackets are added around isotopic values that are not considered reliable for further interpretation. R is for the right side, L is for the left side. * species determination confirmed by ZooMS analysis. Tüb. stands for Tübingen and NU for National University.</p> <p>Table A.4: Results of elemental analysis on bone or dentine (N<sub>bone or dentine</sub>) and collagen (C<sub>coll</sub>, N<sub>coll</sub>, C:N<sub>coll</sub>) and of isotopic analysis on collagen (<em>δ</em><sup>13</sup>C<sub>coll</sub>, <em>δ</em><sup>15</sup>N<sub>coll</sub>) from large bovids (<em>Bos/Bison</em>) and muskox (<em>Ovibos moschatus</em>) at the Serinyà caves. Underlined numbers correspond to outlier data. Brackets are added around isotopic values that are not considered reliable for further interpretation. R is for the right side, L is for the left side. * species determination confirmed by ZooMS analysis. Tüb. stands for Tübingen.</p> <p>Table A.5: Results of elemental analysis on collagen (C<sub>coll</sub>, N<sub>coll</sub>, C:N<sub>coll</sub>) and of isotopic analysis on collagen (<em>δ</em><sup>13</sup>C<sub>coll</sub>,<em>δ</em><sup>15</sup>N<sub>coll</sub>) and radiocarbon dates (<sup>14</sup>C) from horse (<em>Equus ferus</em>), red deer (<em>Cervus elaphus</em>), reindeer (<em>Rangifer tarandus</em>), muskox (<em>Ovibos moschatus</em>), rabbit (<em>Oryctolagus cuniculus</em>) and human (<em>Homo sapiens</em>) at the Serinyà caves. R is for the right side, L is for the left side. * species determination confirmed by ZooMS analysis. na stands for not applicable, nd for not determined and ind for indetermined.</p>
Logratio table of in-situ U-Th-4He/3He dated Fish Canyon zircon
<p>The U-Th-He logratio compositions of 61 Fish Canyon zircons dated by laser microprobe analysis using proton-induced 3He as a proxy for ablation pit volume.</p>
Data from: Snowmelt and laying date shape the parental care strategy of a high-Arctic shorebird
<p>Parental care varies across animal taxa, from uniparental to biparental care, driven by ecological and social factors such as weather, food availability, predation, and partner availability. Understanding this diversity within species can reveal biotic and abiotic conditions allowing uniparental versus biparental strategies. This study examines the impact of biotic and abiotic factors on parental care strategies in Sanderlings (<em>Calidris alba</em>), one of the few species that uses both types of care. Using long-term data from Greenland (2011-2023), path analyses revealed that laying date and snowmelt influence parental care strategies, with indirect climatic effects during migration and on breeding grounds. We observed a greater proportion of uniparental nests in years with delayed laying dates, and a greater proportion of biparental nests in years with delayed snowmelt. These findings underscore the complex interplay between environmental factors and parental care strategies, offering insights into how these strategies may evolve under changing ecological conditions.</p>
Figure 2 in Indotyphlops braminus (Daudin, 1803): distribution and oldest record of collection dates in Oceania, with report of a newly established population in French Polynesia (Tahiti Island, Society Archipelago)
Figure 2. Anterior ventral area of Indotyphlops braminus MNHN-RA 2015.0057 showing the whitish gular coloration. Picture: I. Ineich.
Figure 1 in Indotyphlops braminus (Daudin, 1803): distribution and oldest record of collection dates in Oceania, with report of a newly established population in French Polynesia (Tahiti Island, Society Archipelago)
Figure 1. Two introduced specimens of Indotyphlops braminus from Tahiti Island in French Polynesia. MNHN-RA 2015.0058 above and MNHN-RA 2015.0057 below. Scale bar: 1cm. Picture: I. Ineich.
Lithic, faunal, and radiocarbon dating data from Bukhtarma Cave, East Kazakhstan
<p>Data associated with the paper "<span>A newly dated late Pleistocene and Holocene archaeological assemblage from Bukhtarma Cave in the southern Altai piedmont, East Kazakhstan," containing the zooarchaeological identification and analysis, the lithic analysis, and the radiocarbon dates obtained from the 14C dating lab of the Curt Engelhorn Zentrum für Archäometrie, Mannheim, Germany (co-author S. Lindauer). </span></p>
FIGURE 8 in A new perspective on the molecular dating of the brown trout complex with an extended phylogeographic information on the species in Serbia
FIGURE 8 Simplified palinspastic map for the Pliocene (compiled and modified after Popov et al., 2004, 2006; Neubauer et al., 2015) with the indication of hypothetic BT colonization routes (arrows). Interrupted lines mark migration routes that are, in our opinion, less likely. Green areas represent brackish environments, light blue freshwater lakes or marshes and rivers, dark blue seas, dark gray mountain ranges, and light gray land mass; all geographic features are tentatively positioned. 1 – Ancestral trout originated in the Ponto-Caspian system and crossed from the paleo-Danube into the Western Mediterranean basin via stream capture of Alpine rivers in Pliocene; 2 – Ancestral trout originated in the Balkans basin and colonized other parts of the Mediterranean Basin from here; 3 – Colonization of the Central Alps took place in the Pliocene after the paleo-Rhône separated from the paleo-Danube and reached the Mediterranean; 4 – Atlantic basin was colonized when the Rhine captured Central Alpine rivers; 5 – Atlantic basin was colonized along the Mediterranean coastline and via Gibraltar; 6 – Ponto-Caspian basin was colonized from the Mediterranean basin following a presumed sea corridor in the upper Euphrates valley or using the paleo-Euphrates, which might have been connected with the Mediterranean until the Middle Pliocene; 7 – Ponto-Caspian basin was colonized via a possible Pliocene gateway that connected the Dacic basin and the Aegean Sea; 8 – Ponto-Caspian basin was colonized through the Bosphorus gateway.
FIGURE 6 in A new perspective on the molecular dating of the brown trout complex with an extended phylogeographic information on the species in Serbia
FIGURE 6 Split graph of the Neighbor-Net phylogenetic network analysis of brown trout lineages. The colors of the haplotypes represent different lineages, and the scale bar represents the nucleotide substitutions per site.
FIGURE 4 in A new perspective on the molecular dating of the brown trout complex with an extended phylogeographic information on the species in Serbia
FIGURE 4 Median-joining network of CR mtDNA sequences belonging to Danubian haplogroups. Haplotypes are represented by colored circles whose size is proportional to haplotype frequencies detected and taken from the literature (supplementary tables S2 and S3). Haplotypes from this study are bolded and framed. Mutations are represented by hatch marks on the lines connecting the haplotypes. Missing or theoretical haplotypes are shown as black dots. The maps show the distribution of haplotypes from the network (A – DA-ES haplotypes, B – DA-INT haplotypes, C – DA-BS haplotypes), and their numbering corresponds to that in supplementary table S2.
FIGURE 3 in A new perspective on the molecular dating of the brown trout complex with an extended phylogeographic information on the species in Serbia
FIGURE 3 Reconstruction of the sequence evolution in the Danubian lineage. Defining variable nucleotide sites in the control region are all placed nearby in the central part of the control region, between the nucleotide positions 540-550 of our alignment. The 542 G → C transversion defines the split of the DAES + DA-INT and the DA-BS; 541 G → A split of the DA-ES + DA-INT (excluding DaBS9) from the DaBS9 haplotype; and 548 C → T defines the DA-ES.
figure 2 The dated phylogenetic trees using the cytb gene for G. subgutturosa. Blue bars show 95 in Unraveling goitered gazelle (Gazella subgutturosa) diversification: insights from phylogeography and species distribution modeling
figure 2 The dated phylogenetic trees using the cytb gene for G. subgutturosa. Blue bars show 95% highest posterior density intervals of the estimated node ages; numbers next to the nodes are mean node ages (Mya). The red and green lines show new haplotypes from this study.
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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.