Combined effect of light and temperature on triacylglycerol accumulation in Dicranum elongatum

In the subarctic moss Dicranum elongatum Schleich & Schwaegr., the level of total lipids and triacylglycerols (TAG) was high in late winter and spring and low in autumn and winter. Four-week exposure of field material to continuous light (135μmol m⁻²s⁻¹) at 1°C resulted in a considerable increase in the amount of TAG in the autumn material acclimated to low temperatures and rhythmic light in the field. In contrast, the same treatment did not cause any increase in TAG in the spring material, acclimated to low temperatures and continuous light in the field. Results from experiments, in which moss cultivated for 4 months at 9°C on 12-h photoperiods (135μmol m⁻²s⁻¹) was kept for 3 weeks at low temperatures (9°C and −3°C) either in continuous light (135 or 70 μmol m⁻²s⁻¹) or with 12-h photoperiods (135 μmol m⁻²s⁻¹), indicated that the TAG level was higher at higher light intensity. At 9°C it was also higher in continuous light of both intensities than in rhythmic light. These results strongly suggest that decreasing irradiance and decreasing daylength limits the accumulation of TAG in D. elongatum during autumn in the subarctic.     

Field test of resource regulation by the bud-galling sawfly, Euura mucronata, on Salix cinerea

The attack by the bud-galling sawfly, Euura mucronata , on its willow host was simulated by removing every other living bud from previous year's shoots in a natural stand of Salix cinerea . The impact of simulated attack on the growth of the willow and the subsequent attack by E. mucronata was estimated after one growing season. Experimental bud-killing resulted in a growth reaction in S. cinerea characterized by significant increase in the length of new shoots produced by the remaining buds Also the number of buds and E. mucronata galls per shoot were significantly higher on bud-removal branches as compared with control branches. The overall survival of E. mucronata larvae was better on long shoots than on short shoots. The result shows that sawfly attack increases the amount of high quality resources for the subsequent generation of the same sawfly as predicted by "resource regulation hypothesis". We conclude that these highly specialized insect herbivores have adapted to utilize and to maintain the willow's juvenile traits. Rapid regrowth of willows after damage may have originally arisen as an adaptation in response to other, less specific pressures such as mammal browsing or snow and ice damage.     

Naloxone and TRH affect regional blood flows in the anesthetized rabbit

The cardiovascular effects of IV naloxone and a subsequent administration of TRH IV were studied in the rabbit. Naloxone caused a vasodilation in the myocardium and adrenal glands. Naloxone elicited an increment in cerebral blood flow in several regions which attenuated the cerebrovasodilating effect of TRH in a few regions. The blockade of endogenous opioids with naloxone did not modify the peripheral vasoconstricting effect of TRH or affect the vascular effects of TRH mediated by the peripheral sympathetic nerves. The results indicate that naloxone has a vasodilating effect in the myocardium and CNS in anesthetized rabbits. The major part of the cardiovascular effect of TRH is not dependent on mechanisms sensitive to naloxone.     

Production of protoplasts from the fungi Curvularia inaequalis and Trichoderma reesei

Summary Protoplast formation in Curvularia inaequalis was achieved using non-commercial and commercial snail gut enzymes or Trichoderma harzianum enzymes. The cells were grown for enzyme treatment on cellophane sheets or in liquid cultures for varying periods of time. The production of T. harzianum enzymes is discussed. The highest protoplast yields were 2.6x10⁷ protoplasts/ml enzyme solution. Protoplasts were shown to have zero to four nuclei. Protoplast regeneration was succesfully carried out in semisolid agar.     

Accumulation and Disintegration of Starch in the Chloroplasts of Stellaria media Grown under Constant Illumination

The persent paper contains a study un the starch content of the chloroplasts of the leaves of Stellaria media, performed by hsitochemical methods. Three leaves were collected at short intervals, fixed and cut in 10 μ sections, and stained according to the PAS-procedure. The starch content of single chloroplasts was measured by a microscope photometer. The chemical composition of the stainable material was demonstrated by enzyme specific experiments. At the end of a 12 hours' dark period the chloroplasts contained only traces of starch. Light caused the starch accumulation to begin and after a time chloroplasts seemed to be filled with starch. Subsequently, however, a sudden decrease in the starch content of the chloroplasts took place, in spite of constant illumination. A rather high level of starch content was restored in a few hours. The author puts forward some ideas about the nature of the factors causing the transitory disintegration of starch in illuminated leaves. The induction or the activation of certain enzymes seems to be the most probable explanalion.     

The development of non-separation time-resolved fluoroimmunoassays for the measurement of urinary metabolites

We describe the principles of a new generation of sequential or simultaneous time-resolved fluoroimmunoassays, namely, simple, rapid, liquid-phase non-separation procedures which may be applied to the measurement of urinary steroid and drug metabolites. As an example, a method for the measurement of estrone-3-glucuronide in undiluted urine is reported. This method has a similar sensitivity, specificity and accuracy to a conventional separation fluoroimmunoassay or radioimmunoassay but in terms of speed, convenience, precision, reliability and clinical utility the new method has many advantages. The labelled antigen is a novel fluorescent europium chelate covalently linked to estrone-3-glucuronide. The antibody-binding reaction involves the incubation of the labelled antigen (2ng) with a limited concentration of polyclonal or monoclonal antibodies to estrone-3-glucuronyl-6-BSA and an aliquot of standard or sample (undiluted urine; 10 μl) in microtitre wells. After a 10 min incubation, the fluorescence which emanates from the antibody-free label is measured in a time-resolved fluorometer and is proportional to the concentration of estrone-3-glucuronide in the standard or sample. The method may be applied for the monitoring of ovarian function in women.