ArticleFrontiers in physiology2013
Trace conditioning in insects-keep the trace!
Article in Frontiers in physiology, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.
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Who cites it
19 citing papers in PubMed.
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- How bumblebees manage conflicting information seen on arrival and departure from flowers.Animal cognition · 2025Article
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- How do real animals account for the passage of time during associative learning?Behavioral neuroscience · 2022Article
- What Behavioral Abilities Emerged at Key Milestones in Human Brain Evolution? 13 Hypotheses on the 600-Million-Year Phylogenetic History of Human Intelligence.Frontiers in psychology · 2021Article
- Fishnition: Developing Models From Cognition Toward Consciousness.Frontiers in veterinary science · 2021Article
- Unlimited Associative Learning and the origins of consciousness: a primer and some predictions.Biology & philosophy · 2020Article
- Odors from phylogenetically-distant plants to Brassicaceae repel an herbivorous Brassica specialist.Scientific reports · 2019Article
- Calcium in Kenyon Cell Somata as a Substrate for an Olfactory Sensory Memory inFrontiers in cellular neuroscience · 2018Article
- Olfactory learning without the mushroom bodies: Spiking neural network models of the honeybee lateral antennal lobe tract reveal its capacities in odour memory tasks of varied complexities.PLoS computational biology · 2017Article
- Trace Conditioning inFrontiers in neural circuits · 2017Article
- The Transition to Minimal Consciousness through the Evolution of Associative Learning.Frontiers in psychology · 2016Article
- Reversing Stimulus Timing in Visual Conditioning Leads to Memories with Opposite Valence in Drosophila.PloS one · 2015Article
- Plasticity in invertebrate sensory systems.Frontiers in physiology · 2013Article
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4 authors.
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Abstract
Trace conditioning is a form of associative learning that can be induced by presenting a conditioned stimulus (CS) and an unconditioned stimulus (US) following each other, but separated by a temporal gap. This gap distinguishes trace conditioning from classical delay conditioning, where the CS and US overlap. To bridge the temporal gap between both stimuli and to form an association between CS and US in trace conditioning, the brain must keep a neural representation of the CS after its termination-a stimulus trace. Behavioral and physiological studies on trace and delay conditioning revealed similarities between the two forms of learning, like similar memory decay and similar odor identity perception in invertebrates. On the other hand differences were reported also, like the requirement of distinct brain structures in vertebrates or disparities in molecular mechanisms in both vertebrates and invertebrates. For example, in commonly used vertebrate conditioning paradigms the hippocampus is necessary for trace but not for delay conditioning, and Drosophila delay conditioning requires the Rutabaga adenylyl cyclase (Rut-AC), which is dispensable in trace conditioning. It is still unknown how the brain encodes CS traces and how they are associated with a US in trace conditioning. Insects serve as powerful models to address the mechanisms underlying trace conditioning, due to their simple brain anatomy, behavioral accessibility and established methods of genetic interference. In this review we summarize the recent progress in insect trace conditioning on the behavioral and physiological level and emphasize similarities and differences compared to delay conditioning. Moreover, we examine proposed molecular and computational models and reassess different experimental approaches used for trace conditioning.
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