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19,493 results for “Populism”
Figure 4 in Population biology of the ghost shrimps, Trypaea australiensis and Biffarius arenosus (Decapoda: Thalassinidea), in Western Port, Victoria.
Figure 4. Carapace length (CL) size frequency distributions for Trypaea australiensis collected at Crib Point, Western Port in 2006-2007. Nonovigerous females are shown by black bars, ovigerous females by grey bars and males by open bars (n = number of shrimp collected). Individuals are grouped into size classes by rounding to the closest mm from two decimal places. Arrows show mean CL of the cohorts using FISAT II.
Figure 2 in Population biology of the ghost shrimps, Trypaea australiensis and Biffarius arenosus (Decapoda: Thalassinidea), in Western Port, Victoria.
Figure 2. Carapace length (CL) size frequency distributions for Trypaea australiensis collected at Warneet, Western Port in 2004-2005. Non-ovigerous females are shown by black bars, ovigerous females by grey bars and males by open bars (n = number of shrimp collected). Individuals are grouped into size classes by rounding to the closest mm from two decimal places. Arrows show mean CL length of the cohorts identified using FISAT II
Figure 3 in Population biology of the ghost shrimps, Trypaea australiensis and Biffarius arenosus (Decapoda: Thalassinidea), in Western Port, Victoria.
Figure 3. Carapace length (CL) size frequency distributions for Trypaea australiensis collected at Warneet, Western Port in 2006-2007. Non-ovigerous females are shown by black bars, ovigerous females by grey bars and males by open bars (n = number of shrimp collected). Individuals are grouped into size classes by rounding to the closest mm from two decimal places. Arrows show the mean CL length of cohorts identified using FISAT II.
FIG. 5 in Expressed sex ratio in populations of the moss Hamatocaulis vernicosus (Mitt.) Hedenäs (Scorpidiaceae) in the Czech Republic with consideration of its cryptic species
FIG. 5. — The sex ratio in mixed population at locality Zhůří 1. Unbordered pie charts refer to clade 1, bordered ones represent clade 2. The patch in the larger circle contained plants of both clades, so this patch must be excluded from evaluating sex ratio in separated clades.
FIG. 3 in Expressed sex ratio in populations of the moss Hamatocaulis vernicosus (Mitt.) Hedenäs (Scorpidiaceae) in the Czech Republic with consideration of its cryptic species
FIG. 3. — Rates of male (blue), female (red) and non-expressing (green) plants at studied localities of Hamatocaulis vernicosus (Mitt.) Hedenäs clade 1 and 2.
FIG. 2 in Expressed sex ratio in populations of the moss Hamatocaulis vernicosus (Mitt.) Hedenäs (Scorpidiaceae) in the Czech Republic with consideration of its cryptic species
FIG. 2. — The expressed sex ratio at studied localities of H. vernicosus (Mitt.) Hedenäs. In mixed populations,only single-clade patches were used for the assessment.
FIG. 4 in Expressed sex ratio in populations of the moss Hamatocaulis vernicosus (Mitt.) Hedenäs (Scorpidiaceae) in the Czech Republic with consideration of its cryptic species
FIG. 4.— Sex ratio at localities with co-occurring cryptic species. All, without distinguished clades; cl. 1, clade 1; cl. 2, clade 2; Šimanov, Šimanovské rašeliniště. Only barcoded shoots were used to create this graph.
FIG. 1 in Expressed sex ratio in populations of the moss Hamatocaulis vernicosus (Mitt.) Hedenäs (Scorpidiaceae) in the Czech Republic with consideration of its cryptic species
FIG. 1.— The sex expression of Hamatocaulis vernicosus (Mitt.) Hedenäs in the Czech Republic at individual localities assessed at two levels of pooling hierarchy ("shoots at localities" and "patches at localities").
FIG. 3 in Study of a new population of the Argentinian endemic species Riella choconensis Hässel (Riellaceae, Marchantiophyta) reveals a novel anatomical structure of the female involucre in Riella
FIG. 3. — LM and SEM images of spores of Riella choconensis Hässel. A, distal view; B, spines from distal side; C, spines from proximal side; D, distal view; E, spines from distal side; F, spines from proximal side; G, distal view; H, Spines and reticulum from distal pole; I, spines from distal side and rugose spore surface; J, distal view; K, spines and reticulum from distal pole; L, spines from distal side and rugose spore surface; M, proximal view; N, proximal spore surface and spines; O, proximal spines and rugose-granulose spore surface; P, Proximal view; Q, transition between distal and proximal side, showing the equatorial row of distal spines; R, Proximal spines and rugose spore surface (A-F made with LM; G-R made with SEM; A-C, I, from VAL-Briof. 11724; G-H, M-O, from VAL-Briof. 11725; D-F, J-L, P-R, from BA 33609). Scale bars: A, D, 50 μm; B, C, E, F, H, K, N, Q, 10 μm; G, J, M, P, 30 μm; I, L, O, 5 μm; R, 8 μm.
FIG. 2 in Study of a new population of the Argentinian endemic species Riella choconensis Hässel (Riellaceae, Marchantiophyta) reveals a novel anatomical structure of the female involucre in Riella
FIG. 2. — Habitat, LM and SEM images of Riella choconensis Hässel A, view of the Laguna de los Juncos; B, circinate apex of a male individual thallus showing a continuous row of antheridia; C, cells from thallus wing showing an oil cell with a single, rough oil body; D, apex of a female individual thallus showing three developing sporophytes; E, female involucre enclosing a sporophyte; F, apex of female involucre occluded by inflated cells; G, cross-section of female involucre showing the bistratose wall; H, female involucre; I, Apex of female involucre (B-G made with LM from VAL-Briof. 11724; H,I made with SEM from VAL-Briof. 11725), Scale bars: B, D, 1 mm; C, 20 μm; E, 500 μm; F, 200 μm; G, 50 μm; H, 300 μm; I, 70 μm.
FIG. 1 in Study of a new population of the Argentinian endemic species Riella choconensis Hässel (Riellaceae, Marchantiophyta) reveals a novel anatomical structure of the female involucre in Riella
FIG. 1. — Distribution of the five Argentinian species of Riella Mont. The inset map shows the geographical location of records of each species designated by a different symbol across the different provinces in Central Argentina. Previously known records of Riella choconensis Hässel are designated by a diamond (type locality) and new record by a star. The map indicates names and administrative boundaries of Argentinian provinces (grey lines) which are at some instances coincident with rivers (blue lines).
Figure 1 in Phylogenetic placement of a recently discovered population of the threatened alpine she-oak skink Cyclodomorphus praealtus (Squamata: Scincidae) in Victoria
Figure 1: Elevation map of the mainland Australian alpine region indicating the five major populations of Cyclodomorphus praealtus, including the new location of Wellington Plains. Elevation is indicated by light, mid and dark grey areas at 500 m intervals, with highest elevations at or above 1500 m above sea level. Adapted from fig. 1; Koumoundouros et al. (2009).
Figure 3 in Phylogenetic placement of a recently discovered population of the threatened alpine she-oak skink Cyclodomorphus praealtus (Squamata: Scincidae) in Victoria
Figure 3: Population structure of Victorian Cyclodomorphus praealtus according to ND4 mitochondrial haplotype network. Black indicates individuals from Lankey Plain, dark grey indicates those from Mt Hotham, white indicates those from Bogong High Plains and diagonal stripes indicate those from Wellington Plains. The network structure indicates 3 haplogroups (i, ii and iii) within Victoria. Each circle represents a unique haplotype, with the circle size indicative of frequency and sample sizes within each circle. Empty circles represent missing haplotypes and differ by one base pair from the closest haplotype.
Figure 2 in Phylogenetic placement of a recently discovered population of the threatened alpine she-oak skink Cyclodomorphus praealtus (Squamata: Scincidae) in Victoria
Figure 2: A Bayesian consensus tree of the mtDNA ND4 sequences, depicting the relationship between unique haplotypes at each locality (Bogong High Plains, Lankey Plain, Mt Hotham, Wellington Plains and Kosciuszko National Park) for Cyclodomorphus praealtus. Bayesian posterior probabilities are shown at major nodes.
Fig.3 in Ancyrophora gracilis L , 1892 and Actinocephalus permagnus Wellmer, 1910 (Eugregarinorida: Apicomplexa) in natural populations of ground beetles (Coleoptera, Carabidae) - hosts preferences, intensity and seasonal dynamic
Fig.3. The mean density ± SE of Actinocephalus permagnus (circle) and Ancyrophora gracilis (square) in consecutive seasons
Fig. 1 in Ancyrophora gracilis L , 1892 and Actinocephalus permagnus Wellmer, 1910 (Eugregarinorida: Apicomplexa) in natural populations of ground beetles (Coleoptera, Carabidae) - hosts preferences, intensity and seasonal dynamic
Fig. 1. Mean density of Actinocephalus permagnus (AT) and Ancyrophora gracilis (AC) in relation to host size classes. circle – medium sized, squares – broad sized hosts
Figure 4 in Within-plant distribution and rapid assessment of sugarcane rust mite population on sugarcane canopy
Figure 4 Relationship between sugarcane rust mite density and counting speed of the imprinting technique.
Figure 3 in Within-plant distribution and rapid assessment of sugarcane rust mite population on sugarcane canopy
Figure 3 Within-plant distribution of sugarcane rust mite population based on the imprinting tech- nique (mean ± SEM). The numbers within brackets are the proportions of mite populations within plants. Means across leaves with the same capital letters are not significantly different and means with the same lower letters on a given leaf position are not significantly different (Tukey,P <0.05).
Figure 5 in Within-plant distribution and rapid assessment of sugarcane rust mite population on sugarcane canopy
Figure 5 Physiological parameters of sugarcane canopy (mean±SEM).A=photosynthetic rate, gsw =stomatal conductance,Ci =intercellular CO2, E=transpiration, WUE=water use efficiency.
FIGURE 4 in Exploring the phylogenetic signal in the cranial variation of European populations of grayling (Actinopterygii, Salmonidae)
FIGURE 4 PCA of the grayling dorsal cranium. Wireframe diagrams (magnified 3 times) illustrate shape differences along PC1 and PC2 axes.
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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.