As a bio-inspired vision sensor, spike camera records light intensity by accumulating photons and firing a spike once a preset threshold is reached. For high-light regions, the accumulated photons may reach the threshold multiple times within a readout interval, while only one spike can be stored and read out, resulting in incorrect intensity representation and a limited dynamic range. Multi-level (ML) spike camera enhances the dynamic range by introducing a spike-firing counter (SFC) to count spikes within each readout interval for each pixel, and uses different spike symbols to represent the arrival of different amounts of photons. However, when the light intensity becomes even higher, each pixel requires an SFC with a higher bit depth, causing great cost to the manufacturing process. To address these issues, we propose time-encoding (TE) spike camera, which transforms the counting of spikes to recording of the time at which a specific number of spikes (i.e., an overflow) is reached.

As a bio-inspired vision sensor, spike camera records light intensity by accumulating photons and firing a spike once a preset threshold is reached. For high-light regions, the accumulated photons may reach the threshold multiple times within a readout interval, while only one spike can be stored and read out, resulting in incorrect intensity representation and a limited dynamic range. Multi-level (ML) spike camera enhances the dynamic range by introducing a spike-firing counter (SFC) to count spikes within each readout interval for each pixel, and uses different spike symbols to represent the arrival of different amounts of photons. However, when the light intensity becomes even higher, each pixel requires an SFC with a higher bit depth, causing great cost to the manufacturing process. To address these issues, we propose time-encoding (TE) spike camera, which transforms the counting of spikes to recording of the time at which a specific number of spikes (i.e., an overflow) is reached.

In our experiments, the proposed method achieved a test classification accuracy of 96.5%

Forthenotations of directions, we use the convention that both the incident and outgoing rays point away from a scattering location. Spherical Harmonics (SH) are orthonormal basis defined on complex numbersovertheunitsphere. Since they were designed for scenes with solid objects, we adapt them to cope with participating media. Our implementation of the Neural Reflectance Field [2] baseline uses the same neural network architecture and positional encoding asinthe original paper. In addition, we employ a visibility MLP [3]tocompute a1-Dvisibility anda1-Dexpected termination depth.

Biotechnology can benefit from dynamic control to improve production efficiency. In this context, optogenetics enables modulation of gene expression using light as an external input, allowing fine-tuning of protein levels to unlock dynamic metabolic control and regulation of cell growth. Optogenetic systems can be actuated by light intensity. However, relying solely on intensity-driven control (i.e., signal amplitude) may fail to properly tune optogenetic bioprocesses when the dose-response relationship (i.e., light intensity versus gene-expression strength) is steep. In these cases, tunability is effectively constrained to either fully active or fully repressed gene expression, with little intermediate regulation. Pulse-width modulation, a concept widely used in electronics, can alleviate this issue by alternating between fully ON and OFF light intensity within forcing periods, thereby smoothing the average response and enhancing process controllability. Naturally, optimizing pulse-width-modulated optogenetics entails a switching-time optimal control problem with a binary input over many forcing periods. While this can be formulated as a mixed-integer program on a refined time grid, the number of decision variables can grow rapidly with increasing time-grid resolution and number of forcing periods, compromising tractability. Here, we propose an alternative solution based on reinforcement learning. We parametrize control actions via the duty cycle, a continuous variable that encodes the ON-to-OFF switching time within each forcing period, thereby respecting the intrinsic binary nature of the light intensity.

The application of spectral-shifting films in greenhouses to shift green light to red light has shown variable growth responses across crop species. However, the yield enhancement of crops under altered light quality is related to the collective effects of the specific biophysical characteristics of each species. Considering only one attribute of a crop has limitations in understanding the relationship between sunlight quality adjustments and crop growth performance. Therefore, this study aims to comprehensively link multiple plant phenotypic traits and daily light integral considering the physiological responses of crops to their growth outcomes under SF using artificial intelligence. Between 2021 and 2024, various leafy, fruiting, and root crops were grown in greenhouses covered with either PEF or SF, and leaf reflectance, leaf mass per area, chlorophyll content, daily light integral, and light saturation point were measured from the plants cultivated in each condition. 210 data points were collected, but there was insufficient data to train deep learning models, so a variational autoencoder was used for data augmentation. Most crop yields showed an average increase of 22.5% under SF. These data were used to train several models, including logistic regression, decision tree, random forest, XGBoost, and feedforward neural network (FFNN), aiming to binary classify whether there was a significant effect on yield with SF application. The FFNN achieved a high classification accuracy of 91.4% on a test dataset that was not used for training. This study provide insight into the complex interactions between leaf phenotypic and photosynthetic traits, environmental conditions, and solar spectral components by improving the ability to predict solar spectral shift effects using SF.

It consists of various corner cases.

We cut off the gradient from the render loss to the visibility network. Our inference uses the same setting as the training. Specifically, we implement the dual-network design with a coarse network and a fine network. For the "env + point" illumination, we set the number of first indirect bounces to 32 . F .1 Scenes trained on the "point" Each test view has a new point light.