Experimental Demonstration of Real-Time 400G Coherent Transmission over 300m OM3 MMF

We experimentally demonstrate real-time coherent transmission up to 400Gbps over 300m OM3 multimode fibers, showing resilience to connector offsets up to 3-6 µm and fiber mechanical shaking using rigorous TIA-455-203 procedures

100 Gbps PON L-band downstream transmission using IQ-MZM CD digital pre-compensation and DD ONU receiver

We propose a downstream direct-detection 100G-PON solution aided by chromatic dispersion digital pre-compensation using an IQ-MZM, allowing L-band operation and 29 dB power budget with low ONU complexity and without requiring single-sideband modulation

Introduction to the JOCN special issue on future PON architectures enabled by advanced technology

This JOCN Special Issue, which spans the September and October 2020 issues, investigates the future of passive optical networks (PONs) in light of new enabling technologies that are currently under consideration. The papers present a broad overview of topics of current interest, across both the physical and network layers. They investigate how new technologies (e.g., higher-speed direct detection transceivers, coherent systems, advanced digital signal processing, and new optoelectronic components) and new network-layer approaches may drive the medium- to long-term evolution of PONs

Analysis and experiments on C band 200G coherent PON based on Alamouti polarization-insensitive receivers

Passive optical network (PON) based on coherent detection has attracted a great deal of attention in recent years as a future solution for 100+ Gbps per wavelength. Particularly for 200G-PON, one of the most attractive options would be to switch to QAM transmission and coherent detection, due to its well know advantages compared to the Direct-Detection approaches used so far in PON. However, coherent technology, extensively used in core networks, has costs that are still perceived as too high for the access ecosystem. In order to perform cost reduction, some groups have studied the option of coherent polarization-independent (PI) detection, since it halves the number of optoelectronic components in the receiver front end. In this paper, we thus present a detailed simulative and experimental investigation of polarization-independent receivers to achieve 200 Gbps transmission in C band using the Alamouti polarization time block coding (PTBC). Our goal is to show what would be the system requirements in terms of optoelectronic bandwidths, laser phase noise and ultimate power budget limitations. We study two different modulation formats: quadrature phase-shift keying (QPSK) and 16 quadrature amplitude modulation (16QAM). We also compare heterodyne and homodyne/intradyne solutions through simulations. As a summarizing result, we experimentally show that 200G PON based on 50 Gbaud-16QAM single-polarization Alamouti coded signals would be possible with today state-of-the-art coherent technologies, demonstrating an Optical Distribution Network loss above 33 dB with 25 km fiber length, a very promising result that is compliant with the PON power budget E1 class

The three-body recombination of a condensed Bose gas near a Feshbach resonance

In this paper, we study the three-body recombination rate of a homogeneous dilute Bose gas with a Feshbach resonance at zero temperature. The ground state and excitations of this system are obtained. The three-body recombination in the ground state is due to the break-up of an atom pair in the quantum depletion and the formation of a molecule by an atom from the broken pair and an atom from the condensate. The rate of this process is in good agreement with the experiment on $^{23}$Na in a wide range of magnetic fields.Comment: 10 pages, 2 figures, to be published in Phys. Rev.

Proportion of various types of thyroid disorders among newborns with congenital hypothyroidism and normally located gland: A regional cohort study

Objective To determine the proportion of the various types of thyroid disorders among newborns detected by the neonatal TSH screening programme, with a normally located thyroid gland.Patients and methods Of the 882 575 infants screened in our centre between 1981 and 2002, 85 infants with a normally located gland had persistent elevation of serum TSH values (an incidence of 1/10 383). Six of these 85 patients were lost to follow-up and were therefore excluded from the study. During follow-up, patients were classified as having permanent or transient hypothyroidism.Results Among the 79 patients included in the study, transient (n = 30, 38% of cases) and permanent (n = 49, 62% of cases) congenital hypothyroidism (CH) was demonstrated during the follow-up at the age of 0.7 +/- 0.6 years and 2.6 +/- 1.8 years (P < 0.0001), respectively. The proportion of premature births was significantly higher in the group with transient CH (57%) than in the group with permanent CH (2%) (P < 0.0001). A history of iatrogenic iodine overload was identified during the neonatal period in 69% of transient cases. Among permanent CH cases (n = 49), patients were classified as having a goitre (n = 27, 55% of cases), a normal sized and shaped thyroid gland (n = 14, 29% of cases) or a hypoplastic gland (n = 8, 16% of cases). The latter patients demonstrated global thyroid hypoplasia (n = 3), a right hemithyroid (n = 2), hypoplasia of the left lobe (n = 2), or asymmetry in the location of the two lobes (n = 1). Patients with a normal sized and shaped thyroid gland showed a significantly less severe form of hypothyroidism than those with a goitre or a hypoplastic thyroid gland (P < 0.0002). Among permanent CH cases, those with a goitre (n = 27) had an iodine organification defect (n = 10), Pendred syndrome (n = 1), a defect of thyroglobulin synthesis (n = 8), or a defect of sodium iodine symporter (n = 1), and in seven patients no aetiology could be determined. Among permanent cases with a normal sized and shaped thyroid gland (n = 14), a specific aetiology was found in only one patient (pseudohypoparathyroidism) and two patients had Down's syndrome. Among those with a globally hypoplastic gland, a TSH receptor gene mutation was found in two patients.Conclusions A precise description of the phenotype can enhance our understanding of various forms of neonatal hypothyroidism as well as their prevalence and management. It also helps to identify cases of congenital hypothyroidism of unknown aetiology, which will need to be investigated in collaboration with molecular biologists