Pay Phone Protections in a Smartphone Society: The Need to Restrict Searches of Modern Technology Incident to Arrest

Since their development in the 1980s, cell phones have become ubiquitous in modern society. Today, cell phones feature large data-storage capacities and can access various types of personal media, making them pocket-sized windows into intimate aspects of an individual’s life. Yet many courts treat cell phones as if they were ordinary physical containers, allowing police officers to search the contents of an arrestee’s cell phone incident to an arrest. The warrantless search of electronic devices incident to an arrest, however, cannot be justified on the same grounds as a similar search of physical containers. The government does not have a strong interest in searching a cell phone incident to an arrest because the search is exceedingly unlikely to reveal a concealed weapon or prevent the destruction of evidence. Moreover, given the personal nature of cell phones, individuals have a much greater expectation of privacy in their cell phones than they do in physical containers stored on their persons. This Note argues that search of a cell phone incident to arrest should no longer be blindly governed by the same precedent that controls other searches incident to arrest, and it urges the Supreme Court to engage in a fresh and thoughtful balancing of the interests at stake. Only by creating new doctrine can the Supreme Court adequately protect these important interests and restore fidelity to the Fourth Amendment principles that should govern searches incident to arrest

Scan-less full-field fluorescence-lifetime dual-comb microscopy using two-dimensional spectral mapping and frequency multiplexing of dual-optical-comb beats

Fluorescence lifetime imaging microscopy (FLIM) is a powerful tool for quantitative fluorescence imaging because fluorescence lifetime is independent of concentration of fluorescent molecules or excitation/detection efficiency and is robust to photobleaching. However, since FLIM is based on point-to-point measurements, mechanical scanning of a focal spot is needed for forming an image, which hampers rapid imaging. In this article, we demonstrate scan-less full-field FLIM based on a one-to-one correspondence between two-dimensional (2D) image pixels and frequency-multiplexed RF signals. A vast number of dual-optical-comb beats between dual optical frequency combs is effectively adopted for 2D spectral mapping and high-density frequency multiplexing in radio-frequency region. Bimodal images of fluorescence amplitude and lifetime are obtained with high quantitativeness from amplitude and phase spectra of fluorescence RF comb modes without the need for mechanical scanning. The proposed method will be useful for rapid quantitative fluorescence imaging in life science.Comment: 38 pages, 8 figures, 1 tabl

Full-field fluorescence lifetime dual-comb microscopy using spectral mapping and frequency multiplexing of dual-comb optical beats

Fluorescence lifetime imaging microscopy (FLIM) is a powerful tool for quantitative fluorescence imaging because fluorescence lifetime is independent of concentration of fluorescent molecules or excitation/detection efficiency and is robust to photobleaching. However, since most FLIMs are based on point-to-point measurements, mechanical scanning of a focal spot is needed for forming an image, which hampers rapid imaging. Here, we demonstrate scan-less full-field FLIM based on a one-to-one correspondence between two-dimensional (2D) image pixels and frequency-multiplexed radio frequency (RF) signals. A vast number of dual-comb optical beats between dual optical frequency combs are effectively adopted for 2D spectral mapping and high-density frequency multiplexing in the RF region. Bimodal images of fluorescence amplitude and lifetime are obtained with high quantitativeness from amplitude and phase spectra of fluorescence RF comb modes without the need for mechanical scanning. The parallelized FLIM will be useful for rapid quantitative fluorescence imaging in life science

Optical image amplification in dualcomb microscopy

Dual-comb microscopy (DCM), based on a combination of dual-comb spectroscopy (DCS) with two-dimensional spectral encoding (2D-SE), is a promising method for scan-less confocal laser microscopy giving an amplitude and phase image contrast with the confocality. However, signal loss in a 2D-SE optical system hampers increase in image acquisition rate due to decreased signal-to-noise ratio. In this article, we demonstrated optical image amplification in DCM with an erbium-doped fiber amplifier (EDFA). Combined use of the image-encoded DCS interferogram and the EDFA benefits from not only the batch amplification of amplitude and phase images but also significant rejection of amplified spontaneous emission (ASE) background. Effectiveness of the optical-image-amplified DCM is highlighted in the single-shot quantitative nanometer-order surface topography and the real-time movie of polystyrene beads dynamics under water convection. The proposed method will be a powerful tool for real-time observation of surface topography and fast dynamic phenomena