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4,028 results for “Behaviour”
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.
figure 10 in Morphology and mating behaviour in the millipede Megaphyllum unilineatum (C.L. Koch, 1838) (Myriapoda, Diplopoda, Julida) under laboratory conditions
figure 10 Canonical variate analysis (cva) of differences in promere shape between males with different mating status (bars: grey – mated males; white –non-mated males).
figure 9 in Morphology and mating behaviour in the millipede Megaphyllum unilineatum (C.L. Koch, 1838) (Myriapoda, Diplopoda, Julida) under laboratory conditions
figure 9 Canonical variate analysis (cva) of differences in walking leg shape between males and females with different mating status (rectangles: black – mated males, white – non-mated males; circles: black – mated females, white – non-mated females).
figure 7 in Morphology and mating behaviour in the millipede Megaphyllum unilineatum (C.L. Koch, 1838) (Myriapoda, Diplopoda, Julida) under laboratory conditions
figure 7 Canonical variate analysis (cva) of differences in antennal shape between males and females with different mating status (rectangles: black – mated males, white – non-mated males; circles: black – mated females, white – non-mated females).
figure 8 in Morphology and mating behaviour in the millipede Megaphyllum unilineatum (C.L. Koch, 1838) (Myriapoda, Diplopoda, Julida) under laboratory conditions
figure 8 Canonical variate analysis (cva) of differences in head shape between males and females with different mating status (rectangles: black – mated males, white – non-mated males; circles: black – mated females, white – non-mated females). Downloaded from Brill.com 06/24/2024 12:52:58AM via Open Access. This is an open access article distributed under the terms of the CC-BY 4.0 license. https://creativecommons.org/licenses/by/4.0/
figure 3 in Morphology and mating behaviour in the millipede Megaphyllum unilineatum (C.L. Koch, 1838) (Myriapoda, Diplopoda, Julida) under laboratory conditions
figure 3 Individuals of both sexes and sequences of sexual behaviour in M. unilineatum. A – male; B – female; C, D, E – contact; F, G, H, I, J, K – extrusion of gonopods (arrows); L, M, N – copulation. photo by B. Ilić
figure 2 in Morphology and mating behaviour in the millipede Megaphyllum unilineatum (C.L. Koch, 1838) (Myriapoda, Diplopoda, Julida) under laboratory conditions
figure 2 Digitalized landmarks on antenna (A) and leg (C) of the species M. unilineatum are shown, as well as digitalized landmarks and semi-landmarks on its head (B), promere (D), and opisthomere (E). See supplementary text S1 for descriptions of landmarks and Downloaded semi-landmarksfrom.Brill.com 06/24/2024 12:52:58AM via Open Access. This is an open access article distributed under the terms of the CC-BY 4.0 license. https://creativecommons.org/licenses/by/4.0/
figure 6 in Morphology and mating behaviour in the millipede Megaphyllum unilineatum (C.L. Koch, 1838) (Myriapoda, Diplopoda, Julida) under laboratory conditions
figure 6 Morphological variation in centroid size (CS) of antennae (A), head (B), walking legs (C), promeres (D), and opisthomeres (E) between individuals with different mating status. The median with the first and the third quartiles is shown (in boxes), together with the range of variation and outliers.
figure 5 in Morphology and mating behaviour in the millipede Megaphyllum unilineatum (C.L. Koch, 1838) (Myriapoda, Diplopoda, Julida) under laboratory conditions
figure 5 Morphological variation of body mass (A), body length (B), antennal length (C), walking leg length (D), trunk width (E), and trunk height (F) between males and females with different mating status. Morphological variation of flagellum length (FL) between mated and non-mated males (G) is also depicted. The median with the first and the third quartiles is shown (in boxes), together with the range of variation and outliers.
figure 4 in Morphology and mating behaviour in the millipede Megaphyllum unilineatum (C.L. Koch, 1838) (Myriapoda, Diplopoda, Julida) under laboratory conditions
figure 4 Percentage of copulations in female and male choice tests (grey bars – mating with previous partner; white bars – mating with new partner).
Fig. 1 in First description of the breeding biology and behaviour of the near threatened northern sooty woodpecker Mulleripicus funebris (Valenciennes 1826) (Piciformes: Picidae) in Luzon Island, Philippines
Fig. 1 - Cavity nest excavated by the northern sooty woodpecker: a) nest entrance; b) nest contents. / Nido scavato dal picchio fuligginoso: a) ingresso del nido; b) contenuto del nido. (Photo: / Foto: Erwin S. Quijano, 29 May 2022).
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.