Intracavity interrogation of an array of fiber Bragg gratings.

In this work, we explore the interrogation of an array of fiber Bragg gratings as part of a laser cavity. A semiconductor optical amplifier in a sigma-shaped fiber cavity provides gain and is gated periodically at a rate that matches the roundtrip time associated with each grating of the array. The interrogator exhibits clear laser properties such as a threshold and linewidth narrowing. Besides improving the signal-to-noise ratio and enabling the re-use of wavelengths, it is found that this interrogation scheme enables monitoring of weak gratings spaced by less than 1 cm. Intracavity grating interrogation studied here is found to be a simple and powerful way to increase the number of sensor points for industrial applications.

C-cavity fiber laser employing a chirped fiber Bragg grating for electrically gated wavelength tuning.

We present a novel C-cavity concept for tunable lasers. The laser is based on a semiconductor optical amplifier (SOA), serving both as a gain medium as well as a modulator, and a chirped fiber Bragg grating (C-FBG) which acts as the end mirrors on both cavity ends. Driving the SOA with a pulse pair with variable delay enables wavelength tuning by targeting different regions in the C-FBG with the circulating pulse. The cavity design allows for wide tuning while maintaining a constant repetition rate, we show a tuning range of 35 nm -limited by the C-FBG's reflection bandwidth. Time-multiplexed operation with four different wavelengths is also demonstrated. Furthermore, the laser performance and dynamics under different operating conditions are analyzed and discussed.

1.57 µm fiber source for atmospheric CO2 continuous-wave differential absorption lidar.

We present an efficient fiber source designed for continuous-wave differential absorption light detection and ranging (CW DIAL) of atmospheric CO2-concentration. It has a linewidth of 3 MHz, a tuning range of 2 nm over the CO2 absorption peaks at 1.572 µm, and an output power of 1.3 W limited by available pump power. Results from the initial CW DIAL testing are also presented and discussed.

Continuously tunable, narrow-linewidth laser based on a semiconductor optical amplifier and a linearly chirped fiber Bragg grating.

We describe a simple, narrow-linewidth, tunable fiber-based laser with a high degree of tuning accuracy. A polarization independent semiconductor optical amplifier (SOA) is used as the gain medium in a unidirectional fiber ring cavity with a circulator connected to a 6-meter long chirped fiber Bragg grating (CFBG). The laser wavelength is chosen by setting the modulation frequency of the SOA the same as the harmonics of the fundamental repetition rate of the light reflected at a specific point on the CFBG. Careful management of the drive current and pulse width helps to generate laser light of narrow linewidth (less than 0.03 nm) with low power variation (1.46 dB) over a tuning range of 40 nm.

Atmospheric CO2 sensing using Scheimpflug-lidar based on a 1.57-µm fiber source.

A molecular laser-radar system, based on the Scheimpflug principle, has been constructed and demonstrated for remote sensing of atmospheric CO2 concentrations using Differential Absorption Lidar (DIAL) in the (30012←00001) absorption band. The laser source is a Continues Wave (CW) Distributed-FeedBack (DFB) diode laser seeding an Erbium-doped fiber amplifier, emitting narrowband (3 MHz) tunable radiation with an output power of 1.3 W at 1.57 µm. The laser beam is expanded and transmitted to the atmosphere. The atmospheric backscattered signal is collected with a Newtonian telescope and detected with a linear InGaAs array detector satisfying the Scheimpflug condition. We present range-resolved measurements of atmospheric CO2 concentration from a test range of 2 km located in the city of Lund, Sweden. We discuss and provide scalable results for CO2 profiling with the Scheimpflug-lidar method.

Samp1 is functionally associated with the LINC complex and A-type lamina networks.

The transmembrane inner nuclear membrane (INM) protein Samp1 is required for anchoring centrosomes near the nuclei. Using high-resolution fluorescence microscopy we show that Samp1 is distributed in a distinct and characteristic pattern in the nuclear envelope (NE), where it partially colocalizes with the LINC complex protein Sun1. By studying the localization of Samp1 deletion mutants and fusion proteins, we conclude that the cysteine-rich N-terminal half of Samp1 is nucleoplasmically exposed and is responsible for targeting to the INM. It contains four conserved CxxC motifs with the potential to form zinc fingers. The distribution of cysteine-to-alanine substitution mutants, designed to prevent zinc finger formation, showed that NE localization of Samp1 depends on intact CxxC motifs. Overexpression of Samp1 zinc finger mutants produced an abnormal dominant phenotype characterized by disrupted organization of a selective subset NE proteins, including emerin, Sun1, endogenous Samp1 and, in some cases, lamin A/C, but not lamin B, Sun2 or nucleoporins. Silencing of Samp1 expression showed that emerin depends on Samp1 for its correct localization in the NE. Our results demonstrate that Samp1 is functionally associated with the LINC complex protein Sun1 and proteins of the A-type lamina network.

A comparative study of an Yb-doped fiber gain-managed nonlinear amplifier seeded by femtosecond fiber lasers.

In this work, we show that the nonlinear evolution of femtosecond seed pulses with different parameters (temporal and spectral shapes, repetition rate, pulse energy) in an Yb-fiber amplifier leads to gain-managed nonlinear amplification, enabling robust generation of high-peak-power and nearly transform-limited pulses after external compression. We demonstrate a compressed pulse duration of 33 fs with an energy of 80.5 nJ and a peak power of 2.29 MW for a source with a repetition rate of 30 MHz. For a second seed source with a repetition rate of 125 MHz, we obtained a pulse duration of 51 fs with an energy of 22.8 nJ and a peak power of 420 kW. Numerical simulations incorporating rate equations and nonlinear propagation in the amplifier provide evolutions that agree well with the experimental results. The discrepancies in the amplifier's absorption edge appearing at low repetition rates and higher pump powers are attributed to the temperature dependence of the amplifier's gain cross-sections. Here, we experimentally verify this attribution and thus underline the importance of accounting for the fiber core temperature for precise modelling of the short-wavelength spectral edge of the output pulses in nonlinear Yb-fiber amplifiers. We also measure, for the first time, the relative intensity noise of an amplifier operating in the gain-managed nonlinear regime. The measurements reveal a significant contribution of the amplification process to the overall output noise of the system.

Report of the Joint Workshop on Induced Special Regions.

The Joint Workshop on Induced Special Regions convened scientists and planetary protection experts to assess the potential of inducing special regions through lander or rover activity. An Induced Special Region is defined as a place where the presence of the spacecraft could induce water activity and temperature to be sufficiently high and persist for long enough to plausibly harbor life. The questions the workshop participants addressed were: (1) What is a safe stand-off distance, or formula to derive a safe distance, to a purported special region? (2) Questions about RTGs (Radioisotope Thermoelectric Generator), other heat sources, and their ability to induce special regions. (3) Is it possible to have an infected area on Mars that does not contaminate the rest of Mars? The workshop participants reached a general consensus addressing the posed questions, in summary: (1) While a spacecraft on the surface of Mars may not be able to explore a special region during the prime mission, the safe stand-off distance would decrease with time because the sterilizing environment, that is the martian surface would progressively clean the exposed surfaces. However, the analysis supporting such an exploration should ensure that the risk to exposing interior portions of the spacecraft (i.e., essentially unsterilized) to the martian surface is minimized. (2) An RTG at the surface of Mars would not create a Special Region but the short-term result depends on kinetics of melting, freezing, deliquescence, and desiccation. While a buried RTG could induce a Special Region, it would not pose a long-term contamination threat to Mars, with the possible exception of a migrating RTG in an icy deposit. (3) Induced Special Regions can allow microbial replication to occur (by definition), but such replication at the surface is unlikely to globally contaminate Mars. An induced subsurface Special Region would be isolated and microbial transport away from subsurface site is highly improbable.

A case of extreme weight loss due to mesenteric ischemia and antiphospholipid syndrome.

Mesenteric ischemia and antiphospholipid syndrome is a rare combination but should be suspected as a differential diagnosis. This may be presented as diffuse abdominal pain typically after food intake, diarrhea, and weight loss. Early recognition is warranted, and nutrition, stenting, and anticoagulant treatments are indicated.

Endothelial cell-surface tissue transglutaminase inhibits neutrophil adhesion by binding and releasing nitric oxide.

Nitric oxide (NO) produced by endothelial cells in response to cytokines displays anti-inflammatory activity by preventing the adherence, migration and activation of neutrophils. The molecular mechanism by which NO operates at the blood-endothelium interface to exert anti-inflammatory properties is largely unknown. Here we show that on endothelial surfaces, NO is associated with the sulfhydryl-rich protein tissue transglutaminase (TG2), thereby endowing the membrane surfaces with anti-inflammatory properties. We find that tumor necrosis factor-α-stimulated neutrophil adherence is opposed by TG2 molecules that are bound to the endothelial surface. Alkylation of cysteine residues in TG2 or inhibition of endothelial NO synthesis renders the surface-bound TG2 inactive, whereas specific, high affinity binding of S-nitrosylated TG2 (SNO-TG2) to endothelial surfaces restores the anti-inflammatory properties of the endothelium, and reconstitutes the activity of endothelial-derived NO. We also show that SNO-TG2 is present in healthy tissues and that it forms on the membranes of shear-activated endothelial cells. Thus, the anti-inflammatory mechanism that prevents neutrophils from adhering to endothelial cells is identified with TG2 S-nitrosylation at the endothelial cell-blood interface.

Accurate modeling of high-repetition rate ultrashort pulse amplification in optical fibers.

A numerical model for amplification of ultrashort pulses with high repetition rates in fiber amplifiers is presented. The pulse propagation is modeled by jointly solving the steady-state rate equations and the generalized nonlinear Schrödinger equation, which allows accurate treatment of nonlinear and dispersive effects whilst considering arbitrary spatial and spectral gain dependencies. Comparison of data acquired by using the developed model and experimental results prove to be in good agreement.

An integral protein of the inner nuclear membrane localizes to the mitotic spindle in mammalian cells.

Here, we characterize a transmembrane protein of the nuclear envelope that we name spindle-associated membrane protein 1 (Samp1). The protein is conserved in metazoa and fission yeast and is homologous to Net5 in rat and Ima1 in Schizosaccharomyces pombe. We show that, in human cells, the protein is a membrane-spanning polypeptide with an apparent molecular mass of 43 kDa. This is consistent with a predicted polypeptide of 392 amino acids that has five transmembrane segments and its C-terminus exposed to the nucleoplasm. During interphase, Samp1 was specifically distributed in the inner nuclear membrane. Post-transcriptional silencing of Samp1 expression resulted in separation of centrosomes from the nuclear envelope, indicating that it is functionally connected to the cytoskeleton. At the onset of mitosis, most of the protein dispersed out into the ER, as expected. However, during mitosis, a significant fraction of the protein specifically localized to the polar regions of the mitotic spindle. We demonstrate for the first time, in human cells, the existence of a membranous structure overlapping with the mitotic spindle. Interestingly, another integral inner nuclear membrane protein, emerin, was absent from the spindle-associated membranes. Thus, Samp1 defines a specific membrane domain associated with the mitotic spindle.

Neisseria gonorrhoeae isolates with reduced susceptibility to cefixime and ceftriaxone: association with genetic polymorphisms in penA, mtrR, porB1b, and ponA.

The recent emergence and transmission of Neisseria gonorrhoeae isolates with reduced susceptibility to expanded-spectrum cephalosporins such as cefixime and ceftriaxone have been reported. The aim of this study was to determine the correlation of different polymorphisms in the penA, mtrR, porB1b (penB), and ponA genes of N. gonorrhoeae with reduced susceptibility to cefixime and ceftriaxone. Eighteen gonococcal isolates with reduced cefixime and ceftriaxone susceptibility (Cef(i)) and two susceptible isolates were characterized using serovar determination, antibiograms, N. gonorrhoeae multiantigen sequence typing (NG-MAST), and sequencing of penA, mtrR, porB1b, and ponA alleles. For the Cef(i) isolates (n = 18), the MICs of cefixime and ceftriaxone ranged between 0.032 to 0.38 mug/ml and 0.064 to 0.125 mug/ml, respectively. These isolates were assigned five different serovars and six divergent NG-MAST sequence types. Eleven isolates (61%) with higher MICs of cefixime and ceftriaxone contained a nearly identical penA mosaic allele and previously described polymorphisms in mtrR (a single nucleotide [A] deletion in the promoter), penB (mutations in porB1b encoding loop 3 of PorB1b), and ponA (ponA1 polymorphism). The remaining seven Cef(i) isolates (39%), which had somewhat lower MICs of cefixime and ceftriaxone, contained an aspartic acid insertion (Asp-345a) in PBP 2 in conjunction with alterations of 4 to 10 amino acid residues in the C-terminal region of the transpeptidase domain of penA. In conclusion, an unambiguous association between penA mosaic alleles, in conjunction with genetic polymorphisms in mtrR, porB1b, and ponA, and greater reduced susceptibility to cefixime and ceftriaxone was identified.