Pollen grains display a wide range of variation in aperture number and arrangement (pattern) in angiosperms. Apertures are well-defined areas of the pollen wall surface that permit pollen tube germination. For low aperture numbers, aperture patterns are characteristic of the major taxonomic divisions of angiosperms. This paper presents a developmental model that explains most of the aperture patterns that are recorded in angiosperms. It is based on the analysis of the different events that occur during meiosis and lead to microspore differentiation. It demonstrates that variation occurring during meiosis in angiosperms is sufficient to produce the core morphological set of the most commonly observed pollen morphologies.
Each Ficus species depends on a specific mutualistic wasp for pollination. The wasp breeds on the fig, each larva destroying a female flower. It is, however, not known why the wasps have not evolved the ability to use all female flowers. In "dioecious" figs, the wasp can only breed in the female flowers of the "male" trees, so that pollination of a female tree is always lethal. The wasps should therefore be selected to avoid female trees. Field data is presented showing that the fruiting phenology of the dioecious fig Ficus carica is such that this selection does not occur: syconia are not receptive at the same time on "male" and female trees. Most wasps are forced to emerge from the syconia of "male" trees at a time when they will not be able to reproduce, whether they avoid female trees or not. This aspect of the life cycle of the wasp, although noticed, has been obscured in most previous studies. It is shown that the fruiting phenology of Ficus carica, which stabilizes the symbiosis, is the result of short-term selective pressures on the male function of the trees. Such selective pressures suggest a possible pathway from monoecy to dioecy in Ficus under seasonal climates.
Association or linkage studies involving control and long-lived populations provide information on genes that influence longevity. However, the relationship between allele-specific differences in survival and the genetic structure of aging cohorts remains unclear. We model a heterogeneous cohort comprising several genotypes differing in age-specific mortality. In its most general form, without any specific assumption regarding the shape of mortality curves, the model permits derivation of a fundamental property underlying abrupt age-related changes in the composition of a cohort. The model is applied to sex-specific survival curves taken from period life tables, and Gompertz-Makeham mortality coefficients are calculated for the French population. Then, adjustments are performed under Gompertz-Makeham mortality functions for three genotypes composing a heterogeneous cohort, under the constraint of fitting the resultant mortality to the real French population mortality obtained from life tables. Multimodal curves and divergence after the 8th decade appear as recurrent features of the frequency trajectories. Finally, a fit to data previously obtained at the angiotensin-converting-enzyme locus is realized, explaining what had seemed to be paradoxical results-namely, that the frequency of a genotype known as a cardiovascular risk factor was increased in centenarians. Our results help explain the well-documented departure from Gompertz-Makeham mortality kinetics at older ages. The implications of our model are discussed in the context of known genetic effects on human longevity and age-related pathologies. Since antagonistic pleiotropy between early and late survival emerges as a general rule, extrapolating the effects measured for a gene in a particular age class to other ages could be misleading.
The authors collected Sahelian sorghum landraces of Burkina Faso in 1984 and 74 of these accessions were characterized in 1985-1986 at Gampela in Burkina Faso (West Africa). The five races of cultivated sorghum were represented in this zone but 63.5% of the accessions were Guinea type. Great intra-and inter-accession variability was found. Plants were tall and had long panicles and small to intermediate seeds. There was a strong association between days-to-flowering, number of internodes, panicle length and height. The 100-kernel weight showed an antagonism with days to flowering and tillering. Multivariate analyses were made which enabled the accessions to be classified into four groups. The group most adapted to the sahelian zone, 'sahelian group', was semi-late, developed intermediate size of vegetative organs, had moderate tillering and had the best yield per plant.
To establish the genetic relationship among Sahelian sorghum [Sorghum bicolor (L.) Moench S.L.] landraces from Burkina Faso were submitted to electrophoretic analysis for 10 enzymatic systems and 18 loci. Four enzymatic systems (ADH, LAP, MDH, PGD) and five loci revealed polymorphism both within and among landraces. Thirty-eight per cent of the landraces were monomorphic in all the 18 loci. The genotypic frequencies in most of the landraces deviated markedly from Hardy-Weinberg proportions due to a major heterozygote deficit, the landrace being homozygous or a mixture of homozygotes. Multivariate analysis yielded three main groups, containing native landraces and five minors, containing introduced cultivars, randomly distributed over the territory. The pattern of allelic occurrence was random and unrelated to external selection pressures. The major diversity among landraces appears to be from genetic shift caused by farmers' selection of their seeds. It could also be due to the low rates of outcrossing (19%) and migration (0.06) prevailing in the set.
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