Demographic genetics of the American beech (Fagus grandifolia Ehrh.) III. Genetic substructuring of coastal plain population in Maryland

Spatiotemporal genetic substructurings were investigated in the American beech population of the east-central coastal plain in Maryland. All trees including seedlings, various sizes of juveniles, and mature trees within the study site (10 × 100 m) were mapped, diameters measured, and leaves collected for allozyme analyses. Eleven polymorphic loci in eight enzyme systems were examined: 6Pgdh2, 6Pgdh3, Acp2, Adh1, Adh2, Fum, Got1, Got3, Lap, Pgi, and Pgm2. A total of 1945 trees were analyzed and 595 multilocus genotypes were detected. Six size-classes and 10 spatial blocks were discriminated for spatiotemporal analyses. Parameters for genetic variations (heterozygosity, Simpson's index, Shannon-Weaver's index, and inbreeding coefficient) decreased in larger size-classes. These genetic parameters fluctuated in spatial blocks of 10 m intervals, in which certain alleles were characteristic of specific blocks. The spatial autocorrelation by Moran's I and coancestry revealed the ranges of genetic relatedness to be only 20–30 m. Multilocus genotype analyses showed that higher genetic variations occur in larger size-classes and at gap openings where seed shadows for mother trees are overlapped. The relationships among reproductive trees, seedlings and juveniles suggested that the seed dispersal range of the American beech is normally in the range of 30–40 m. The mechanisms of a remarkably high genetic polymorphism maintained in this once artificially disturbed and grazed forest are discussed as related to conservation biology.     

Genetic structure within a Japanese stone pine (Pinus pumila regel) population on Mt. Aino-dake in central Honshu, Japan

In previous investigations, natural layering of Japanese stone pine (Pinus pumila) was suggested by the occurrence of adventitious roots. However, there is no genetic evidence so far that this species actually produces offspring by natural layering. We, therefore, investigated clonal structure and spatial genetic structure within a 38×18 m plot on Mt. Aino-dake, using allozyme, random amplified polymorphic DNA (RAPD), and inter-simple sequence repeat (ISSR) analyses. We found 24 genets, with stems found to be genetically identical in multiple tests, which extended later-ally against the direction of the slope, indicating that there were clonal structures originating from elongation of ramified stems and subsequent natural layering. The results suggest, however, that less than one third of the 200 stems analyzed from this site were clonaly propagated. We also analyzed spatial genetic structure by spatial autocorrelation. Many of the spatial autocorrelation coefficients were significantly positive in short distance classes. We concluded that the species has genetic structures which largely originate from clonal propagation and avian seed dispersal.     

Population dynamics of a phytophagous lady-beetle,Epilachna vigintioctopunctata (Fabricius), living in spatio-temporally heterogeneous habitats. III. Effects of habitat structure on population dynamics

Temporal changes in the population size of a phytophagous lady-beetle were analyzed to identify mechanisms affecting lady-beetle population dynamics at different spatial scales. The study area (15 ha) included 18 habitat patches. The major host plants were potato for first generation larvae and eggplant for second generation larvae. The habitat patches were classified into three groups according to the major host plants in each patch: P-E patches (both host plants available), P patches (potato only), and E patches (eggplant only). The winter disappearance of adults in the whole study area, and larval mortality in E patches were apparently the most important factors disturbing the overall population density. Density-dependent movement of females appeared to have the greatest stabilizing effect on the yearly fluctuation of population density. Rate of increase of female adults from the first to the second generation,R, was generally higher on eggplants in E patches than in P-E patches because the adult density of the first generation was much higher in P-E patches. The yearly fluctuation of adult density in each generation tended to be less in patches with all habitat components necessary for the full life cycle (P-E patches). However, such patches were not favorable for first generation females, as indicated by the lower rate of increase from the first to the second generation. The density and stability of lady-beetle populations is discussed in relation to habitat structure.