Über die negativ-phototaktische Reaktion von Euglena

Zusammenfassung Die negativ-phototaktischen Reaktionen von Euglena gracilis sind reine Schock-Reaktionen. Beim Schwimmen zu ausreichend hohen Lichtintensitäten oder bei plötzlicher Erhöhung der Lichtintensität im Gesamtfeld tritt eine solche Reaktion auf. Die weitere Schwimmrichtung ist von der Richtung des Gefälles der Lichtintensität unabhägig.Das Ergebnis spricht für die Annahme, daß nur bei physiologisch starker periodischer Verdunklung des Photorezeptors (meist durch den Augenfleck) positive Phototaxis eintreten kann, während sonst der Lichtzutritt zum Photoreceptor ausschließlich negative Reaktionen bedingt.     

Oxygen consumption of brown noddy (Anous stolidus) embryos in a quasiequilibrium state at lowered ambient temperatures

1. The oxygen consumption (MO2) of the semi-precocial Brown Noddy embryos at different stages of development was measured at 36 degrees C and again after 5-hr exposure to lowered ambient temperatures (30 and 32 degrees C). 2. The MO2 measured in a quasiequilibrium state was equal to the value predicted by a temperature coefficient of 2. 3. In contrast to precocial chickens, the semi-precocial Noddy had no apparent metabolic response to cooling before hatching.     

Comparative model analysis of central shunts in vertebrate cardiovascular systems

The incomplete double circulation of air-breathing fishes and lungfishes, amphibians, reptiles and embryonic birds and mammals has been analyzed using a simplified mode comprising the intra- and extracardiac shunts and compartments for the gas exchange (gills, lungs, skin, etc.) as well as systemic tissue gas exchange. The intracardiac shunting is defined and given common symbols for all species of animals analyzed. Two types of equations, fluid-flow and mass-flow equations, are derived for each model, which are solved to give shunting rate as a function of blood O2 content of the principal cardiac compartments and vessels. The model analysis not only offers possibility for an overall average evaluation of central shunts, but also suggests which blood samples must be determined for evaluation of the shunt patterns.     

Glycosis in the eggs of the echiuroid, Urechis unicinctus and the oyster, Crassostrea gigas. Rate-limiting steps and activation at fertilization.

The content of glycolytic intermediates and of adenine nucleotides was measured in eggs of the echiuroid, Urechis unicinctus and the oyster, Crassostrea gigas, before and after fertilization. On the whole, the profile of the change in each glycolytic intermediate in Urechis eggs upon fertilization was found to be essentially similar to that in oyster eggs. Calculation of the mass action ratio for each glycolytic step from the amounts of glycolytic intermediates determined suggests that there are at least three limiting enzymes in the glycolysis system in unfertilized and fertilized eggs of each species examined. Phosphorylase (EC 2.4.1.1), phosphofructokinase (EC 2.7.1.11), and pyruvate kinase (EC 2.7.1.40) may be rate-limiting enzymes for the glycolysis system in Urechis eggs as well as in oyster eggs. These enzymes are thought to be activated upon fertilization, though even the reactions of the enzymes in fertilized eggs do not reach a state of equilibrium. In eggs of Urechis and oyster, phosphorylase is the first enzyme to be activated following fertilization. In Urechis eggs, pyruvate kinase is activated after the instant increase in the phosphorylase activity upon fertilization, followed by phosphofructokinase activation. In oyster eggs, however, pyruvate kinase and phosphofructokinase seem to be stimulated simultaneously, subsequent to phosphorylase activation upon fertilization. The mechanism controlling phosphorylase and pyruvate kinase activity is unknown, but the phosphofructokinase activity in both species may be regulated by the intracellular concentration of adenine nucleotides, since the enzyme activity is enhanced along with a decline in the phosphate potential in the eggs of both Urechis and of oyster.     

Osmotic and ionic regulation in Nitella

When the osmotic value of an internodal cell of Nitella flexiliswas modified by the method of transcellular osmosis, the normalosmotic value was chiefly restored by the release or absorptionof K⁺. The release or uptake of Na⁺ was observed only when themodification of osmotic value was significant. Both the uptakeand release of K⁺ were linearly dependent on the degree of modificationof the osmotic value. The effectiveness of alkali metal cationsin restoring the osmotic value in cells of lower osmotic valueswas in the order K⁺>Rb⁺>Na⁺, Cs⁺>Li⁺. The absorptionof K⁺ by cells of lower osmotic values depended strongly ontemperature, while the release of K⁺ from cells of higher osmoticvalues did not. To clarify whether the Nitella cell regulates the osmotic valueor regulates the concentration of K⁺ in the vacuole, the cellsap was exchanged for artificial cell saps whose osmotic valuesand ionic concentrations were varied independent of each other.It was shown that in Nitella two regulating mechanisms are operating,one which regulates the osmotic value of the cell sap irrespectiveof the level of vacuolar K⁺ (0.1–140 mM) and another whichregulates the vacuolar K⁺-level when it is abnormaly high (>160mM). Both mechanisms are assumed to operate in order to keepthe concentration of K⁺ in the cytoplasm at a constant level.The presence of Na⁺ (0–100 mM) and Ca²⁺ (5–40 mM)did not affect the movement of K⁺ during osmoregulation. ¹Present address: Sanki Engineering Limited, Nagaokakyo, Kyoto,Japan. (Received December 19, 1973; )     

Fruitless and doublesex coordinate to generate male-specific neurons that can initiate courtship

Biologists postulate that sexual dimorphism in the brain underlies gender differences in behavior, yet direct evidence for this has been sparse. We identified a male-specific, fruitless (fru)/doublesex (dsx)-coexpressing neuronal cluster, P1, in Drosophila. The artificial induction of a P1 clone in females effectively provokes male-typical behavior in such females even when the other parts of the brain are not masculinized. P1, located in the dorsal posterior brain near the mushroom body, is composed of 20 interneurons, each of which has a primary transversal neurite with extensive ramifications in the bilateral protocerebrum. P1 is fated to die in females through the action of a feminizing protein, DsxF. A masculinizing protein Fru is required in the male brain for correct positioning of the terminals of P1 neurites. Thus, the coordinated actions of two sex determination genes, dsx and fru, confer the unique ability to initiate male-typical sexual behavior on P1 neurons.