Light/fluorescence microscopy of cells & tissues, and electron/cryo-EM imaging of macromolecular structures — a metadata catalog with a durable link back to the source archive, not a hosted image gallery. These are primary research datasets (often multi-GB to multi-TB), so this platform never downloads or stores the underlying imaging data itself. Datasets already in either source archive are ingested via accession paste/CSV at /mirroring by a Continental Admin (no automated harvesting — neither source archive supports geography-filterable search); a dataset not yet in either archive can instead be submitted directly below by any node operator, for Continental Admin review. Either way, whoever submits an accession or a self-submitted dataset is the one asserting African origin — this platform does not verify it.
Using lacZ reporter mouse models, we mapped expression of the HH ligand SHH, HH receptors, and GLI transcription factors in fungiform, circumvallate and foliate taste papillae in early and late postnatal and adult stages. In adults we also studied the soft palate, and the geniculate and trigeminal ganglia, which extend afferent fibers to the anterior tongue.
3D light-sheet microscopy data for SELMA3D 2026 challenge - contiguous structures - training subset with annotations
BioImage Archive:S-BIAD2106 · Ying Chen (Ludwig-Maximilians-Universität München) · Spialia ali
This dataset is the training set with annotations of contiguous structures for SELMA3D 2026 challenge. The SELMA3D 2026 challenge focuses on self-supervised learning for 3D light-sheet microscopy (LSM) image segmentation. Its objective is to encourage the development of generalizable models capable of serving multiple 3D LSM image segmentation tasks. This dataset contains 3D image patches of different contiguous structures including blood vessels, nerves and axons. Each patch includes corresponding pixel-wise annotations for the structures.
Automated confocal feedback imaging of Plasmodium berghei liver stage translation
BioImage Archive:S-BIAD1040 · Kirsten K. Hanson (The University of Texas at San Antonio) · Plasmodium malariae
Protein synthesis is a core cellular process, necessary throughout the complex lifecycle of Plasmodium parasites, thus specific translation inhibitors would be a valuable class of antimalarial drugs, capable of both treating symptomatic infections in the blood and providing chemoprotection by targeting the initial parasite population in the liver, preventing both human disease and parasite transmission back to the mosquito host. As increasing numbers of antiplasmodial compounds are identified that converge mechanistically at inhibition of cytoplasmic translation, regardless of molecular target or mechanism, it would be useful to gain deeper understanding of how their effectiveness as liver stage translation inhibitors relates to their chemoprotective potential. Here, we probed that relationship using the P. berghei-HepG2 liver stage infection model. Using o-propargyl puromycin-based labeling of the nascent proteome in P. berghei-infected HepG2 monolayers coupled with automated confocal feedback microscopy to generate unbiased, single parasite image sets of P. berghei liver stage translation, we determined translation inhibition EC50s for five compounds, encompassing parasite-specific aminoacyl tRNA synthetase inhibitors, compounds targeting the ribosome in both host and parasite, as well as DDD107498, which targets Plasmodium eEF2, and is a leading antimalarial candidate compound being clinically developed as cabamiquine. Compounds were then tested at equivalent effective concentrations to compare the parasite response to, and recovery from, a brief period of translation inhibition in early schizogony.
A large collection of Scanning Electron Microscopy images of protists and their taxonomic annotations from the Marquesas Island area (Tara Oceans survey, Southern Pacific Ocean).
Tara Expeditions are global scientific voyages that probe morphological and molecular diversity, evolution and ecology of marine plankton to explore how they are impacted by changes in the Earth's climate. The first expeditions collected samples of marine plankton containing viruses, bacteria, archaea, protists and planktonic metazoans living in the photic layer of the world's oceans. These expeditions, the first taking place between 2009 and 2013, include Tara Oceans: a global view, and Tara Oceans Polar Circle, both of which followed the same sampling protocol.
This dataset includes 1074 pictures of 284 planktonic taxa (mainly microalgae and other Ciliate and Radiolarian protists) collected from the vicinity of the Marquesas Islands in the Southern Pacific Ocean during the Tara Oceans expedition. Multiple samples particularly of the size fractions 5-20 and 20 180 um from four sites and two depths were processed with different methods and studied in detail using scanning electron microscopy.
Manuscript abstract:
Malaria transmission relies on sporozoite formation in the mosquito midgut and subsequent salivary gland invasion. Despite their importance, the cell biology of these processes remains poorly understood. We apply Mosquito Tissue Ultrastructure Expansion Microscopy (MoTissU-ExM), which physically expands infected mosquito tissues while preserving host and parasite ultrastructure. MoTissU-ExM reveals parasite structures and organelles, including features previously seen only by electron microscopy and novel structures not observed before. We use MoTissU-ExM to investigate sporozoite formation and salivary gland invasion, focusing on rhoptries - secretory organelles critical for host cell invasion. We establish a timeline for rhoptry biogenesis, show that two rhoptries are consumed during salivary gland invasion, and provide the first evidence that rhoptry pairs are specialized for different invasion events. We further characterize RON11 as the first protein involved in sporozoite rhoptry biogenesis; its disruption produces sporozoites that specifically fail to invade salivary gland epithelial cells, blocking parasite transmission.
Dataset description:
This dataset contains all microscopy data associated with the linked publication "Unlocking new understanding of Plasmodium sporozoite biology with expansion microscopy".
All samples were prepared by ultrastructure-expansion microscopy (U-ExM).
All samples were imaged on either a Zeiss LSM900 or LSM980 microscope, using either Airyscan-SR or Airyscan-MPLX modes.
File names will include the magnification of the objective lens used as follows:
5x = EC Plan-Neofluar 5x/0.16NA Air
10x = Ziess Plan-Apochromat 10x/0.45NA air
20x = Ziess Plan-Apochromat 20x/0.8NA air
40x = Zeiss C-Apochromat 40x/1.2NA water-immersion autocorr M27
63x = Zeiss Plan-Apochromat 63x/1.4NA oil-immersion M27
Images are of mosquito tissues, or isolated parasites, from three Plasmodium species - berghei (Pb), falciparum (Pf), and yoelii (Py).
Images are sorted and named as follows (folder name, file name)
Plasmodium species > Tissue type/site of isolation > Parasite strain > Species abbreviation, MG/SG, Harvest day(dpi), Dye/Fluorophores (405nm -> 647nm), Objective, Image number (1->X), as (airyscan)
For example, the third image taken of a P. berghei oocyst with the RON11iKD parasite line, that was harvested on Day 14 post infection, stained with NHS Ester AF405, BODIPY-FL, anti-Tubulin AF555, and Sytox Red, and imaged on the 40x-objective would be listed as follows:
Plasmodium berghei > Infected midguts > RON11iKD > RON11KD MG 14dpi NHSBFlTub-SytR 40x 1 as
The majority of images in this dataset are z-stacked images, but for many oocysts a single-slice image of the whole oocyst was taken. When this is the case, the single-slice image will be indicated with "SNAP".
A list of the acronyms and abbreviations used in file names are as follows
MG = Midgut
SG = Salivary gland
Spz = Sporozoite
HC = Haemocoel
dpi = Days post infection
NHS = NHS Ester Alexa Fluor 405
BFl = Bodipy-FL-Ceramide
BTRc = Bodipy-TR-Ceramide
SytR = Sytox Deep Red
Tub = anti-tubulin antibody
CSP = anti-circumsporozoite protein antibody
RAP1 = anti-rhoptry associated protein 1 antibody
iKD = Inducible knockdown
Ctrl = Control
KD = Knockdown
RON4 = anti-rhoptry neck protein 4 antibody
GFP = anti-green fluorescent protein antibody
WGA = Wheat germ aglutinnin
BIP = anti-BiP antibody
ERD2 = anti-ERD2 antibody
Heterochrony of axis segmentation underlies extreme morphogenesis in the Japanese eel
BioImage Archive:S-BIAD3325 · (EMBL Heidelberg) · Spialia ali
Heterochrony is a major mode of vertebrate body plan evolution, yet its molecular and cellular basis remains poorly characterized. Here, we show that axis segmentation in Anguilla japonica —a species that forms 120 vertebrae—is driven by the temporal extension of somitogenesis. This is achieved through the prolonged maintenance of axial progenitors in the tail beyond the hatching stage, coupled to an extreme segment scaling regime that operates under the constraint of minimal axis growth. We identify delayed Hox13 activation and sustained Oct4 expression as molecular signatures of the prolonged segmentation program. Furthermore, we describe two spatially distinct axial progenitor pools that expand stemness in the tail. These findings reveal how the modulation of stemness in time and space drives extreme morphological evolution in vertebrates.
BioImage Archive:S-BIAD1504 · Roger Vila (Institut de Biologia Evolutiva) · Spialia ferax
Lepidoptera, i.e. butterflies and moths, are vital components of the global ecosystem. Project Psyche is a scientific research project established to sequence the genomes of all butterflies and moths of Europe; helping to conserve, protect and drive innovation.