Determination of changes in mass and volume of linseed oil during drying

Plates of stainless steel were coated with a thin film of seven different types of oxidative drying oils in order to follow the development charge in mass and volume during 42 days of curing. The plates were weighed in air and in water, and the volumes determined by applying Archimedes’ principle. All of the oils gained considerably in mass, with a maximum of 12% within seven days. The volume, however, decreased with large individual differences from one oil to another. A cold-pressed raw linseed oil decreased in volume by almost 15% whereas the volume of an alkali-refined linseed oil only decreased by a few percent. It is well known that linseed oil-based coatings are prone to crocodiling (surface crack formation), it is suggested that the severity of this phenomenon may be related to the volumetric reduction of the binder during curing. The described method is suggested as a simple means of screening linseed oil binders for formulation and development purposes.     

Estimation of Intrinsic Volumes from Digital Grey-Scale Images

Local algorithms are common tools for estimating intrinsic volumes from black-and-white digital images. However, these algorithms are typically biased in the design based setting, even when the resolution tends to infinity. Moreover, images recorded in practice are most often blurred grey-scale images rather than black-and-white. In this paper, an extended definition of local algorithms, applying directly to grey-scale images without thresholding, is suggested. We investigate the asymptotics of these new algorithms when the resolution tends to infinity and apply this to construct estimators for surface area and integrated mean curvature that are asymptotically unbiased in certain natural settings.     

Social relations and extent and severity of coronary artery disease. The Stockholm Female Coronary Risk Study

Peak bone mass is a major determinant of risk of osteoporotic fracture. Family and twin studies have found a strong genetic component to the determination of bone mineral density (BMD). However, BMD is a complex trait whose expression is confounded by environmental influences and polygenic inheritance. The number, locations, and effects of the individual genes contributing to natural variation in this trait are all unknown. Experimental animal models provide a means to circumvent complicating environmental factors, and the development of dense genetic maps based on molecular markers now provides opportunities to resolve quantitative genetic variation into individual regions of the genome influencing a given trait (quantitative trait loci, QTL). To begin to identify the heritable determinants of BMD, we have examined genetically distinct laboratory mouse strains raised under strict environmental control. Mouse whole-body bone mineral content by dual-energy X-ray absorptiometry (DXA) correlated strongly with skeletal calcium content by ashing, and peak whole-body BMD by DXA in female mice occurred at approximately 80-90 days of age. We therefore determined mean body weight and peak whole body BMD values in 12-week-old female mice from a panel of 24 recombinant inbred (RI) BXD strains, derived from a cross between C57BL/6 and DBA/2 progenitors. The distribution of body weight and BMD values among the strains clearly indicated the presence of strong genetic influences on both of these traits, with an estimated narrow sense heritability of 60% and 35%, respectively. The patterns of differences in body weight and peak whole body BMD in the BXD strains were then integrated with a large database of genetic markers previously defined in the RI BXD strains to generate chromosome map sites for QTL. After correction for redundancy among the significant correlations, QTL analysis of the BXD RI strain series provisionally identified 10 chromosomal sites linked to peak bone mass development in the female. Several of the identified sites map near genes encoding hormones, structural proteins, and cell surface receptors that are intricately involved in skeletal homeostasis. Four QTL for body weight were also identified. One of these loci was also strongly linked to inherited variation in BMD. This finding suggests that body weight and peak BMD may be influenced by linked genes or perhaps by common genes with pleiotropic effects. Our phenotyping in the RI BXD strains has allowed us to map a number of specific genetic loci strongly related to the acquisition of peak BMD. Confirmation of these findings will likely result in the understanding of which genes control skeletal health.