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Searching for the Memory Trace in a Mini-Brain, the Honeybee

https://doi.org/10.1101/lm.38801
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What this work says

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

inferredcites →https://doi.org/10.1006/nlme.1997.3801openalex-snapshot
Temporal Determinants of Olfactory Long-Term Retention in Honeybee Classical Conditioning: Nonmonotonous Effects of the Training Trial Interval
inferredcites →https://doi.org/10.1006/nlme.1998.3834openalex-snapshot
Some Historical Background of Topics in This Conference
inferredcites →https://doi.org/10.1007/978-3-642-86666-1_14openalex-snapshot
Learning and Memory in the Honeybee
inferredcites →https://doi.org/10.1007/bf00192658openalex-snapshot
Pattern recognition in bees: orientation discrimination
inferredcites →https://doi.org/10.1007/bf00298776openalex-snapshot
Absolute anzahl und verteilung der zellen im him der honigbiene
inferredcites →https://doi.org/10.1007/bf00368172openalex-snapshot
Time course of short-term memory depends on associative events
inferredcites →https://doi.org/10.1007/bf01138799openalex-snapshot
Formation of long term olfactory memory in honeybees does not require protein synthesis
inferredcites →https://doi.org/10.1007/s003590050296openalex-snapshot
Tactile learning in the honeybee
inferredcites →https://doi.org/10.1007/s003590050392openalex-snapshot
Memory dynamics in the honeybee
inferredcites →https://doi.org/10.1007/s100710100080openalex-snapshot
Learning in honey bees with brain lesions: how partial mushroom-body ablations affect sucrose responsiveness and tactile antennal learning
inferredcites →https://doi.org/10.1016/0022-1910(61)90060-9openalex-snapshot
Classical conditioned response in the honey bee
inferredcites →https://doi.org/10.1016/s0022-1910(99)00194-8openalex-snapshot
Odour representation in honeybee olfactory glomeruli shows slow temporal dynamics: an optical recording study using a voltage-sensitive dye
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
inferredcites →https://doi.org/10.1016/s0166-2236(96)01019-3openalex-snapshot
The neural basis of associative reward learning in honeybees
inferredcites →https://doi.org/10.1016/s0896-6273(00)00002-7openalex-snapshot
Timing Is Everything
inferredcites →https://doi.org/10.1016/s0896-6273(00)00017-9openalex-snapshot
Prolonged Activation of cAMP-Dependent Protein Kinase during Conditioning Induces Long-Term Memory in Honeybees
inferredcites →https://doi.org/10.1016/s0896-6273(00)80073-2openalex-snapshot
Inhibition of Nitric Oxide Synthase Impairs a Distinct Form of Long-Term Memory in the Honeybee, Apis mellifera
inferredcites →https://doi.org/10.1016/s0896-6273(00)80987-3openalex-snapshot
Cognitive Neuroscience and the Study of Memory
inferredcites →https://doi.org/10.1016/s1364-6613(00)01601-6openalex-snapshot
Cognitive architecture of a mini-brain: the honeybee
inferredcites →https://doi.org/10.1037//0033-295x.101.4.587openalex-snapshot
Similarity and discrimination: A selective review and a connectionist model.
inferredcites →https://doi.org/10.1037/0735-7036.97.2.107openalex-snapshot
Classical conditioning of proboscis extension in honeybees (Apis mellifera).
inferredcites →https://doi.org/10.1038/281368a0openalex-snapshot
Behavioural access to short-term memory in bees
inferredcites →https://doi.org/10.1038/35073582openalex-snapshot
The concepts of ‘sameness’ and ‘difference’ in an insect
inferredcites →https://doi.org/10.1038/366059a0openalex-snapshot
An identified neuron mediates the unconditioned stimulus in associative olfactory learning in honeybees
inferredcites →https://doi.org/10.1038/377725a0openalex-snapshot
Bee foraging in uncertain environments using predictive hebbian learning
inferredcites →https://doi.org/10.1038/382458a0openalex-snapshot
Symmetry perception in an insect
inferredcites →https://doi.org/10.1038/387285a0openalex-snapshot
Representations of odours and odour mixtures visualized in the honeybee brain
inferredcites →https://doi.org/10.1038/4576openalex-snapshot
Associative learning modifies neural representations of odors in the insect brain
inferredcites →https://doi.org/10.1038/8144openalex-snapshot
The glomerular code for odor representation is species specific in the honeybee Apis mellifera
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/10.1098/rspb.2000.1097openalex-snapshot
Two spatial memories for honeybee navigation
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.7.3.151openalex-snapshot
Contextual Modulation of Memory Consolidation
inferredcites →https://doi.org/10.1111/j.1365-3032.1980.tb00244.xopenalex-snapshot
Localization of short‐term memory in the brain of the bee, Apis mellifera
inferredcites →https://doi.org/10.1126/science.275.5306.1593openalex-snapshot
A Neural Substrate of Prediction and Reward
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/10.1146/annurev.ps.33.020182.001405openalex-snapshot
Behavioral Studies of Associative Learning in Animals
inferredcites →https://doi.org/10.1162/jocn.1992.4.3.208openalex-snapshot
Configural and Elemental Associations and the Memory Coherence Problem
inferredcites →https://doi.org/10.1242/jeb.195.1.91openalex-snapshot
The Olfactory Memory of the Honeybee Apis Mellifera:II. Blocking Between Odorants in Binary Mixtures
inferredcites →https://doi.org/10.1242/jeb.200.19.2513openalex-snapshot
Visually Mediated Odometry in Honeybees
inferredcites →https://doi.org/10.1242/jeb.202.13.1839openalex-snapshot
No evidence for olfactory blocking in honeybee classical conditioning
inferredcites →https://doi.org/10.1242/jeb.203.18.2797openalex-snapshot
Blocking and the detection of odor components in blends
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.15-03-01617.1995openalex-snapshot
Learning and memory in the honeybee
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/10.3758/bf03328970openalex-snapshot
Negative patterning in classical conditioning: Summation of response tendencies to isolable and configurai components
inferredcites →https://doi.org/10.4159/9780674043404openalex-snapshot
The Wisdom of the Hive
inferredcites →https://doi.org/10.4159/harvard.9780674418776openalex-snapshot
The Dance Language and Orientation of Bees

What points at this work

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

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A Mosquito Brain Like a Sieve: Evaluating the Memory Persistence in Mosquito Larvae
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Age‐dependent transcriptional and epigenomic responses to light exposure in the honey bee brain
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CHARACTERIZATION OF NICOTINE ACETYLCHOLINE RECEPTOR SUBUNITS IN THE COCKROACH Periplaneta americana MUSHROOM BODIES REVEALS A STRONG EXPRESSION OF β1 SUBUNIT: INVOLVEMENT IN NICOTINE‐INDUCED CURRENTS
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The remote roots of consciousness in fruit-fly selective attention?
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Organization of the honey bee mushroom body: Representation of the calyx within the vertical and gamma lobes
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Common design of mushroom bodies in bees and flies?
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Segregation of visual input to the mushroom bodies in the honeybee (Apis mellifera)
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A new ascending sensory tract to the calyces of the honeybee mushroom body, the subesophageal‐calycal tract
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Developmental changes in expression patterns of two dopamine receptor genes in mushroom bodies of the honeybee, Apis mellifera
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A taste for learning?
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Copper/zinc superoxide dismutase‐like immunoreactivity in the metamorphosing brain of the sphinx moth Manduca sexta
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Mushroom body volumes and visual interneurons in ants: Comparison between sexes and castes
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Developmental expression of a tyramine receptor gene in the brain of the honey bee, Apis mellifera
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Synaptogenesis in the mushroom body calyx during metamorphosis in the honeybeeApis mellifera: An electron microscopic study
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Dual olfactory pathway in the honeybee, Apis mellifera
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Anatomical organization of antennal lobe projection neurons in the moth Heliothis virescens
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Topographic organization of sensory afferents of Johnston's organ in the honeybee brain
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Sprouting interneurons in mushroom bodies of adult cricket brains
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Modular subdivision of mushroom bodies by kenyon cells in the silkmoth
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Ground plan of the insect mushroom body: Functional and evolutionary implications
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Anisometric brain dimorphism revisited: Implementation of a volumetric 3D standard brain inManduca sexta
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CaMKII is differentially localized in synaptic regions of kenyon cells within the mushroom bodies of the honeybee brain
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A multisensory centrifugal neuron in the olfactory pathway of heliothine moths
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Topographically distinct visual and olfactory inputs to the mushroom body in the Swallowtail butterfly, Papilio xuthus
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The brain of Cataglyphis ants: Neuronal organization and visual projections
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Open‐Source Automation of the Proboscis Extension Response Assay: From Odor Delivery to Deep Learning Behavior Analysis
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Eph receptor and ephrin signaling in developing and adult brain of the honeybee (Apis mellifera)
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Visual experience and age affect synaptic organization in the mushroom bodies of the desert ant Cataglyphis fortis
inferred← citeshttps://doi.org/10.1002/dneu.22290openalex-snapshot
Neuronal plasticity in the mushroom body calyx during adult maturation in the honeybee and possible pheromonal influences
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New life in an old idea: The synaptic plasticity and memory hypothesis revisited
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Stratification and synaptogenesis in the mushroom body of the honeybee, Apis mellifera
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Hydroxyurea‐induced partial mushroom body ablation does not affect acquisition and retention of olfactory differential conditioning in honeybees
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Neural substrates of memory: From synapse to system
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Hygienic behavior in the honey bee (Apis mellifera L.) and the modulatory role of octopamine
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Eph receptor and ephrin signaling in developing and adult brain of the honeybee (Apis mellifera)
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Invertebrate learning and cognition: relating phenomena to neural substrate
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Learning and cognition in insects
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Category Learning as a Cognitive Foundation of Language Evolution
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Plasticity in the Auditory System of Insects
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Biomedical Research with Honey Bees
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Focusing on Dynamics: When an Exception Becomes a Rule
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Associative Mechanisms
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Associative Mechanisms
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Dynamics of Odor-Evoked Activity Patterns in the Olfactory System
inferred← citeshttps://doi.org/10.1007/978-3-319-55065-7_1759openalex-snapshot
Associative Mechanisms
inferred← citeshttps://doi.org/10.1007/978-3-540-88464-4_1openalex-snapshot
Perception for Action in Insects
inferred← citeshttps://doi.org/10.1007/978-3-8274-2618-5_10openalex-snapshot
Lernen und Gedächtnis
inferred← citeshttps://doi.org/10.1007/978-4-431-54331-2_2openalex-snapshot
Classical Conditioning of the Proboscis Extension Reflex in the Honeybee
inferred← citeshttps://doi.org/10.1007/978-4-431-56469-0_6openalex-snapshot
Insect Brains: Minute Structures Controlling Complex Behaviors
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The Digital Honey Bee Brain Atlas
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Neurogenomic and Neurochemical Dissection of Honey Bee Dance Communication
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Elucidating the Path from Genotype to Behavior in Honey Bees: Insights from Epigenomics
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Testing Mathematical Laws of Behavior in the Honey Bee
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The Impact of Induced Plant Volatiles on Plant-Arthropod Interactions
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Foraging
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Social Association Brings Out the Altruism in an Ant
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Encoding of plant odour information in insects: peripheral and central mechanisms
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Reconsolidation and the fate of consolidated memories
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Clique formation of super-sister honeybee workers ( Apis mellifera ) in experimental groups
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Getting to the start line: how bumblebees and honeybees are visually guided towards their first floral contact
inferred← citeshttps://doi.org/10.1007/s00040-018-0641-8openalex-snapshot
A new protocol for measuring spatial learning and memory in the honey bee Apis mellifera: effects of behavioural state and cGMP
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Olfactory host finding, intermediate memory and its potential ecological adaptation in Nasonia vitripennis
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Africanized honeybees are slower learners than their European counterparts
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Recency preference of odour memory retrieval in honeybees
inferred← citeshttps://doi.org/10.1007/s00359-003-0469-0openalex-snapshot
Physiological and morphological characterization of honeybee olfactory neurons combining electrophysiology, calcium imaging and confocal microscopy
inferred← citeshttps://doi.org/10.1007/s00359-005-0619-7openalex-snapshot
Selective modulation of task performance by octopamine in honey bee (Apis mellifera) division of labour
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Appetitive odor learning does not change olfactory coding in a subpopulation of honeybee antennal lobe neurons
inferred← citeshttps://doi.org/10.1007/s00359-006-0160-3openalex-snapshot
Olfactory conditioning of proboscis activity in Drosophila melanogaster
inferred← citeshttps://doi.org/10.1007/s00359-007-0208-zopenalex-snapshot
Central gustatory projections and side-specificity of operant antennal muscle conditioning in the honeybee
inferred← citeshttps://doi.org/10.1007/s00359-007-0235-9openalex-snapshot
Behavioral and neural analysis of associative learning in the honeybee: a taste from the magic well
inferred← citeshttps://doi.org/10.1007/s00359-009-0449-0openalex-snapshot
Effect of age, behaviour and social environment on honey bee brain plasticity
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Comparison of learning and memory of Apis cerana and Apis mellifera
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Glomerular interactions in olfactory processing channels of the antennal lobes
inferred← citeshttps://doi.org/10.1007/s00359-014-0904-4openalex-snapshot
Multisensory integration of colors and scents: insights from bees and flowers
inferred← citeshttps://doi.org/10.1007/s00359-019-01320-wopenalex-snapshot
Cross-modal transfer in visual and nonvisual cues in bumblebees
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Comparative biology of spatial navigation in three arachnid orders (Amblypygi, Araneae, and Scorpiones)
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Ecdysone receptor expression in developing and adult mushroom bodies of the ant Camponotus japonicus
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Three-dimensional organization of the glomeruli in the antennal lobe of the parasitoid wasps Cotesia glomerata and C. rubecula
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Novel antennal lobe substructures revealed in the small hive beetle Aethina tumida
inferred← citeshttps://doi.org/10.1007/s00441-015-2299-0openalex-snapshot
Brief sensory experience differentially affects the volume of olfactory brain centres in a moth
inferred← citeshttps://doi.org/10.1007/s10071-006-0032-9openalex-snapshot
Categorization of visual stimuli in the honeybee Apis mellifera
inferred← citeshttps://doi.org/10.1007/s10071-014-0733-4openalex-snapshot
How images may or may not represent flowers: picture–object correspondence in bumblebees (Bombus impatiens)?
inferred← citeshttps://doi.org/10.1007/s10071-014-0750-3openalex-snapshot
Peak shift in honey bee olfactory learning
inferred← citeshttps://doi.org/10.1007/s10071-024-01926-xopenalex-snapshot
How bumblebees manage conflicting information seen on arrival and departure from flowers
inferred← citeshttps://doi.org/10.1007/s10071-026-02065-1openalex-snapshot
Olfactory learning in two Amblypygi species Paraphrynus laevifrons and Phrynus pseudoparvulus
inferred← citeshttps://doi.org/10.1007/s10144-009-0185-xopenalex-snapshot
The effect of learning and search images on predator–prey interactions
inferred← citeshttps://doi.org/10.1007/s10158-007-0045-3openalex-snapshot
Characterization of a metabotropic glutamate receptor in the honeybee (Apis mellifera): implications for memory formation
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Sublethal imidacloprid effects on honey bee flower choices when foraging
inferred← citeshttps://doi.org/10.1007/s10841-021-00335-6openalex-snapshot
Sublethal doses of glyphosate impair olfactory memory retention, but not learning in the honey bee (Apis mellifera scutellata)
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Aversive learning-induced plasticity throughout the adult mammalian olfactory system: insights across development
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Effects of Chronic Morphine Treatment on an Odor Conditioning Paradigm, Locomotor Activity and Sucrose Responsiveness in Honeybees (Apis mellifera)
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The Role of Associative Learning in Ant Learning and Memory
inferred← citeshttps://doi.org/10.1007/s11055-007-0084-6openalex-snapshot
Electrophysiological characteristics of a population of mushroom body neurons in Apis Mellifera honeybees in kynurenine deficiency
inferred← citeshttps://doi.org/10.1007/s11055-008-0052-9openalex-snapshot
Comparative analysis of the locations of the NR1 and NR2 NMDA receptor subunits in honeybee (Apis mellifera) and fruit fly (Drosophila melanogaster, Canton-S wild-type) cerebral ganglia
inferred← citeshttps://doi.org/10.1007/s11055-014-9890-9openalex-snapshot
Morphological Basis of a Conditioned Reflex in the Honeybee Apis Mellifera L.
inferred← citeshttps://doi.org/10.1007/s11829-020-09743-yopenalex-snapshot
Neuroactive nectar: compounds in nectar that interact with neurons
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Effects of morphine on associative memory and locomotor activity in the honeybee (Apis mellifera)
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Previous exposures to cues from conspecifics and ladybird beetles prime antipredator responses in pea aphids Acyrthosiphon pisum (Hemiptera: Aphididae)
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The molecular signalling processes underlying olfactory learning and memory formation in honeybees
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Age-mediated and environmentally mediated brain and behavior plasticity in the stingless bee Melipona quadrifasciata anthidioides
inferred← citeshttps://doi.org/10.1016/b0-12-370878-8/00158-0openalex-snapshot
Segmental Organization of Cephalic Ganglia in Arthropods
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Analysis of Learning in Invertebrates
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Learning
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Associative Learning and Unlearning
inferred← citeshttps://doi.org/10.1016/b978-0-12-386892-3.00007-xopenalex-snapshot
Memory Reconsolidation and Extinction in Invertebrates
inferred← citeshttps://doi.org/10.1016/b978-0-12-397179-1.00020-8openalex-snapshot
Learning and Memory
inferred← citeshttps://doi.org/10.1016/b978-0-12-415823-8.00004-6openalex-snapshot
Exploring Brain Connectivity in Insect Model Systems of Learning and Memory
inferred← citeshttps://doi.org/10.1016/b978-0-12-415823-8.00007-1openalex-snapshot
Computational Analyses of Learning Networks
inferred← citeshttps://doi.org/10.1016/b978-0-12-415823-8.00026-5openalex-snapshot
A Multidisciplinary Approach to Learning and Memory in the Crab Neohelice (Chasmagnathus) granulata
inferred← citeshttps://doi.org/10.1016/b978-0-12-415823-8.00036-8openalex-snapshot
Behavioral and Neural Analyses of Punishment Learning in Honeybees
inferred← citeshttps://doi.org/10.1016/b978-0-12-415823-8.00038-1openalex-snapshot
Learning and Recognition of Identity in Ants
inferred← citeshttps://doi.org/10.1016/b978-0-12-809324-5.21022-5openalex-snapshot
Behavioral Analysis of Learning and Memory in Honeybees ☆
inferred← citeshttps://doi.org/10.1016/b978-0-12-809324-5.21024-9openalex-snapshot
Behavioral Analysis of Learning and Memory in Cephalopods ☆
inferred← citeshttps://doi.org/10.1016/b978-0-12-809324-5.21124-3openalex-snapshot
In Search of Engram Cells
inferred← citeshttps://doi.org/10.1016/b978-0-323-91793-3.00005-5openalex-snapshot
Introduction
inferred← citeshttps://doi.org/10.1016/b978-0-443-15754-7.00068-7openalex-snapshot
Behavioral and neural analysis of associative learning in the honey bee
inferred← citeshttps://doi.org/10.1016/b978-0-444-63350-7.00003-6openalex-snapshot
Mixture Processing and Odor-Object Segregation in Insects
inferred← citeshttps://doi.org/10.1016/b978-012148660-0/50019-6openalex-snapshot
Learning and Memory: Basic Mechanisms
inferred← citeshttps://doi.org/10.1016/b978-012370509-9.00005-xopenalex-snapshot
Sensitization and Habituation: Invertebrate
inferred← citeshttps://doi.org/10.1016/b978-012370509-9.00066-8openalex-snapshot
Behavioral Analysis of Learning and Memory in Drosophila
inferred← citeshttps://doi.org/10.1016/b978-012370509-9.00067-xopenalex-snapshot
Behavioral and Neural Analysis of Associate Learning in the Honeybee
inferred← citeshttps://doi.org/10.1016/b978-012370509-9.00069-3openalex-snapshot
Behavioral Analysis of Learning and Memory in Cephalopods
inferred← citeshttps://doi.org/10.1016/b978-044452977-0/50003-6openalex-snapshot
The Remote Roots of Consciousness in Fruit-fly Selective Attention?††“The remote roots of consciousness in fruit-fly selective attention” by Bruno van Swinderen appeared in BioEssays 27:321-330 (2005). Reprinted with permission of Wiley-Liss, Inc., a subsidiary of John Wiley & Sons, Inc.
inferred← citeshttps://doi.org/10.1016/bs.aiip.2014.12.006openalex-snapshot
Insect Reward Systems
inferred← citeshttps://doi.org/10.1016/j.anbehav.2005.09.016openalex-snapshot
Differences in memory dynamics between two closely related parasitoid wasp species
inferred← citeshttps://doi.org/10.1016/j.anbehav.2006.03.011openalex-snapshot
Individual olfactory learning in Camponotus ants
inferred← citeshttps://doi.org/10.1016/j.anbehav.2009.09.008openalex-snapshot
Gender differences, responsiveness and memory of a potentially painful event in hermit crabs
inferred← citeshttps://doi.org/10.1016/j.anbehav.2010.11.002openalex-snapshot
Natural variation in learning and memory dynamics studied by artificial selection on learning rate in parasitic wasps
inferred← citeshttps://doi.org/10.1016/j.anbehav.2011.12.025openalex-snapshot
Repeated unrewarded scent exposure influences the food choice of stingless bee foragers, Melipona scutellaris
inferred← citeshttps://doi.org/10.1016/j.asd.2005.04.003openalex-snapshot
Organization and evolutionary trends of primary olfactory brain centers in Tetraconata (Crustacea+Hexapoda)
inferred← citeshttps://doi.org/10.1016/j.asd.2008.03.002openalex-snapshot
Higher order visual input to the mushroom bodies in the bee, Bombus impatiens
inferred← citeshttps://doi.org/10.1016/j.asd.2008.05.005openalex-snapshot
Tritocerebral tract input to the insect mushroom bodies
inferred← citeshttps://doi.org/10.1016/j.asd.2010.12.002openalex-snapshot
Comparison of microglomerular structures in the mushroom body calyx of neopteran insects
inferred← citeshttps://doi.org/10.1016/j.asd.2012.02.005openalex-snapshot
Neuropeptides in insect mushroom bodies
inferred← citeshttps://doi.org/10.1016/j.asd.2024.101345openalex-snapshot
Sensory pathway in aquatic basal polyneoptera: Antennal sensilla and brain morphology in stoneflies
inferred← citeshttps://doi.org/10.1016/j.aspen.2025.102476openalex-snapshot
Effects of ethanol exposure and withdrawal on olfactory sensitivity and learning and memory in honeybees(Apis mellifera)
inferred← citeshttps://doi.org/10.1016/j.bandc.2008.07.007openalex-snapshot
Multiple memory stores and operant conditioning: A rationale for memory’s complexity
inferred← citeshttps://doi.org/10.1016/j.bbi.2005.09.004openalex-snapshot
Insecta immune–cognitive interactions
inferred← citeshttps://doi.org/10.1016/j.bbr.2003.11.014openalex-snapshot
Ethological analyses of crayfish behavior: a new invertebrate system for measuring the rewarding properties of psychostimulants
inferred← citeshttps://doi.org/10.1016/j.bbr.2005.02.008openalex-snapshot
The influence of training length on generalization of visual feature assemblies in honeybees
inferred← citeshttps://doi.org/10.1016/j.bbr.2006.10.019openalex-snapshot
The trial-spacing effect in olfactory patterning discriminations in honeybees
inferred← citeshttps://doi.org/10.1016/j.bbr.2012.04.014openalex-snapshot
Consumption of an acute dose of caffeine reduces acquisition but not memory in the honey bee
inferred← citeshttps://doi.org/10.1016/j.bbrc.2006.11.020openalex-snapshot
In vivo gene transfer into the honeybee using a nucleopolyhedrovirus vector
inferred← citeshttps://doi.org/10.1016/j.beproc.2005.02.019openalex-snapshot
Simple heuristics and rules of thumb: Where psychologists and behavioural biologists might meet
inferred← citeshttps://doi.org/10.1016/j.brainres.2011.07.032openalex-snapshot
Transient dynamics between displaced fixed points: An alternate nonlinear dynamical framework for olfaction
inferred← citeshttps://doi.org/10.1016/j.brainresrev.2003.09.003openalex-snapshot
Complexities of a simple system: new lessons, old challenges and peripheral questions for the gill withdrawal reflex of Aplysia
inferred← citeshttps://doi.org/10.1016/j.cbpb.2005.04.014openalex-snapshot
Honey bees as a model for understanding mechanisms of life history transitions
inferred← citeshttps://doi.org/10.1016/j.cell.2005.09.037openalex-snapshot
Drosophila DPM Neurons Form a Delayed and Branch-Specific Memory Trace after Olfactory Classical Conditioning
inferred← citeshttps://doi.org/10.1016/j.cell.2006.01.011openalex-snapshot
Small Brains, Bright Minds
inferred← citeshttps://doi.org/10.1016/j.celrep.2020.01.086openalex-snapshot
Redefining Single-Trial Memories in the Honeybee
inferred← citeshttps://doi.org/10.1016/j.cois.2017.08.003openalex-snapshot
Using virtual reality to study visual performances of honeybees
inferred← citeshttps://doi.org/10.1016/j.conb.2003.10.015openalex-snapshot
Cognitive neuroethology: dissecting non-elemental learning in a honeybee brain
inferred← citeshttps://doi.org/10.1016/j.conb.2004.10.014openalex-snapshot
An engram found? Evaluating the evidence from fruit flies
inferred← citeshttps://doi.org/10.1016/j.conb.2006.10.009openalex-snapshot
Intermediate-term processes in memory formation
inferred← citeshttps://doi.org/10.1016/j.conb.2018.10.014openalex-snapshot
How foresight might support the behavioral flexibility of arthropods
inferred← citeshttps://doi.org/10.1016/j.cub.2005.08.024openalex-snapshot
Deconstructing Memory in Drosophila
inferred← citeshttps://doi.org/10.1016/j.cub.2008.01.056openalex-snapshot
The Octopus Vertical Lobe Modulates Short-Term Learning Rate and Uses LTP to Acquire Long-Term Memory
inferred← citeshttps://doi.org/10.1016/j.cub.2021.10.067openalex-snapshot
Cold-induced anesthesia impairs path integration memory in dung beetles
inferred← citeshttps://doi.org/10.1016/j.cub.2022.07.062openalex-snapshot
Ecology dictates the value of memory for foraging bees
inferred← citeshttps://doi.org/10.1016/j.cub.2022.08.043openalex-snapshot
Pollinator cognition: Framing bee memories in an ecological context
inferred← citeshttps://doi.org/10.1016/j.cub.2022.10.017openalex-snapshot
Transient active zone remodeling in the Drosophila mushroom body supports memory
inferred← citeshttps://doi.org/10.1016/j.endend.2012.04.001openalex-snapshot
10.1016/j.endend.2012.04.001
inferred← citeshttps://doi.org/10.1016/j.endend.2012.04.002openalex-snapshot
10.1016/j.endend.2012.04.002
inferred← citeshttps://doi.org/10.1016/j.endend.2012.04.003openalex-snapshot
10.1016/j.endend.2012.04.003
inferred← citeshttps://doi.org/10.1016/j.endend.2012.04.004openalex-snapshot
10.1016/j.endend.2012.04.004
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10.1016/j.endend.2012.04.006
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10.1016/j.endend.2012.04.007
inferred← citeshttps://doi.org/10.1016/j.gene.2004.09.010openalex-snapshot
Apisα2, Apisα7-1 and Apisα7-2: three new neuronal nicotinic acetylcholine receptor α-subunits in the honeybee brain
inferred← citeshttps://doi.org/10.1016/j.ibmb.2012.02.005openalex-snapshot
Functional characterization of transmembrane adenylyl cyclases from the honeybee brain
inferred← citeshttps://doi.org/10.1016/j.jhazmat.2023.133218openalex-snapshot
Environmental exposure to metallic pollution impairs honey bee brain development and cognition
inferred← citeshttps://doi.org/10.1016/j.jinsphys.2006.09.006openalex-snapshot
Acute ethanol ingestion produces dose-dependent effects on motor behavior in the honey bee (Apis mellifera)
inferred← citeshttps://doi.org/10.1016/j.jinsphys.2009.09.007openalex-snapshot
Associative learning in ants: Conditioning of the maxilla-labium extension response in Camponotus aethiops
inferred← citeshttps://doi.org/10.1016/j.jinsphys.2011.06.005openalex-snapshot
Myosins and DYNLL1/LC8 in the honey bee (Apis mellifera L.) brain
inferred← citeshttps://doi.org/10.1016/j.jinsphys.2016.05.007openalex-snapshot
Inhibiting DNA methylation alters olfactory extinction but not acquisition learning in Apis cerana and Apis mellifera
inferred← citeshttps://doi.org/10.1016/j.jinsphys.2020.104014openalex-snapshot
Impact of sublethal exposure to synthetic and natural acaricides on honey bee (Apis mellifera) memory and expression of genes related to memory
inferred← citeshttps://doi.org/10.1016/j.jinsphys.2020.104177openalex-snapshot
Floral tea polyphenols can improve honey bee memory retention and olfactory sensitivity
inferred← citeshttps://doi.org/10.1016/j.jinsphys.2024.104650openalex-snapshot
Habituation leads to short but not long term memory formation in mosquito larvae
inferred← citeshttps://doi.org/10.1016/j.jip.2009.06.013openalex-snapshot
Chronic bee paralysis: A disease and a virus like no other?
inferred← citeshttps://doi.org/10.1016/j.jviromet.2008.06.027openalex-snapshot
In situ hybridization assays for localization of the chronic bee paralysis virus in the honey bee (Apis mellifera) brain
inferred← citeshttps://doi.org/10.1016/j.lmot.2014.10.007openalex-snapshot
The effects of acute stress on learning and memory in bumblebees
inferred← citeshttps://doi.org/10.1016/j.lmot.2014.11.001openalex-snapshot
Honeypot visitation enables scent learning and heightens forager response in bumblebees (Bombus impatiens)
inferred← citeshttps://doi.org/10.1016/j.neucom.2004.01.164openalex-snapshot
Odor interactions and learning in a model of the insect antennal lobe
inferred← citeshttps://doi.org/10.1016/j.neulet.2012.08.052openalex-snapshot
Whole-cell recording from Kenyon cells in silkmoths
inferred← citeshttps://doi.org/10.1016/j.neulet.2013.02.021openalex-snapshot
Involvement of nitric oxide in memory formation in microbrains
inferred← citeshttps://doi.org/10.1016/j.neunet.2012.11.013openalex-snapshot
Modeling the insect mushroom bodies: Application to a delayed match-to-sample task
inferred← citeshttps://doi.org/10.1016/j.neuroimage.2004.08.048openalex-snapshot
In vivo 3D MRI of insect brain: cerebral development during metamorphosis of Manduca sexta
inferred← citeshttps://doi.org/10.1016/j.neuron.2012.04.007openalex-snapshot
Dopamine Is Required for Learning and Forgetting in Drosophila
inferred← citeshttps://doi.org/10.1016/j.neuroscience.2008.10.039openalex-snapshot
Memory consolidation and reconsolidation in an invertebrate model: The role of the GABAergic system
inferred← citeshttps://doi.org/10.1016/j.nlm.2008.07.017openalex-snapshot
Acute ethanol ingestion impairs appetitive olfactory learning and odor discrimination in the honey bee
inferred← citeshttps://doi.org/10.1016/j.nlm.2009.06.007openalex-snapshot
Growth and pruning of mushroom body Kenyon cell dendrites during worker behavioral development in the paper wasp, Polybia aequatorialis (Hymenoptera: Vespidae)
inferred← citeshttps://doi.org/10.1016/j.nlm.2011.08.010openalex-snapshot
Context-dependent olfactory learning monitored by activities of salivary neurons in cockroaches
inferred← citeshttps://doi.org/10.1016/j.nlm.2013.09.011openalex-snapshot
Dopamine interferes with appetitive long-term memory formation in honey bees
inferred← citeshttps://doi.org/10.1016/j.nlm.2020.107278openalex-snapshot
Degradation of an appetitive olfactory memory via devaluation of sugar reward is mediated by 5-HT signaling in the honey bee
inferred← citeshttps://doi.org/10.1016/j.pbb.2003.09.023openalex-snapshot
Effects of NMDA receptor antagonists on olfactory learning and memory in the honeybee (Apis mellifera)
inferred← citeshttps://doi.org/10.1016/j.pbb.2012.08.001openalex-snapshot
Evidence for a role of GABA- and glutamate-gated chloride channels in olfactory memory
inferred← citeshttps://doi.org/10.1016/j.pestbp.2003.10.001openalex-snapshot
Imidacloprid impairs memory and brain metabolism in the honeybee (Apis mellifera L.)
inferred← citeshttps://doi.org/10.1016/j.pestbp.2011.09.005openalex-snapshot
Neonicotinoid insecticides imidacloprid and clothianidin affect differently neural Kenyon cell death in the cockroach Periplaneta americana
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