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Fig. 1 in The invasive white ginger lily (Hedichium coronarium) simplifies the trait composition of an insect assemblage in the littoral zone of a Savanna reservoir
Fig. 1. Location and characterization of plant composition banks of Fazzari reservoir in the Brazilian Savanna (Cerrado Biome, Brazil).
Fig. 3 in The invasive white ginger lily (Hedichium coronarium) simplifies the trait composition of an insect assemblage in the littoral zone of a Savanna reservoir
Fig. 3. The average values of CWM-trait values of aquatic insect assemblages in invaded and non-invaded banks by white ginger lily of a reservoir in Brazilian Savanna (Cerrado Biome). A – CWM-FFG, B – CWM-feed, C – CWM-habit, D – CWM body length. CWM, Community level Weight-Mean.
Fig. 3 in Diurnal flight periodicity of a Neotropical ant assemblage (Hymenoptera, Formicidae) in the Atlantic Forest
Fig. 3. The relationship between hour and flight activity of ant subfamilies from a Neotropical assemblage captured through a 24 h time scale. The solid lines were obtained by the locally weighted smoother (function loess in R).
Fig. 4 in Diurnal flight periodicity of a Neotropical ant assemblage (Hymenoptera, Formicidae) in the Atlantic Forest
Fig. 4. Phenologies of flight activity of common species of a Neotropical ant assemblage in Atlantic Forest, southeastern of Brazil. Phenologies are the pooled activity from four Malaise traps and hourly sampling from five days.
Fig. 2 in Spatial variation of dung beetle assemblages associated with forest structure in remnants of southern Brazilian Atlantic Forest
Fig. 2. Principal coordinates analysis (PCoA) of dung beetle species based on Bray–Curtis similarity and environmental variables based on Euclidean distance. The analysis was performed using presence–absence (a), abundance (b) and biomass (c) data of dung beetles, and 15 environmental variables (d). ANH: Anhatomirim Environmental Protection Area; ITA: Permanent Protection Areas of Itapema; PER: Peri Lagoon Municipal Park; RAT: Permanent Protection Areas of Ratones.
Fig. 2 in Dung beetle (Coleoptera, Scarabaeidae) assemblage of a highly fragmented landscape of Atlantic forest: from small to the largest fragments of northeastern Brazilian region
Fig. 2. Non-Metric Multidimensional Scaling (NMDS) ordination of fragments of Trapiche, CIMNC and Coimbra, based on dung beetle species composition.
Figure 1 in Effects of forest conversion on tce assemblages' structure of aquatic insects in subtropical regions
Figure 1. Location of tce micro-basin and sampled streams in forested area (F1, F2, and F3) and converted area (C1, C2, and C3) at Parque Estadual do Turvo and adjacent areas, in soutcern Brazil.
Figure 3 in Effects of forest conversion on tce assemblages' structure of aquatic insects in subtropical regions
Figure 3. Ordination diagram of NMDS of Epcemeroptera, Plecoptera, and Triccoptera assemblages at streams in forested area (F) and converted area (C). Numbers 1-3 refer to tce stream; R refers to rocky bottom substrate, and L refers to leaf litter substrate.
Fig. 5 in Benthic Foraminiferal Assemblages and Biotopes in a Coastal Lake: The Case Study of Lake Varano (Southern Italy)
Fig. 5. Distribution of the most abundant species in Lake Varano. The sampling stations are shown here as black dots.
Fig. 3 in Benthic Foraminiferal Assemblages and Biotopes in a Coastal Lake: The Case Study of Lake Varano (Southern Italy)
Fig. 3. Grain size and geochemistry of sediments from Lake Varano. The sampling stations are shown here as black dots.
Fig. 2 in Benthic Foraminiferal Assemblages and Biotopes in a Coastal Lake: The Case Study of Lake Varano (Southern Italy)
Fig. 2. Main physicochemical parameters of the bottom water of Lake Varano. The sampling stations are shown here as black dots.
Text-fig. 4. Dendrogram (Ward's method, squared Euclidean distance) showing the relationship between the studied fossil vegetation assemblages of Hrádek/N. (48), Wackersdorf (49), Berzdorf and Wiesa (50) and the Mydlovary Fm. (51) and the studied modern vegetation units from SE China and Japan (Teodoridis et al. 2011a, 2012, Appendix – this volume). in A Review Of The Early Miocene Mastixioid Flora Of The Kristina Mine At Hrádek Nad Nisou In North Bohemia (The Czech Republic)
Text-fig. 4. Dendrogram (Ward's method, squared Euclidean distance) showing the relationship between the studied fossil vegetation assemblages of Hrádek/N. (48), Wackersdorf (49), Berzdorf and Wiesa (50) and the Mydlovary Fm. (51) and the studied modern vegetation units from SE China and Japan (Teodoridis et al. 2011a, 2012, Appendix – this volume).
Fig. 5 in Foraminiferal Assemblages And Facies Associations In The Upper Jurassic Carbonates From Ardeu Unit (Metaliferi Mountains, Romania)
Fig. 5 Upper Jurassic dasycladalean algae (a-c, e-g), incertae sedis (d), cyanobacteria (h), sponges (j-k), and crustaceans (l) from the Ardeu Unit. a, b Salpingoporella pymaea (Gümbel) (a - Sample 39, b - Sample 167). c Petrascula sp. (Sample 7). d Thaumatoporella parvovesiculifera (Raineri) (arrows) (Sample 56). e Clypeina sulcata (Alth) (Sample 159). f-i Salpingoporella annulata Carozzi (f - Sample 67, i - Sample 41). g Neoteutloporella socialis (Praturlon) (Sample 193). h Rivularia-type cyanobacteria (Sample 69). j Calcistella jachenhausenensis Reitner (Sample 19). k Thalamopora lusitanica Termier & Termier (Sample 79). l Carpathocancer sp. (Sample 61).
Fig. 3 Upper Jurassic foraminifers from the Ardeu Unit. a-c in Foraminiferal Assemblages And Facies Associations In The Upper Jurassic Carbonates From Ardeu Unit (Metaliferi Mountains, Romania)
Fig. 3 Upper Jurassic foraminifers from the Ardeu Unit. a-c Bramkampella arabica Redmond (a - Sample 65, b - Sample 172, c - Sample 146). d Undetermined lituolid (Sample 41). e Kaminskia-type foraminifer with fine canaliculated wall (Sample 66). f-h Everticyclammina praekelleri Banner & Highton (Sample 65). i Alveosepta jaccardi (Schrodt) (Sample 49). j-l Ammobaculites sp. (j - Sample 65, k - Sample 110, l - Sample 95). m-n Charentia evoluta (Gorbachik) (m - Sample 32, n - Sample 45). o-p Protopeneroplis striata Weynschenk (o - Sample 153, p - Sample 212).
Fig. 4 Upper Jurassic foraminifers from the Ardeu Unit. a-c in Foraminiferal Assemblages And Facies Associations In The Upper Jurassic Carbonates From Ardeu Unit (Metaliferi Mountains, Romania)
Fig. 4 Upper Jurassic foraminifers from the Ardeu Unit. a-c Mohlerina basiliensis (Mohler) (a - Sample 31, b - Sample 14, c - Sample 7). d-e Coscinoconus alpinus Leupold (d - Sample 17, e - Sample 21). f Coscinoconus sp. (Sample 110). g-h Troglotella incrustans Wernli & Fookes (g - Sample 10, h - Sample 85). i Troglotella incrustans associated with a Lithocodium aggregatum oncoid (Sample 85). j-k Redmondoides lugeoni (Septfontaine) (j - Sample 138, k - Sample 45). l Lenticulina sp. (Sample 145). m Nautiloculina bronnimanni Arnaud-Vanneau & Peybernès (Sample 174). n Coscinophragma sp. (Sample 182). o Haddonia sp. (Sample 53). p Neokilianina rahonensis (Foury & Vincent) (Sample 115).
Fig. 1 in A Belated Addition To The Paper: & Avram: "The Lower Cretaceous Ammonite Assemblages In The Dâmbovicioara Region", Published In Acta Palaeontologica Romaniae, 4 (2004), Pp. 331-341 Patrulius
Fig. 1 Geological Map of the Dâmbovicioara Region. Legend: 1, Quaternary (alluvial deposits, terraces, gravelites); 2, the Podu Dâmboviței Sandstone (Upper Albian); the Gura Văii Conglomerate (Upper Apțian); 4-6, the Dâmbovicioara Formation: 4*), Valea Muierii Member (uppermost Hauterivian-lowermost Apțian); 5*), Dealul Sasului Member (uppermost Valanginian-Upper Hauterivian); 6, Cetatea Neamțului Member (Upper Valanginian); 7, the Upper Bajocian-Berriasian-? Lower Valanginian deposits; 8, Crystalline basement; 9, boundary of the Quaternary deposits; 10, lithostratigraphic boundary; 11, fault; 12, gorge; 13, cave; 14 ruins of the "Neamțului" fortress; 15, the "Dealul Sasului" Inn; 16, winter-stable, sheep-fold; 17, routes: a, the Bran-Rucăr highway; b, the old comercial route between Vallachia and Transylvania; c, forest roads and paths (noted when necesary for the location of the sites); 18, fossiliferous sites. *) in 4 and 5: a = interbeds of reefal limestones and breccias.
Fig. 4 in A community analysis approach to parasite transmission in multi-host systems: Assemblages of small mammal prey and Echinococcus multilocularis in an urban area in North America
Fig. 4. Map showing the geographic distribution of three small mammal assemblage types predicted for the City of Calgary area by a multinomial logistic regression (MLR) model associating the environmental variables to assemblage types, developed from data collected in 2012 and 2013 (Liccioli et al., 2014). Note how large portion of BWM and NHP were classified as assemblage 1 as expected, but also large portion of FCPP, where it was not expected.
Fig. 1 in A community analysis approach to parasite transmission in multi-host systems: Assemblages of small mammal prey and Echinococcus multilocularis in an urban area in North America
Fig. 1. Study sites for the characterization of the small mammal assemblages in urban Calgary, AB, Canada in 2012–2013, showing the location of five areas in Urban Calgary and detailed map of Bowmont, Southland Lowlands, and Weaselhead. Bowmont (BM), Fishcreek Provincial Park (FCPP), Nose Hill Park (NHP), Southland Lowlands (SL), and Weaselhead (WSH).
Fig. 2 in A community analysis approach to parasite transmission in multi-host systems: Assemblages of small mammal prey and Echinococcus multilocularis in an urban area in North America
Fig. 2. Dendrograms derived from the Bray-Curtis similarity of small mammal assemblages in five parks and natural areas in urban Calgary, AB, Canada, 2012–2013. a) Dendrogram using abundance data and group-average clustering algorithm. The dashed line indicates the cluster cut-off line of 45% similarity. Symbols for each site indicate the prevalence of definitive hosts (EmDH) and presence (1) or absence (0) of infected small mammals (EmIH). b) Dendrogram using abundance data and complete-linkage clustering algorithm. Note how it is similar to the dendrogram using group-average algorithm. c) Dendrogram using proportion data and group-average clustering algorithm. Note how all BM sites are in single cluster and all NHP sites and most sites are in another cluster, similar to the dendrogram using abundance data.
Text-fig. 2. Taphonomic and pathological phenomena of bear bones from Middle Pleistocene deposits from Vykopaná chodba in Za Hájovnou Cave (Moravia, the Czech Republic). a – fragment of left mandibula with pathological condylar process; b – thoracic vertebra with pathological rib facet; c – Mc III dext. with exostoses; d – fragment of juvenile right ulna with bite marks; e – gnawed right tibia with bite marks on proximal part; f – gnawed left calcaneus with bite marks. in Basic Population And Taphonomic Analysis Of Bear Assemblages From Za Hájovnou Cave (Moravia, The Czech Republic): A Fossil Record From 1987-2007
Text-fig. 2. Taphonomic and pathological phenomena of bear bones from Middle Pleistocene deposits from Vykopaná chodba in Za Hájovnou Cave (Moravia, the Czech Republic). a – fragment of left mandibula with pathological condylar process; b – thoracic vertebra with pathological rib facet; c – Mc III dext. with exostoses; d – fragment of juvenile right ulna with bite marks; e – gnawed right tibia with bite marks on proximal part; f – gnawed left calcaneus with bite marks.
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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.