Plasticity‐related genes in brain development and amygdala‐dependent learning

Learning about motivationally important stimuli involves plasticity in the amygdala, a temporal lobe structure. Amygdala‐dependent learning involves a growing number of plasticity‐related signaling pathways also implicated in brain development, suggesting that learning‐related signaling in juveniles may simultaneously influence development. Here, we review the pleiotropic functions in nervous system development and amygdala‐dependent learning of a signaling pathway that includes brain‐derived neurotrophic factor (BDNF), extracellular signaling‐related kinases (ERKs) and cyclic AMP‐response element binding protein (CREB). Using these canonical, plasticity‐related genes as an example, we discuss the intersection of learning‐related and developmental plasticity in the immature amygdala, when aversive and appetitive learning may influence the developmental trajectory of amygdala function. We propose that learning‐dependent activation of BDNF, ERK and CREB signaling in the immature amygdala exaggerates and accelerates neural development, promoting amygdala excitability and environmental sensitivity later in life.     

Asymmetric interspecific aggression in New Guinean songbirds that replace one another along an elevational gradient

A common pattern in tropical avifaunas is for closely related species to inhabit largely parapatric elevational distributions such that they replace one another along the elevational gradient. A long‐standing hypothesis for this pattern is that parapatry is maintained by interspecific interference competition mediated by interspecific aggression. However, empirical tests of this hypothesis remain scarce. We used reciprocal playback experiments to measure interspecific aggression in five species‐pairs of New Guinean passerine elevational replacements. We found evidence of interspecific aggression in three species‐pairs. In these three cases, interspecific aggression was asymmetric, with the lower elevation species more aggressive towards the upper elevation species than vice versa. Two patterns suggest that this interspecific aggression is a learned response to the presence of a heterospecific competitor rather than misdirected intraspecific aggression or an evolved response to a competitor. First, when present, interspecific aggression was always strongest at the upper elevation range margin of the lower elevation species (i.e. in the elevational zone in which the two species were found in close proximity and thus interacted with each other), and diminished over very short distances away from this zone. Secondly, the two species‐pairs that did not exhibit interspecific aggression had narrow ‘no man's land’ gaps between their elevational distributions such that heterospecifics did not encounter one another, possibly explaining the lack of interspecific aggression in these examples. Our results support the hypothesis that interspecific aggression is one factor influencing elevational limits in species‐pairs of New Guinean elevational replacements.     

Prediction of taxon occurrence: a test on taxon‐specific change point values of stream benthic invertebrates

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