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19,493 results for “Populism”
Fig. 11 in Reproductive and population dynamics of the Bay whiff Citharichthys spilopterus Günther, 1862 (Pleuronectiformes: Paralichthyidae) in the Mamanguá Inlet, Rio de Janeiro, Brazil
Fig. 11. Temporal variation of the mean values of the gonadosomatic relationship (GSR) of the Bay whiff in the Mamanguá Inlet. Bars= standard deviation.
Fig. 7 in Reproductive and population dynamics of the Bay whiff Citharichthys spilopterus Günther, 1862 (Pleuronectiformes: Paralichthyidae) in the Mamanguá Inlet, Rio de Janeiro, Brazil
Fig. 7. Bay whiff oocytes at different developmental stages: a)chromatin-nucleolar (CN), perinucleolar (PN), yolk vesicles and mature stages (M), H-E, 40 X; b) yolk vesicles and secondary yolk stage, and α and β atresia, H-E, 40 X; c) primary yolk stage and early β atresia, H-E, 40 X; d) high numbers of α and β atresia, H-E, 10 X; e) and f) post-ovulatory follicles (POF), H-E, 40 X.
Fig. 4 in Reproductive and population dynamics of the Bay whiff Citharichthys spilopterus Günther, 1862 (Pleuronectiformes: Paralichthyidae) in the Mamanguá Inlet, Rio de Janeiro, Brazil
Fig. 4. Mean values of the alometric condition factor (K) and "K estimated to C. spilopterus in the Mamanguá Inlet.
Fig. 2. T-S in Reproductive and population dynamics of the Bay whiff Citharichthys spilopterus Günther, 1862 (Pleuronectiformes: Paralichthyidae) in the Mamanguá Inlet, Rio de Janeiro, Brazil
Fig. 2. T-S diagram for the Mamanguá Inlet based on (a) surface and (b) bottom data of temperature and salinity from March 1990 to March 1992. Lines represent the values of the South Atlantic Central Waters, calculated from coefficients of the mean T-S expressions based in Miranda (1985).
Fig. 3 in Reproductive and population dynamics of the Bay whiff Citharichthys spilopterus Günther, 1862 (Pleuronectiformes: Paralichthyidae) in the Mamanguá Inlet, Rio de Janeiro, Brazil
Fig. 3. Spatial variation of the average length of Citharichthys spilopterus in the Mamanguá Inlet. Bars= standard deviation.
Fig. 9 in Reproductive and population dynamics of the Bay whiff Citharichthys spilopterus Günther, 1862 (Pleuronectiformes: Paralichthyidae) in the Mamanguá Inlet, Rio de Janeiro, Brazil
Fig. 9. Rates of follicular atresia in the ovaries of C. spilopterus captured at Mamanguá Inlet: a) percentage of females presenting á or older atresia; b) maximum rates of atresia by females in each oceanographic station on March and May 1990.
Fig. 6 in Reproductive and population dynamics of the Bay whiff Citharichthys spilopterus Günther, 1862 (Pleuronectiformes: Paralichthyidae) in the Mamanguá Inlet, Rio de Janeiro, Brazil
Fig. 6. Proportion of males (a) and females (b) of the Bay whiff in each macroscopic maturity stage considered in this study. Stars means significantly different - tested by Chisquare (χ2).
Fig. 1 in Reproductive and population dynamics of the Bay whiff Citharichthys spilopterus Günther, 1862 (Pleuronectiformes: Paralichthyidae) in the Mamanguá Inlet, Rio de Janeiro, Brazil
Fig. 1. Sampled area for Citharichthys spilopterus in the Mamanguá Inlet, Rio de Janeiro, Brazil. Modified from Bernardes (1995). Five oceanographic stations and four satations in the margins of the beaches are indicated with numbers.
Fig. 1 in Comparative dietary analysis of two populations of Mimagoniates rheocharis (Characidae: Glandulocaudinae) from two streams of Southern Brazil
Fig. 1. Percent composition of dietary items found in the stomachs of Mimagoniates rheocharis. (a) Station 1, March 1998 to March 1999 and (b) Station 2, January 1998 to February 1999.
Figure 2. Phylogenetic relationships among the 29 in Molecular phylogeny and phylogeography of the Greek populations of the genus Orthometopon (Isopoda, Oniscidea) based on mitochondrial DNA sequences
Figure 2. Phylogenetic relationships among the 29 specimens of Orthometopon species. Individuals from two other terrestrial isopod species were used as outgroup taxa: Ligidium sp. and Armadillidium vulgare. Phylogenetic analyses, maximum parsimony (MP), maximum likelihood (ML), and Bayesian inference (BI), all produced trees with the same topology. Only the BI tree is presented here. Numbers above the branches indicate bootstrap values in the MP and ML analyses, respectively (MP/ML). Numbers below the branches indicate the posterior probabilities of the Bayesian analysis (BI).
Figure 1 in Molecular phylogeny and phylogeography of the Greek populations of the genus Orthometopon (Isopoda, Oniscidea) based on mitochondrial DNA sequences
Figure 1. Map showing the sampling localities of the 29 specimens used for the DNA analysis. The numbers correspond to those listed in Table 1.
Abb. 26-29 in Carabidae (Coleoptera) associated with gypsy moth, Lymantria dispar (L.) (Lepidoptera: Lymantriidae), populations subjected to Bacillus thuringiensis Berliner treatments in Pennsylvania.
Abb. 26-29: Chorebus transversus (NIXON) (26) Kopf, Mesosoma und Metasoma mit Vorder- und Hinterflügel lateral, (27) Basis eines Fühlers, (28) Mandibel, (29) Metasoma dorsal.
Abb. 23-25 in Carabidae (Coleoptera) associated with gypsy moth, Lymantria dispar (L.) (Lepidoptera: Lymantriidae), populations subjected to Bacillus thuringiensis Berliner treatments in Pennsylvania.
Abb. 23-25: Chorebus iphias (NIXON) (23) Kopf und Mesosoma lateral, (24) Mandibel, (25) Vorderflügel.
Abb. 20-22 in Carabidae (Coleoptera) associated with gypsy moth, Lymantria dispar (L.) (Lepidoptera: Lymantriidae), populations subjected to Bacillus thuringiensis Berliner treatments in Pennsylvania.
Abb. 20-22: Lepton pajori nov.sp. (20) Mesosoma und Metasoma mit Vorder- und Hinterflügel lateral, (21) Mandibel, (22) Hinterbein.
Abb. 17-19 in Carabidae (Coleoptera) associated with gypsy moth, Lymantria dispar (L.) (Lepidoptera: Lymantriidae), populations subjected to Bacillus thuringiensis Berliner treatments in Pennsylvania.
Abb. 17-19: Lepton maehongsonensis nov.sp. (17) Kopf dorsal, (18) Mesopleurum und Metapleurum, (19) Vorder- und Hinterflügel.
Abb. 14-16 in Carabidae (Coleoptera) associated with gypsy moth, Lymantria dispar (L.) (Lepidoptera: Lymantriidae), populations subjected to Bacillus thuringiensis Berliner treatments in Pennsylvania.
Abb. 14-16: Lepton lusakaensis nov.sp. (14) Kopf, Mesosoma und Metasoma lateral, (15) Hinterbein, (16) Vorder- und Hinterflügel.
Abb. 9-13 in Carabidae (Coleoptera) associated with gypsy moth, Lymantria dispar (L.) (Lepidoptera: Lymantriidae), populations subjected to Bacillus thuringiensis Berliner treatments in Pennsylvania.
Abb. 9-13: Coelalysia zambiae nov.sp. (9) Basis eines Fühlers, (10) Mandibel, (11) Hinterbein, (12) Metascutum bis T1 dorsal, (13) Metasoma lateral.
Abb. 5-8 in Carabidae (Coleoptera) associated with gypsy moth, Lymantria dispar (L.) (Lepidoptera: Lymantriidae), populations subjected to Bacillus thuringiensis Berliner treatments in Pennsylvania.
Abb. 5-8: Coelalysia tanzaniae nov.sp. (5) Basis und Mitte eines Fühlers, (6) Hinterbein, (7) Propodeum und T1, (8) Vorder- und Hinterflügel.
Abb. 1-4 in Carabidae (Coleoptera) associated with gypsy moth, Lymantria dispar (L.) (Lepidoptera: Lymantriidae), populations subjected to Bacillus thuringiensis Berliner treatments in Pennsylvania.
Abb. 1-4: Coelalysia nigricapite nov.sp. (1) Seite des Pronotum und Mesopleurum lateral, (2) Praescutellarfurche, Scutellum und Postaxillae, (3) Metascutum bis T1 dorsal, (4) Vorder- und Hinterflügel.
Effects of population density on static allometry between horn length and body mass in mountain ungulates
<p class="MsoNoSpacing">Little is known about the effects of environmental variation on allometric relationships of condition-dependent traits, especially in wild populations. We estimated sex-specific static allometry between horn length and body mass in four populations of mountain ungulates that experienced periods of contrasting density over the course of the study. These species displayed contrasting sexual dimorphism in horn size; high dimorphism in <i>Capra ibex</i> and <i>Ovis canadensis</i> and low dimorphism in <i>Rupicapra rupicapra</i> and <i>Oreamnos americanus</i>. The effects of density on static allometric slopes were weak and inconsistent while allometric intercepts were generally lower at high density, especially in males from species with high sexual dimorphism in horn length. These results confirm that static allometric slopes are more canalized than allometric intercepts against environmental variation induced by changes in population density, particularly when traits appear more costly to produce and maintain.</p>
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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.