New evidence of broader diets for archaic Homo populations in the northwestern Mediterranean.

Investigating diet breadth is critical for understanding how archaic Homo populations, including Neanderthals, competed for seasonally scarce resources. The current consensus in Western Europe is that ungulates formed the bulk of the human diet during the Lower and Middle Paleolithic, while small fast prey taxa were virtually ignored. Here, we present a multisite taphonomic study of leporid assemblages from Southern France that supports frequent exploitation of small fast game during marine isotope stages 11 to 3. Along with recent evidence from Iberia, our results indicate that the consumption of small fast game was more common prior to the Upper Paleolithic than previously thought and that archaic hominins from the northwestern Mediterranean had broader diets than those from adjacent regions. Although likely of secondary importance relative to ungulates, the frequent exploitation of leporids documented here implies that human diet breadths were substantially more variable within Europe than assumed by current evolutionary models.

Mitigating pattern dependent nonlinearity in SiP IQ-modulators via iterative learning control predistortion.

Silicon based Mach Zehnder modulators, unlike lithium niobate, suffer from nonlinear pattern-dependent behavior beyond simple intersymbol interference. We experimentally demonstrate a novel predistortion method based on the iterative learning control (ILC) technique to address this issue using quasi-real-time adaptation with hardware-in-the-loop. We compare bit error rate performance to that of linear solutions at several M-QAM modulation levels and baud rates. We demonstrate 256QAM at 20 Gbaud which linear compensation alone cannot achieve. For 40 Gbaud 128QAM, we improve power sensitivity by 4.4 dB. We combine optical compensation with ILC to improve power sensitivity by ∼ 5 dB for 60 Gbaud 32QAM.

Dual phase-shift Bragg grating silicon photonic modulator operating up to 60 Gb/s.

We demonstrate PAM-4 and OOK operation of a novel silicon photonic modulator. The modulator design is based on two phase-shifts in a Bragg Grating structure driven in a push pull configuration. Back-to-back PAM-4 modulation is demonstrated below the FEC threshold at up to 60 Gb/s. OOK modulation is also shown up to 55 Gb/s with MMSE equalization and up to 50 Gb/s without equalization. Eye diagrams and BER curves at different bit rates are provided for both PAM-4 and OOK modulations. To our knowledge, this structure is the fastest silicon photonic modulator based on Bragg gratings, reaching modulation speed comparable to the fastest Mach-Zehnder modulators and micro-ring modulators.

Few-mode fiber with inverse-parabolic graded-index profile for transmission of OAM-carrying modes.

A novel type of few-mode fiber, characterized by an inverse-parabolic graded-index profile, is proposed for the robust transmission of cylindrical vector modes as well as modes carrying quantized orbital angular momentum (OAM). Large effective index separations between vector modes (>2.1 × 10(-4)) are numerically calculated and experimentally confirmed in this fiber over the whole C-band, enabling transmission of OAM(+/-1,1) modes for distances up to 1.1 km. Simple design rules are provided for the optimization of the fiber parameters.

Characterization of OAM fibers using fiber Bragg gratings.

The reflectogram of a fiber grating is used to characterize vector modes of an optical fiber supporting orbital angular momentum states. All modes, with a minimal effective index separation around 10(-4), are simultaneously measured. OAM states are reflected by the FBG, along with a charge inversion, at the center wavelength of the Bragg reflection peak of the corresponding fiber vector mode.

Flexible sixteen monopole antenna array for microwave breast cancer detection.

Radar based microwave imaging (MI) has been widely studied for breast cancer detection in recent times. Sensing dielectric property differences of tissues over a wide frequency band has been made possible by ultra-wideband (UWB) techniques. In this paper, a flexible, compact monopole antenna on a 100 µm Kapton polyimide is designed, using a high frequency structure simulator (HFSS), to be in contact with biological breast tissues over the 2-5GHz frequency range. The antenna parameters are optimized to obtain a good impedance match over the required frequency range. The designed antenna size is 18mm × 18mm. Further, a flexible conformal 4×4 ultra-wideband antenna array, in a format similar to that of a bra, was developed for a radar-based breast cancer detection system.

BER performance of implant-to-air high-speed UWB data communications for neural recording systems.

Implant-to-air ultra-wideband communication systems are interesting for neural recording systems due to their low power consumption and high data-rates. In this paper we investigate the performance of an implant-to-air wireless link using a realistic model of the biological channel for neural recording systems. We propose an optimized fifth-derivative Gaussian pulse as a transmitted waveform for different modulations: binary phase shift keying (BPSK), on-off keying (OOK) and differential phase shift keying (DPSK). Monitoring of neural responses with high resolution in the brain requires a high data rate link as the number of electrodes is increased. Each electrode needs a data rate around 800 kb/s to support its neural channel. As we target more than 512 electrodes, we require a data link higher than 400 Mbps.

Monitoring activation of ribonuclease L by 2',5'-oligoadenylates using purified recombinant enzyme and intact malignant glioma cells.

A wide range of methods have been developed to study RNase L activation in cell-free systems and in intact cells. Many of the original methods were developed in the laboratory of I. Kerr in the early 1980s (e.g., see Knight et al.). Additional methods described in this article were developed or adapted from research in other fields after the cloning of RNase L and the appreciation of its role in apoptosis. These methods provide the basic techniques needed to induce RNase L activation in vitro and to measure some of its biological effects in living mammalian cells.

Caspase-dependent apoptosis by 2',5'-oligoadenylate activation of RNase L is enhanced by IFN-beta.

The 2',5'-oligoadenylate (2-5A) system is an interferon (IFN)-regulated RNA decay pathway that provides innate immunity against viral infections. The biologic action of the 2-5A system is mediated by RNase L, an endoribonuclease that becomes enzymatically active after binding to 2-5A. RNase L is also implicated in mediating apoptosis in response to both viral and nonviral inducers. To study the cellular effects of RNase L activation directly, 2-5A was transfected into the human ovarian cancer cell line, Hey1B. Activation of RNase L by 2-5A resulted in specific 18S rRNA cleavage and induction of apoptosis, as measured by TUNEL and annexin V binding assays. In contrast, the dimeric form of 2-5A, ppA2'p5'A, neither activated RNase L nor caused apoptosis. Treatment with IFN-beta prior to 2-5A transfection enhanced cellular RNase L levels (< or = 2.2-fold) and increased the proportion of cells undergoing apoptosis (by < or =40%). However, rRNA cleavages after 2-5A transfections were not enhanced by IFN-beta pretreatments, indicating that basal levels of RNase L were sufficient for this activity. Apoptosis in response to RNase L activation was accompanied by cytochrome c release from mitochondria. Induction of apoptosis by either 2-5A alone or by the combination of 2-5A and IFN-beta was effectively blocked with either the pancaspase inhibitor, Z-VAD-fmk, or with the caspase 3 inhibitor, DEVD-fmk. Therefore, activation of RNase L by 2-5A leads to cytochrome c release into the cytoplasm and then to caspase activation and apoptosis. These results suggest potential uses for 2-5A in augmenting the anticancer activities of IFN.

Mapping the active sites of 3-phosphoglycerate kinase and glycerol kinase with monoammine chromium(III) ATP.

The 12 isomers of monoammine chromium(III) ATP have been used to probe the ATP binding sites of yeast 3-phosphoglycerate kinase and glycerol kinase from Candida mycoderma. Inhibition studies of 3-phosphoglycerate kinase show a dramatic decrease in isomer binding only when the ammonia is in the Delta axial facial anti position. This suggests an open site architecture with only one strong contact point between the coordination sphere and the enzyme surface. These results agree well with the computer modeling studies of bidentate chromium ATP into the nucleotide site determined by X-ray crystallography [McPhillips, T., et al. (1996) Biochemistry 35, 4118-4127]. Both methods describe an open site strongly supporting the validity of the inhibition studies. Inhibition studies of glycerol kinase show significant decreases in binding for all the tested ammonia positions, suggesting a closed site architecture with many contacts between the coordination sphere and the surface of the enzyme. This is in good agreement with X-ray studies [Hurley, T., et al. (1993) Science 259, 673-677] on the Escherichia coli glycerol kinase. Inhibition studies of hexokinase previously reported [Rawlings, J., et al. (1993) Biochemistry 32, 11204-11210] more closely resemble those of 3-phosphoglycerate kinase, suggesting the surprising result that however closely hexokinase and glycerol kinase are related structurally the site around the coordination sphere in hexokinase is functionally open like that of 3-phosphoglycerate kinase.