Page 106 - Zoo Animal Learning and Training
P. 106

78  Box A3   Makinng Sense oouScents:  loactorry  erception inuAnimals

  VetBooks.ir  considerably depending on the particular   signals from potential prey (Gillingham and
                                                     Clark 1981), and elephants transfer potential
            message being sent, and olfactory signals
            have been shown to convey a staggering
                                                     (Rasmussen and Schulte 1998). In fact, the
            amount of information on factors such as   signals  there  using  the  tip  of  their  trunk
            sex,  age, condition,  reproductive status,   typical ‘flehmen’ response of cats and many
            group membership and even individual iden-  ungulates, whereby they lift and curl the nose
            tity (e.g. see Epple et al. 1987). But how are   whilst raising and contorting their lips, relates
            these olfactory signals perceived?       to the stimulation of the vomeronasal organ
                                                     with urine from conspecifics. Overall, the
                                                     vomeronasal organ appears to be particularly
              Scent Perception                       important in modulating reproduction and
                                                     social behaviour, and many neurons are acti-
            Successful olfactory communication relies on   vated by urinary‐borne chemicals signalling
            the receipt and accurate discrimination of   physiological state.
            scent signals, all of which is handled by spe-
            cialised  olfactory  processing  equipment,
            which is divided into two discrete systems.     Perception and Learning
            The first, the main olfactory system, is the
            olfactory bulb, and this receives information   Using this olfactory  equipment, receivers
            passed along millions of olfactory receptor   must be able to extract and categorise the rel-
            neurons travelling from the nose to the brain.   evant olfactory information from encoun-
            Neurons expressing the same olfactory recep-  tered odours, all within environments infused
            tor are clustered together in individual glo-  with irrelevant and potentially confusing
            meruli in the olfactory bulb, forming a kind of   smells. Correct categorisation, or recognition,
            layer  that  has  been  described  as  a  spatial   of different odours may be important in many
            odour map (Uchida et al. 2000). Importantly,   aspects of social life, including the modulation
            in the context of learning and perception, the   of competitive relationships and the mainte-
            olfactory  bulb  appears  to  exhibit  enormous   nance of stable social groups, navigation and
            plasticity  in  response  to  experience  with   reproduction. Although innate responses to
            scents, and exposure to odours can modify   some chemical signals are known, novel
            the perceptions of those odours enormously   odours are generally more difficult to discrim-
            (e.g. Wilson and Stevenson 2003). In the sec-  inate than familiar ones (Rabin 1988). In fact,
            ond system, the accessory olfactory system,   learning is perhaps the most important com-
            the vomeronasal organ or Jacobson’s organ   ponent of olfactory perception. Unsurprisingly,
            (Keverne 1999), is responsible for scent detec-  human adults and older children perform bet-
            tion and is usually found in the main nasal   ter at odour discrimination tasks than young
            chamber of many but not all amphibians, rep-  children (Lehrner et al. 1999), but importantly
            tiles, and mammals. Neurons from the vome-  improvement in the discrimination often
            ronasal organ connect it to the accessory   improves after exposure to that odour, whilst
            olfactory bulb in the brain, which ultimately   discrimination of other odours remains poor
            feeds the hypothalamus via the amygdala. As   (Rabin 1988). This suggests that maturity of
            in the olfactory bulb, odours are detected fol-  the  receptor  system  itself  is  not  driving  the
            lowing binding to receptors, but in this case   observed odour improvement in discrimina-
            the signals are non‐volatile and so are received   tion with age. Rather it is specific experience
            in the liquid phase. Additionally, animals may   or  learning  that  enhances  olfactory  percep-
            exhibit various specialist behaviours in order   tion. In fact, under conditions where a per-
            to transfer signals to the vomeronasal organ.   son’s capability for memory is reduced, such
            For example, snakes touch their tongue to the   as is the case in Alzheimer’s disease, the ability
            vomeronasal organ after ‘tasting’ the air for   to perceive odour quality is itself lost or
   101   102   103   104   105   106   107   108   109   110   111