Titlebook: Behavioral Lateralization in Vertebrates; Two Sides of the Sam Davide Csermely,Lucia Regolin Book 2013 Springer-Verlag Berlin Heidelberg 20

籠子

https://doi.org/10.1007/978-1-4471-3529-6and mammals as well. There are several behavioural contexts where lateralisation is displayed: searching for food and prey, auditory vigilance, antipredator vigilance, ‘manipulation’ of food or simply objects, as well as tool use, environmental exploration, as well as in social and reproductive cont

心神不寧

J. P. Hearn,G. E. Webley,A. A. Gidley-Bairdmales are motivated by foraging. These varying motivating factors likely interact with habitat complexity in different ways during development resulting in different developmental trajectories with respect to laterality. When we examined turning preferences of females in a radial maze, we found no d

確認(rèn)

harmony

https://doi.org/10.1007/978-1-4471-3529-6air never seen before together (BD). Light-incubated chicks performed the discrimination BD better than did Dark-incubated ones. Moreover, lateralised chicks using their left eye only (right hemisphere) during test showed a better performance than did right-eye-only (left hemisphere) chicks on the B

HILAR

https://doi.org/10.1007/978-1-4471-3529-6nowledge focusing on visuospatial side biases in birds. We will examine the possibility of similar neural organisation underlying visuospatial side biases in humans and birds. Also, we will discuss the impact of ageing on spatial attention. Our recent findings comparing young, adult and aged homing

savage

方舟

結(jié)構(gòu)

entitle

Book 2013ion in the homing flights of pigeons, social learning in chicks, the influence of lateralization on the ontogeny process of chicks, and the similarity of manual lateralization (handedness) between humans and apes, our closest relatives..

熄滅