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Figure 7 in Is there a chance for conservation breeding? Ex situ management, reproduction, and early life stages of the Harlequin toad Atelopus flavescens Duméril & Bibron, 1841 (Amphibia: Anura: Bufonidae)
Figure 7. Color patterns of Atelopus flavescens at the amphibian breeding unit at the Cologne Zoo: Four females (above) and males (below) in ventral and dorsal views. Photographs by D. Karbe.
Figure 6 in Is there a chance for conservation breeding? Ex situ management, reproduction, and early life stages of the Harlequin toad Atelopus flavescens Duméril & Bibron, 1841 (Amphibia: Anura: Bufonidae)
Figure 6. Total length (mm) of larger tadpole of Atelopus flavescens from first clutch in relation to age in days; water temperature 22-24 °C.
Figure 4 in Is there a chance for conservation breeding? Ex situ management, reproduction, and early life stages of the Harlequin toad Atelopus flavescens Duméril & Bibron, 1841 (Amphibia: Anura: Bufonidae)
Figure 4. Hatched larvae of Atelopus flavescens (from first egg deposition): (A) - (B) hatchlings at Gosner stage 20 (13 December 2010), (C) lateral view of tadpole at stages 24-25 (27 December 2010, 22 days after egg deposition), (D) ventral view of tadpole at stage 25 (3 January 2011, 29 days after egg deposition). Photographs by D. Karbe.
Figure 3 in Is there a chance for conservation breeding? Ex situ management, reproduction, and early life stages of the Harlequin toad Atelopus flavescens Duméril & Bibron, 1841 (Amphibia: Anura: Bufonidae)
Figure 3. First clutch of Atelopus flavescens at the amphibian breeding unit at the Cologne Zoo: (A) freshly deposited spawn under water surface on stones or filamentous algae (5 to 6 December 2010), (B) cream-colored eggs one day after deposition (6 December 2010), (C) developing embryos at Gosner stage <18 (9 December 2010), (D) embryos at stage 19 (10 December 2010). Photographs by D. Karbe.
Figure 2 in Is there a chance for conservation breeding? Ex situ management, reproduction, and early life stages of the Harlequin toad Atelopus flavescens Duméril & Bibron, 1841 (Amphibia: Anura: Bufonidae)
Figure 2. Atelopus flavescens at the amphibian breeding unit at the Cologne Zoo: (A) adult male, (B) calling male, and (C) couple in amplexus. Photograph (A) (B) by T. Ziegler and (C) by D. Karbe.
Figure 1 in Is there a chance for conservation breeding? Ex situ management, reproduction, and early life stages of the Harlequin toad Atelopus flavescens Duméril & Bibron, 1841 (Amphibia: Anura: Bufonidae)
Figure 1. Atelopus flavescens terraria in the amphibian breeding unit at the Cologne Zoo from different perspectives (A) - (D); both terraria have artificial streams in the foreground. Photographs by D. Karbe.
Figure 5 in Is there a chance for conservation breeding? Ex situ management, reproduction, and early life stages of the Harlequin toad Atelopus flavescens Duméril & Bibron, 1841 (Amphibia: Anura: Bufonidae)
Figure 5. Tadpoles of Atelopus flavescens: (A) ventral view of larva at Gosner stage 28 (22 February 2011, 79 days after egg deposition; from first clutch; larger larva), (B) lateral view of tadpole at stages 34-36 (22 April 2011, 96 days after egg deposition; from second clutch), (C) ventral view of tadpole at stage 41 (26 April 2011, 100 days after egg deposition; from second clutch), (D) tadpole at stage 42 (15 April 2011, 131 days after egg deposition; smaller larva). Photographs by D. Karbe.
The dataset of article "Early Detection of Cognitive Impairment in End-Stage Renal Disease Patients Undergoing Hemodialysis: Insights from Resting-State Functional Connectivity Analysis"
<p>This is a file as dataset of the article "Early Detection of Cognitive Impairment in End-Stage Renal Disease Patients Undergoing Hemodialysis: Insights from Resting-State Functional Connectivity Analysis".</p> <p>It includes fMRI brain imaging data of subjects included in the case group (ESRD group) and healthy control group (HC group).</p>
Figure 7 in The early stages and breeding sites of four rare saproxylic hoverflies (Diptera: Syrphidae) from Spain
Figure 7. Typical Mallota-shaped puparium of M. dusmeti, lacking the detachable thoracic plate and the drawomitted long tail in lateral view, with head to the left. Scale bar: 4 mm.
Figures 8, 9 in The early stages and breeding sites of four rare saproxylic hoverflies (Diptera: Syrphidae) from Spain
Figures 8, 9. Head skeletons in lateral view. (8) Mallota dusmeti. (9) Myolepta difformis. Scale bar: 1.2 mm.
Figures 3–6 in The early stages and breeding sites of four rare saproxylic hoverflies (Diptera: Syrphidae) from Spain
Figures 3–6. Closely related Ferdinandea species posterior respiratory processes (prp) showing the tube sculpture and the spiracular plate, in dorsal and apical views, respectively. (3, 4) Ferdinandea cuprea. (5, 6) Ferdinandea fumipennis. Scale bars: 1 mm.
Figures 1, 2 in The early stages and breeding sites of four rare saproxylic hoverflies (Diptera: Syrphidae) from Spain
Figures 1, 2. Mandibular sclerite detail from closely related Ferdinandea species head skeletons in lateral view. (1) Ferdinandea cuprea. (2) Ferdinandea fumipennis. Scale bar: 1 mm.
Figures 14–17 in The early stages and breeding sites of four rare saproxylic hoverflies (Diptera: Syrphidae) from Spain
Figures 14–17. Myolepta spp. SEMs. (14) M. difformis anterior spiracle. (15) M. difformis pupal spiracle in dorsal view. (16) M. difformis prp apical end showing laterally the spiracular plate and setae (notice the white patches, always coating extensively Myolepta species puparia). (17) M. obscura prp showing remains of the typical Myolepta white coating (dorsal view). Scale and other photo data are shown at the bottom of each figure.
Figures 10–13 in The early stages and breeding sites of four rare saproxylic hoverflies (Diptera: Syrphidae) from Spain
Figures 10–13. Mallota dusmeti SEMs. (10) Posterior end of the puparium showing the diagnostic conspicuous projections on the lateral ridges (ventral view). (11) Anterior spiracle (both were damaged in the unique available specimen). (12) Pupal spiracle in dorso-lateral view. (13) Detail of pupal spiracle surface. Scale and other photo data are shown at the bottom of each figure.
Text-fig. 6. Scanning electron micrographs of multicarpellate and apocarpous floral structures from the Early Cretaceous Puddledock locality, Virginia, USA (a, b: PP43701, Puddledock sample 001; c: PP43000x, Puddledock sample 073). a) Anacostia? sp., strongly compressed, elongated receptacle with spirally arranged carpels (red dots; not all shown); note larger size compared to the other floral structures; b) Numerous Anacostia type pollen grains in proximal view from the base of floral structure in (a); note graded reticulum over the proximal pole of the pollen grains; c) Elongated receptacle with numerous carpels in a spiral arrangement, possibly representing an earlier developmental stage of Anacostia? sp. Scale bars = 1 mm (a, c), 10 µm (b). in Multiparted, Apocarpous Flowers From The Early Cretaceous Of Eastern North America And Portugal
Text-fig. 6. Scanning electron micrographs of multicarpellate and apocarpous floral structures from the Early Cretaceous Puddledock locality, Virginia, USA (a, b: PP43701, Puddledock sample 001; c: PP43000x, Puddledock sample 073). a) Anacostia? sp., strongly compressed, elongated receptacle with spirally arranged carpels (red dots; not all shown); note larger size compared to the other floral structures; b) Numerous Anacostia type pollen grains in proximal view from the base of floral structure in (a); note graded reticulum over the proximal pole of the pollen grains; c) Elongated receptacle with numerous carpels in a spiral arrangement, possibly representing an earlier developmental stage of Anacostia? sp. Scale bars = 1 mm (a, c), 10 µm (b).
Cowpea GWAS drought stress in early vegetative stage
<p>The GWAS outputs for Cowpea (<em>Vigna unguiculata</em>) responses to drought stress at early vegetative stress. The cowpea seedlings (miniCore population) were exposed to drought stress at 17 days after germination using the weight of the pot and AAWEsmo device, developed in Julkowska Lab, Boyce Thompson Institute. The seedlings were kept at 60 and 10% of soil water holding capacity for 2 weeks and the data on cowpea shoot size, evapotranspiration and photosystem II efficiency was collected. The data was assembled and curated (https://rpubs.com/mjulkowska/Cowpea2022alltraits), and subsequently used for GWAS. The GWAS data was analyzed, and the most interesting associations were selected (https://rpubs.com/mjulkowska/Cowpea2022Gwas). </p> <p>The raw data was collected by Hayley Sussman, with help of Olga Khmelnitsky, while GWAS was performed by Magdalena Julkowska, using ASReml script developed by Arthur Korte (https://github.com/arthurkorte/GWAS), adapted for cowpea. </p>
Fig. 7 in New data on the early stages and behaviour of the endangered species Callophrys mystaphia (Lepidoptera: Lycaenidae) and its first larval parasitoid, Cotesia sp. (Hymenoptera: Braconidae)
Fig. 7. Distribution map of Callophrys mystaphia Miller, 1913 (black circle: records based on scientific papers, empty circle: records of butterfly watchers) and Rheum ribes (square).
Fig. 2 in New data on the early stages and behaviour of the endangered species Callophrys mystaphia (Lepidoptera: Lycaenidae) and its first larval parasitoid, Cotesia sp. (Hymenoptera: Braconidae)
Fig. 2. Feeding larvae of Callophrys mystaphia Miller, 1913 on Rheum ribes host plant. (a–b – fully grown larvae, 20.vi.2020; c–d – final instar larvae approaching pupation, 4.vi.2020).
Fig. 6. a in New data on the early stages and behaviour of the endangered species Callophrys mystaphia (Lepidoptera: Lycaenidae) and its first larval parasitoid, Cotesia sp. (Hymenoptera: Braconidae)
Fig. 6. a – Parasitised larva of Callophrys mystaphia Miller, 1913; b–c – cocoons of the parasitoid; c – intentionally removed larva to reveal the cocoons, d–g – reared parasitoids of the genus Cotesia (Braconidae: Microgastrinae) from various perspectives.
Fig. 1 in New data on the early stages and behaviour of the endangered species Callophrys mystaphia (Lepidoptera: Lycaenidae) and its first larval parasitoid, Cotesia sp. (Hymenoptera: Braconidae)
Fig. 1. Habitus of Callophrys mystaphia Miller, 1913 (a – 29.iv.2020 during a field study, b–c – stretched specimen).
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.