THE TIME AND SITE OF THE SEMIDOMINANT LETHAL ACTION OF “Wo” IN LYCOPERSICON ESCULENTUM

Huang , P. C. (California Inst. Technol., Pasadena), and E. F. Paddock . The time and site of the semidominant lethal action of “Wo” in Lycopersicon esculentum. Amer. Jour. Bot. 49(4): 388–393. Illus. 1962.—The semidominant lethal gene, Wo (Woolly), in Lycopersicon esculentum has been investigated with specific attention to its lethal action. The primary lethal action is believed to occur prior to the torpedo stage of embryonic development (approximately 22 days after anthesis). The presumed WoWo embryos cease to grow before any cambial differentiation or organogenesis can be recognized. Their accompanying endospermous cells, however, continue to divide, this resulting in full-sized seeds. The death of these embryos probably occurs near the time of maturation of the seeds (approximately 52 days after anthesis or when the ovulary turns orange-red). The mechanism of death of the embryo apparently lies in and is specific to the embryo; hence, this is a case of autogenously determined embryonic lethality.     

WAVE LENGTH OF LIGHT AND PHOTIC INHIBITION OF STEREOTROPISM IN TENEBRIO LARV?

A definite intensity of white light is required (about 136 m.c.) to produce negative phototropic orientation of creeping Tenebrio larvæ away from contact with a vertical glass surface. This gives a measure of stereotropism in terms of phototropism, or reciprocally. The effectiveness of light for the suppression of stereotropism varies with wave length. It is therefore simple to obtain a measure of the relation between wave length and stimulating efficiency in this case of phototropic orientation. By determinations of the minimal energy required to inhibit stereotropism with different regions of the spectrum, it is found that the maximum effectiveness is sharply localized in the neighborhood of 535µµ. The curve connecting stimulating efficiency with wave length, while giving a picture of the effective absorption by the photosensory receptors, probably does not permit accurate characterization of the essential photosensitive material.     

THE OCCURRENCE OF “ROOT GAPS” IN THE RHIZOME SOLENOSTELE AND LEAF TRACE OF DENNSTAEDTIA CICUTARIA

The vascular system of the rhizome axes of Dennstaedtia cicutaria consists of a solenostele with an amphicribral vascular bundle centrally located in the pith. Each leaf has a single trace which is an amphicribral vascular bundle. At each node of an axis there is a complex consisting of the main axis, leaf base, and a branch axis attached to the basiscopic margin of the leaf base. Numerous roots are present on the rhizomes and the abaxial side of the leaf bases. Parenchymatous gaps occur in the rhizome solenostele and the leaf trace directly above the departure of some of the root traces. These gaps are termed root gaps. In some instances the root gaps are confluent. However, not all of the root traces have an associated root gap. The leaf trace is inserted laterally on the main and branch axes at the node so that the acroscopic leaf trace margin anastomoses with the main axis of the vascular system and the basiscopic margin with that of the branch axis. Two leaf gaps are associated with each leaf trace, one occurring in the main axis solenostele and the other in the branch axis solenostele. The medullary bundle of each axis anastomoses with each leaf trace at its point of attachment to the rhizome solenostele. Thus, the medullary bundle forms a continuous vascular strand from leaf trace to leaf trace in any given rhizome axis.