Tracing of mono- and polysynaptic afferent connections between the main olfactory bulb and higher-order brain regions in the mouse

With our model parameters, oscillations in this regime have higher frequency, typically in the gamma range (50Hz-90Hz) but their frequency is highly sensitive to the level of

We assessed respectively the trends, uses, mode of action and metabolites (Simon-Delso et al. 2014); the environmental fate and exposure (Bonmatin et al. 2014); effects on non-

experiments which showed that a visual stimulus previously asso- ciated with an odorant is able to activate primary olfactory cortical regions ( Gottfried et al., 2002, 2004 ) in

associated with ash urns in Chalcidice, more exactly in Kriaritsi Sykia and in Nea Skioni (Asouchidou 2011, 34–40; Tsigarida/Mantazi 2004); in southern Pieria, the burial mounds

This morphological plasticity may be influenced by peptides involved in food intake regulation such as NPY, and may participate to the adaptation of olfactory sensitivity to

٥ ٢ ( نﺎﻤﻀﻟا ﺔﻳﺮﻈﻧ : ﻪﻴﻘﻔﻟا حﱰﻘﻳ ) كرﺎﺘﺳ ( سﺎﺳأ نﻮﻜﻳ نا ﻞﻛ ﻦﻋ لﺄﺴﻳ نﺎﺴﻧﻹا نأ ﻮﻫ ﺔﻣﺎﻋ ﺔﻴﻧﺪﳌا ﺔﻴﻟوﺆﺴﳌا ﺊﻄﳐ ﲑﻏ وأ ًﺎﺌﻄﳐ نﺎﻛ اذإ ﺎﻤﻋ ﺚﺤﺒﻟا نود ﻪﻟاﻮﻣﺄﺑ

10–12, the following eight variables are eval- uated at each site: 2-m temperature, 2-m specific hu- midity, latent heat flux, sensible heat flux, surface short- wave

The olfactory tubercle excepted (Fig 2. b1), all the olfactory regions receiving bulbar projections via the lateral olfactory tract showed retrogradely labeled cells (Fig 2;