2026-07-28 カリフォルニア大学バークレー校（UCB）
Overview of the researchers’ large-scale compressive microscope. (a) The imaging system uses an engineered diffractive optical element to generate a distributed multi-spot point spread function (PSF) at the image plane. Images are captured by an array of 48 sensors arranged in a grid, with gaps between individual sensors. (b) The system forward model is a masked convolution with the PSF, which compressively encodes the parts of the image that would normally fall on the gap areas. A computational inverse problem then recovers the full-scale image. (Image courtesy of the researchers)
＜関連情報＞
- https://engineering.berkeley.edu/news/2026/07/bringing-it-all-into-focus/
- https://www.nature.com/articles/s41566-026-01974-4
センサーアレイ全体にわたる回折多重化による大規模圧縮顕微鏡法 Large-scale compressive microscopy via diffractive multiplexing across a sensor array
Kevin C. Zhou,Chaoying Gu,Muneki Ikeda,Tina M. Hayward,Nicholas Antipa,Rajesh Menon,Roarke Horstmeyer,Saul Kato & Laura Waller
Nature Photonics Published:28 July 2026
DOI:https://doi.org/10.1038/s41566-026-01974-4
Abstract
Microscopes face a trade-off between spatial resolution, field of view and frame rate—improving one of these properties typically requires sacrificing others, owing to the limited spatiotemporal throughput of the sensor. To overcome this, we propose a new microscope that achieves snapshot gigapixel-scale imaging with a sensor array and a diffractive optical element. We improve spatiotemporal throughput in two ways. First, we capture data with an array of 48 sensors, resulting in 48× more pixels than a single sensor. Second, we use point spread function engineering and compressive sensing algorithms to fill in the missing information from the gaps between the individual sensors in the array, further increasing the spatiotemporal throughput of the system by an additional >5.4×. The array of sensors is modelled as a single large-format ‘super sensor’, with erasures corresponding to the gap areas between sensors. The sensor array is placed at the output of a (nearly) 4f imaging system, with a diffractive optical element in the Fourier plane that generates a distributed multi-spot point spread function. This enables encoding of information from the entire super-sensor area, including the gaps. We then perform a large-scale regularized reconstruction using a direct fully shift-variant convolutional forward model, assuming that the object is sparse in some domain. Our microscope can achieve ~3 μm resolution over >5.2 cm2 field of view at up to 120 fps, culminating in an effective total spatiotemporal throughput of 25.2 billion pixels per second. We demonstrate the versatility of our microscope in two different modes: structural imaging via dark-field contrast and functional fluorescence imaging of calcium dynamics across dozens of freely moving Caenorhabditis elegans.
