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Figure 2 in First estimate of the fecundity of Ogcocephalus cubifrons (Lophiiformes) with notes on spawning behaviour
Figure 2. – Ova of Ogcocephalus cubifrons, 50x magnification showing the beginning of cleavage indicating the beginning of embryogenesis, and red oil droplet.
FIGURE 5 in Dancing with the devil: courtship behaviour, mating evidences and population structure of the Mobula tarapacana (Myliobatiformes: Mobulidae) in a remote archipelago in the Equatorial Mid-Atlantic Ocean
FIGURE 5 | Distinct courtship behaviors of sicklefin devil rays Mobula tarapacana observed in the Saint Peter and Saint Paul Archipelago. A. Female being chased by two males. B. Male overlapping female. C. Male trying to overlap on female. D. Male overlaps the female with two more males chasing. E–F. Sequence of male following female.
FIGURE 3 in Dancing with the devil: courtship behaviour, mating evidences and population structure of the Mobula tarapacana (Myliobatiformes: Mobulidae) in a remote archipelago in the Equatorial Mid-Atlantic Ocean
FIGURE 3 | Female (grey) and male (black) Mobula tarapacana size distribution (disk width- DW, in meters) per month, in the Saint Peter and Saint Paul Archipelago (SPSPA), from December 2008 to June 2016. Red dashed line= size at maturity for males (White et al., 2006); blue dashed line= size at maturity for females (Notarbartolo di Sciara, 1988).
Fig. 3 in Impact of ecotourism on the fish fauna of Bonito region (Mato Grosso do Sul State, Brazil): ecological, behavioural and physiological measures
Fig. 3. Image illustrating under water visibility at the beginning of the snorkeling excursion and the presence of tourists (Lima, 2008).
Fig. 1 in Impact of ecotourism on the fish fauna of Bonito region (Mato Grosso do Sul State, Brazil): ecological, behavioural and physiological measures
Fig. 1. Map showing the location of the study area: Sucuri River (C), município of Bonito area (B), Brazil (A). Adapted from Miranda & Coutinho (2004).
Fig. 8 in Impact of ecotourism on the fish fauna of Bonito region (Mato Grosso do Sul State, Brazil): ecological, behavioural and physiological measures
Fig. 8. Variation of behaviour patterns between before (8h00) and after (9h00) the first disturbance of tourists in the river (mean and SEM) for M. bonita; (a) Tourism and (b) No Tourism. Lighter bars = 8h00; darker bars = 9h00 (Mann-Whitney U-test). N = 70; * p <0.05; ** p <0.01.
Fig. 9 in Impact of ecotourism on the fish fauna of Bonito region (Mato Grosso do Sul State, Brazil): ecological, behavioural and physiological measures
Fig. 9. Variation (mean and SEM) of cortisol responses to restraining stress in Moenkhausia bonita individuals at the No Tourism and Tourism sites (Mann-Whitney U-test, N = 6; Z = -2.95; p <0.005).
Figure 1 in Breeding and reproductive behaviour of the neo-tropical opossum, Didelphis marsupialis insularis, Allen 1902 under captive conditions
Figure 1. Design and layout of Adult Units using a Single Corridor Layout. Source: Tardieu and Garcia, 2018).
Figure 2 in Breeding and reproductive behaviour of the neo-tropical opossum, Didelphis marsupialis insularis, Allen 1902 under captive conditions
Figure 2. Photo of opossum breeding unit showing – (A) Human Access panel to Male; (B) Male Cage; (C & D) Male Access panels to females; (E) Female Cage; (F) Human Access panel to Female.
Fig. 1 in Large theropod dinosaur footprint associations in western Gondwana: Behavioural and palaeogeographic implications
Fig. 1. Location of the large theropod trackbeds: track 1 indicates the Querulpa Chico locality while track 2 indicates the Chacarilla locality.
Fig. 5 in Large theropod dinosaur footprint associations in western Gondwana: Behavioural and palaeogeographic implications
Fig. 5. Photographs of Early Cretaceous theropod footprints from the Querulpa Chico tracksite, Peru. A–I refer to the individual trackways in Fig. 4, and the number to the particular print in the trackway. Arrows point to hallux impressions. Scale bars 0.5 m.
Fig. 6. Early Cretaceous Chacarilla tracksite, Chile. A in Large theropod dinosaur footprint associations in western Gondwana: Behavioural and palaeogeographic implications
Fig. 6. Early Cretaceous Chacarilla tracksite, Chile. A. Line drawing and photographs of the Chacarilla theropod tracksite, showing orientations and distribution of trackways. B. Schematic map of trackways 3 and 4, crossed perpendicularly by trackways 1, 5 and 2 (unidentified trackway). Scale bars in A 5 m.
Fig. 3 in Large theropod dinosaur footprint associations in western Gondwana: Behavioural and palaeogeographic implications
Fig. 3. Measurements taken in situ on footprints and trackways. Anteroposterior track length: distance between the distal tip of digit III and the proximal boundary of the sole; mediolateral track width: distance between the distal tip of lateral digits measured perpendicular to the track axis; pace angle: angle formed by the two segments joining three consecutive tracks; pace, distance between two consecutive tracks; stride length: distance between two consecutive tracks on the same side (left or right) of the trackway.
Dataset: Towards a two-step assessment of the chloride ingress behaviour of new cementitious binders
<p>Data and results to accompany the publication:</p> <p> </p> <p><strong>Towards a two-step assessment of the chloride ingress behaviour of new cementitious binders</strong></p> <p><strong>William Wilson<sup>a,b,</sup><sup>⁎</sup>, Fabien Georget<sup>a,c</sup>, Karen L. Scrivener<sup>a</sup></strong></p> <p><strong>Cement and Concrete Research, Volume 184, July 2024, 107594</strong></p> <p> </p> <p><sup>a</sup>Laboratory of Construction Materials, EPFL, Lausanne, Switzerland</p> <p><sup>b</sup>Université de Sherbrooke, Sherbrooke, Canada</p> <p><sup>c</sup>Institute of Building Materials Research, RWTH Aachen, Aachen, Germany</p> <p> </p> <p>*Corresponding author: william.wilson@usherbrooke.ca</p>
Fig. 6.- Anthrenus angustefasciatus final larval instar case. 6a in Behavioural and feeding observations of some Anthrenus Geoffroy, 1767 species (Coleoptera, Dermestidae) and identification using final larval instar cases
Fig. 6.- Anthrenus angustefasciatus final larval instar case. 6a.- Dorsal aspect (scale bar = 1 mm). 6b.- Lateral aspect (scale bar = 1 mm). 6c.- Head capsule (scale bar = 1 mm). 6d.- Arrow-headed hastisetae on terminal segments (scale bar = 100 µm).
Fig. 5.- Anthrenus amandae final larval instar case. 5a in Behavioural and feeding observations of some Anthrenus Geoffroy, 1767 species (Coleoptera, Dermestidae) and identification using final larval instar cases
Fig. 5.- Anthrenus amandae final larval instar case. 5a.– Dorsal aspect (scale bar = 1 mm). 5b.- Lateral aspect (scale bar = 1 mm). 5c.- Head capsule (scale bar = 1 mm). 5d.- Arrow-headed hastisetae on terminal segments (scale bar = 100 µm).
Fig. 7.- Anthrenus isabellinus final larval instar case. 7a in Behavioural and feeding observations of some Anthrenus Geoffroy, 1767 species (Coleoptera, Dermestidae) and identification using final larval instar cases
Fig. 7.- Anthrenus isabellinus final larval instar case. 7a.- Dorsal aspect (scale bar = 1 mm). 7b.- Lateral aspect (scale bar = 1 mm). 7c.- Head capsule (scale bar = 1 mm). 7d.- Arrow-headed hastisetae on terminal segments (scale bar = 100 µm).
Fig. 4.- Anthrenus amandae. 4a in Behavioural and feeding observations of some Anthrenus Geoffroy, 1767 species (Coleoptera, Dermestidae) and identification using final larval instar cases
Fig. 4.- Anthrenus amandae. 4a.– Quiescent in final larval instar case. 4b.– Rotation in final larval instar case to split sutures in head capsule to facilitate eclosion. Scale bars = 1 mm in both cases.
Fig. 1.- Dorsal aspect. 1a.- Anthrenus amandae. 1b.- Anthrenus angustefasciatus. 1c in Behavioural and feeding observations of some Anthrenus Geoffroy, 1767 species (Coleoptera, Dermestidae) and identification using final larval instar cases
Fig. 1.- Dorsal aspect. 1a.- Anthrenus amandae. 1b.- Anthrenus angustefasciatus. 1c.- Anthrenus isabellinus. Scale bar = 1 mm in all cases.
Fig. 1 in Short communication Antecedent description and depiction of the recently described cetacean behaviour of trap/tread-water feeding inferred from a nineteenth-century sighting of a 'sea monster' in the Gulf of Suez, Egypt
Fig. 1 - Illustration of a nineteenth-century encounter with a purported sea monster observed in the Gulf of Suez (Andrews, 1879). The vertical body position and open mouth of what is obviously a baleen whale (the rightward animal in the group) closely resembles the photographs and digital reconstructions of the recently described, so-called 'new' or 'first' descriptions of the stationary hunting behaviour of trap/tread-water feeding, as shown in Iwata et al. (2017), McMillan et al. (2018), McCarthy et al. (2023a, 2023b), and Lu (2023). The illustration, drawn in concordance to the eyewitness report, is emblematic of the instance of such whales 'rapidly closing them [their mouths] to trap prey' (McCarthy et al., 2023a). Note the presence of seabirds, something common to all modern recorded instances of such feeding documented in humpback whales, an association which may be related to shoaling fish being driven to seek the apparent shelter of the whale's open mouth (McMillan et al., 2018).
ScienceDex guides
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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.