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Colonization of plant roots by arbuscular mycorrhizal (AM) fungi is a primary factor determining mycorrhizal associations. This study aimed to investigate the variation in AM colonization among maize genotypes and in response to plant breeding programs. Three types of maize (Zea mays) germplasms composed of 141 inbred lines, 38 hybrids, and 76 landraces were grown in replicated field experiments in Sapporo, Japan, for two cropping years to evaluate the percentage of root length colonized by indigenous AM fungi. The percent colonization varied greatly and continuously among maize genotypes. Inbred lines that originated (released) in particular locations (e.g., Tokachi, Japan) and years (e.g., 1960s) showed significantly larger values than other lines. Inter-location differences were also observed for landraces. The direction of the year-ofrelease effect on colonization depended on the origin. No significant differences were observed between leaf-blight-disease-resistant near-isogenic inbred lines and their parents. Modern hybrids showed significantly greater values than inbred lines and older landraces. Evaluating numerous, diverse genotypes demonstrated that AM colonization of maize plants varies with germplasm type, origin (country and location), and year of release, and that modern plant breeding programs do not necessarily lead to the suppression of colonization.

We compared the abundance of litter categories (coarse particulate organic matter 1-16 mm, leaves Ͼ16 mm, and small woody detritus 16-100 mm) and macroinvertebrate assemblages between natural litter patches in pools and riffles in a headwater stream. Litter patches in pools were formed under conditions of almost no current (Ͻ6 cms Ϫ1 ), but in riffles they were formed under variable current velocities (13-89 cm s Ϫ1 ). Although the abundance of each litter category exhibited seasonal change, leaves were more abundant in riffles, and coarse particulate organic matter and small woody detritus were more abundant in pools throughout the study period. Macroinvertebrate assemblages in pools and riffles also changed seasonally but distinctly differed from each other. Shredders, collector-gatherers, and predators were the dominant functional groups in abundance in both pools and riffles, but the dominant shredders were caddisflies in pools and stoneflies in riffles. It is considered that the hydraulic conditions affected macroinvertebrate assemblages directly and indirectly through influences on the characteristics of litter retained in the patches. Our results suggest that the relative abundance of litter patches in pools and riffles largely affects the macroinvertebrate community structure of the headwater stream.

Rice ( Oryza sativa L.) plants develop vertically with shoot elongation and horizontally with tillering. The purpose of this study was to identify and characterize genomic regions influencing the rice plant architecture by quantitative trait locus (QTL) analysis for the component traits: culm length (CL), panicle length (PnL), panicle number (PnN) and tiller number (TN). For this QTL analysis, 191 recombinant inbred lines (F(7)) derived from a cross of Milyang 23 (M23) and Akihikari (AK) were grown in 1995, 1996 and 1997 (May-Oct) in Joetsu, Japan (temperate climate), and in the 2000 dry season (Jan-Apr), the 2000 wet season (Jun-Oct) and the 2001 dry season in Los Baños, The Philippines (tropical climate). Results showed that rice plant architecture was influenced by 19 genomic regions categorized into five groups. In Group I, two regions (on chrs. 6 and 11) affected shoot elongation (CL and PnL) and tillering (PnN and TN) in opposite directions more significantly in Los Baños than in Joetsu. In Group II, two regions (chrs. 3 and 12) affected shoot elongation, whereas in Group III, five regions [chrs. 1 (two), 2, 3 and 9] affected only culm length (CL). Expressions of four regions of Group III were influenced by either tropical or temperate environments. In Group IV, seven regions (chrs. 1, 2, 4, 5, 6, 8 and 9) controlled panicle development (PnN or PnL), and in Group V, three regions (chrs. 1, 2 and 3) regulated tillering (PnN or TN). Characterizing these 19 genomic regions provided a detailed analysis of rice plant architecture with emphasis on the multiple effect and environmental responsive regions.