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Figure 1 in Nidicolous tadpoles rather than direct development in Malagasy frogs of the genus Gephyromantis
Figure 1. Photographs of the oral disc of the preserved voucher specimens of tadpoles described in this paper (stained with methylene blue). (A) Gephyromantis granulatus (ZSM 298/2008 – Tad 2004-75); (B) G. sculpturatus (ZSM 16/2008 – ZCMV 4833); (C) G. tschenki (ZSM 142/2007 – ZCMV 4335); (D) G. ventrimaculatus (ZSM 852/2007 – ZCMV 4927); (E) G. ambohitra (ZSM 756/2004 – FGMV 2003-1946); (F) G. asper (ZSM 1912/2007 – ZCMV 3401); (G) G. azzurae (ZSM 1922/2007 – T 2007-511); (H) G. corvus ZSM 0674/2008 – T 001); (I) G. pseudoasper (ZSM 707/2004 – FGMV 2003-1919). The scale bars represent 1 mm.
Figure 9 in Can hair width and scale pattern and direction of dorsal scapular mammalian hair be a relatively simple means to identify species?
Figure 9. Scanning electron micrographs of mammalian hair. Little pocket mouse underfur (A); muskrat guard hair (B) and underfur (C); gold mantled ground squirrel guard hair (D, E) and underfur (F).
Figure 3 in Can hair width and scale pattern and direction of dorsal scapular mammalian hair be a relatively simple means to identify species?
Figure 3. Scanning electron micrographs of mammalian hair. Striped skunk guard hair (A, C) and underfur (B, D); American badger guard hair (E) and underfur (F).
Figure 4 in Can hair width and scale pattern and direction of dorsal scapular mammalian hair be a relatively simple means to identify species?
Figure 4. Scanning electron micrographs of mammalian hair. Northern raccoon guard hair (A) and underfur (B); American black bear guard hair (C) and underfur (D); pallid bat underfur (E, F).
Figure 1 in Can hair width and scale pattern and direction of dorsal scapular mammalian hair be a relatively simple means to identify species?
Figure 1. Scanning electron micrographs of mammalian hair. Bighorn sheep guard hair (A) and underfur (B); elk guard hair (C) and underfur (D); white tailed deer guard hair (E) and underfur (F).
Figure 8 in Can hair width and scale pattern and direction of dorsal scapular mammalian hair be a relatively simple means to identify species?
Figure 8. Scanning electron micrographs of mammalian hair. North American porcupine guard hair (A–C); northern pocket gopher underfur (D, E); little pocket mouse guard hair (F).
Figure 7 in Can hair width and scale pattern and direction of dorsal scapular mammalian hair be a relatively simple means to identify species?
Figure 7. Scanning electron micrographs of mammalian hair. White tailed jackrabbit guard hair (A) and underfur (B); American beaver guard hair (C) and underfur (D); North American porcupine guard hair (E, F).
Figure 2 in Can hair width and scale pattern and direction of dorsal scapular mammalian hair be a relatively simple means to identify species?
Figure 2. Scanning electron micrographs of mammalian hair. Coyote guard hair (A) and underfur (B); red fox guard hair (C) and underfur (D); cougar guard hair (E) and underfur (F).
Figure 5 in Can hair width and scale pattern and direction of dorsal scapular mammalian hair be a relatively simple means to identify species?
Figure 5. Scanning electron micrographs of mammalian hair. Pallid bat underfur (A); Virginia opossum guard hair (B) and underfur (C); Merriam's shrew guard hair (D, E) and underfur (F).
Figure 6 in Can hair width and scale pattern and direction of dorsal scapular mammalian hair be a relatively simple means to identify species?
Figure 6. Scanning electron micrographs of mammalian hair. Merriam's shrew guard hair (A); broad-footed mole guard hair (C, F) and underfur (B, D, E).
Figure 7 in Reproduction, development and parental care in two direct-developing flatworms (Platyhelminthes: Polycladida: Acotylea)
Figure 7. Imogine zebra parental care: (A) covering newly laid eggs, (B) attacking a gastropod near a recently laid egg plate, scale bars, 1 mm. Imogine zebra, ventral views: (C) before oviposition, showing egg-filled uteri (u), filled ventral glands (gl), and gonopore (gp), scale bar 5 mm; (D) immediately after oviposition, showing marked decrease in gland contents, scale bar 2 mm.
Figure 4 in Reproduction, development and parental care in two direct-developing flatworms (Platyhelminthes: Polycladida: Acotylea)
Figure 4. Relationship between adult length (in mm) and (A) egg production and (B) the number of egg batches in Pleioplana atomata and Imogine zebra.
Figure 5 in Reproduction, development and parental care in two direct-developing flatworms (Platyhelminthes: Polycladida: Acotylea)
Figure 5. Imogine zebra, developmental stages. (A) egg blebbing, (B) two-cell to eight-cell stage, (C) 16-cell stage, (D) 32-cell stage, (E) solid morulae, (F) gastrulation by epiboly, arrowhead indicates blastopore, (G) embryo with one pair of eyes (arrowheads), (H) embryos with noticeable pharynges, (I) embryo with two pairs of eyes, (J) juvenile worm hatching out of eggshell. Scale bars (C, D, I) 50 mm, all others 100 mm.
Figure 3 in Reproduction, development and parental care in two direct-developing flatworms (Platyhelminthes: Polycladida: Acotylea)
Figure 3. Egg masses: (A) Pleioplana atomata, (B) Imogine zebra. Scale bars, 500 mm. Pleioplana atomata: (C) two eggs per egg capsule, scale bar 150 mm, (D) conjoined hatchlings, scale bar 100 mm.
Figure 1 in Reproduction, development and parental care in two direct-developing flatworms (Platyhelminthes: Polycladida: Acotylea)
Figure 1. Pleioplana atomata reproductive behaviour: (A) initial encounters, (B) and (C) reciprocal prodding of ventral surface, and (D) copulation. Images are video stills.
Figure 8 in Reproduction, development and parental care in two direct-developing flatworms (Platyhelminthes: Polycladida: Acotylea)
Figure 8. Variation in mean hatching rate (¡1 SE) per batch of eggs with and without parental care in Pleioplana atomata and Imogine zebra. (A, C) Treatment 1 – egg hatching rate for all batches per individual; black bars – with parental care, white bars – without parental care, (B, D) Treatment 2 – three egg batches with parental care and three batches without parental care per individual.
Figure 2 in Reproduction, development and parental care in two direct-developing flatworms (Platyhelminthes: Polycladida: Acotylea)
Figure 2. Imogine zebra reproductive behaviour: (A) initial encounter and gliding over each other, (B) prodding of dorsal surface, (C) unilateral sperm transfer, (D) sperm transfer among multiple animals, (E) spermatophores on dorsal surface. Images are video stills.
Figure 6 in Reproduction, development and parental care in two direct-developing flatworms (Platyhelminthes: Polycladida: Acotylea)
Figure 6. Hatchlings (A) Pleioplana atomata and (B) Imogine zebra, arrowheads indicate caudal cilia. Scale bars, 100 mm.
Identification of PIAS1-direct interacting proteins through DSP-based crosslinking
<p>As a conserved post-translational modification, SUMOylation has been shown to play important roles in chromatin related biological processes including transcription. However, how the SUMOylation machinery associates with chromatin is not clear. To underatand how nuclear matrix associated SUMO enzymes regulate chromatin related function, we attempted to identify the direct interacting proteins of PIAS1, a major SUMO E3 protein. We made use of the crosslinking reagent dithiobis succinimidyl propionate (DSP), which is a water-insoluble, membrane-permeable homobifunctional N-hydroxysuccimide ester that can reversibly cross-link different proteins by primary amines in cells.</p>
Figure 1 in Direct development of the bush frog Raorchestes longchuanensis (Yang and Li 1978) under laborary conditions in Southern China
Figure 1. The map of the study area. Red star denotes Yinjiang, Yunnan, China, the locality of Raorchestes longchuanensis.
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.