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Figure 2 from: Tajovsky K, Hosek J, Hofmeister J, Wytwer J (2012) Assemblages of terrestrial isopods (Isopoda, Oniscidea) in a fragmented forest landscape in Central Europe. ZooKeys 176: 189-198. https://doi.org/10.3897/zookeys.176.2296
Figure 2 - Epigeic activity (columns) (total catch per 5 traps per year) and numbers of species (white squares) of isopods at the sites studied in the different fragments of woodland.
Figure 1 from: Tajovsky K, Hosek J, Hofmeister J, Wytwer J (2012) Assemblages of terrestrial isopods (Isopoda, Oniscidea) in a fragmented forest landscape in Central Europe. ZooKeys 176: 189-198. https://doi.org/10.3897/zookeys.176.2296
Figure 1 - Total population densities (ind.m-2 ± SE) (columns) and numbers of species (white squares) in the isopod assemblages at the sites sampled in the different fragments of woodland.
Figure 1 from: Vilisics F, Bogyó D, Sattler T, Moretti M (2012) Occurrence and assemblage composition of millipedes (Myriapoda, Diplopoda) and terrestrial isopods (Crustacea, Isopoda, Oniscidea) in urban areas of Switzerland. ZooKeys 176: 199-214. https://doi.org/10.3897/zookeys.176.2153
Figure 1 - Abundances of isopods and millipedes in Zurich, Lucerne and Lugano in logarithmic scale. Dashed line separates isopods (on the left) from millipedes. Black bars represent abundances, white circles show the species' incidences per all sites per city.
Figure 1 from: (2011) Sub-fossil beetle assemblages associated with the "mammoth fauna" in the Late Pleistocene localities of the Ural Mountains and West Siberia. ZooKeys 100: 149-169. https://doi.org/10.3897/zookeys.100.1524
Figure 1 - Geographical location of the study sites in the Ural Mountains and Western Siberia. Numbers of sites: 1 Syoyakha-Mutnaya 2 430 km from Ob 3 Aganskiy uval-1290/2 4 Mega 5 Lokosovo 6 Kul'egan-2247 Point I 7 Kul'egan -2247 Point II 8 Skorodum 9 Andriyshino 10 Nizhnyaya Tavda 11 Mal'kovo 12 Nikitino 13 Shurala. Bold line - Borders of vegetation types, reconstructed for the beginning of MIS 2 on the basis of palynological data: I periglacial tundra II periglacial steppe and forest-steppe III boreal forest and parklands (after Grichuk and Borisova 2009)
Figure 2 from: Mossakowski D, Dormann W (2011) A plea for using qualitative aspects in the interpretation of ecological field data as revealed by carabid beetle assemblages of a pristine salt marsh. ZooKeys 100: 273-286. https://doi.org/10.3897/zookeys.100.1532
Figure 2 - IndVals at different levels in the UPGMA tree. Result for a single species, Dicheirotrichus gustavii, calculated by the original IndVal program. Eight values of the nine levels are significant. Data: abundance/frequency data. 7/4: a total of seven specimens were found in four of the five traps. Sites 102 and 103 are omitted.
Figure 1 from: Mossakowski D, Dormann W (2011) A plea for using qualitative aspects in the interpretation of ecological field data as revealed by carabid beetle assemblages of a pristine salt marsh. ZooKeys 100: 273-286. https://doi.org/10.3897/zookeys.100.1532
Figure 1 - Result of a cluster analysis using Relative Euclidean distances and Ward's method. Most traps of the site at the lowest elevation (-20 cm below MHW) cluster with those of 100 cm above MHW. Arrow: One trap of -20 behaves differently.
Figure 4 from: Sklodowski J, Garbalinska P (2011) Ground beetle (Coleoptera, Carabidae) assemblages inhabiting Scots pine stands of Puszcza Piska Forest: six-year responses to a tornado impact. ZooKeys 100: 371-392. https://doi.org/10.3897/zookeys.100.1360
Figure 4 - Regression distances between carabid assemblages inhabiting post-tornado (disturbed) and control stands during 2003-2008.
Figure 2 from: Sklodowski J, Garbalinska P (2011) Ground beetle (Coleoptera, Carabidae) assemblages inhabiting Scots pine stands of Puszcza Piska Forest: six-year responses to a tornado impact. ZooKeys 100: 371-392. https://doi.org/10.3897/zookeys.100.1360
Figure 2 - Dendrograms of species similarity of carabid beetle assemblages inhabiting tornado-impacted (D) and control stands (C) in age classes I–V (see text) in the first (2003) and last (2008) years of observation. The analysis was performed with the Ward method and Euclidean distance as the measure of similarity.
Figure 1 from: Sklodowski J, Garbalinska P (2011) Ground beetle (Coleoptera, Carabidae) assemblages inhabiting Scots pine stands of Puszcza Piska Forest: six-year responses to a tornado impact. ZooKeys 100: 371-392. https://doi.org/10.3897/zookeys.100.1360
Figure 1 - The proportion of individuals of European carabid species living in tornado-impacted and in control stands during 2003-2008.
Figure 3 from: Mossakowski D, Dormann W (2011) A plea for using qualitative aspects in the interpretation of ecological field data as revealed by carabid beetle assemblages of a pristine salt marsh. ZooKeys 100: 273-286. https://doi.org/10.3897/zookeys.100.1532
Figure 3 - Results of the IndVal procedure depend on the tree used. Data: abundance/frequency of Cillenus lateralis along the elevation gradient. 3/3: a total of three specimens was found in three of the five traps. Sites 102 and 103 are omitted.
Figure 3 from: Sklodowski J, Garbalinska P (2011) Ground beetle (Coleoptera, Carabidae) assemblages inhabiting Scots pine stands of Puszcza Piska Forest: six-year responses to a tornado impact. ZooKeys 100: 371-392. https://doi.org/10.3897/zookeys.100.1360
Figure 3 - The MIB/SPC model of carabid assemblages living in tornado-impacted (D) and control stands (C) during 2003-2008.
Figure 2 from: Kwiatkowski A (2011) Assemblages of carabid beetles (Coleoptera, Carabidae) in humid forest habitats of different stages of succession in the Puszcza Knyszyńska Forest (northeastern Poland). ZooKeys 100: 447-459. https://doi.org/10.3897/zookeys.100.1539
Figure 2 - Relationship between the contribution of forest species and the age of sampled forest stands (Spearman rank correlation coefficient rs=0.696; p=0.001)
Figure 1 from: Kwiatkowski A (2011) Assemblages of carabid beetles (Coleoptera, Carabidae) in humid forest habitats of different stages of succession in the Puszcza Knyszyńska Forest (northeastern Poland). ZooKeys 100: 447-459. https://doi.org/10.3897/zookeys.100.1539
Figure 1 - Location of the sampling plots in the Puszcza Knyszyńska forest. For specifications, see Table 1.
Figure 3 from: Kwiatkowski A (2011) Assemblages of carabid beetles (Coleoptera, Carabidae) in humid forest habitats of different stages of succession in the Puszcza Knyszyńska Forest (northeastern Poland). ZooKeys 100: 447-459. https://doi.org/10.3897/zookeys.100.1539
Figure 3 - Relationship between the contribution of large zoophages and age of the sampled forest stands (Spearman rank correlation coefficient rs=0.485; p<0.05)
Figure 4 from: Kwiatkowski A (2011) Assemblages of carabid beetles (Coleoptera, Carabidae) in humid forest habitats of different stages of succession in the Puszcza Knyszyńska Forest (northeastern Poland). ZooKeys 100: 447-459. https://doi.org/10.3897/zookeys.100.1539
Figure 4 - Multivariate analysis (RDA) carried out with the dataset (number of the sampling plots as in Table 1). See text for explanations.
Figure 1 from: Pétillon J, Georges A, Fouillet P (2011) Changes in salt-marsh carabid assemblages after an invasion by the native grass Elymus athericus (Link) Kerguélen. ZooKeys 100: 407-419. https://doi.org/10.3897/zookeys.100.1537
Figure 1 - Location of the study sites (Mont St-Michel Bay, France). Codes: F 'Ferme Foucault' R 'la Rive'.
Figure 2 from: Pétillon J, Georges A, Fouillet P (2011) Changes in salt-marsh carabid assemblages after an invasion by the native grass Elymus athericus (Link) Kerguélen. ZooKeys 100: 407-419. https://doi.org/10.3897/zookeys.100.1537
Figure 2 - Changes in the percentage of halophilic species in the salt marsh after the invasion by Elymus athericus.
Figure 4 from: Gandhi K, Epstein M, Koehle J, Purrington F (2011) A quarter of a century succession of epigaeic beetle assemblages in remnant habitats in an urbanized matrix (Coleoptera, Carabidae). ZooKeys 147: 667-689. https://doi.org/10.3897/zookeys.147.1954
Figure 4 - Dendrogram for the similarity/dissimilarity in standardized per trap catches of epigaeic beetle assemblages in sampling years 1980 and 2005 (A) and 1981 and 2005 (B) in cottonwood and oak stands, and old fields.
Figure 2 from: Gandhi K, Epstein M, Koehle J, Purrington F (2011) A quarter of a century succession of epigaeic beetle assemblages in remnant habitats in an urbanized matrix (Coleoptera, Carabidae). ZooKeys 147: 667-689. https://doi.org/10.3897/zookeys.147.1954
Figure 2 - Mean (+SE) standardized total catches of epigaeic beetles (A), and Cyclotrachelus sodalis sodalis LeConte (B) caught in 1980 and 2005 in cottonwood (N = 3) and oak (N =4) stands, and old fields (N = 2).
Figure 3 from: Gandhi K, Epstein M, Koehle J, Purrington F (2011) A quarter of a century succession of epigaeic beetle assemblages in remnant habitats in an urbanized matrix (Coleoptera, Carabidae). ZooKeys 147: 667-689. https://doi.org/10.3897/zookeys.147.1954
Figure 3 - Estimated mean species richness of epigaeic beetles using rarefaction analyses in sampling years 1980 and 2005 (A) and 1981 and 2005 (B) in cottonwood and oak stands, and old fields.
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.