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437 results for “morphological variability”
FIGURE 2 in The intraspecific morphological variability of Styloperla Wu, 1935 (Plecoptera: Styloperlidae)
FIGURE 2. Styloperla inae from Fujian, terminalia of adult, dorsal and ventral view. A–B: male; C–D: female.
FIGURE 12 in The intraspecific morphological variability of Styloperla Wu, 1935 (Plecoptera: Styloperlidae)
FIGURE 12. Aedeagus of Styloperla, dorsal view. A: S. inae from Fujian, B: S. spinicercia from Guangxi; C: S. starki from Zhejiang; D: S. wui from Anhui.
FIGURE 7 in The intraspecific morphological variability of Styloperla Wu, 1935 (Plecoptera: Styloperlidae)
FIGURE 7. Styloperla starki from Zhejiang (Hangzhou, Taihuyuan), male right cercus from different individuals. A–B: basal cercal segment with two apical spines (side by side) and three subapical spines; C–D: basal cercal segment with two apical spines arranged in tandem.
FIGURE 11 in The intraspecific morphological variability of Styloperla Wu, 1935 (Plecoptera: Styloperlidae)
FIGURE 11. Styloperla wui from Anhui (A–C) and Fujian (D), male right cercus from different individuals.
FIGURE 8 in The intraspecific morphological variability of Styloperla Wu, 1935 (Plecoptera: Styloperlidae)
FIGURE 8. Styloperla starki from Zhejiang, male cercus with three small teeth at one side. A–B: male from Quzhou (Qianjiangyuan); C–D: male from Taizhou (Danzhu).
Highly variable (no clear pattern). All portions of the dorsal views were equally used. In head images the area around the eye, the top of the head, the snout and the throat were all used in similar proportions. P. carbonelli Variable for both views. Snout and middle of the dorsum used in dorsal view. Top of the head most frequently (but not strictly) used in lateral view. P. guadarramae Whole body used for dorsal view (but variable); either throat (most common) or ear region used in head lateral views. P. hispanicus Variable. Anterior portion of snout used more frequently than in other species for both dorsal and head lateral views. P. liolepis Highly variable. Whole body used in most dorsal images, area around the eye and throat used in head lateral views, but other patterns common. P. lusitanicus Highly variable. All parts of the dorsum used (but frequently the most posterior part); area around the ear frequently used in head lateral images. P. tunesiacus Highly variable. Dorsal area near the insertion of the posterior limbs used more frequently than in other species; different regions of the head used, often simultaneously. P. Ʋaucheri Highly variable. Different regions of dorsum (from head to the posterior region) used in dorsal images, all portions of the head, but most frequently the throat, used in lateral images. P. Ʋirescens Highly variable. All parts of both images used. Head and anterior part of the dorsum more used than in other species. in Identification of morphologically cryptic species with computer vision models: wall lizards (Squamata: Lacertidae: Podarcis) as a case study
Highly variable (no clear pattern). All portions of the dorsal views were equally used. In head images the area around the eye, the top of the head, the snout and the throat were all used in similar proportions. P. carbonelli Variable for both views. Snout and middle of the dorsum used in dorsal view. Top of the head most frequently (but not strictly) used in lateral view. P. guadarramae Whole body used for dorsal view (but variable); either throat (most common) or ear region used in head lateral views. P. hispanicus Variable. Anterior portion of snout used more frequently than in other species for both dorsal and head lateral views. P. liolepis Highly variable. Whole body used in most dorsal images, area around the eye and throat used in head lateral views, but other patterns common. P. lusitanicus Highly variable. All parts of the dorsum used (but frequently the most posterior part); area around the ear frequently used in head lateral images. P. tunesiacus Highly variable. Dorsal area near the insertion of the posterior limbs used more frequently than in other species; different regions of the head used, often simultaneously. P. Ʋaucheri Highly variable. Different regions of dorsum (from head to the posterior region) used in dorsal images, all portions of the head, but most frequently the throat, used in lateral images. P. Ʋirescens Highly variable. All parts of both images used. Head and anterior part of the dorsum more used than in other species.
Highly variable. Mid-portion of the dorsum used frequently (although other areas as well). Tip of the snout used often, but area around the ear and throat are also relevant. P. carbonelli Variable. In the dorsal view, the tip of the snout is frequently used. In the head lateral view, the tip of the snout is also com- monly used, as well as the most posterior region of the head. P. guadarramae Variable. Mid portion of the dorsum and tip of the snout are the regions used more frequently in dorsal and head lateral views, respectively. P. hispanicus Variable. The head and most anterior part of the dorsum are frequently used in the dorsal view. Snout and/or top of posterior region of head used. P. liolepis Variable. Different parts of the dorsum are used, whereas the tip of the snout is used in most head lateral images. P. lusitanicus Anterior dorsum, in the dorsal view, and both snout and posterior side of the head (in head lateral views) frequently used. P. tunesiacus Variable. Tip of the snout and posterior part of the trunk more used than in other species; snout and top head region behind the eye used with some frequency. P. Ʋaucheri Highly variable. All parts of the dorsum used in dorsal images, various parts of the head (but frequently snout and throat combined) used in head lateral images. P. Ʋirescens Highly variable. All portions of the dorsum used in dorsal images, region around and behind the ear more used than in other species for head lateral images. in Identification of morphologically cryptic species with computer vision models: wall lizards (Squamata: Lacertidae: Podarcis) as a case study
Highly variable. Mid-portion of the dorsum used frequently (although other areas as well). Tip of the snout used often, but area around the ear and throat are also relevant. P. carbonelli Variable. In the dorsal view, the tip of the snout is frequently used. In the head lateral view, the tip of the snout is also com- monly used, as well as the most posterior region of the head. P. guadarramae Variable. Mid portion of the dorsum and tip of the snout are the regions used more frequently in dorsal and head lateral views, respectively. P. hispanicus Variable. The head and most anterior part of the dorsum are frequently used in the dorsal view. Snout and/or top of posterior region of head used. P. liolepis Variable. Different parts of the dorsum are used, whereas the tip of the snout is used in most head lateral images. P. lusitanicus Anterior dorsum, in the dorsal view, and both snout and posterior side of the head (in head lateral views) frequently used. P. tunesiacus Variable. Tip of the snout and posterior part of the trunk more used than in other species; snout and top head region behind the eye used with some frequency. P. Ʋaucheri Highly variable. All parts of the dorsum used in dorsal images, various parts of the head (but frequently snout and throat combined) used in head lateral images. P. Ʋirescens Highly variable. All portions of the dorsum used in dorsal images, region around and behind the ear more used than in other species for head lateral images.
Data and code for: "An open-source GIS approach to understanding dunefield morphologic variability at Kati Thanda (Lake Eyre), central Australia"
<p>Data and reproducabel code</p>
Data from: Neighbour species richness and local structural variability modulate aboveground allocation patterns and crown morphology of individual trees
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Data from: The influence of climatic variability on morphological integration, evolutionary rates, and disparity in the Carnivora
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Data from: Giving taxonomic significance to morphological variability in the bivalve Ptychomya Agassiz
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Data from: The Azores Bullfinch (Pyrrhula murina) has the same unusual and size-variable sperm morphology as the Eurasian Bullfinch (Pyrrhula pyrrhula)
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Data from: Molecular data confirm morphological variability in the widespread foliose lichen Canoparmelia carolinana (Parmeliaceae)
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Data from: Analysis of morphological variability in the clam shrimp Eosestheria middendorfii (Crustacea, Spinicaudata) from the Lower Cretaceous of China, and its implications for spinicaudatan taxonomy
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Data from: Echinorhynchus salmonis Müller, 1784 (Acanthocephala: Echinorhynchidae) from the Bothnian Bay, Baltic Sea: morphological variability and radial asymmetry of proboscis hooks
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Morphological and behavioural differences facilitate tropical butterfly persistence in variable environments
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Supplementary material 3 from: Ossowska E, Guzow-Krzemińska B, Kolanowska M, Szczepańska K, Kukwa M (2019) Morphology and secondary chemistry in species recognition of Parmelia omphalodes group – evidence from molecular data with notes on the ecological niche modelling and genetic variability of photobionts. MycoKeys 61: 39-74. https://doi.org/10.3897/mycokeys.61.38175
: Data type: multimedia
Supplementary material 1 from: Ossowska E, Guzow-Krzemińska B, Kolanowska M, Szczepańska K, Kukwa M (2019) Morphology and secondary chemistry in species recognition of Parmelia omphalodes group – evidence from molecular data with notes on the ecological niche modelling and genetic variability of photobionts. MycoKeys 61: 39-74. https://doi.org/10.3897/mycokeys.61.38175
: Data type: occurrence
Figure 6 from: Ossowska E, Guzow-Krzemińska B, Kolanowska M, Szczepańska K, Kukwa M (2019) Morphology and secondary chemistry in species recognition of Parmelia omphalodes group – evidence from molecular data with notes on the ecological niche modelling and genetic variability of photobionts. MycoKeys 61: 39-74. https://doi.org/10.3897/mycokeys.61.38175
Figure 6 Association network between lichen mycobionts of P. omphalodes group (i.e. Parmelia discordans, P. omphalodes and P. pinnatifida) and photobiont OTUs. The line width is proportional to the number of specimens forming the association with the particular OTU. SUn1 and SUn2 represent unnamed lineages of Trebouxia belonging to clade S.
Figure 3 from: Ossowska E, Guzow-Krzemińska B, Kolanowska M, Szczepańska K, Kukwa M (2019) Morphology and secondary chemistry in species recognition of Parmelia omphalodes group – evidence from molecular data with notes on the ecological niche modelling and genetic variability of photobionts. MycoKeys 61: 39-74. https://doi.org/10.3897/mycokeys.61.38175
Figure 3 Haplotype network showing relationships between ITS rDNA sequences from Parmelia discordans and P. omphalodes. The names of species are followed with herbarium numbers of specimens or GenBank Accession Numbers. Mutational changes are presented as numbers in brackets near lines between haplotypes.
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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.