ライフサイエンスコーパス: alarm pheromone

1 g of critical neural circuits in response to alarm pheromone.

2 ral tests, the chemical structure of a mouse alarm pheromone.

3 lation of genes that mediate the response to alarm pheromone.

4 regarious insect species use aggregation and alarm pheromones.

5 ly tuned, and stereotyped representations of alarm pheromones.

6 ed complete glomerular responses to four ant alarm pheromones.

7 owed reduced diving responses to conspecific alarm pheromone after 7 days, but not after 28 days, ind

8 sive allomones, activity inhibitors, cryptic alarm pheromones, aggregative attractants, robbing agent

9 vidence that aphid perception of conspecific alarm pheromone aids in predator avoidance and thereby b

10 ulated biting of foragers or exposure to bee alarm pheromone also elicited signaling (88-fold and 14-

11 ental stressors, including exposure to aphid alarm pheromone and crowding, and, in one experiment, we

12 le, nest defenders were triggered by the bee alarm pheromone and live hornet presence to heat-ball th

13 foragers could eavesdrop upon heterospecific alarm pheromones, and would detect and avoid conspicuous

14 The bed bug, Cimex lectularius L., emits an alarm pheromone (AP), a 70/30 blend of (E)-2-hexenal and

15 d avoidance of heterospecific alarm signals, alarm pheromones, at food sources in bees.

16 tarily warn the prey or by the production of alarm pheromones by the stressed prey alerting its consp

17 lobe (AL) changes with age in the context of alarm pheromone communication in the clonal raider ant (

18 he defensive behaviour elicited by the bee's alarm pheromone component isoamyl acetate (IAA) is stron

19 bee species can detect and use a specialized alarm pheromone component, benzyl acetate (BA), to avoid

20 hat OBP3 from M. viciae can bind to all four alarm pheromone components and the differential ligand b

21 xamine their molecular interactions with the alarm pheromone components.

22 We next examined responses to individual alarm pheromone compounds.

23 array of antennal sensilla, specifically for alarm pheromone detection and nestmate recognition, shar

24 to release (E)-beta-farnesene (Ebetaf), the alarm pheromone for many pest aphids, using a synthetic

25 Alarm pheromones function in integrating defensive respo

26 e chemical structure of the identified mouse alarm pheromone has similar features as the sulfur-conta

27 Continuous exposure to alarm pheromone in aphid colonies raised on transgenic A

28 This study explores how formic acid, an alarm pheromone in Camponotus aethiops ants, influences

29 (EBF) is the predominant constituent of the alarm pheromone in Myzus persicae (green peach aphid) an

30 This highlights a novel role for alarm pheromones in modulating cognition, with broader i

31 ults suggest that the heightened response to alarm pheromones in older ants occurs via increased sens

32 sentations for five general odorants and two alarm pheromones in young and old ants.

33 n integrating defensive responses; honey bee alarm pheromone is an excellent example of a multicompon

34 f conservation with mammals, even though the alarm pheromone itself is bee-specific.

35 t Apis cerana foragers avoid the distinctive alarm pheromones of A. dorsata and A. mellifera, species

36 The alarm pheromones of many arthropods are also used as def

37 ided BA as strongly as they did to their own alarm pheromone on natural inflorescences.

38 to human or animal odorants, CO(2), sex and alarm pheromones, or other odorants known to attract or

39 We analysed the volatile alarm pheromone produced by attacked workers of the most

40 ials or a closer imitation, in the plant, of alarm pheromone release.

41 For the alarm pheromone response gene set, we found a particular

42 onserved honey bee genes associated with the alarm pheromone response shows overrepresentation of pro

43 entially expressed gene sets associated with alarm pheromone response, the difference between old and

44 However, alarm pheromone responses within individual glomeruli ch

45 Alarm pheromones robustly activated <=6 glomeruli, and a

46 as the sensory organ through which mammalian alarm pheromones signal a threatening situation, the che

47 ated with the natural developmental shift in alarm pheromone-specific responses of an ant.

48 (,)(16) older ants responded more rapidly to alarm pheromones, the chemical signals for danger.

49 n predator attack, individual aphids emit an alarm pheromone to warn the colony of this danger.

50 Both species use alarm pheromones to warn of dangers.

51 ato aphids showed that a reduced response to alarm pheromone was associated with both gene amplificat

52 Alarm pheromones were represented sparsely at all ages.

53 obtained for EHB in response to exposure to alarm pheromone (which provokes aggression) and when com

54 Only two glomeruli became sensitized to alarm pheromones with age, while at the same time becomi