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David F Sherry

Publications and source records attributed to David F Sherry.

5 recordsLinked to original sources

Annual cycle of the black-capped chickadee: seasonality of food-storing and the hippocampus.

Previous research presents a mixed picture of seasonal variation in the hippocampus of food-storing black-capped chickadees. One field study has shown an October peak in hippocampus volume, although laboratory studies conducted to determine whether photoperiod regulates this seasonal growth have failed to find changes in the size of the hippocampus. To resolve the discrepancy between field and lab reports we examined caching activity, hippocampal volume, and neurogenesis in adult male black-capped chickadees at four times over the annual cycle: October, January, April and July. We found that more birds stored food in October than at other times of year, but did not observe a significant change in the size of the hippocampus over the annual cycle. Telencephalon volume, however, was larger in October than in July. Hippocampal neuronal recruitment showed a significant peak in January, but there was no seasonal change in neuronal recruitment in the adjacent hyperpallium apicale. These results indicate that there might be seasonal variation in the recruitment of new neurons into the hippocampus of chickadees without overall seasonal change in hippocampal size.

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Interval timing by an invertebrate, the bumble bee Bombus impatiens.

Sensitivity to temporal information and the ability to adjust behavior to the temporal structure of the environment should be phylogenetically widespread. Some timing abilities, such as sensitivity to circadian cycles, appear in a wide range of invertebrate and vertebrate taxa [1,2]. Interval timing--sensitivity to the duration of time intervals--has, however, only been shown to occur in vertebrates [3,4]. Insect pollinators make a variety of decisions that would appear to require the ability to estimate elapsed durations. We exposed bumble bees to conditions in which proboscis extension was reinforced after a fixed duration had elapsed or after either of two fixed durations had elapsed. Two groups of bees were trained with a short duration (either 6 s or 12 s) and a long duration (36 s) in separate experimental phases (independent timing groups), whereas two other groups were trained with a short duration (either 6 s or 12 s) and long duration (36 s) always intermixed unpredictably (multiple timing groups). On long intervals, independent timing groups waited longer than mixed timing groups to generate the first response and responded maximally near the end of the interval. Multiple timing groups waited the same amount of time on average before generating the first response on both long and short intervals. On individual trials, multiple timing groups appeared to time either the long duration only or both the short and long durations: most trials were characterized by a single burst of responding that began between the short and long duration values or by two bursts of responding with the first burst bracketing the short value and the second burst beginning in anticipation of the long value. These results show that bumble bees learn to time interval durations and can flexibly time multiple durations simultaneously. The results indicate no phylogenetic divide between vertebrates and invertebrates in interval timing ability.

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Annual cycle of the black-capped chickadee: seasonality of singing rates and vocal-control brain regions.

Black-capped chickadees have a rich vocal repertoire including learned calls and the learned fee-bee song. However, the neural regions underlying these vocalizations, such as HVC, area X, and RA (robust nucleus of arcopallium), remain understudied. Here, we document seasonal changes in fee-bee song production and show a marked peak in singing rate during March through May. Despite this, we found only minimal seasonal plasticity in vocal control regions of the brain in males. There was no significant effect of time of year on the size of HVC, X, or RA in birds collected in January, April, July, and October. We then pooled birds into two groups, those with large testes (breeding condition) and those with small testes (nonbreeding), regardless of time of year. Breeding birds had slightly larger RA, but not HVC or X, than nonbreeding birds. Breeding birds had slightly larger HVC and RA, but not X, as a proportion of telencephalon volume than did nonbreeding birds. Birds collected in July had heavier brains than birds at other times of year, and had the greatest loss in brain mass during cryoprotection. The absence of any overall seasonal change in the vocal-control regions of chickadees likely results from a combination of individual differences in the timing of breeding phenology and demands on the vocal-control regions to produce learned calls year-round.

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Neuroecology.

Neuroecology is the study of adaptive variation in cognition and the brain. The origin of neuroecology dates from the 1980s, when researchers in behavioral ecology began to apply the methods of comparative evolutionary biology to cognitive processes and the underlying neural mechanisms of cognition. The comparative approach, however, is much older. It was a mainstay of ethology, it has been part of the study of neuroanatomy since the seventeenth century, and it was used by Darwin to marshal evidence for the theory of natural selection. Neuroecology examines the relations between ecological selection pressures and species or sex differences in cognition and the brain. The goal of neuroecology is to understand how natural selection acts on cognition and its neural mechanisms. This chapter describes the general approach of neuroecology, phylogenetic comparative methods used in the field, and new findings on the cognitive mechanisms and brain structures involved in mating systems, social organization, communication, and foraging. The contribution of neuroecology to psychology and the neurosciences is the information it provides on the selective pressures that have influenced the evolution of cognition and brain structure.

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Neuron production, neuron number, and structure size are seasonally stable in the hippocampus of the food-storing black-capped chickadee (Poecile atricapillus).

Neuronal recruitment in the black-capped chickadee (Poecile atricapillus) hippocampus occurs at a higher rate in the fall than at other times of the year. As a means of determining whether this increase in recruitment results from greater neuron production, chickadees were caught in the wild between October and March and injected with the cell-birth marker 5-bromo-2'-deoxyuridine. Two weeks later, birds were killed by overdose, and hippocampal neuron production, apoptosis, neuron number, and hippocampal volume were determined. Chickadees collected in October, November, January, February, and March did not differ in neuron production, apoptosis, hippocampal volume, or neuron number. These findings indicate that increases in neuronal recruitment in the chickadee hippocampus in the fall do not result from increased neuron production, but instead, enhanced survival of new neurons.

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