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125 results for “Pales”
BOSPLAY AGEN PG SOFT PALING GAMPANG JACKPOT
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- Sternite 1 without a pair of submedian tubercles, tubercles present on sternites 2–4 only (a); general coloration pale to striking yellow with isolated black markings (b) …………………………………7 7. Apex of subtegular ridge concave, laterally flanged (A) ……………………………………………8 - Apex of subtegular ridge convex, without lateral flange (a) ……………………………………9 in A review of the Afrotropical Rhyssinae (Hymenoptera: Ichneumonidae) with the descriptions of five new species
- Sternite 1 without a pair of submedian tubercles, tubercles present on sternites 2–4 only (a); general coloration pale to striking yellow with isolated black markings (b) …………………………………7 7. Apex of subtegular ridge concave, laterally flanged (A) ……………………………………………8 - Apex of subtegular ridge convex, without lateral flange (a) ……………………………………9
Fig. 5 in Distributional Range Extension of the Pale Ornate Jobfish Pristipomoides amoenus (Teleostei: Perciformes: Lutjanidae) in the Western Pacific Ocean, with Notes on Newly Recognized Diagnostic Coloration
Fig. 5. Live individuals of Pristipomoides argyrogrammicus collected from Motobu, Okinawa-jima island, Japan, and reared at Okinawa Churaumi Aquarium (photos by A. Kaneko). A, B, 200 m depth, 26 September 2019; C, 105 mm TL, juvenile, 150 m depth, 1 March 2020.
Fig. 4 in Distributional Range Extension of the Pale Ornate Jobfish Pristipomoides amoenus (Teleostei: Perciformes: Lutjanidae) in the Western Pacific Ocean, with Notes on Newly Recognized Diagnostic Coloration
Fig. 4. Distributional records of Pristipomoides amoenus. Stars and circles represent localities of specimens examined in the present and previous studies, respectively. Open symbol indicates type locality.
Fig. 3 in Distributional Range Extension of the Pale Ornate Jobfish Pristipomoides amoenus (Teleostei: Perciformes: Lutjanidae) in the Western Pacific Ocean, with Notes on Newly Recognized Diagnostic Coloration
Fig. 3. Live individual of Pristipomoides amoenus collected from Tsuken-jima island, Okinawa Islands, Japan, 300 m depth, 14 December 2019, and reared at Okinawa Churaumi Aquarium (photos by A. Kaneko). A, Lateral view; B, dorsal view.
Fig. 2 in Distributional Range Extension of the Pale Ornate Jobfish Pristipomoides amoenus (Teleostei: Perciformes: Lutjanidae) in the Western Pacific Ocean, with Notes on Newly Recognized Diagnostic Coloration
Fig. 2. Preserved specimens of (A–D) Pristipomoides amoenus and (E–H) P. argyrogrammicus. A, KAUM–I. 156091, 177.3 mm SL, Amamioshima island, Kagoshima, Japan; B, D, KAUM–I. 113361, 184.7 mm SL, Dong-gang, Pingtung, Taiwan; C, KAUM–I. 156091, 221.2 mm SL, Amami-oshima island, Kagoshima, Japan; E, KAUM–I. 139296, 141.7 mm SL, Amami-oshima island, Kagoshima, Japan; F, H, KAUM–I. 108166, 210.9 mm SL, Amami-oshima island, Kagoshima, Japan; G, KAUM–I. 51137, 277.6 mm SL, Tokara Islands, Kagoshima, Japan; D, H: dorsal view.
Fig. 1 in Distributional Range Extension of the Pale Ornate Jobfish Pristipomoides amoenus (Teleostei: Perciformes: Lutjanidae) in the Western Pacific Ocean, with Notes on Newly Recognized Diagnostic Coloration
Fig. 1. Fresh specimens of (A–C) Pristipomoides amoenus and (D–F) P. argyrogrammicus. A, KAUM–I. 156091, 177.3 mm SL, Amami-oshima island, Kagoshima, Japan; B, KAUM–I. 113361, 184.7 mm SL, Dong-gang, Pingtung, Taiwan; C, KAUM–I. 156091, 221.2 mm SL, Amami-oshima island, Kagoshima, Japan; D, KAUM–I. 139296, 141.7 mm SL, Amami-oshima island, Kagoshima, Japan; E, KAUM–I. 108166, 210.9 mm SL, Amami-oshima island, Kagoshima, Japan; F, KAUM–I. 51137, 277.6 mm SL, Tokara Islands, Kagoshima, Japan.
Fig. 36. Character 51, discrete pale proximoventral calf spot. State 1 in PHYLOGENETIC SYSTEMATICS OF DART-POISON FROGS AND THEIR RELATIVES (AMPHIBIA: ATHESPHATANURA: DENDROBATIDAE)
Fig. 36. Character 51, discrete pale proximoventral calf spot. State 1, present (imbricolus, AMNH 102082).
Figure 5 in Post-fledging parental care in the pale-breasted thrush, Turdus leucomelas (Passeriformes: Turdidae)
Figure 5. Food provisioning to fledglings of the Pale-breasted Thrush Turdus leucomelas: (A) fledgling (front) swallowing a fruit delivered by the adult; (B) the fledgling (right) receives a piece of an arthropod.
Figure 2 in Post-fledging parental care in the pale-breasted thrush, Turdus leucomelas (Passeriformes: Turdidae)
Figure 2. Food provisioning rate (events per fledgling per hour) in the Pale-breasted Thrush Turdus leucomelas in relation to fledgling age expressed as days from fledging.
Figure 1 in Post-fledging parental care in the pale-breasted thrush, Turdus leucomelas (Passeriformes: Turdidae)
Figure 1. Total number of food provisioning events to fledglings of the Pale-breasted Thrush Turdus leucomelas by each parental sex. Grouped bars refer to fledglings from the same family group (1 to 8) and reflect clutch size, with exception of families 5 and 6 (two fledglings each, one of them non assessed during focal observations). Families 1 and 6 to 8 were assigned as biparental care; in family 7, biparental care was assigned because the male was observed feeding one non focal nestling.
Figure 4 in Post-fledging parental care in the pale-breasted thrush, Turdus leucomelas (Passeriformes: Turdidae)
Figure 4. Age-related variation in the frequency of foraging and vocalization behaviors in fledglings of Turdus leucomelas. The curve in the panel A represents a significant logistic relationship between the variables, and its 95% confidence interval denoted by the shaded area. Bars in both panels represent the relative frequency of the behaviors followed by the number of scans (below bars) within 1-day age intervals (n = 787 in total), with fledgling age corresponding to the number of days after fledging.
Figure 3 in Post-fledging parental care in the pale-breasted thrush, Turdus leucomelas (Passeriformes: Turdidae)
Figure 3. Food provisioning rate (events per fledgling per hour) in the Pale-breasted Thrush Turdus leucomelas. A) effect of brood size and mode of parental care division (uniparental/biparental), and B) by females and males in family groups with biparental food provisioning. Points in B represent the values comprised in the boxplots, in which the box delimit interquartile ranges, the vertical lines indicate minimum and maximum and the horizontal line denotes medians.
Figure 6 in Post-fledging parental care in the pale-breasted thrush, Turdus leucomelas (Passeriformes: Turdidae)
Figure 6. Relative frequency of food items delivered to Turdus leucomelas fledglings in relation to their age (days after fledging). Sample sizes are indicated above bars. "Other" refers to food items like dog food and pieces of bread.
Linked collectors and determiners for: A whiter shade of pale: anchoring the name Paecilaema C. L. Koch, 1839 onto a neotype (Opiliones, Cosmetidae).
Natural history specimen data linked to collectors and determiners held within, "A whiter shade of pale: anchoring the name Paecilaema C. L. Koch, 1839 onto a neotype (Opiliones, Cosmetidae)". Claims or attributions were made on Bionomia by volunteer Scribes, <a href="https://bionomia.net/dataset/d2d146be-d297-4c55-a744-c51d71221e78">https://bionomia.net/dataset/d2d146be-d297-4c55-a744-c51d71221e78</a> using specimen data from the dataset aggregated by the Global Biodiversity Information Facility, <a href="https://gbif.org/dataset/d2d146be-d297-4c55-a744-c51d71221e78">https://gbif.org/dataset/d2d146be-d297-4c55-a744-c51d71221e78</a>. Formatted as a Frictionless Data package.
Fig. 2 in A new pale-spotted species of Hypostomus Lacépède (Siluriformes: Loricariidae) from the rio Tocantins and rio Xingu basins in central Brazil
Fig. 2. Hypostomus faveolus, (a) MZUSP 86790, 77.1 mm SL, rio Araguaia basin, (b) MZUSP 90721, 140.5 mm SL, rio Araguaia basin, (c) MZUSP 91971, 75.0 mm SL, Xingu basin, (d) MZUSP 91971, 158.0 mm SL, rio Xingu basin; (b-d) photographed alive, (a) preserved specimens.
Fig. 1 in A new pale-spotted species of Hypostomus Lacépède (Siluriformes: Loricariidae) from the rio Tocantins and rio Xingu basins in central Brazil
Fig. 1. Hypostomus faveolus, holotype, Brazil, Mato Grosso, Cocalinho, Corixo da Saudade (Corixinho), 25 km NO of Cocalinho on road MT 326, rioAraguaia drainage. MZUSP 90722, 206.0 mm SL.
Figure 1. Specimen PALE-8463 in An Eocene army ant
Figure 1. Specimen PALE-8463 from Eocene age Baltic amber. (a) Photomicrograph of lateral profile view of D. perseus. (Bottom) Micro-CT scan reconstruction of D. perseus, in (b) lateral and (c) frontal view. Scanning primarily resolved internal 'void space' air trapped within the insect cuticle, apparent holes in specimen reflect imperfect infilling of gas. Scale bars 0.5 mm. Specimen images are © President and Fellows of Harvard College, Museum of Comparative Zoology, Harvard University.
Data and code from "A dimmer shade of pale: revealing the faint signature of local assembly processes on the structure of strongly filtered plant communities"
<p>Trait-based ecology suggests that abiotic filtering is the main mechanism structuring the regional species pool in different subsets of habitat-specific species. At more local spatial scales, other ecological processes may add on giving rise to complex patterns of functional diversity (FD). Understanding how assembly processes operating on the habitat-specific species pools produce the locally observed plant assemblages is an ongoing challenge. Here, we evaluated the importance of different processes to community assembly in an alpine fellfield, assessing its effects on local plant trait FD. Using classical randomization tests and linear mixed models, we compared the observed FD with expectations from three null models that hierarchically incorporate additional assembly constraints: stochastic null models (random assembly), independence null models (each species responding individual and independently to abiotic environment), and co-occurrence null models (species responding to environmental variation and to the presence of other species). We sampled species composition in 115 quadrats across 24 locations in the central Pyrenees (Spain) that differed in soil conditions, solar radiation and elevation. Overall, the classical randomization tests were unable to find differences between the observed and expected functional patterns, suggesting that the strong abiotic filters that sort out the flora of extreme regional environments blur any signal of other local processes. However, our approach based on linear mixed models revealed the signature of different ecological processes. In the case of seed mass and leaf thickness, observed FD significantly deviated from the expectations of the stochastic model, suggesting that fine-scale abiotic filtering and facilitation can be behind these patterns. Our study highlights how the hierarchical incorporation of ecological additional constraints may shed light on the dim signal left by local assembly processes in alpine environments.</p>
Data from: Hematological parameters vary with life history stage in the pale-breasted thrush (Turdus leucomelas)
<p>The avian life cycle is composed by a progressive sequence of life history stages (LHS). Changes in energy expenditure and exposure to stressors at different LHS require corresponding changes in behavior, physiology, and morphology. Variation in hematological parameters, such hematocrit (Hct), hemoglobin (Hb), and heterophil to lymphocyte ratio (H/L ratio), can have permissive, stimulatory, and preparative actions to help maintain homeostasis through different LHS. Few studies have examined differences in these parameters among different LHS in free-living birds, with most of them restricted to temperate zones. We collected blood samples and measured hematological parameters every week for over a year from a population of a common resident bird species in southeastern Brazil, the pale–breasted thrush (Turdus leucomelas). Hematocrit and hemoglobin concentration were highest during the onset of the reproduction and lowest during molt. Furthermore, H/L ratios were higher at the end of the reproduction, indicating that the breeding season could be the most stressful period of the year for this population of thrushes. There was no difference between sexes for any hematological parameter at any LHS. These results show that there is a permissive physiological effect for Hct and Hb to facilitate LHS transitions and that reproduction could be the most stressful event for this species. Lastly, these results mirror those from temperate species despite distinct environmental differences between these regions.</p>
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Allen Brain Atlas
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DANDI Archive for NWB datasets
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International Brain Laboratory public data
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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.