Excitation and Disruption of a Giant Molecular Cloud by the Supernova Remnant 3C391

Using the IRAM 30-m telescope, we observed the supernova remnant 3C 391 (G31.9+0.0) and its surroundings in the CO(2-1), HCO+(1-0), CS(2-1), CS(3-2), and CS(5-4) lines. The ambient molecular gas at the distance (9 kpc) of the remnant comprises a giant molecular cloud whose edge is closely parallel to a ridge of bright non-thermal radio continuum, which evidently delineates the blast-wave into the cloud. We found that in a small (0.6 pc) portion of the radio shell, the molecular line profiles consist of a narrow (2 km/s) component, plus a very wide (> 20 km/s) component. Both spectral components peak within 20" of a previously-detected OH 1720 MHz maser. We name this source 3C 391:BML (broad molecular line); it provides a new laboratory, similar to IC 443 but on a larger scale, to study shock interactions with dense molecular gas. The wide spectral component is relatively brighter in the higher-excitation lines. We interpret the wide spectral component as post-shock gas, either smoothly accelerated or partially dissociated and reformed behind the shock. The narrow component is either the pre-shock gas or cold gas reformed behind a fully dissociative shock. Using the 3 observed CS lines, we measured the temperature, CS column density, and H2 volume density in a dense clump in the parent molecular cloud as well as the wide-line and narrow-line portions of the shocked clump. The physical conditions of the narrow-line gas are comparable to the highest-density clumps in the giant molecular cloud, while the wide-line gas is both warmer and denser. The mass of compressed gas in 3C 391:BML is high enough that its self-gravity is significant, and eventually it could form one or several stars

Erratum: Corrigendum: Sequence and comparative analysis of the chicken genome provide unique perspectives on vertebrate evolution

International Chicken Genome Sequencing Consortium. The Original Article was published on 09 December 2004. Nature432, 695–716 (2004). In Table 5 of this Article, the last four values listed in the ‘Copy number’ column were incorrect. These should be: LTR elements, 30,000; DNA transposons, 20,000; simple repeats, 140,000; and satellites, 4,000. These errors do not affect any of the conclusions in our paper. Additional information. The online version of the original article can be found at 10.1038/nature0315

A New Fuzzy Logic Approach to Capacitated Dynamic Dial-a-Ride Problem

Almost all Dial-a-Ride problems (DARP) described in the literature pertain to the design of optimal routes and schedules for n customers who specify pick-up and drop-off times. In this article we assume that the customer is mainly concerned with the drop-off time because it is the most important to the customer. Based on the drop-off time specified by the customer and the customer’s location, a pick-up time is calculated and given to the customer by the dispatching office. We base our formulation on a dynamic fuzzy logic approach in which a new request is assigned to a vehicle. The fuzzy logic algorithm chooses the vehicle to transport the customer by seeking to satisfy two objectives. The first reflects the customer’s preference and minimizes the time a customer spends in the vehicle, and the second reflects the company’s preference and minimizes the distance a vehicle needs to travel to transport the customer. The proposed heuristic algorithm is relatively simple and computationally efficient in comparison with most deterministic algorithms for solving both small and large sized problems

Loss of Sparc in p53-null Astrocytes Promotes Macrophage Activation and Phagocytosis Resulting in Decreased Tumor Size and Tumor Cell Survival

Both the induction of SPARC expression and the loss of the p53 tumor suppressor gene are changes that occur early in glioma development. Both SPARC and p53 regulate glioma cell survival by inverse effects on apoptotic signaling. Therefore, during glioma formation, the upregulation of SPARC may cooperate with the loss of p53 to enhance cell survival. This study determined whether the loss of Sparc in astrocytes that are null for p53 would result in reduced cell survival and tumor formation and increased tumor immunogenicity in an in vivo xenograft brain tumor model. In vitro, the loss of Sparc in p53-null astrocytes resulted in an increase in cell proliferation, but a loss of tumorigenicity. At 7 days after intracranial implantation, Sparc-null tumors had decreased tumor cell survival, proliferation and reduced tumor size. The loss of Sparc promoted microglia/macrophage activation and phagocytosis of tumor cells. Our results indicate that the loss of p53 by deletion/mutation in the early stages of glioma formation may cooperate with the induction of SPARC to potentiate cancer cell survival and escape from immune surveillance