Lake optics and depth limits for photogenesis and photosynthesis in charophyte meadows

Two series of lakes with increasing attenuation were examined for trends in spectral composition. They became the basis for an evaluation of the light environment at the lower boundary (LB) of Nitella meadows in three other series of lakes. Increased attenuation (K _d PAR) was marked by progressive erosion of the blue window and caused primarily by humic substances. An increase in K _d PAR from 0.06 to 0.81 produced, at the floor of the euphotic zone, a shift in K _d min from 440 to 580 nm. Regressions of boundary depths of Nitella meadows on water clarity produced similar slope coefficients for the three series of lakes. Several trends became evident: 1, PAR irradiance at the LB increases with depth of the LB; 2, red light (E _d 660) declines from richness at shallow LB to near extinction in deep water LB in clear lakes; while 3, blue light (K _d 450) increases to an asymptote. Blue light appears to substitute, although less effectively, for red light irradiance in the growth regulation of charophytes. These data support an hypothesis that spectral quality is involved in the determination of lower boundary depths for benthic macro-algae.     

Type C Niemann-Pick disease: dimethyl sulfoxide moderates abnormal LDL-cholesterol processing in mutant fibroblasts

Biochemical and cytochemical studies have revealed that abnormal processing of low-density-lipoprotein (LDL) cholesterol can be reversed in mutant Niemann-Pick C (NP-C) fibroblasts when 2% dimethyl sulfoxide (DMSO) is added to the culture medium. Both the excessive lysosomal accumulation of LDL cholesterol and the delayed induction of cellular homeostatic responses associated with the uptake of LDL by the mutant cells were substantially reversed by DMSO. DMSO appears to accelerate the intracellular mobilization of LDL-derived cholesterol through effects that may reflect enhanced membrane permeability or cholesterol solubilization.     

Endothelial cell junctions

In the course of a freeze-cleave study on intercellular junctions in the regenerating rat liver, we observed an unusual array of intramembranous particles located in regions of contact between endothelial cells lining the hepatic sinusoids. These arrays were characterized by an accumulation of particles which resembled a zonula occludens in their linear deployment but differed in that the contact regions were composed of individual particles which remained separated from each other by regular particle-free intervals.     

Integration of progeny simian virus 40 DNA into the host cell genome

A procedure was developed for the separation of cellular DNA of productively infected monkey kidney cells from free simian virus 40 DNA. The application of this procedure allowed the investigation of progeny viral DNA integration into the host cell DNA by nucleic acid hybridization techniques. The purification consisted of precipitation of the cellular DNA by Hirt's (1967) method, velocity centrifugation in alkaline sucrose gradients, equilibrium centrifugation in ethidium bromide/CsCl solution, and an additional velocity centrifugation in an alkaline sucrose gradient. The efficiency of each step of the procedure was determined by monitoring the amount of contaminating free viral DNA. Purified cellular DNA, isolated from cells late after infection, contained approximately 0/sd006% free viral DNA, but as much as 2% integrated simian virus 40 DNA. This corresponds to more than 20,000 integrated virus genome equivalents per cell, as determined by DNA-DNA reassociation kinetics. Integration of simian virus 40 DNA into the cellular DNA became detectable at 24 hours after infection, and increased with the increase in the rate of viral DNA synthesis.