New breeding gain definitions and their application to the optimization of a molten salt reactor design

The molten salt reactor (MSR) is an attractive breeder reactor. A graphite-moderated MSR can reach breeding because of the online salt processing and refueling. These features give difficulties when the breeding gain (BG) of the MSR is evaluated. The inventory of the core and external stockpiles have to be treated separately in order to quantify the breeding performance of the reactor. In this paper, an improved BG definition is given and it is compared with definitions used earlier. The improved definition was used in an optimization study of the graphite – salt lattice of the core. The aim of the optimization is a passively safe, self-breeder reactor. The fuel channel diameter, graphite volume and thorium concentration were varied while the temperature feedback coefficient of the core, BG – as defined in the paper – and the lifetime of the graphite were calculated. There is a small range of lattices which provide both negative temperature feedback and breeding. Furthermore, breeding is possible only at low power densities in case of the salt processing efficiencies set in this study. In this range of power the lifetime of the graphite is between 12 and 20 years.     

SEDIMENTOLOGICAL AND PALEONTOLOGICAL ANALYSIS OF JURASSIC NORTH SEA DEPOSITS FROM DELTAIC ENVIRONMENTS

Core samples from Well 33/9-3, Norwegian North Sea, have been analysed sedimentologically, palynologically and micro-paleontologically. The cores cover the Toarcian Drake Member of the Dunlin Formation, and nearly the whole thickness of the Middle Jurassic Brent Formation.
The Drake Member is characterized by pro-deltaic depositional conditions. In the Brent Formation, five members are recognized (from below): the Broom, Rannoch and Etive Members represent distributary mouth bar facies; while the Ness and Tarbert Members are recognized as interdistributary bay fill sequences.
The composition of the kerogen assemblages is controlled by the changing energy regimes of the different depositional facies. Terrestrial plant débris are dominant throughout the studied interval. Marine palynomorphs are present in the Drake Member and in the lower part of the Broom Member. The development of rich, arenaceous foraminiferal assemblages in the Drake Member are interpreted as a response to shallow, pro-deltaic conditions. Calcareous foraminifera constitute only a small, accessorial part of these assemblages.     

Lipid composition of commercially canned single-strength orange juice

The lipid composition of commercially canned single-strength orange juice ranged from 84–101 mg/100 ml juice (overall mean 95 ± 6). Phospholipid phosphorus, expressed as mg/100 ml juice, showed a range of from 1.56–1.95, while phospholipid phosphorus/lipid values (as µg-P/mg lipid) were within a very narrow range, 18.9 ± 1.1. The percentage distribution of lipid classes in these juices was 24–35% neutral lipids, 18–23% resin acids and glycolipids, and 43–53% phospholipids and other polar lipids. Five fatty acids, i.e. C₁₆, C_16:1, C_18:1, C_18:2, and C_18:3, accounted for over 93% of all fatty acids. The relative percentages of C_18:2 and C_18:3 differed between seasonal juices. The lipid composition does not warrant inclusion in nutritional labeling; however, lipid levels may be useful in detecting adulteration.     

Stable association of PYK2 and p130(Cas) in osteoclasts and their co-localization in the sealing zone

Bone resorption is initiated by osteoclast attachment to the mineralized matrix, cytoskeletal reorganization, cellular polarization, and the formation of the sealing zone. The present study examines the interaction between PYK2 and p130(Cas) (Crk-associated substrate), suggested to be part of the signaling pathway initiated by osteoclast adhesion. Using murine osteoclast-like cells (OCLs) and their mononuclear precursors (pOCs), generated in a co-culture of bone marrow and osteoblastic MB1.8 cells, we show that: 1) p130(Cas) is tyrosine-phosphorylated upon adhesion of pOCs to vitronectin or ligation of beta3 integrins; 2) p130(Cas) colocalizes with PYK2 and the cytoskeletal proteins F-actin, vinculin, and paxillin in the podosomal-rich ring-like structures of OCLs plated on glass and in the sealing zone in actively resorbing OCLs on bone; 3) p130(Cas) and PYK2 form a stable complex in pOCs, independent of tyrosine phosphorylation of either molecule, and this complex is present in Src (-/-) OCLs, in which neither protein is phosphorylated or associated with the osteoclast adhesion structure; 4) the association of p130(Cas) and PYK2 is mediated by the SH3 domain of p130(Cas) and the C-terminal domain of PYK2. These findings suggest that p130(Cas) and its association with PYK2 may play an important role in the adhesion-dependent signaling that leads to cytoskeletal reorganization and formation of the sealing zone during osteoclast activation.     

Bit-stuffing algorithms and analysis for run-length constrained channels in two and three dimensions

A rigorous derivation is given of the coding rate of a variable-to-variable length bit-stuffing coder for a two-dimensional (1,/spl infin/)-constrained channel. The coder studied is "nearly" a fixed-to-fixed length algorithm. Then an analogous variable-to-variable length bit-stuffing algorithm for the three-dimensional (1,/spl infin/)-constrained channel is presented, and its coding rate is analyzed using the two-dimensional method. The three-dimensional coding rate is demonstrated to be at least 0.502, which is proven to be within 4% of the capacity.     

Fat distribution and insulin response in prepubertal African American and white children

Ethnic differences in obesity-related disease prevalence may relate to differences in fat distribution or metabolism. We conducted a study in 73 African American and white children to examine the relation between fat distribution and insulin and to determine whether ethnic differences in fat distribution or in adiposity-insulin relations contribute to differences in insulin concentrations. Fasting and postchallenge insulin concentrations were determined by oral-glucose-tolerance test, total body fat by dual-energy X-ray absorptiometry, and subcutaneous abdominal (SAAT) and intraabdominal (IAAT) adipose tissue by computerized tomography. African Americans had greater fasting insulin (x +/- SD: 79 +/- 37 compared with 55 +/- 23 pmol/L, P < 0.01), incremental 30-min insulin (567 +/- 438 compared with 300 +/- 304 pmol/L, P < 0.001), and incremental area under the insulin curve (AUC; 262 +/- 209 compared with 164 +/- 156 pmol/L, P < 0.01). In multiple linear regression, fasting insulin was independently related to total fat within both ethnic groups (model R2 = 0.42 and 0.52 for African Americans and whites, respectively), incremental 30-min insulin to total fat and IAAT in whites only (model R2 = 0.71), and AUC to SAAT in African Americans only (model R2 = 0.49). Adjusting insulin indexes for adiposity did not eliminate the significant effect of ethnicity. In general, relations between adiposity and insulin were stronger in whites than in African Americans. African American children had higher insulin concentrations than white children after total body fat, IAAT, and SAAT were controlled for. However, strong relations between adiposity (total and abdominal) and insulin in both groups suggest that obesity may contribute to disease risk regardless of ethnicity.