Light beams carrying orbital angular momentum (OAM) in free space or within optical fibers have a wide range of applications in optics; however, exciting these modes with both high purity and low loss generally requires demanding optimization of excitation conditions in a high dimensional space. Furthermore, mechanical drift can significantly degrade the mode purity over time, which may limit practical deployment of OAM modes in concrete applications. Here, combining an iterative wavefront matching approach and a genetic algorithm, we demonstrate rapid and automated excitation of OAM modes with optimized purity and reduced loss.
View Article and Find Full Text PDFThe brain's remarkable properties arise from the collective activity of millions of neurons. Widespread application of dimensionality reduction to multi-neuron recordings implies that neural dynamics can be approximated by low-dimensional "latent" signals reflecting neural computations. However, can such low-dimensional representations truly explain the vast range of brain activity, and if not, what is the appropriate resolution and scale of recording to capture them? Imaging neural activity at cellular resolution and near-simultaneously across the mouse cortex, we demonstrate an unbounded scaling of dimensionality with neuron number in populations up to 1 million neurons.
View Article and Find Full Text PDFThe brain's remarkable properties arise from collective activity of millions of neurons. Widespread application of dimensionality reduction to multi-neuron recordings implies that neural dynamics can be approximated by low-dimensional "latent" signals reflecting neural computations. However, what would be the biological utility of such a redundant and metabolically costly encoding scheme and what is the appropriate resolution and scale of neural recording to understand brain function? Imaging the activity of one million neurons at cellular resolution and near-simultaneously across mouse cortex, we demonstrate an unbounded scaling of dimensionality with neuron number.
View Article and Find Full Text PDFTwo-photon microscopy has enabled high-resolution imaging of neuroactivity at depth within scattering brain tissue. However, its various realizations have not overcome the tradeoffs between speed and spatiotemporal sampling that would be necessary to enable mesoscale volumetric recording of neuroactivity at cellular resolution and speed compatible with resolving calcium transients. Here, we introduce light beads microscopy (LBM), a scalable and spatiotemporally optimal acquisition approach limited only by fluorescence lifetime, where a set of axially separated and temporally distinct foci record the entire axial imaging range near-simultaneously, enabling volumetric recording at 1.
View Article and Find Full Text PDFCalcium imaging using two-photon scanning microscopy has become an essential tool in neuroscience. However, in its typical implementation, the tradeoffs between fields of view, acquisition speeds, and depth restrictions in scattering brain tissue pose severe limitations. Here, using an integrated systems-wide optimization approach combined with multiple technical innovations, we introduce a new design paradigm for optical microscopy based on maximizing biological information while maintaining the fidelity of obtained neuron signals.
View Article and Find Full Text PDFDispersion control is a critical functionality required in systems involving ultra-short (∼100 fs) pulses, and we demonstrate the use of chirped long-period fiber gratings for this purpose. The operation principles of this device share many attributes with the more established fiber Bragg grating technology for dispersion compensation, but with the added benefit of record low loss (0.2 dB) and the potential of being free from group-delay ripple distortions.
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