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Massed and Spaced Learning in Honeybees: The Role of CS, US, the Intertrial Interval, and the Test Interval

https://doi.org/10.1101/lm.40001
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What this work says

Outgoing claims: the papers this work cites, builds on, or argues with.

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Temporal Determinants of Olfactory Long-Term Retention in Honeybee Classical Conditioning: Nonmonotonous Effects of the Training Trial Interval
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Context Shift and Protein Synthesis Inhibition Disrupt Long-Term Habituation after Spaced, but Not Massed, Training in the CrabChasmagnathus
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Das Ged�chtnis der Honigbiene f�r Spektralfarben
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Formation of long term olfactory memory in honeybees does not require protein synthesis
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Memory dynamics in the honeybee
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Learning in honey bees with brain lesions: how partial mushroom-body ablations affect sucrose responsiveness and tactile antennal learning
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The relationship between sugar flow and foraging and recruiting behaviour of honey bees (Apis mellifera L.)
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C/EBP is an immediate-early gene required for the consolidation of long-term facilitation in Aplysia
inferredcites →https://doi.org/10.1016/0092-8674(94)90398-0openalex-snapshot
Genetic dissection of consolidated memory in Drosophila
inferredcites →https://doi.org/10.1016/0092-8674(94)90399-9openalex-snapshot
Induction of a dominant negative CREB transgene specifically blocks long-term memory in Drosophila
inferredcites →https://doi.org/10.1016/0092-8674(95)90213-9openalex-snapshot
Aplysia CREB2 represses long-term facilitation: Relief of repression converts transient facilitation into long-term functional and structural change
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CREB as a Memory Modulator: induced expression of a dCREB2 activator isoform enhances long-term memory in drosophila
inferredcites →https://doi.org/10.1016/b978-0-12-268330-5.50013-5openalex-snapshot
Memory and the Brain
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Production of the Fos protein after contextual fear conditioning of C57BL/6N mice
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The spacing effect: Consolidation or differential encoding?
inferredcites →https://doi.org/10.1016/s0163-1047(05)80020-2openalex-snapshot
Color learning and memory in honey bees are not affected by protein synthesis inhibition
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Prolonged Activation of cAMP-Dependent Protein Kinase during Conditioning Induces Long-Term Memory in Honeybees
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Inhibition of Nitric Oxide Synthase Impairs a Distinct Form of Long-Term Memory in the Honeybee, Apis mellifera
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Serotonin Induces Temporally and Mechanistically Distinct Phases of Persistent PKA Activity in Aplysia Sensory Neurons
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Spaced training induces normal long-term memory in CREB mutant mice
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Distribution-of-trials effects in Pavlovian conditioning: An apparent involvement of inhibitory backward conditioning with short intertrial intervals.
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Contextual conditioning with massed versus distributed unconditional stimuli in the absence of explicit conditional stimuli.
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Heritable variation for latent inhibition and its correlation with reversal learning in honeybees (Apis mellifera).
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A comparison of contextual and generalized auditory-cue fear conditioning: evidence for similar memory processes.
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Interactive contributions of intracellular calcium and protein phosphatases to massed-trials learning deficits in Hermissenda.
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Characteristics of associative learning in younger and older adults: Evidence from an episodic priming paradigm.
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Judgments of frequency and recognition memory in a multiple-trace memory model.
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Classical conditioning of proboscis extension in honeybees (Apis mellifera).
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The principles of psychology, Vol I.
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Review of Die Assoziationsfestigkeit in ihrer Abhängigkeit von der Verteilung der Wiederholungen.
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Rank order as a psycho-physical method.
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Behavioural access to short-term memory in bees
inferredcites →https://doi.org/10.1038/35021052openalex-snapshot
Fear memories require protein synthesis in the amygdala for reconsolidation after retrieval
inferredcites →https://doi.org/10.1038/83976openalex-snapshot
Spaced stimuli stabilize MAPK pathway activation and its effects on dendritic morphology
inferredcites →https://doi.org/10.1046/j.1460-9568.1998.00319.xopenalex-snapshot
Long- but not medium-term retention of olfactory memories in honeybees is impaired by actinomycin D and anisomycin
inferredcites →https://doi.org/10.1097/00001756-199412300-00015openalex-snapshot
Long-term habituation of an appetitive reflex in the honeybee
inferredcites →https://doi.org/10.1101/lm.4.5.429openalex-snapshot
Backward inhibitory learning in honeybees: a behavioral analysis of reinforcement processing.
inferredcites →https://doi.org/10.1101/lm.5.1.1openalex-snapshot
What Do the Mushroom Bodies Do for the Insect Brain? An Introduction
inferredcites →https://doi.org/10.1101/lm.5.1.146openalex-snapshot
Multiple Sites of Associative Odor Learning as Revealed by Local Brain Microinjections of Octopamine in Honeybees
inferredcites →https://doi.org/10.1101/lm.5.1.90openalex-snapshot
Early Development of Mushroom Bodies in the Brain of the Honeybee Apis mellifera as Revealed by BrdU Incorporation and Ablation Experiments
inferredcites →https://doi.org/10.1101/lm.5.3.246openalex-snapshot
Differential Induction of Long-Term Synaptic Facilitation by Spaced and Massed Applications of Serotonin at Sensory Neuron Synapses of Aplysia californica
inferredcites →https://doi.org/10.1101/lm.7.3.151openalex-snapshot
Contextual Modulation of Memory Consolidation
inferredcites →https://doi.org/10.1126/science.175.4020.451openalex-snapshot
Long-Term Habituation of a Defensive Withdrawal Reflex in Aplysia
inferredcites →https://doi.org/10.1126/science.182.4116.1039openalex-snapshot
Long-Term Sensitization of a Defensive Withdrawal Reflex in Aplysia
inferredcites →https://doi.org/10.1146/annurev.ne.09.030186.002251openalex-snapshot
Invertebrate Learning and Memory: From Behavior to Molecules
inferredcites →https://doi.org/10.1146/annurev.ne.19.030196.002115openalex-snapshot
Learning and Memory in Honeybees: From Behavior to Neural Substrates
inferredcites →https://doi.org/10.1152/jn.1992.67.3.588openalex-snapshot
Habituation of an appetitive reflex in the honeybee
inferredcites →https://doi.org/10.1242/jeb.161.1.367openalex-snapshot
The Olfactory Memory of the Honeybee Apis Mellifera: I. Odorant Modulation of Short- and Intermediate-Term Memory After Single-Trial Conditioning
inferredcites →https://doi.org/10.1242/jeb.200.14.2045openalex-snapshot
The Olfactory Memory of The Honeybee Apis Mellifera: III. Bilateral Sensory Input is Necessary for Induction and Expression of Olfactory Blocking
inferredcites →https://doi.org/10.1242/jeb.201.14.2213openalex-snapshot
Visual Modulation of Olfactory Learning in Honeybees
inferredcites →https://doi.org/10.1242/jeb.203.8.1351openalex-snapshot
Sensory Preconditioning in Honeybees
inferredcites →https://doi.org/10.1523/jneurosci.13-04-01379.1993openalex-snapshot
Inhibition of brain protein synthesis by cycloheximide does not affect formation of long-term memory in honeybees after olfactory conditioning
inferredcites →https://doi.org/10.1523/jneurosci.18-11-04384.1998openalex-snapshot
Induction of a Specific Olfactory Memory Leads to a Long-Lasting Activation of Protein Kinase C in the Antennal Lobe of the Honeybee
inferredcites →https://doi.org/10.1523/jneurosci.20-08-02944.2000openalex-snapshot
Learning Performance of Normal and MutantDrosophilaafter Repeated Conditioning Trials with Discrete Stimuli
inferredcites →https://doi.org/10.3758/bf03198931openalex-snapshot
Trial spacing effects in pavlovian conditioning: A role for local context
inferredcites →https://doi.org/10.3758/bf03205285openalex-snapshot
Factors governing one-trial contextual conditioning
inferredcites →https://doi.org/10.4324/9781032722375-5openalex-snapshot
Theoretical Implications of the Spacing Effect 1

What points at this work

Incoming claims: where this work appears in other papers’ reference lists and arguments.

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Effects of cold immobilization and recovery period on honeybee learning, memory, and responsiveness to sucrose
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Inhibiting DNA methylation alters olfactory extinction but not acquisition learning in Apis cerana and Apis mellifera
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Appetitive olfactory learning and memory in the honeybee depend on sugar reward identity
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Spaced Training Forms Complementary Long-Term Memories of Opposite Valence in Drosophila
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Influence of mRNA and protein synthesis inhibitors on the long-term memory acquisition of classically conditioned earthworms
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Spacing and Testing Effects
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The Dynamics of Learning and Allocation of Study Time to a Region of Proximal Learning.
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Iron-induced oxidative stress modulates olfactory learning and memory in honeybees.
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Humor in advertisements enhances product liking by mere association.
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Neuroligin-associated microRNA-932 targets actin and regulates memory in the honeybee
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Memory reactivation improves visual perception
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The massed-spaced learning effect in non-neural human cells
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Duration between rewards controls the rate of behavioral and dopaminergic learning
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Spatial-Memory Formation After Spaced Learning Involves ERKs1/2 Activation Through a Behavioral-Tagging Process
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Suitability of drone olfactory sensitivity as a selection trait for Varroa-resistance in honeybees
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Dynamically expressed single ELAV/Hu orthologue elavl2 of bees is required for learning and memory
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Low doses of neonicotinoid pesticides in food rewards impair short-term olfactory memory in foraging-age honeybees
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Towards a Theory of Learning for Naming Rehabilitation: Retrieval Practice and Spacing Effects
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The AmCREB gene is an ortholog of the mammalian CREB/CREM family of transcription factors and encodes several splice variants in the honeybee brain
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Synchronizing education to adolescent biology: ‘let teens sleep, start school later’
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Rapid Associative Learning and Stable Long-Term Memory in the SquidEuprymna scolopes
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Memory of conspecifics in male salamanders Plethodon cinereus: Implications for territorial defense
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Evidence for instantaneous e-vector detection in the honeybee using an associative learning paradigm
inferred← citeshttps://doi.org/10.1098/rspb.2013.0528openalex-snapshot
Reception and learning of electric fields in bees
inferred← citeshttps://doi.org/10.1098/rspb.2017.1323openalex-snapshot
A possible structural correlate of learning performance on a colour discrimination task in the brain of the bumblebee
inferred← citeshttps://doi.org/10.1098/rspb.2023.2274openalex-snapshot
Transcriptomic responses to location learning by honeybee dancers are partly mirrored in the brains of dance-followers
inferred← citeshttps://doi.org/10.1101/2021.06.24.449637openalex-snapshot
Dynamically expressed ELAV is required for learning and memory in bees
inferred← citeshttps://doi.org/10.1101/2024.03.07.583937openalex-snapshot
Asynchronous temporal variance in learning behaviour and neural gene expression in a butterfly
inferred← citeshttps://doi.org/10.1101/2025.02.17.638520openalex-snapshot
Long-term memory formation impacts dietary energy intake but not metabolic rate in honeybees
inferred← citeshttps://doi.org/10.1101/420968openalex-snapshot
Characterization of the olfactory system in Apis dorsata , an Asian honey bee
inferred← citeshttps://doi.org/10.1101/lm.024711.111openalex-snapshot
Invertebrate learning and memory: Fifty years of olfactory conditioning of the proboscis extension response in honeybees
inferred← citeshttps://doi.org/10.1101/lm.026245.112openalex-snapshot
A role of protein degradation in memory consolidation after initial learning and extinction learning in the honeybee (Apis mellifera)
inferred← citeshttps://doi.org/10.1101/lm.026906.112openalex-snapshot
Two waves of transcription are required for long-term memory in the honeybee
inferred← citeshttps://doi.org/10.1101/lm.033118.113openalex-snapshot
Molecular mechanisms underlying formation of long-term reward memories and extinction memories in the honeybee (Apis mellifera)
inferred← citeshttps://doi.org/10.1101/lm.035600.114openalex-snapshot
Duration of the unconditioned stimulus in appetitive conditioning of honeybees differentially impacts learning, long-term memory strength, and the underlying protein synthesis
inferred← citeshttps://doi.org/10.1101/lm.040964.115openalex-snapshot
Involvement of phosphorylated Apis mellifera CREB in gating a honeybee's behavioral response to an external stimulus
inferred← citeshttps://doi.org/10.1101/lm.043513.116openalex-snapshot
Interaction of inhibitory and facilitatory effects of conditioning trials on long-term memory formation
inferred← citeshttps://doi.org/10.1101/lm.053396.121openalex-snapshot
Distributed learning episodes create a context fear memory outside the hippocampus that depends on perirhinal and anterior cingulate cortices
inferred← citeshttps://doi.org/10.1101/lm.1132008openalex-snapshot
Distributed learning enhances relational memory consolidation
inferred← citeshttps://doi.org/10.1101/lm.1419109openalex-snapshot
Side-specific reward memories in honeybees
inferred← citeshttps://doi.org/10.1101/lm.1445609openalex-snapshot
Long-term memory shapes the primary olfactory center of an insect brain
inferred← citeshttps://doi.org/10.1101/lm.192506openalex-snapshot
Protein synthesis-dependent long-term memory induced by one single associative training trial in the parasitic waspLariophagus distinguendus
inferred← citeshttps://doi.org/10.1101/lm.2224411openalex-snapshot
Aversive olfactory learning and associative long-term memory in Caenorhabditis elegans
inferred← citeshttps://doi.org/10.1101/lm.2232711openalex-snapshot
Average group behavior does not represent individual behavior in classical conditioning of the honeybee
inferred← citeshttps://doi.org/10.1101/lm.44802openalex-snapshot
Interaction between Amount and Pattern of Training in the Induction of Intermediate- and Long-Term Memory for Sensitization in Aplysia
inferred← citeshttps://doi.org/10.1101/lm.63604openalex-snapshot
Associative Mechanosensory Conditioning of the Proboscis Extension Reflex in Honeybees
inferred← citeshttps://doi.org/10.1101/lm.785608openalex-snapshot
Distinct neural mechanisms mediate olfactory memory formation at different timescales
inferred← citeshttps://doi.org/10.1101/lm.81504openalex-snapshot
Spontaneous Recovery After Extinction of the Conditioned Proboscis Extension Response in the Honeybee
inferred← citeshttps://doi.org/10.1111/1744-7917.13119openalex-snapshot
Formation characteristics of long‐term memory in Bactrocera dorsalis
inferred← citeshttps://doi.org/10.1111/j.1439-0310.2004.01060.xopenalex-snapshot
Memory of Social Partners in Hermit Crab Dominance
inferred← citeshttps://doi.org/10.1111/j.1570-7458.2012.01253.xopenalex-snapshot
Demonstration of long‐term memory in the parasitic wasp Nasonia vitripennis
inferred← citeshttps://doi.org/10.1111/j.1601-183x.2005.00134.xopenalex-snapshot
Differential translation and fragile X syndrome
inferred← citeshttps://doi.org/10.1111/j.1601-183x.2009.00482.xopenalex-snapshot
Parametric and genetic analysis of Drosophila appetitive long‐term memory and sugar motivation
inferred← citeshttps://doi.org/10.1111/oik.05405openalex-snapshot
Petrol exhaust pollution impairs honey bee learning and memory
inferred← citeshttps://doi.org/10.1126/science.1228806openalex-snapshot
Caffeine in Floral Nectar Enhances a Pollinator's Memory of Reward
inferred← citeshttps://doi.org/10.1152/jn.90459.2008openalex-snapshot
Monoaminergic Modulation of the Na+-Activated K+Channel in Kenyon Cells Isolated From the Mushroom Body of the Cricket (Gryllus bimaculatus) Brain
inferred← citeshttps://doi.org/10.1152/physiol.00009.2006openalex-snapshot
Synaptic Plasticity In Vitro and In Silico: Insights into an Intracellular Signaling Maze
inferred← citeshttps://doi.org/10.1186/1741-7007-7-30openalex-snapshot
Early calcium increase triggers the formation of olfactory long-term memory in honeybees
inferred← citeshttps://doi.org/10.1186/s13041-020-00667-5openalex-snapshot
Fear response-based prediction for stress susceptibility to PTSD-like phenotypes
inferred← citeshttps://doi.org/10.1201/b20027-34openalex-snapshot
References
inferred← citeshttps://doi.org/10.1242/jeb.01474openalex-snapshot
Olfactory learning by means of trophallaxis inApis mellifera
inferred← citeshttps://doi.org/10.1242/jeb.034140openalex-snapshot
Thermal learning in the honeybee,Apis mellifera
inferred← citeshttps://doi.org/10.1242/jeb.074898openalex-snapshot
Associative learning in the dengue vector mosquito,Aedes aegypti: avoidance of a previously attractive odor or surface color that is paired with an aversive stimulus
inferred← citeshttps://doi.org/10.1242/jeb.083931openalex-snapshot
Exposure to multiple cholinergic pesticides impairs olfactory learning and memory in honeybees
inferred← citeshttps://doi.org/10.1242/jeb.115105openalex-snapshot
Diurnal oscillation of vocal development associated with clustered singing by juvenile songbirds
inferred← citeshttps://doi.org/10.1242/jeb.161489openalex-snapshot
Nosema ceranae parasitism impacts olfactory learning and memory and neurochemistry in honey bees (Apis mellifera)
inferred← citeshttps://doi.org/10.1242/jeb.164731openalex-snapshot
Honeybees in a virtual reality environment learn unique combinations of colour and shape
inferred← citeshttps://doi.org/10.1242/jeb.168344openalex-snapshot
The reluctant visitor: an alkaloid in toxic nectar can reduce olfactory learning and memory in Asian honey bees
inferred← citeshttps://doi.org/10.1242/jeb.173062openalex-snapshot
Correction: Honeybees in a virtual reality environment learn unique combinations of colour and shape
inferred← citeshttps://doi.org/10.1242/jeb.179622openalex-snapshot
Length of stimulus presentation and visual angle are critical for efficient visual PER conditioning in the restrained honey bee,Apis mellifera
inferred← citeshttps://doi.org/10.1242/jeb.205.10.1429openalex-snapshot
Temporal determinants of long-term retention of olfactory memory in the cricket Gryllus bimaculatus
inferred← citeshttps://doi.org/10.1242/jeb.244340openalex-snapshot
The gut parasite Nosema ceranae impairs olfactory learning in bumblebees
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A Normative Theory of Forgetting: Lessons from the Fruit Fly
inferred← citeshttps://doi.org/10.1371/journal.pone.0013504openalex-snapshot
In the Laboratory and during Free-Flight: Old Honey Bees Reveal Learning and Extinction Deficits that Mirror Mammalian Functional Decline
inferred← citeshttps://doi.org/10.1371/journal.pone.0037666openalex-snapshot
Visual Associative Learning in Restrained Honey Bees with Intact Antennae
inferred← citeshttps://doi.org/10.1371/journal.pone.0117205openalex-snapshot
The Spacing Principle for Unlearning Abnormal Neuronal Synchrony
inferred← citeshttps://doi.org/10.1371/journal.pone.0118708openalex-snapshot
The Sound and the Fury—Bees Hiss when Expecting Danger
inferred← citeshttps://doi.org/10.1371/journal.pone.0134248openalex-snapshot
Dumb and Lazy? A Comparison of Color Learning and Memory Retrieval in Drones and Workers of the Buff-Tailed Bumblebee, Bombus terrestris, by Means of PER Conditioning
inferred← citeshttps://doi.org/10.1371/journal.pone.0198322openalex-snapshot
Metabolic enzymes in glial cells of the honeybee brain and their associations with aging, starvation and food response
inferred← citeshttps://doi.org/10.1371/journal.pone.0226393openalex-snapshot
Do bumblebees have signatures? Demonstrating the existence of a speed-curvature power law in Bombus terrestris locomotion patterns
inferred← citeshttps://doi.org/10.1371/journal.pone.0232862openalex-snapshot
Optimization and validation of a modified radial-arm water maze protocol using a murine model of mild closed head traumatic brain injury
inferred← citeshttps://doi.org/10.1371/journal.pone.0262441openalex-snapshot
Differential gene expression analysis following olfactory learning in honeybee (Apis mellifera L.)
inferred← citeshttps://doi.org/10.1523/jneurosci.1151-11.2011openalex-snapshot
Role of Cerebellar Cortical Protein Synthesis in Transfer of Memory Trace of Cerebellum-Dependent Motor Learning
inferred← citeshttps://doi.org/10.1523/jneurosci.1331-12.2013openalex-snapshot
Mushroom Body Extrinsic Neurons in the Honeybee Brain Encode Cues and Contexts Differently
inferred← citeshttps://doi.org/10.1523/jneurosci.1893-05.2005openalex-snapshot
Coding for the Initiation of Pseudopregnancy by Temporally Patterned Activation of Amygdalar NMDA Receptors
inferred← citeshttps://doi.org/10.1523/jneurosci.23-12-05370.2003openalex-snapshot
Modulation of Early Olfactory Processing by an Octopaminergic Reinforcement Pathway in the Honeybee
inferred← citeshttps://doi.org/10.1523/jneurosci.23-24-08539.2003openalex-snapshot
Identification of Individual Neurons Reflecting Short- and Long-Term Visual Memory in an Arthropodo
inferred← citeshttps://doi.org/10.1523/jneurosci.23-30-09842.2003openalex-snapshot
Extinction Requires New RNA and Protein Synthesis and the Soma of the Cell Right Pedal Dorsal 1 inLymnaea stagnalis
inferred← citeshttps://doi.org/10.1523/jneurosci.4534-12.2013openalex-snapshot
Protein Phosphatase-Dependent Circadian Regulation of Intermediate-Term Associative Memory
inferred← citeshttps://doi.org/10.15332/erdi.v4i1.555openalex-snapshot
EL AULA COMO UN LECHO DE PROCUSTO: SOFISMAS YMANIPULACIÓN EN ENSEÑANZA DE LENGUAS EXTRANJERAS
inferred← citeshttps://doi.org/10.17169/refubium-16879openalex-snapshot
From behavioral plasticity to neuronal computation
inferred← citeshttps://doi.org/10.18174/24227openalex-snapshot
Associative learning in two closely related parasitoid wasps: a neuroecological approach
inferred← citeshttps://doi.org/10.21203/rs.3.rs-267700/v1openalex-snapshot
The use of A. mellifera drone's olfactory sensitivity towards pathological odours as a selection trait in the breeding against V. destructor
inferred← citeshttps://doi.org/10.2139/ssrn.5360168openalex-snapshot
Effectiveness of Different Conditioning Methods to Improve Host Searching of Commercially Sold Mealybug Parasitoids
inferred← citeshttps://doi.org/10.3109/10253890.2011.596864openalex-snapshot
Stress modulation of cognitive and affective processes
inferred← citeshttps://doi.org/10.3389/fnbeh.2010.00186openalex-snapshot
Memory Formation in Reversal Learning of the Honeybee
inferred← citeshttps://doi.org/10.3389/fnbeh.2013.00029openalex-snapshot
APIS—a novel approach for conditioning honey bees
inferred← citeshttps://doi.org/10.3389/fnbeh.2014.00238openalex-snapshot
Properties and mechanisms of olfactory learning and memory
inferred← citeshttps://doi.org/10.3389/fnbeh.2014.00313openalex-snapshot
Rapid learning dynamics in individual honeybees during classical conditioning
inferred← citeshttps://doi.org/10.3389/fnbeh.2015.00198openalex-snapshot
GABAergic feedback signaling into the calyces of the mushroom bodies enables olfactory reversal learning in honey bees
inferred← citeshttps://doi.org/10.3389/fnbeh.2017.00080openalex-snapshot
Appetitive Olfactory Learning and Long-Term Associative Memory in Caenorhabditis elegans
inferred← citeshttps://doi.org/10.3389/fnbeh.2021.741439openalex-snapshot
Individual Scores for Associative Learning in a Differential Appetitive Olfactory Paradigm Using Binary Logistic Regression Analysis
inferred← citeshttps://doi.org/10.3389/fncom.2016.00044openalex-snapshot
Anti-kindling Induced by Two-Stage Coordinated Reset Stimulation with Weak Onset Intensity
inferred← citeshttps://doi.org/10.3389/fnhum.2013.00589openalex-snapshot
Making long-term memories in minutes: a spaced learning pattern from memory research in education
inferred← citeshttps://doi.org/10.3389/fnhum.2018.00400openalex-snapshot
Making Memories: Why Time Matters
inferred← citeshttps://doi.org/10.3389/fnins.2020.00231openalex-snapshot
Pollen Alters Amino Acid Levels in the Honey Bee Brain and This Relationship Changes With Age and Parasitic Stress
inferred← citeshttps://doi.org/10.3389/fnint.2015.00059openalex-snapshot
Effects of Floral Scents and Their Dietary Experiences on the Feeding Preference in the Blowfly, Phormia regina
inferred← citeshttps://doi.org/10.3389/fphys.2018.00376openalex-snapshot
Short-Term Dosage Regimen for Stimulation-Induced Long-Lasting Desynchronization
inferred← citeshttps://doi.org/10.3389/fpsyg.2018.00989openalex-snapshot
Learning Spatial Aversion Is Sensory-Specific in the Hematophagous Insect Rhodnius prolixus
inferred← citeshttps://doi.org/10.3389/fpsyg.2020.01850openalex-snapshot
EEG Correlates of Learning From Speech Presented in Environmental Noise
inferred← citeshttps://doi.org/10.3390/ani11123365openalex-snapshot
The Sometimes Context-Specific Habituation: Theoretical Challenges to Associative Accounts
inferred← citeshttps://doi.org/10.3390/ijms23158527openalex-snapshot
Anesthesia Resistant Memories in Drosophila, a Working Perspective
inferred← citeshttps://doi.org/10.3390/insects11090572openalex-snapshot
Effect of Immune Inducers on Nosema ceranae Multiplication and Their Impact on Honey Bee (Apis mellifera L.) Survivorship and Behaviors
inferred← citeshttps://doi.org/10.3390/insects16040358openalex-snapshot
Honey Bees Can Use Sequence Learning to Predict Rewards from a Prior Unrewarded Visual Stimulus
inferred← citeshttps://doi.org/10.3390/insects5020377openalex-snapshot
Contrasting Effects of Histone Deacetylase Inhibitors on Reward and Aversive Olfactory Memories in the Honey Bee
inferred← citeshttps://doi.org/10.3758/s13428-019-01324-zopenalex-snapshot
Modeling list-strength and spacing effects using version 3 of the retrieving effectively from memory (REM.3) model and its superimposition-of-similar-images assumption
inferred← citeshttps://doi.org/10.3791/2282openalex-snapshot
Behavioural Pharmacology in Classical Conditioning of the Proboscis Extension Response in Honeybees (Apis mellifera)
inferred← citeshttps://doi.org/10.3791/2282-vopenalex-snapshot
Behavioural Pharmacology in Classical Conditioning of the Proboscis Extension Response in Honeybees (Apis mellifera)
inferred← citeshttps://doi.org/10.3986/fbg0041openalex-snapshot
Dancing with carniolan bee / Plešemo s kranjsko čebelo
inferred← citeshttps://doi.org/10.4161/cib.3.2.10621openalex-snapshot
Reward expectations in honeybees
inferred← citeshttps://doi.org/10.4257/oeco.2020.2401.04openalex-snapshot
COMO TREINAR SUA ABELHA: MÉTODOS APLICADOS À BIOLOGIA COGNITIVA DA POLINIZAÇÃO
inferred← citeshttps://doi.org/10.6084/m9.figshare.13064334openalex-snapshot
Additional file 1 of Fear response-based prediction for stress susceptibility to PTSD-like phenotypes
inferred← citeshttps://doi.org/10.6084/m9.figshare.13064337openalex-snapshot
Additional file 2 of Fear response-based prediction for stress susceptibility to PTSD-like phenotypes
inferred← citeshttps://doi.org/10.64898/2026.02.12.705541openalex-snapshot
Time between learning events shapes functional connectivity in spatial memory, a brain-wide analysis
inferred← citeshttps://doi.org/10.70675/50008b08z15a7z43d1z980ez9cc83dd99e57openalex-snapshot
La cognition des larves de moustique comme indicateur biologique de la qualité des écosystèmes aquatiques
inferred← citeshttps://doi.org/10.70675/92d94500zc831z4aeazb12bz167bf032dd4eopenalex-snapshot
Modularity and Plasticity of olfactory learning and memory in Drosophila
inferred← citeshttps://doi.org/10.7554/elife.61907openalex-snapshot
Reconsidering the evidence for learning in single cells
inferred← citeshttps://doi.org/10.7717/peerj.3858openalex-snapshot
Learning performance and brain structure of artificially-reared honey bees fed with different quantities of food
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