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1 ve ant communities during an invasion by the Argentine ant.
2 emical analyses of the trails laid by living Argentine ants and find that (Z)-9-hexadecenal is not pr
3 Although the inherent dispersal abilities of Argentine ants are limited, in the last century, human-m
4 osition as estimated by delta(15)N values of Argentine ants compare with those of other ants at the s
5 vior unique to introduced populations of the Argentine ant contribute to the elevated population dens
6 umile is among the most carnivorous of ants, Argentine ants from California occupied lower trophic po
12 vior and population genetics of the invasive Argentine ant (Linepithema humile) in its native and int
14 invasion of South African shrublands by the Argentine ant (Linepithema humile) leads to a shift in c
15 , we reconstruct the invasion history of the Argentine ant (Linepithema humile), a widespread invasiv
16 pread and well-studied species, the invasive Argentine ant (Linepithema humile), which was accomplish
18 nio rerio), and in existing rich datasets of argentine ants (Linepithema humile) and sticklebacks (Ga
19 d an 8-year record of stable isotope data on Argentine ants (Linepithema humile) from southern Califo
24 n for the ecological dominance of introduced Argentine ant populations is their ability to dominate f
26 ional classes reveals unique features of the Argentine ant's biology, as well as similarities to Apis
27 and biregional comparisons indicate that the Argentine ant's relative trophic position is reduced at
28 These results support the hypothesis that Argentine ants shift their diet after establishment as a
33 ed that (Z)-9-hexadecenal strongly attracted Argentine ant workers in a multi-choice olfactometer, su
34 ere, we show that the cuticular chemistry of Argentine ant workers, Linepithema humile, undergoes rap
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