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Richard G. Baird

Publications and source records attributed to Richard G. Baird.

3 recordsLinked to original sources

Asynchronous-spectral fusion fluorescence microscopy for microsecond-scale behavioral dynamics

Event-based image sensors provide microsecond temporal resolution but lack spectral discrimination, whereas diffractive spectral imagers encode wavelength information at conventional frame rates. We introduce a fluorescence microscopy architecture that fuses asynchronous event streams with diffraction-encoded CMOS measurements to decouple temporal and spectral sampling. The system achieves ~3.9 um spatial resolution over a 0.5 mm field of view, effective temporal resolution down to 100 us, and differentiates fluorophores whose emission peaks are separated by only 23 nm. By synchronizing and computationally merging both sensing modalities, we enable spectrally resolved tracking at 100,000 frames/s without scanning or filter switching.

physics.optics

HAMscope: a snapshot Hyperspectral Autofluorescence Miniscope for real-time molecular imaging

We introduce HAMscope, a compact, snapshot hyperspectral autofluorescence miniscope that enables real-time, label-free molecular imaging in a wide range of biological systems. By integrating a thin polymer diffuser into a widefield miniscope, HAMscope spectrally encodes each frame and employs a probabilistic deep learning framework to reconstruct 30-channel hyperspectral stacks (452 to 703 nm) or directly infer molecular composition maps from single images. A scalable multi-pass U-Net architecture with transformer-based attention and per-pixel uncertainty estimation enables high spatio-spectral fidelity (mean absolute error ~ 0.0048) at video rates. While initially demonstrated in plant systems, including lignin, chlorophyll, and suberin imaging in intact poplar and cork tissues, the platform is readily adaptable to other applications such as neural activity mapping, metabolic profiling, and histopathology. We show that the system generalizes to out-of-distribution tissue types and supports direct molecular mapping without the need for spectral unmixing. HAMscope establishes a general framework for compact, uncertainty-aware spectral imaging that combines minimal optics with advanced deep learning, offering broad utility for real-time biochemical imaging across neuroscience, environmental monitoring, and biomedicine.

physics.optics

Dynamic Spectral fluorescence microscopy via Event-based & CMOS image-sensor fusion

We present a widefield fluorescence microscope that integrates an event-based image sensor (EBIS) with a CMOS image sensor (CIS) for ultra-fast microscopy with spectral distinction capabilities. The EBIS achieves temporal resolution of $\sim10\thinspaceμ$s ($\sim\thinspace$50,000 frames/s), while the CIS provides diffraction-limited spatial resolution. A diffractive optical element encodes spectral information into a diffractogram, which is recorded by the CIS. The diffractogram is processed using a deep neural network to resolve the fluorescence of two beads, whose emission peaks are separated by only 7 nm and exhibit an 88\% spectral overlap. We validate our microscope by imaging the capillary flow of fluorescent beads, demonstrating a significant advancement in ultra-fast spectral microscopy. This technique holds broad potential for elucidating foundational dynamic biological processes.

physics.optics