ライフサイエンスコーパス: Argentine ant

1 ve ant communities during an invasion by the Argentine ant.

2 imental co-infection of its insect host, the Argentine ant.

3 conducted in native fynbos plots invaded by Argentine ants.

4 locomotion for walking in low-slip animals (Argentine ant, 4.7% slip ratio of slipping to total moti

5 the release of fipronil-treated ants reduced Argentine ant abundance by >90% within 24 h.

6 emical analyses of the trails laid by living Argentine ants and find that (Z)-9-hexadecenal is not pr

7 Although the inherent dispersal abilities of Argentine ants are limited, in the last century, human-m

8 osition as estimated by delta(15)N values of Argentine ants compare with those of other ants at the s

9 vior unique to introduced populations of the Argentine ant contribute to the elevated population dens

10 umile is among the most carnivorous of ants, Argentine ants from California occupied lower trophic po

11 The Argentine ant genome contains fewer immune genes than Dr

12 Distinctive features of the Argentine ant genome include remarkable expansions of gu

13 alysis demonstrate that fipronil is toxic to Argentine ants in extremely small (nanogram) quantities

14 The spread of the Argentine ant involves two discrete modes.

15 while the number of weak non-native invasive Argentine ant Linepithema humile workers increases acros

16 tive and eight introduced populations of the Argentine ant Linepithema humile.

17 A queen and worker of the Argentine ant Linepithema humile.

18 We utilized the Argentine ant (Linepithema humile) as a model system to

19 vior and population genetics of the invasive Argentine ant (Linepithema humile) in its native and int

20 The Argentine ant (Linepithema humile) is recognized as one

21 invasion of South African shrublands by the Argentine ant (Linepithema humile) leads to a shift in c

22 , we reconstruct the invasion history of the Argentine ant (Linepithema humile), a widespread invasiv

23 pread and well-studied species, the invasive Argentine ant (Linepithema humile), which was accomplish

24 rizes introduced populations of the invasive Argentine ant (Linepithema humile).

25 nio rerio), and in existing rich datasets of argentine ants (Linepithema humile) and sticklebacks (Ga

26 d an 8-year record of stable isotope data on Argentine ants (Linepithema humile) from southern Califo

27 The Argentine ant, Linepithema humile, has invaded urban, ag

28 Argentine ant management typically entails the applicati

29 In sites with the Argentine ant, native ant communities appear random or w

30 In sites without the Argentine ant, native ant communities exhibit significan

31 n for the ecological dominance of introduced Argentine ant populations is their ability to dominate f

32 t does not occur in detectable quantities in Argentine ant recruitment trails.

33 ional classes reveals unique features of the Argentine ant's biology, as well as similarities to Apis

34 and biregional comparisons indicate that the Argentine ant's relative trophic position is reduced at

35 These results support the hypothesis that Argentine ants shift their diet after establishment as a

36 Using laboratory colonies of the Argentine ant, they show that there are component Allee

37 nd iridomyrmecin are major components of the Argentine ant trail pheromone.

38 Z)-9-hexadecenal as the key component of the Argentine ant trails.

39 Laboratory choice tests confirmed that Argentine ants were attracted to artificial trails compr

40 ed that (Z)-9-hexadecenal strongly attracted Argentine ant workers in a multi-choice olfactometer, su

41 ere, we show that the cuticular chemistry of Argentine ant workers, Linepithema humile, undergoes rap