The distinction between the two systems should not be thought of

The distinction between the two systems should not be thought of in terms of a “black and white” phenomenon anymore, as recent molecular and genomic information points to the fact that a line of distinction is not as sharp as it was once thought to be, but it is blurred by different shades of grey. (Asian Pac J Allergy Immunol 2014;32:3-15)”
“Elevation confers limitations on distribution of

organisms through correlated variations in temperature, moisture, radiations and precipitation. The elevation gradients of terricolous lichen species richness in Garhwal, western Himalaya were assessed using generalized additive models, in order to compare distribution patterns of different growth-forms, photobiont types, and dominant families. A total of 148 terricolous lichen Selleckchem HIF inhibitor species belonging to 42 genera and 19 families AZD1208 were recorded. The total species richness showed unimodal relationship with elevation, where the highest species richness was observed at mid elevations (3,200 m). The species richness of lichens with green algae (chlorolichens) and of lichens with cyanobacteria (cyanolichens) also exhibited significant unimodal elevational patterns with cyanolichens peaked at somewhat lower (2,800-2,900 m) elevation than

chlorolichens (3,200 m). Growth forms showed statistically significant relationship of species richness to elevation, with crustose and squamulose lichens reaching their maxima at higher elevation than foliose, fruticose and dimorphic terricolous lichens. Unimodal pattern of species richness was also followed by six dominant families, with these families reaching maximum richness at different elevations. Elevational variation in topography, climate, and competition from vascular plant communities, together with the tolerance of specific growth forms to zoo-anthropogenic pressures, shape the distribution of terricolous lichens in the Garhwal

Himalaya.”
“We report on a young pregnant woman developing distal leg edema and hypoalbuminemia, who was lately diagnosed with AL amyloidosis. Fetal growth retardation led to a caesarian section in the 27th week see more of gestation. A live birth healthy female, 710 g weight, was admitted to the neonatal intensive care unit and survived. Thereafter the mother underwent specific chemotherapy achieving only a partial and transient response, and eventually died due to sepsis. Interestingly, amyloidotic material was found on the maternal but not on the fetal side of the placenta.\n\nExperimental data show suppression of AA amyloid formation during pregnancy and suggest a protective role of the placenta on the offspring. However, most reported cases deal with pregnant women diagnosed with AA amyloidosis associated with Familial Mediterranean Fever and describe growth retardation of the fetus, worsening renal function and preeclampsia.\n\nTo the best of our knowledge, this is the first report of AL amyloidosis diagnosed in a pregnant woman.

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