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6,175 results for “Composition”
Figure 7 from: Sublett CA, Cook JL, Janovec JP (2019) Species richness and community composition of sphingid moths (Lepidoptera: Sphingidae) along an elevational gradient in southeastern Peru. Zoologia 36: 1-11. https://doi.org/10.3897/zoologia.36.e32938
Figure 7 Breakpoint regression analysis for (log)elevation with estimated species richness. Vitobamba (800 m), which was the break point, is included in both graphs. The characteristic mid-elevation unimodal richness pattern can be seen with the increase in species richness with elevation up to Vitobamba (r2 = 0.953, p = 0.139), and the decrease in species richness with elevation above Vitobamba (r2 = 0.999, p = 0.003).
Figure 2 from: Sublett CA, Cook JL, Janovec JP (2019) Species richness and community composition of sphingid moths (Lepidoptera: Sphingidae) along an elevational gradient in southeastern Peru. Zoologia 36: 1-11. https://doi.org/10.3897/zoologia.36.e32938
Figure 2 The relationship between elevation and species richness. There is a clear low-elevation skewed unimodal pattern, which peaks around 800 m.
FIGURE 3. Adult Hapalogenys analis, 142 in Phylogenetic position of the fish genera Lobotes, Datnioides and Hapalogenys, with a reappraisal of acanthuriform composition and relationships based on adult and larval morphology
FIGURE 3. Adult Hapalogenys analis, 142 mm SL, Saikung, Hong Kong. Photo by J.E. Randall.
FIGURE 2 in Phylogenetic position of the fish genera Lobotes, Datnioides and Hapalogenys, with a reappraisal of acanthuriform composition and relationships based on adult and larval morphology
FIGURE 2. Adult Datnioides pulcher, ca. 250 mm SL, aquarium specimen. Photo by B. Lee.
FIGURE 4. Larval Lobotes surinamensis, 5.9 in Phylogenetic position of the fish genera Lobotes, Datnioides and Hapalogenys, with a reappraisal of acanthuriform composition and relationships based on adult and larval morphology
FIGURE 4. Larval Lobotes surinamensis, 5.9 mm SL (after Watson 1996).
FIGURE 6. Larval Hapalogenys nitens, 7.3 in Phylogenetic position of the fish genera Lobotes, Datnioides and Hapalogenys, with a reappraisal of acanthuriform composition and relationships based on adult and larval morphology
FIGURE 6. Larval Hapalogenys nitens, 7.3 mm SL, from Japan (after Kinoshita 1988).
Figure 2 from: Costa-Campos CE, Freire EMX (2019) Richness and composition of anuran assemblages from an Amazonian savanna. ZooKeys 843: 149-169. https://doi.org/10.3897/zookeys.843.33365
Figure 2 Rainfall data and minimum and maximum temperatures at the Experimental Field of the Brazilian Agricultural Research Corporation – EMBRAPA, municipality of Macapá, Amapá State, northern Brazil between January and December 2009, 2010, and 2013.
Figure 5 from: Costa-Campos CE, Freire EMX (2019) Richness and composition of anuran assemblages from an Amazonian savanna. ZooKeys 843: 149-169. https://doi.org/10.3897/zookeys.843.33365
Figure 5 Dendrogram of similarity between the savanna area physiognomies, sampled in the Experimental Field of the Brazilian Agricultural Research Corporation – EMBRAPA, municipality of Macapá, Amapá State. Group A (open woodland savanna, OW), Group B (Parkland savanna, PS), and Group C (grassland savanna, GS and scrub grassland savanna, SG).
Figure 4 from: Costa-Campos CE, Freire EMX (2019) Richness and composition of anuran assemblages from an Amazonian savanna. ZooKeys 843: 149-169. https://doi.org/10.3897/zookeys.843.33365
Figure 4 The species accumulation curves sampled in the savanna area from the Experimental Field of the Brazilian Agricultural Research Corporation – EMBRAPA, municipality of Macapá, Amapá State, northern Brazil, for each of the sampled physiognomies: A grassland savanna B scrub grassland savanna C parkland savanna D open woodland savanna, based on the number of individuals representing the observed (Sobs) and estimated species richness (Jackknife 1).
Figure 1 from: Costa-Campos CE, Freire EMX (2019) Richness and composition of anuran assemblages from an Amazonian savanna. ZooKeys 843: 149-169. https://doi.org/10.3897/zookeys.843.33365
Figure 1 Maps showing the Amapá state and sampling sites in the Experimental Field of the Brazilian Agricultural Research Corporation – EMBRAPA, municipality of Macapá, Amapá State, northern Brazil.
Figure 3 from: Costa-Campos CE, Freire EMX (2019) Richness and composition of anuran assemblages from an Amazonian savanna. ZooKeys 843: 149-169. https://doi.org/10.3897/zookeys.843.33365
Figure 3 Anurans recorded in the savanna area from the Experimental Field of the Brazilian Agricultural Research Corporation – EMBRAPA, municipality of Macapá, Amapá State, northern Brazil: ARhinellamajorBRhinella sp. CR.marinaDBoanamultifasciataEB.punctataFB.ranicepsGDendropsophuscf.walfordiHOsteocephalustaurinusIScinaxfuscomarginatusJS.nebulosusKS.ruberLS.x-signatusMTrachycephalustyphoniusNPseudopaludicolabolivianaOAdenomerahylaedactylaPLeptodactylusfuscusQL.macrosternumRL.pentadactylusSL.podicipinusTPithecopushypochondrialis, and UElachistocleishelianneae.
Figure 6 from: Costa-Campos CE, Freire EMX (2019) Richness and composition of anuran assemblages from an Amazonian savanna. ZooKeys 843: 149-169. https://doi.org/10.3897/zookeys.843.33365
Figure 6 Order by MDS of physiognomies in the savanna area physiognomies, sampled in the Experimental Field of the Brazilian Agricultural Research Corporation – EMBRAPA, municipality of Macapá, Amapá State generated from the Bray-Curtis similarity matrix. Grassland savanna (GS); scrub grassland savanna (SG); parkland savanna (PS); open woodland savanna (OW).
Supplementary material 3 from: Petřík P, Sádlo J, Hejda M, Štajerová K, Pyšek P, Pergl J (2019) Composition patterns of ornamental flora in the Czech Republic. NeoBiota 52: 87-109. https://doi.org/10.3897/neobiota.52.39260
: Data type: statistical data
Supplementary material 2 from: Petřík P, Sádlo J, Hejda M, Štajerová K, Pyšek P, Pergl J (2019) Composition patterns of ornamental flora in the Czech Republic. NeoBiota 52: 87-109. https://doi.org/10.3897/neobiota.52.39260
: Data type: measurement
Supplementary material 1 from: Petřík P, Sádlo J, Hejda M, Štajerová K, Pyšek P, Pergl J (2019) Composition patterns of ornamental flora in the Czech Republic. NeoBiota 52: 87-109. https://doi.org/10.3897/neobiota.52.39260
: Data type: species data
Fig. 3 in Variability Of The Phenotypic Composition Of Cepaea Hortensis (Gastropoda, Helicidae) In Western Ukraine: In Space And Time
Fig. 3. Location of all (main and additional) sites in Lviv, where only the variants of shell coloration common for Western Ukraine (A) or any other coloration variants (B) were registered in 2015–2021.
Fig. 2 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. 2. The average values of FD indices of aquatic insect assemblages in invaded and non-invaded bank by white ginger lily of a reservoir in Brazilian Savanna (Cerrado Biome). A – FDis, B – FEve, C – FDiv. FD, Functional Diversity; FDis, Functional Dispersion; FEve, Functional Evenness; FDiv, Functional Divergence.
Figure 3 in The amount of mulch increases the abundance, and its composition the species diversity of springtails in crop rotation on chernozem soils
Figure 3. Effect of the mulch amount and composition on groups of life forms. – epigeic, – hemiedaphic, — euedaphic. (A) plant residues of peas, (B) plant residues of wheat.
Figure 5 in The amount of mulch increases the abundance, and its composition the species diversity of springtails in crop rotation on chernozem soils
Figure 5. Species-treatment plot resulting from redundancy analyses (RDA) of Collembola community composition.
Figure 5 in Seasonal composition and population density of zooplankton in Lake Karaboğaz from the Kızılırmak Delta (Samsun, Turkey)
Figure 5. Canonical correspondence ordination of the zooplankton samples collected at 6 different stations and associated environmental parameters. Biplots of the species (occurrence frequency of>63%) and the environmental parameters. A = Coronatella rectangula, B = Chydorus sphaericus, C = Colurella adriatica, D = Keratella quadrata, E = Lecane closterocerca, F = Lecane luna, G = Notholca acuminata, H = Polyarthra vulgaris, J = Brachionus calyciflorus, K = Colurella obtusa, L = Cephalodella ventripes, and M = Lepadella quadricarinata.
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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.