Aggression pheromone as alarm
pheromone:
Alarm pheromone information is
transmitted, via projection neurons, in ants to the lateral horn and the
calyces of the mushroom body of the protocerebrum. These neurons may
participate in the control of aggressive behavior, which is sensitized by alarm
pheromones and is triggered by non-pheromonal sensory stimuli associated with a
potential enemy (Mizunami et al.,2010).
Alarm pheromone as Aggression
pheromone:
Honey bees (Hymenoptera: Apidae, Apini) produce alarm
pheromone in the sting gland and a pheromone that has sometimes been described
as an alarm pheromone in their mandibular glands, but which does not galvanize
colony aggression (Vallet et al.,
1991; Couvillon et al., 2010). In the
highly social bees (honey bees and stingless bees), alarm pheromones can
increase aggression and flight activity at the nest entrance, a defensive
response (Boch and Shearer, 1971; Roubik, 1989). Honeybees became adapted to synthetic alarm pheromone
components dispensed within their hives and were less inclined to sting. The
reduction in the stinging response of honeybee colonies which were adapted to 6
or 8 alarm pheromone components was no more than in colonies adapted to 3
components only, synthetic alarm pheromones to reduce aggression (Free,
1988).
Alarm
pheromones play an important role in social insects and enhance collective
fitness by providing information about dangers such as predators (Billen and
Morgan, 1998). For example, honey bees can use alarm pheromones to co-ordinate
colony defense (Free, 1987; Pirk et al.,
2011). The behavioral responses can
be classified into (1) initial
preparatory phase of alarm behavior, (2) alarm behavior and (3) aggression
against a potential enemy (Makoto Mizunami et al.,2010). Aggressive behaviour increases with age when the honey bees are
exposed to alarm pheromone ( Alaux
et al.,2009). Not only it it
increases the aggressive behaviour,but also increases metabolism in honey bees
(Southwick and Moritz, 1985) and
higher cytochrome c oxidase activity in rodents and lizards (Sakata et al.,2005). Intrestingly, a reduced
metabolism and aggression has been reported for some parts of the human brain (Anckarsa¨ter,
2006). Melanocortins in the preputial glands can alter the excretion of
aggression-modifying pheromonesn (Caldwell and Lepri, 2002.).
The ‘one gland – two
functions hypothesis’ has developed (Kerr and da Cruz, 1961) in meliponine communication. If one assumes
that mandibular gland secretions do indeed induce both scent trail following to
distant food sources in newly recruited worker bees and defensive/aggressive
behaviour in the same workers near the nest. Almost all workers attracted to target 1 became its
aggressors, probably due to
the presence of alarm pheromones. Thus, pupal odor seems to act as a chemical
signal to indicate the presence of pupae in the nest, attracting the workers
which would care for and defend the pupae against predators. Although pupal
odor does not elicit alarm behavior, it appears to interact with alarm
pheromones by potentiating their effects (Manzoli-Palma et al.,1998).
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