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1 s no evidence that gametophytes later become hermaphroditic.
2 of the fern Ceratopteris are either male or hermaphroditic.
3 of the fern Ceratopteris are either male or hermaphroditic.
4 stems in plants have evolved many times from hermaphroditic ancestors (including monoecious plants wi
5 Separate sexes have evolved repeatedly from hermaphroditic ancestors in flowering plants, and thus s
8 ous species harbor many old haplotypes while hermaphroditic and dioecious species have little to no n
9 the proportion of female progeny produced by hermaphroditic and female plants will show more extreme
11 ng reproductive status to longevity: In both hermaphroditic and gonochoristic Caenorhabditis, mating
12 e measured morphological differences between hermaphroditic and male morph flowers in P. incarnata an
13 on analysis and behavioral observations that hermaphroditic C. briggsae and gonochoristic C. remanei
14 y contrast, we show that in the convergently hermaphroditic Caenorhabditis briggsae, GLD-1 acts to pr
15 specific transcriptional master regulator of hermaphroditic cell identity tra-1, which represses the
17 tis elegans come into association with their hermaphroditic counterparts they cease foraging behavior
18 velop into females can be respecified toward hermaphroditic development if submitted to dauer-inducin
20 e or transport of sperm, including the small hermaphroditic duct (site of sperm storage before mating
22 wers in P. incarnata were of similar size to hermaphroditic flowers, and there was little evidence of
24 (cox1), for multiple populations of several hermaphroditic, gynodioecious, and dioecious species in
26 ion were previously isolated and include the hermaphroditic (her), the transformer (tra) and feminiza
29 Gynodioecy, the co-occurrence of female and hermaphroditic individuals within a population, is an im
30 species consist primarily or exclusively of hermaphroditic individuals, gonochoristic males occur at
32 use one of two different mating systems-male/hermaphroditic, like the model organism Caenorhabditis e
37 oward male function is a general response of hermaphroditic modular organisms to impaired prospects f
38 , the coexistence of functionally female and hermaphroditic morphs within plant populations, often ha
41 This cost is eliminated by the production of hermaphroditic offspring in the self-fertilizing nematod
46 of progeny sex ratios produced by female and hermaphroditic plants in small and large populations of
48 sex ratios showed that progeny sex ratios of hermaphroditic plants were strongly influenced by popula
50 ther situations; and the 'mating systems' of hermaphroditic populations, inbreeding, outcrossing or i
51 ditis, and may reduce the number of males in hermaphroditic populations; neither males nor females of
53 moth species known only from O'ahu, visited hermaphroditic Schiedea kaalae and S. hookeri and remove
55 avoidance, the magnitude of which depends on hermaphroditic selfing rates and the strength of inbreed
56 y response to the frequency of unisexuals in hermaphroditic sex allocation, and they verify the quant
58 ave male and female sexes), but self-fertile hermaphroditic species are not uncommon, and parthenogen
59 sts, P. brevipalpis strongly preferred these hermaphroditic species over two subdioecious species cap
64 61 ESTs from two developmental stages of the hermaphroditic strain of S. mediterranea; this collectio
68 aptive significance of self-fertilization in hermaphroditic taxa, and both scenarios have been invoke
70 inguish two types of systems: 'sex systems', hermaphroditic versus male/female and other situations;
74 gonochoric with DUI, one gonochoric and one hermaphroditic without DUI) and of the related gonochori
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