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1 t notorious invasive pests, the red imported fire ant.
2 , AK cDNA was obtained from the red imported fire ant.
3 energy production and its utilization in the fire ant.
4 AB2, and Gp-9 in workers of the red imported fire ant.
5 le genetic adaptations in lizards invaded by fire ants.
6 is prevalent, it completely replaces native fire ants.
7 induce transitions in social organization in fire ants.
8 different developmental stages and castes of fire ants.
9 caste specifically regulated in red imported fire ants.
10 resumed odorant-binding protein gene Gp-9 in fire ants.
11 equilibrium between the two loci in polygyne fire ants.
12 we focus on the young 'social' supergene of fire ants, a powerful system for disentangling the effec
13 psin alkaloids extracted from two species of fire ants against the protozoan parasite Trypanosoma cru
15 te configuration of the enantiomers of these fire ant alkaloids could be determined via VCD spectrosc
25 ovide insights into the development of novel fire ant baiting systems that can be placed on tree trun
26 gate potential lizard adaptation to invasive fire ants by generating whole-genome sequences from 420
27 irst structure of an ant proteolytic enzyme, fire ant chymotrypsin, was determined to atomic resoluti
28 t a diverse set of molecular markers in 2144 fire ant colonies from 75 geographic sites worldwide rev
31 tory experiment, the performance of mice-fed fire ant colonies was poor when compared to colonies tha
34 +/- 0.23 L), supporting our hypothesis that fire ants construct environments that simplify their con
35 the absence of disturbance and on their own, fire ants do not invade the forest habitats of native an
36 native ant abundance and diversity, whereas fire ants, even in the absence of disturbance, diminishe
38 attern, nitrogen isotopic data revealed that fire ants from populations in the United States occupy a
39 lts indicate that plowing, in the absence of fire ants, greatly diminished total native ant abundance
40 lishing and maintaining colonies of imported fire ants (IFA) (Hymenoptera: Formicidae) in the laborat
42 to the recent discovery of the red imported fire ant in Sicily, Genovesi et al. highlight the delay
44 o-dimensional columns of Solenopsis invicta, fire ants, in which the local activity, density and alig
46 Thus, significant recent social evolution in fire ants is consistent with theoretical expectations ba
47 r, a major feature of social organization in fire ants, is associated with worker genotypes at the ge
48 en workers and larvae simulated those of the fire ant (larvae signal for feedings at rates depending
50 genies built from the genomes of 365 haploid fire ant males, we show that the supergene variant respo
52 rt, edema, and redness in response to wasps, fire ants, mosquitoes, bees, cuts, abrasions, and plant
55 ther solenopsin A, a venom alkaloid from the fire ant, possessed agonistic or antagonistic QS signali
56 her invertebrates that can serve as prey for fire ants, potentially showcasing an interesting case of
58 oratory experiments to quantify red imported fire ant recruitment to rodent carrion and determine whe
59 here is a discrepancy between high levels of fire ant recruitment to vertebrate carrion and the poor
62 se time-lapse photography to investigate how fire ants S. invicta link their bodies together to build
70 various scales in native populations of the fire ant Solenopsis invicta using two classes of nuclear
71 chitectural characteristics with that of the fire ant Solenopsis invicta, but the two show no detecta
72 fined spaces, we study the locomotion of the fire ant Solenopsis invicta, which constructs subterrane
75 ection mutualisms involving the red imported fire ant (Solenopsis invicta) aids the success of this p
79 able in number (180) to those of the eyes of fire ants (Solenopsis fugax) and bark beetles (Hylastes
83 e mixed reproductive systems in the tropical fire ant, Solenopsis geminata, in a population with thre
86 hether transferrin genes in the red imported fire ant, Solenopsis invicta, are similarly induced by m
89 eriment, we combined additions of the exotic fire ant, Solenopsis invicta, with 2 disturbance treatme
92 ested insect species, including red imported fire ants, Solenopsis invicta Buren, black imported fire
93 ts, Solenopsis invicta Buren, black imported fire ants, Solenopsis richteri Forel, little black ants,
94 nces of males from native populations of six fire ant species and show that variation in social organ
95 ation by Gp-9 is conserved in South American fire ant species exhibiting social polymorphism and sugg
99 Available reports suggest that each year, fire ants sting more than 50% of persons in endemic area
102 ocial antagonism shaped the evolution of the fire ant supergene, resulting in distinct patterns of ge
105 overexpressed in workers of the red imported fire ant using PCR-selected subtractive hybridization an
107 or social and ecological trait in Solenopsis fire ants: whether colonies have one queen or multiple q
108 in the different castes of the red imported fire ant, which may be linked to their different mission
109 hornets, European and American paper wasps, fire ants, white-faced hornets, and Polybia wasps were r
110 issue specifically regulated in red imported fire ants with a descending order of worker> alate (wing