Interannual predictability of Arctic sea ice in a global climate model: regional contrasts and temporal evolution

The predictability of the Arctic sea ice is investigated at the interannual time scale using decadal experiments performed within the framework of the fifth phase of the Coupled Model Intercomparison Project with the CNRM-CM5.1 coupled atmosphere–ocean global climate model. The predictability of summer Arctic sea ice extent is found to be weak and not to exceed 2 years. In contrast, robust prognostic potential predictability (PPP) up to several years is found for winter sea ice extent and volume. This predictability is regionally contrasted. The marginal seas in the Atlantic sector and the central Arctic show the highest potential predictability, while the marginal seas in the Pacific sector are barely predictable. The PPP is shown to decrease drastically in the more recent period. Regarding sea ice extent, this decrease is explained by a strong reduction of its natural variability in the Greenland–Iceland–Norwegian Seas due to the quasi-disappearance of the marginal ice zone in the center of the Greenland Sea. In contrast, the decrease of predictability of sea ice volume arises from the combined effect of a reduction of its natural variability and an increase in its chaotic nature. The latter is attributed to a thinning of sea ice cover over the whole Arctic, making it more sensitive to atmospheric fluctuations. In contrast to the PPP assessment, the prediction skill as measured by the anomaly correlation coefficient is found to be mostly due to external forcing. Yet, in agreement with the PPP assessment, a weak added value of the initialization is found in the Atlantic sector. Nevertheless, the trend-independent component of this skill is not statistically significant beyond the forecast range of 3 months. These contrasted findings regarding potential predictability and prediction skill arising from the initialization suggest that substantial improvements can be made in order to enhance the prediction skill.     

The Tuxtuac,Mexico, Meteorite,an LL5 Chondrite Fall

Abstract— The Tuxtuac meteorite fell in Zacatecas state, Mexico, on 16 October 1975, at 1820 hours. Two partly crusted masses, weighing 1924 g and 2340 g, were recovered. The stone is an ordinary chondrite, LL5, with olivine Fa₃₀ and 19.22 weight % total iron. The silicates contain numerous voids and a froth-like mesostasis is present within some chondrules. Metal phases present are kamacite (5.7–6.4% Ni, 6–7% Co) and high nickel metal (taenite 37–41% Ni, 1.7 ± 0.3% Co; tetrataenite 47–52% Ni, 0.8–1.4% Co). The stone is unusual for an LL-group chondrite in that it exhibits neither large-scale brecciation features nor dark veins.     

An Aeronautical Temporal GIS for Post-Flight Assessment of Navigation Performance

This paper describes the design and development of an experimental GIS prototype that may be used to assist experienced pilots, student pilots and flight instructors for post-flight evaluation of navigation performance. The system is developed as a GIS experimental application which employs geographical data derived from the Digital Chart of the World integrated with airspace data derived from the ICAO 1:500,000 Aeronautical Chart. Real-time data are collected and integrated within a monitoring computing environment from external sensors which include GPS, altitude and relative motion sensors. This enables the generation of multi-layered digital maps and navigation data capable of being rapidly re-configured to enhance visualization by abstraction. The integration of real time navigation data with geographical data facilitates airborne decision-making, cockpit management, and makes a valuable contribution to flight safety.     

Rhodamine exclusion activity in primary cultured turbot (Scophthalmus maximus) hepatocytes

Cellular detoxification by direct processes has been investigated in fish by studying the ability of hepatocytes prepared from juvenile aquarium-reared turbot (Scophthalmus maximus) to actively exclude the fluorescent dye rhodamine B (RB). Cell viability was studied by measurements of non-specific esterase activity using fluorescein diacetate. This revealed that turbot hepatocytes can be cultured for a few days with a viability decreasing to 38% after 24 h. The 24-h cultured cells have been used to study the rhodamine B exclusion activity using confocal laser microscopy. Hepatocytes accumulated the dye in a competitive manner with verapamil, thus suggesting that they express a transport system similar to the P-glycoprotein-mediated multixenobiotic resistance process. Incubation of cells with 1 μM RB and 20 μM verapamil led to a 26% increase of cellular fluorescence as compared to the accumulation in absence of competitor. Rhodamine B accumulated in the whole cytoplasm, with more concentrated areas that might correspond to the lysosomal compartment and the cell membrane.     

Rhodamine exclusion activity in primary cultured turbot (Scophthalmus maximus) hepatocytes

Cellular detoxification by direct processes has been investigated in fish by studying the ability of hepatocytes prepared from juvenile aquarium-reared turbot (Scophthalmus maximus) to actively exclude the fluorescent dye rhodamine B (RB). Cell viability was studied by measurements of non-specific esterase activity using fluorescein diacetate. This revealed that turbot hepatocytes can be cultured for a few days with a viability decreasing to 38% after 24 h. The 24-h cultured cells have been used to study the rhodamine B exclusion activity using confocal laser microscopy. Hepatocytes accumulated the dye in a competitive manner with verapamil, thus suggesting that they express a transport system similar to the P-glycoprotein-mediated multixenobiotic resistance process. Incubation of cells with 1 microM RB and 20 microM verapamil led to a 26% increase of cellular fluorescence as compared to the accumulation in absence of competitor. Rhodamine B accumulated in the whole cytoplasm, with more concentrated areas that might correspond to the lysosomal compartment and the cell membrane.