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Figure 1 in Host instars preference, density-dependent parasitism and behavioral perspective of parasitoids (Aphidius colemani, Aphidius matricariae and Aphelinus abdominalis) in Aphis glycines and Aphis gossypii
Figure 1: Comparison of parasitoids (Ad.colemani, Ad.matricariae and Al.abdominalis) on different ages (nymphal instars) of the(A) As.glycines (n= 30) and (B) As. gossypii (n= 30).
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 1 in Efficiency of pitfall traps and snap traps in small terrestrial mammals depends on their diet composition
Figure 1. RDA biplot (first two axes) summarizing the effect of sampling method (triangles) on community composition (arrows) of small mammals. The first two eigenvalues were 0.23 and 0.36, respectively.
Figure 9 in The web amount and quality of web spiders (Agelenidae, Pholcidae), Agelena labyrinthica (Clerck, 1757) and Holocnemus pluchei (Scopoli, 1763), depending on food and temperature
Figure 9. Amounts of food consumed by Holocnemus pluchei at 25–30 °C (1: Drosophyla melanogaster; 2: food caught with insect net).
Figure 8 in The web amount and quality of web spiders (Agelenidae, Pholcidae), Agelena labyrinthica (Clerck, 1757) and Holocnemus pluchei (Scopoli, 1763), depending on food and temperature
Figure 8. Food amounts of Holocnemus pluchei at 20–25 °C (1: Drosophila melanogaster; 2: food caught with insect net).
Figure 7 in The web amount and quality of web spiders (Agelenidae, Pholcidae), Agelena labyrinthica (Clerck, 1757) and Holocnemus pluchei (Scopoli, 1763), depending on food and temperature
Figure 7. Food amounts of Agelena labyrinthica at 25–30°C (1: Drosophila melanogaster; 2: food caught with insect net).
Figure 6 in The web amount and quality of web spiders (Agelenidae, Pholcidae), Agelena labyrinthica (Clerck, 1757) and Holocnemus pluchei (Scopoli, 1763), depending on food and temperature
Figure 6. Food amounts of Agelena labyrinthica at 20–25°C (1:Drosophila melanogaster; 2: food caught with insect net). Table 4. The Mann–Whitney U test results of the amounts of food consumed under different conditions.
Figure 20 in Biogeography of marine tintinnid ciliates (Ciliophora, Tintinnida): a Scale-Dependent Model
Figure 20. Results of cluster analysis (Simpson index) of species compositions of tintinnid ciliates in the world's oceans; in nodes of dendrogram, the results of bootstrap-analysis are marked.
Figure 10 in Biogeography of marine tintinnid ciliates (Ciliophora, Tintinnida): a Scale-Dependent Model
Figure 10. Results of cluster analysis (Simpson index) of species compositions of tintinnid ciliates in the Atlantic Ocean; in nodes of dendrogram, the results of bootstrap-analysis are marked.
Figure 23. A in Biogeography of marine tintinnid ciliates (Ciliophora, Tintinnida): a Scale-Dependent Model
Figure 23. A log-log plots of semivariance versus distance for tintinnid alpha-diversity (A – for distances ranged 100 to 2,500 km; B – for distances ranged 1,500 to 16,000 km). DF – fractal dimension; r - correlation coefficient.
Figure 5 in Biogeography of marine tintinnid ciliates (Ciliophora, Tintinnida): a Scale-Dependent Model
Figure 5. Species accumulation curve for tintinnid ciliates diversity in the Black Sea and the Sea of Azov.
Figure 8 in Biogeography of marine tintinnid ciliates (Ciliophora, Tintinnida): a Scale-Dependent Model
Figure 8. Results of cluster analysis (Simpson index) of species compositions of tintinnid ciliates in the Mediterranean Sea; in nodes of dendrogram, the results of bootstrap-analysis are marked.
Figure 14 in Biogeography of marine tintinnid ciliates (Ciliophora, Tintinnida): a Scale-Dependent Model
Figure 14. Results of cluster analysis (Simpson index) of species compositions of tintinnid ciliates in the Indian Ocean; in nodes of dendrogram, the results of bootstrap-analysis are marked.
Figure 6 in Biogeography of marine tintinnid ciliates (Ciliophora, Tintinnida): a Scale-Dependent Model
Figure 6. Results of cluster analysis (Simpson index) of species compositions of tintinnid ciliates in the Black Sea and the Sea of Azov; in nodes of dendrogram, the results of bootstrap-analysis are marked.
Figure 3 in Biogeography of marine tintinnid ciliates (Ciliophora, Tintinnida): a Scale-Dependent Model
Figure 3. Results of cluster analysis (Simpson index) of species compositions of tintinnid ciliates in the Sevastopol Bay; in nodes of dendrogram, the results of bootstrap-analysis are marked.
Figure 2 in Biogeography of marine tintinnid ciliates (Ciliophora, Tintinnida): a Scale-Dependent Model
Figure 2. Species accumulation curve for tintinnid ciliates collected in Sevastopol Bay of the Black Sea.
ScienceDex guides
Understand access before you commit
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.