Find research datasets worth reusing
Search datasets from major research repositories and use ShareScore to quickly assess how well each record supports discovery, access, and reuse.
684
datasets available to search
ShareScore release 0.9.0
Dataset results
684 results for “Functional morphology”
Figures 5–6. Aporus hirsutus hunting behavior. 5 in Nesting behavior, ecology, and functional morphology of the trapdoor spider-hunting spider wasp Aporus (Plectraporus) hirsutus (Banks) (Hymenoptera: Pompilidae)
Figures 5–6. Aporus hirsutus hunting behavior. 5) Aporus hirsutus female digging into sand, using her mandibles and foretarsal digging rake, apparently searching for host Aptostichus simus, sandy coastal back dunes, Santa Barbara County, CA; 12 June 2014; A. Abela. Photograph © Alice Abela. 6) Aptostichus simus trapdoor being propped open by a twig. Note the flimsy silk and sand consistency of the trapdoor and sides of entrance, Montaña de Oro State Park, San Luis Obispo, CA; 5 July 2020; A. Abela. Photograph © Alice Abela.
Figures 3–4. Aporus hirsutus adult feeding. 3 in Nesting behavior, ecology, and functional morphology of the trapdoor spider-hunting spider wasp Aporus (Plectraporus) hirsutus (Banks) (Hymenoptera: Pompilidae)
Figures 3–4. Aporus hirsutus adult feeding. 3) Aporus hirsutus female taking nectar from flowers of Eriogonum parvifolium, Vandenberg Air Force Base, Santa Barbara County, CA; 6 August 2014; A. Abela. Photograph © Alice Abela. 4) Aporus hirsutus female with immobilized Aptostichus simus, immature, on sand, Surf Beach at Vandenberg Air Force Base, Santa Barbara County, CA; 28 March 2015; A. Abela. The wasp appressed her mouthparts and basal antennal segments to the paralyzed prey and, apparently, used this individual only for adult feeding. Photograph © Alice Abela.
Figure 11 in Nesting behavior, ecology, and functional morphology of the trapdoor spider-hunting spider wasp Aporus (Plectraporus) hirsutus (Banks) (Hymenoptera: Pompilidae)
Figure 11. Aporus (Plectraporus) hirsutus (Banks) degree of body hairiness (Wasbauer and Kimsey 1985; this study).
Data for "Examining functional impact and trophic morphology of small, sand-sifting fishes on coral reefs"
<p>This data is the product of the study published as "<strong>Examining functional impact and trophic morphology of small, sand-sifting fishes on coral reefs </strong>"</p> <p>It contains:<br> Feeding depth count of the two fish species used</p> <p>Granulometry on the experimental sediment</p> <p>Gut content analysis of the 8 fish used in the experiment. Measurements of maximum and minimum size of each individual prey item noted.</p> <p>Feeding experiment count data. ID and count data of meiobenthos (benthic meiofauna) found during the feeding experiment. The benthic community was assessed in 3 replicates for each fish individual at each timepoint. See the methods in publications for details or contact the Ole Brodnicke or Camilla Hansen for details. </p>
Figure 7 in Morphology, feeding and behaviour of British Magelona (Annelida: Magelonidae), with discussions on the form and function of abdominal lateral pouches
Figure 7. Various palp positions observed for Magelona mirabilis from in situ experiments. Third picture depicts debris collecting on and in between the palps.
Figure 3 in Morphology, feeding and behaviour of British Magelona (Annelida: Magelonidae), with discussions on the form and function of abdominal lateral pouches
Figure 3. Experimental set-up: A, aquarium tank and cooling system; B, Magelona johnstoni Berwick-upon-Tweed (NMW.Z. 2013.037.0001): live animal in capillary tube. Photo: A.S.Y. Mackie.
Figure 10 in Morphology, feeding and behaviour of British Magelona (Annelida: Magelonidae), with discussions on the form and function of abdominal lateral pouches
Figure 10. Abdominal posteriorly opening pouches from several specimens of Magelona johnstoni: A–B, initiation of new pouches represented by small 'holes' (lateral view) (A: NMW.Z.2013.037.0008e; B: NMW.Z.2013.037.0010d); C, first pouch (~6 chaetigers) from pygidium (lateral view) (NMW.Z.2013.037.0011d); D, first pouch from a regenerating tail (ventral/posterior view) (NMW.Z.2013.037.0008c); E, third pouch (~10 chaetigers) from pygidium (posterior view) (NMW.Z.2013.037.0011d); F, posteriorly opening pouch of an abdominal fragment (lateral posterior view) (NMW.Z.1998.028). Photos: K. Mortimer.
Figure 2 in Morphology, feeding and behaviour of British Magelona (Annelida: Magelonidae), with discussions on the form and function of abdominal lateral pouches
Figure 2. Magelona mirabilis Berwick-upon-Tweed (NMW.Z. 2013.037.0020): A, whole animal; B, anterior (ventral view); C, palp; D, prostomium (ventral view, showing mouth); E, posterior. All MgCl -relaxed. Photos: A.S.Y. Mackie.
Figure 6 in Morphology, feeding and behaviour of British Magelona (Annelida: Magelonidae), with discussions on the form and function of abdominal lateral pouches
Figure 6. In situ picture of the posterior thorax and anterior abdomen of living Magelona johnstoni (chaetigers 7–14, dorsal view).
Figure 9 in Morphology, feeding and behaviour of British Magelona (Annelida: Magelonidae), with discussions on the form and function of abdominal lateral pouches
Figure 9. Lateral view of Magelona johnstoni between chaetigers 9 (to the left of the picture) and chaetiger 11 (to the right), showing anteriorly opening abdominal pouches between chaetigers 10 and 11. Arrows indicate water flow around the pouches and lamellae, as observed during capillary tube experiments.
Figure 5 in Morphology, feeding and behaviour of British Magelona (Annelida: Magelonidae), with discussions on the form and function of abdominal lateral pouches
Figure 5. Magelona johnstoni Berwick-upon-Tweed: A, prostomium and first two chaetigers (ventral view), showing mouth surrounded by one upper (UL) and two lower lips (LL), and the proboscis (Pb, not everted) (NMW.Z.1999.021.0020a); B, papillae of mid-palp region (NMW.Z.2013.037.0008c); C, left-hand anteriorly opening pouch located between chaetigers 10 and 11 (lateral view, DF = dorsal flap, VF = ventral flap, LO = lateral organ, CM = convoluted membrane) (NMW.Z.2013.037.0011b); D, close-up view of convoluted membrane; E, transverse section through the body and anteriorly opening pouch situated between chaetigers 10 and 11 (posterior half of pouch and parapodia of chaetiger 11) (NotoL = notopodial lamellae, NeuroL = neuropodial lamellae) (NMW.Z.2013.037.0010c); F, anterior half of same pouch (NMW.Z.2013.037.0010b). Photos: K. Mortimer.
Figure 1 in Morphology, feeding and behaviour of British Magelona (Annelida: Magelonidae), with discussions on the form and function of abdominal lateral pouches
Figure 1. Magelona johnstoni Berwick-upon-Tweed (A, C, D, G: NMW.Z. 2013.037.0018; B: NMW.Z. 2013.037.0001; E, F: NMW.Z. 2013.037.0017; H: NMW.Z. 2013.037.0015): A, whole animal; B, anterior (dorsal view); C, anterior (ventral view); D, anterior (lateral view); E, palp; F, prostomium (ventral view, showing mouth); G, prostomium (ventral view, 'proboscis' everted); H, posterior section of female showing eggs. All MgCl -relaxed. Photos: A.S.Y. Mackie.
Figure 8 in Morphology, feeding and behaviour of British Magelona (Annelida: Magelonidae), with discussions on the form and function of abdominal lateral pouches
Figure 8. Showing two individuals of Magelona johnstoni simultaneously making lateral sinuous movements of the thorax (outside the burrow) (dorsal views).
Figure 4 in Morphology, feeding and behaviour of British Magelona (Annelida: Magelonidae), with discussions on the form and function of abdominal lateral pouches
Figure 4. Feeding in Magelona johnstoni: A, feeding position within the burrow (ventral view), indicating four zones where different methods are utilised to move food particles along the palp; B, looping of the palp at the surface (zone 1), in order to pass food particles along the palp (lateral view); C, similar process to that shown in B but utilising coiling of the palp (lateral view, papillae omitted for clarity); D, sequence showing the process of passing food particles from papillae to papillae along palp in zone 2; E, food particles being passed between papillae of both palps in zone 3; F, region where food particles are dropped towards mouth (ventral view) in zone 4.
Fig. 1 in Eukaryotic Microbial Communities Associated with Rock-dwelling Foliose Lichens: A Functional Morphological and Microecological Analysis
Fig. 1. Photograph of a portion of a Flavoparmelia thallus showing an example of a radially oriented lobe with three segments sampled in analyzing the microbial communities: A – inner, B – middle, and C – outer. Scale bar: 5 mm.
Fig. 6 in Functional morphology and biomechanics of the cynodont Trucidocynodon riograndensis from the Triassic of Southern Brazil: Pectoral girdle and forelimb
Fig. 6. Movements in the left shoulder and elbow of Trucidocynodon riograndensis. Maximal (A) and minimal (B) humeral adduction, in dorsal view; humeral protraction in lateral view (C), humeral rotation in anterior view (D); elbow flexion in lateral view (E), medial translation of ulna during elbow flexion in anterior view (F). Darker shaded steps, in E and F the radius was not figured.
Fig. 5 in Functional morphology and biomechanics of the cynodont Trucidocynodon riograndensis from the Triassic of Southern Brazil: Pectoral girdle and forelimb
Fig. 5. Movements in the pectoral girdle of Trucidocynodon riograndensis. Right clavicle/interclavicle articulation, in ventral view, front upward (A); right clavicle/scapulocoracoid articulation, in dorsal (B), anterior (C), and lateral (D) views.
Fig. 4 in Functional morphology and biomechanics of the cynodont Trucidocynodon riograndensis from the Triassic of Southern Brazil: Pectoral girdle and forelimb
Fig. 4. Muscular reconstruction of pectoral region and forelimb of Trucidocynodon riograndensis in lateral (A) and ventral (B) views (only the muscles discussed in the text are labeled).
Fig. 2 in Functional morphology and biomechanics of the cynodont Trucidocynodon riograndensis from the Triassic of Southern Brazil: Pectoral girdle and forelimb
Fig. 2. The holotype of the non-mammalian cynodont Trucidocynodon riograndensis Oliveira, Soares, and Schultz, 2010 (UFRGS PV-1051-T) from Carnian (Upper Triassic) of Agudo municipality, state of Rio Grande do Sul, Brazil.
Fig. 1. A in Functional morphology and biomechanics of the cynodont Trucidocynodon riograndensis from the Triassic of Southern Brazil: Pectoral girdle and forelimb
Fig. 1. A. Map of South America with the state of Rio Grande do Sul shaded. B. Location of the Agudo municipality (arrow) in the state of Rio Grande do Sul, where Middle and Upper Triassic rocks crop out. C. Sequence stratigraphy of Brazilian rocks containing Triassic vertebrates, with the Hyperodapedon Assemblage Zone highlighted (modified from Horn et al. 2014).
ScienceDex guides
Understand access before you commit
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.