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1 , AK cDNA was obtained from the red imported fire ant.
2 energy production and its utilization in the fire ant.
3 AB2, and Gp-9 in workers of the red imported fire ant.
4 t notorious invasive pests, the red imported fire ant.
5 is prevalent, it completely replaces native fire ants.
6 induce transitions in social organization in fire ants.
7 different developmental stages and castes of fire ants.
8 caste specifically regulated in red imported fire ants.
9 resumed odorant-binding protein gene Gp-9 in fire ants.
10 equilibrium between the two loci in polygyne fire ants.
12 te configuration of the enantiomers of these fire ant alkaloids could be determined via VCD spectrosc
17 irst structure of an ant proteolytic enzyme, fire ant chymotrypsin, was determined to atomic resoluti
18 t a diverse set of molecular markers in 2144 fire ant colonies from 75 geographic sites worldwide rev
22 +/- 0.23 L), supporting our hypothesis that fire ants construct environments that simplify their con
23 the absence of disturbance and on their own, fire ants do not invade the forest habitats of native an
24 native ant abundance and diversity, whereas fire ants, even in the absence of disturbance, diminishe
26 attern, nitrogen isotopic data revealed that fire ants from populations in the United States occupy a
27 lts indicate that plowing, in the absence of fire ants, greatly diminished total native ant abundance
30 Thus, significant recent social evolution in fire ants is consistent with theoretical expectations ba
31 r, a major feature of social organization in fire ants, is associated with worker genotypes at the ge
32 en workers and larvae simulated those of the fire ant (larvae signal for feedings at rates depending
35 rt, edema, and redness in response to wasps, fire ants, mosquitoes, bees, cuts, abrasions, and plant
38 ther solenopsin A, a venom alkaloid from the fire ant, possessed agonistic or antagonistic QS signali
41 se time-lapse photography to investigate how fire ants S. invicta link their bodies together to build
45 various scales in native populations of the fire ant Solenopsis invicta using two classes of nuclear
46 chitectural characteristics with that of the fire ant Solenopsis invicta, but the two show no detecta
47 fined spaces, we study the locomotion of the fire ant Solenopsis invicta, which constructs subterrane
50 ection mutualisms involving the red imported fire ant (Solenopsis invicta) aids the success of this p
54 able in number (180) to those of the eyes of fire ants (Solenopsis fugax) and bark beetles (Hylastes
58 hether transferrin genes in the red imported fire ant, Solenopsis invicta, are similarly induced by m
61 eriment, we combined additions of the exotic fire ant, Solenopsis invicta, with 2 disturbance treatme
63 ested insect species, including red imported fire ants, Solenopsis invicta Buren, black imported fire
64 ts, Solenopsis invicta Buren, black imported fire ants, Solenopsis richteri Forel, little black ants,
65 ation by Gp-9 is conserved in South American fire ant species exhibiting social polymorphism and sugg
67 Available reports suggest that each year, fire ants sting more than 50% of persons in endemic area
70 overexpressed in workers of the red imported fire ant using PCR-selected subtractive hybridization an
72 in the different castes of the red imported fire ant, which may be linked to their different mission
73 hornets, European and American paper wasps, fire ants, white-faced hornets, and Polybia wasps were r
74 issue specifically regulated in red imported fire ants with a descending order of worker> alate (wing
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