Effects of Indole-3-acetic Acid and Gibberellin on Synchronous Cultures of Chlorella fusca

The applicability of synchronous cultures of Chlorella fusca as a reproducible experimental system for the study of growth regulators has been investigated using indole-3-acetic acid (IAA) and gibberellin.

• 1 None of these compounds stimulated growth or sporulation.
• 2 IAA inhibited growth and sporulation at concentrations higher than 6 × 10^?5M, the effect increasing with increasing acidity. Gibberellin had no effect.

     

Changes in non-protein nitrogen metabolism during tobacco mosaic virus biosynthesis

1. Discs cut from tobacco leaf tissue infected with tobacco mosaic virus and cultured in water contain less non-protein nitrogen than comparable uninfected discs during the time at which TMV is formed. This deficiency disappears when virus formation ceases. Discs cultured in nutrient solution form about twice as much TMV as discs cultured in water. The maximum non-protein nitrogen deficiency is comparable in magnitude to the amount of virus synthesized. 2. The largest difference between injected and uninfected tissue occurs in the ammonia content. Smaller, but significant differences in amide content are found. Infected discs cultured in water show no significant differences from control discs in free amino acid content; infected discs cultured in nutrient solution develop a small deficiency in amino acid nitrogen. 3. The general patterns of change in composition of the pool of soluble nitrogen are similar in both infected and uninfected discs. 4. The data indicate that the bulk of the nitrogen incorporated into virus protein is withdrawn from the leaf's pool of soluble nitrogen; virus is formed de novo from ammonia nitrogen and non-nitrogenous carbon sources. The effect of virus infection on host nitrogen metabolism appears to be due to the formation of virus rather than to its presence.     

Trap‐jaws revisited: the mandible mechanism of the ant Acanthognathus

Abstract.Ants of the genus Acanthognathus stalk small insects and catch their prey by a strike with their long, thin mandibles. The mandibles close in less than 2.5 ms and this movement is controlled by a specialized closer muscle. In Acanthognathus , unlike other insects, the mandible closer muscle is subdivided into two distinct parts: as in a catapult, a large slow closer muscle contracts in advance and provides the power for the strike while the mandibles are locked open. When the prey touches specialized trigger hairs, a small fast closer muscle rapidly unlocks the mandibles and thus releases the strike. The fast movement is steadied by large specialized surfaces in the mandible joint and the sensory‐motor reflex is controlled by neurones with particularly large, and thus fast‐conducting, axons.