No abstract

An experiment was conducted to determine the effects of nutritional level and flower location on factors related to flower, pollen, and ovule production, and to determine what developmental patterns would be modified to mediate any observed changes. Plants subjected to high nutrient levels developed larger leaves, more branches, more flowers on both the main stem and the branches, and opened their first flowers 6 days sooner than plants at lower levels of nutrients. Total flower number increased from 72.2 to 626 .8 per plant, with most of the increase produced on the primary branches. The number of pollen grains in the entire androecium averaged 14,685, but significantly increased with higher nutrient levels and decreased with the stage of plant maturity (nodal position on the plant). The number of ovules also increased with nutrient level and decreased with maturity stage. Average ovule number decreased from about 129 in flowers at nodes produced early in the growth cycle to about 100 in flowers produced at later nodes. Despite highly significant plasticity in numbers of both pollen and ovules, the Pollen/ Ovule Ratio (average 132.7) did not vary significantly with either nutrient level or plant maturity stage. Path analysis, which decomposes correlation coefficients into direct and indirect effects of factors influencing development, indicated that nutrient level had a very strong direct effect on the number of primary branches and on the number of primary-branch flowers, as well as very strong indirect effects on the latter. The primary-branch flowers directly determined over 67% of the total flower number, and indirectly determined about 24%jointly with secondary-branch flowers, and over 3% jointly with main-stem flowers. The direct effects of secondary-branch flowers and mainstem flowers were 3.8% and 0.3%, respectively. The relationship among components of yield is slightly additive. Direct determination of yield was 74.6% by the number of flowers per plant, 0.6% by the number of ovules per flower, 3.8% by the number of seeds per ovule, and 1.1 % by the weight per seed. The proportion of yield jointly determined by flower number and the developed seeds per ovule was 15.3%. It was concluded that allocation of resources increases to both male and female functions under conditions of high nutrient levels, and pollen/ ovule ratios are consistent within a plant despite significant plasticity in numbers of pollen grains and ovules.

Observations of the habitats and relative flowering of a Clarkia species with hairy flower buds and several with hairless flower buds led to the hypothesis that long hairs on flower buds regulate bud temperature. This hypothesis predicts that hairless buds would be warmer and develop faster than hairy buds, which would be cooler, develop more slowly, and avoid high temperature stress. The hypothesis was tested by comparing flower bud growth rates and temperatures in three genetically similar biotypes of Clarkia unguiculata and in all six species of section Phaeostoma. Flower buds of the three biotypes included hairy (HY) and hairless (HN) from the same coastal population and densely hairy (HD) from an interior locality. The six species included C. unguiculata with densely hairy buds (HD) and five related species with hairless buds. Contrary to expectations, HY buds grew more rapidly than HN buds. HD buds grew more rapidly than either and also more rapidly than the hairless buds of five related species. Again contrary to expectations, the three biotypes of C. unguiculata had equivalent temperature relations, with bud temperatures mostly somewhat below air temperatures. In a comparative experiment, bud temperatures in C. unguiculata approximated air temperatures while bud temperatures in five related species mostly fell well below air temperatures. Thus, predictions of the hypothesis were not borne out. Long bud hairs apparently have minimal effect on bud growth rates and temperatures, and we conclude that physiological adaptations are more important. Bud cooling mechanisms are discussed.

A study of the water requirement of nine strains of vine‐mesquite (Panicum obtusum H. B. K.) was conducted in the greenhouse for 126 days. Three herbage clippings were made. Least‐squares analyses of dry herbage yield, transpiration, and water requirement (a ratio of transpiration to herbage yield) indicated no statistically significant differences among strains in either water requirement or herbage yield during any of the growth periods or in the whole experiment. However, there were significant differences in transpiration by the strains throughout the test. Although large and highly significant negative genetic correlations were obtained between herbage yield and water requirement, the lack of significant differences among strains in these two traits suggests that high herbage yield cannot be used with confidence as a guide in selecting for low water requirement in these accessions of vine‐mesquite.