Exclusive selection for yield raises, the harvest index of self-pollinated crops with little or no gain in total bipmass. In addition to selection for yield, it is suggested that efficient breeding for higher yield requires simultaneous selection for yield's three major, genetically controlled physiological components. The following are needed: (1) a superior rate of biomass accumulation. (2) a superior rate of actual yield accumulation in order to acquire a high harvest index, and (3) a time to harvest maturity that is neither shorter nor longer than the duration of the growing season. That duration is provided by the environment, which is the fourth major determinant of yield. Simultaneous selection is required because genetically established interconnections among the three major physiological components cause: (a) a correlation between the harvest index and days to maturity that is usually negative; (b) a correlation between the harvest index and total biomass that is often negative, and (c) a correlation between biomass and days to maturity that is usually positive. All three physiological components and the correlations among them can be quantified by yield system analysis (YSA) of yield trials. An additive main effects and multiplicative interaction (AMMI) statistical analysis can separate and quantify the genotype × environment interaction (G × E) effect on yield and on each physiological component that is caused by each genotype and by the different environment of each yield trial. The use of yield trials to select parents which have the highest rates of accumulation of both biomass and yield, in addition to selecting for the G × E that is specifically adapted to the site can accelerate advance toward the highest potential yield at each geographical site. Higher yield for many sites will raise average regional yield. Higher yield for multiple regions and continents will raise average yield on a world-wide basis. Genetic and physiological bases for lack of indirect selection for biomass from exclusive selection for yield are explained.

The hypothesis tested was that lack of photoperiod gene activity allows inherent partitioning of photosynthate to continued growth of the earliest potential buds, flowers, pods, and seeds (the organs that give rise to the yield). Alternatively, and competitively, photoperiod gene activity causes the photosynthate to be partitioned predominantly toward continued growth of new vegetative organs plus later initiation of more reproductive (yield) organs. This hypothesis was tested by comparing an insensitive and a photoperiod-sensitive bean (Phaseolus vulgaris L.) cultivar and their F1 with F2 segregates of undetermined genotype. Randomly derived homozygous F8 segregates were also compared. The F8 generation included one photoperiod-insensitive and one photoperiod-sensitive genotype in a 1:1 ratio, which verified control by one photoperiod gene. Under long daylength (LD), in addition to early versus late flowering and maturity, the two genotypes expressed opposite levels of 23 other traits that would be changed by competitive partitioning of the photosynthate. In contrast, under short daylength (SD), both genotypes flowered and matured early, and both expressed the levels for all 25 traits that the photoperiod-insensitive genotype expressed in both SD and LD. The photoperiod gene interacted with daylength to control the levels of all three major physiological components of yield: the aerial biomass, harvest index, and days to maturity. Included among the other traits with levels altered by daylength-modulated photoperiod gene activity were: the number of branches, nodes, leaves and leaf area, the rate of yield accumulation, and sink activity.

Fruit of tomato (Lycopersicon esculentum Mill.) hybrids heterozygous for the alc ripening mutation stored on average 60% (3.6 days) longer at 20C than that of their normal-ripening parents. There were no detrimental effects of the alc heterozygous condition on fruit color, firmness, or size. The background into which alc was introduced also affected fruit quality and shelf life. These results indicate hybrids heterozygous for the alc ripening mutant can produce commercially acceptable fruit with significantly longer shelf life than their normal-ripening parents.

Effects by photoperiod gene(s) and daylength on crop yield and its three major physiological components (aerial biomass, harvest index, and days to harvest maturity) are reviewed for bean (Phaseolus vulgaris L.) and peanut (Arachis hypogaea L.). In these plus many other cited crops, photoperiod sensitive gene(s) delay days to flowering and/or days to maturity in non-promotive daylength while simultaneously lowering the harvest index. Thus, for many crops, earlier maturity is associated with higher harvest index, and/or it has been shown that photoperiod gene(s) control partitioning of photosynthate toward reproductive growth versus toward competitive partitioning to continued vegetative growth. Our conclusion is that photoperiod gene control over this partitioning precedes and is causal of the photoperiodgene control over days to flowering and maturity. This implies shifts from commonly accepted paradigms about effects by photoperiod and about breeding for higher yield. These paradigm shifts suggest more efficient ways to breed for cultivar adaption to the specific growing season duration and environment of each geographical site and for higher crop yield.

The plastochron index was used to compare the effects by daylength, mean temperature, and diurnal temperature fluctuation, on the rate of node development of five indeterminate common bean (Phaseolas vulgaris L.) genotypes grown in eight growth chamber environments. Regression analysis described temporal trends in the plastochron index. Regression curves for the various genotype—environment combinations were compared using canonical variates analysis. At a constant 17C, extending daylength from 12 to 14 or 16 hr had no effect on rate of node development. The rate of node development increased at a constant 23C when daylength was lengthened from 12 to 14 or 16 hr. The increase in rate of node development was more pronounced in genotypes with higher photoperiod sensitivity, as measured by delay of flowering. Temperature rise from 17 to 23 to 29C also increased the rate of node development, with genotypes again exhibiting differential response. Diurnal fluctuation of 6C about a mean of 23C had the same node development rate as a constant 23C.