On the public citation graph

Brain composition in Heliconius butterflies, post-eclosion growth and experience dependent neuropil plasticity

0 signed · 105 inferred · view as graph

Inferred edges come from two machine sources: sweeps of open repository metadata (mostly SSRN and Zenodo), and a bulk OpenAlex citation snapshot. Every row below is labelled with the one it came from. Neither is a complete citation index — absence here is not evidence of absence.

Is this your work? Sign in with ORCID and put your name on the claims that are yours.
Claim with ORCID
Reference health. See whether every reference in this work resolves to a known work and none has been retracted — and get a dated CiteStamped badge you can embed.
See reference health

What this work says

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

inferredcites →https://doi.org/10.1002/(sici)1096-9861(19981228)402:4<520::aid-cne6>3.0.co;2-kopenalex-snapshot
Mushroom bodies of the cockroach: Their participation in place memory
inferredcites →https://doi.org/10.1002/(sici)1096-9861(19990712)409:4<647::aid-cne9>3.0.co;2-3openalex-snapshot
Multimodal efferent and recurrent neurons in the medial lobes of cockroach mushroom bodies
inferredcites →https://doi.org/10.1002/(sici)1096-9861(19990920)412:2<229::aid-cne4>3.0.co;2-eopenalex-snapshot
Morphologic representation of visual and antennal information in the ant brain
inferredcites →https://doi.org/10.1002/cne.10180openalex-snapshot
Digital atlases of the antennal lobe in two species of tobacco budworm moths, the oriental Helicoverpa assulta (male) and the American Heliothis virescens (male and female)
inferredcites →https://doi.org/10.1002/cne.10285openalex-snapshot
Organization of the honey bee mushroom body: Representation of the calyx within the vertical and gamma lobes
inferredcites →https://doi.org/10.1002/cne.1045openalex-snapshot
Subdivisions of hymenopteran mushroom body calyces by their afferent supply
inferredcites →https://doi.org/10.1002/cne.20644openalex-snapshot
Three-dimensional average-shape atlas of the honeybee brain and its applications
inferredcites →https://doi.org/10.1002/cne.20692openalex-snapshot
Consistent organization of glomeruli in the antennal lobes of related species of heliothine moths
inferredcites →https://doi.org/10.1002/cne.20698openalex-snapshot
Organization of Kenyon cells in subdivisions of the mushroom bodies of a lepidopteran insect
inferredcites →https://doi.org/10.1002/cne.21194openalex-snapshot
Anatomical organization of antennal lobe projection neurons in the moth Heliothis virescens
inferredcites →https://doi.org/10.1002/cne.21948openalex-snapshot
Ground plan of the insect mushroom body: Functional and evolutionary implications
inferredcites →https://doi.org/10.1002/cne.22150openalex-snapshot
Anisometric brain dimorphism revisited: Implementation of a volumetric 3D standard brain inManduca sexta
inferredcites →https://doi.org/10.1002/cne.22471openalex-snapshot
Implementation of pigment‐dispersing factor‐immunoreactive neurons in a standardized atlas of the brain of the cockroachLeucophaea maderae
inferredcites →https://doi.org/10.1002/cne.23054openalex-snapshot
Anatomical basis of sun compass navigation I: The general layout of the monarch butterfly brain
inferredcites →https://doi.org/10.1002/cne.23214openalex-snapshot
Anatomical basis of sun compass navigation II: The neuronal composition of the central complex of the monarch butterfly
inferredcites →https://doi.org/10.1002/cne.23711openalex-snapshot
Brain composition in Godyris zavaleta, a diurnal butterfly, Reflects an increased reliance on olfactory information
inferredcites →https://doi.org/10.1002/cne.902200108openalex-snapshot
Invariance and sex‐specific variations of the glomerular organization in the antennal lobes of a moth,Mamestra brassicae, and a butterfly,Pieris brassicae
inferredcites →https://doi.org/10.1002/dneu.20374openalex-snapshot
Learning with half a brain
inferredcites →https://doi.org/10.1002/dneu.20574openalex-snapshot
Experience‐dependent plasticity in the mushroom bodies of the solitary bee Osmia lignaria (Megachilidae)
inferredcites →https://doi.org/10.1002/dneu.20579openalex-snapshot
Mas‐allatotropin in the developing antennal lobe of the sphinx moth Manduca sexta: Distribution, time course, developmental regulation, and colocalization with other neuropeptides
inferredcites →https://doi.org/10.1002/neu.10256openalex-snapshot
Limits on volume changes in the mushroom bodies of the honey bee brain
inferredcites →https://doi.org/10.1002/neu.20235openalex-snapshot
Age‐dependent and task‐related volume changes in the mushroom bodies of visually guided desert ants, Cataglyphis bicolor
inferredcites →https://doi.org/10.1006/nlme.1995.1019openalex-snapshot
Volume Changes in the Mushroom Bodies of Adult Honey Bee Queens
inferredcites →https://doi.org/10.1007/bf00216202openalex-snapshot
Local interneurons associated with the mushroom bodies and the central body in the brain of Acheta domesticus
inferredcites →https://doi.org/10.1007/bf00299935openalex-snapshot
Host location and exploitation by the cleptoparasitic wasp Argochrysis armilla: the role of learning (Hymenoptera: Chrysididae)
inferredcites →https://doi.org/10.1007/bf00345321openalex-snapshot
Resource heterogeneity and patterns of movement in foraging bumblebees
inferredcites →https://doi.org/10.1007/bf00347978openalex-snapshot
Patterns of pollen exploitation by Heliconius butterflies
inferredcites →https://doi.org/10.1007/bf00384782openalex-snapshot
Pollen flow in Psiguria warscewiczii: a comparison of Heliconius butterflies and hummingbirds
inferredcites →https://doi.org/10.1007/bf00610683openalex-snapshot
Processing of antennal information in extrinsic mushroom body neurons of the bee brain
inferredcites →https://doi.org/10.1007/bf00614495openalex-snapshot
Threshold and odor specificity of pheromone-sensitive neurons in the deutocerebrum ofAntheraea pernyi andA. polyphemus (Saturnidae)
inferredcites →https://doi.org/10.1007/bf01053299openalex-snapshot
Mushroom body development in nymphalid butterflies: A correlate of learning?
inferredcites →https://doi.org/10.1007/s00359-009-0449-0openalex-snapshot
Effect of age, behaviour and social environment on honey bee brain plasticity
inferredcites →https://doi.org/10.1007/s00441-004-1016-1openalex-snapshot
Standard three-dimensional glomeruli of the Manduca sexta antennal lobe: a tool to study both developmental and adult neuronal plasticity
inferredcites →https://doi.org/10.1007/s00441-008-0620-xopenalex-snapshot
Standardized atlas of the brain of the desert locust, Schistocerca gregaria
inferredcites →https://doi.org/10.1007/s00441-009-0756-3openalex-snapshot
Constancy and variability of glomerular organization in the antennal lobe of the silkmoth
inferredcites →https://doi.org/10.1007/s10905-005-3701-7openalex-snapshot
Absence of Learning and Local Specialization on Host Plant Selection by Heliconius erato
inferredcites →https://doi.org/10.1016/0198-9715(90)90050-4openalex-snapshot
Statistical power analysis for the behavioral sciences
inferredcites →https://doi.org/10.1016/j.anbehav.2013.12.027openalex-snapshot
Larval feeding choices in heliconians: induced preferences are not constrained by performance and host plant phylogeny
inferredcites →https://doi.org/10.1016/j.asd.2005.01.008openalex-snapshot
Evolution of insect mushroom bodies: old clues, new insights
inferredcites →https://doi.org/10.1016/j.asd.2008.05.005openalex-snapshot
Tritocerebral tract input to the insect mushroom bodies
inferredcites →https://doi.org/10.1016/j.cub.2009.08.023openalex-snapshot
Are Bigger Brains Better?
inferredcites →https://doi.org/10.1016/j.jneumeth.2008.04.031openalex-snapshot
Confocal microscopy in large insect brains: Zinc–formaldehyde fixation improves synapsin immunostaining and preservation of morphology in whole-mounts
inferredcites →https://doi.org/10.1016/j.jphysparis.2014.07.004openalex-snapshot
The insect mushroom body, an experience-dependent recoding device
inferredcites →https://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)
inferredcites →https://doi.org/10.1016/s0020-7322(98)00022-1openalex-snapshot
Mouthparts of heliconius butterflies (LEPIDOPTERA : NYMPHALIDAE) : a search for anatomical adaptations to pollen-feeding behavior
inferredcites →https://doi.org/10.1016/s0163-1047(05)80025-1openalex-snapshot
Development and experience lead to increased volume of subcompartments of the honeybee mushroom body
inferredcites →https://doi.org/10.1016/s0959-4388(00)00147-1openalex-snapshot
Behavioral functions of the insect mushroom bodies
inferredcites →https://doi.org/10.1016/s0960-9822(02)00656-5openalex-snapshot
The Drosophila Standard Brain
inferredcites →https://doi.org/10.1023/a:1007814618149openalex-snapshot
Behavioral Adaptations to Pollen-Feeding in Heliconius Butterflies (Nymphalidae, Heliconiinae): An Experiment Using Lantana Flowers
inferredcites →https://doi.org/10.1038/364238a0openalex-snapshot
Selective neuroanatomical plasticity and division of labour in the honeybee
inferredcites →https://doi.org/10.1038/44766openalex-snapshot
Inferring the historical patterns of biological evolution
inferredcites →https://doi.org/10.1038/nature11041openalex-snapshot
Butterfly genome reveals promiscuous exchange of mimicry adaptations among species
inferredcites →https://doi.org/10.1046/j.1365-2311.2002.00434.xopenalex-snapshot
Patterns of pollen feeding and habitat preference among Heliconius species
inferredcites →https://doi.org/10.1046/j.1439-0310.1999.372-2.xopenalex-snapshot
Machiavellian Intelligence II: Extensions and Evaluations
inferredcites →https://doi.org/10.1073/pnas.0407858101openalex-snapshot
Mechanism and circuitry for clustering and fine discrimination of odors in insects
inferredcites →https://doi.org/10.1073/pnas.0508430102openalex-snapshot
Coevolution of generalist feeding ecologies and gyrencephalic mushroom bodies in insects
inferredcites →https://doi.org/10.1073/pnas.69.6.1403openalex-snapshot
Pollen Feeding and Reproductive Biology of Heliconius Butterflies
inferredcites →https://doi.org/10.1080/01677060802471627openalex-snapshot
The Wuerzburg Hybridoma Library against Drosophila Brain
inferredcites →https://doi.org/10.1093/chemse/bjt008openalex-snapshot
Organization of the Olfactory System of Nymphalidae Butterflies
inferredcites →https://doi.org/10.1093/molbev/msr121openalex-snapshot
MEGA5: Molecular Evolutionary Genetics Analysis Using Maximum Likelihood, Evolutionary Distance, and Maximum Parsimony Methods
inferredcites →https://doi.org/10.1093/nar/gkh340openalex-snapshot
MUSCLE: multiple sequence alignment with high accuracy and high throughput
inferredcites →https://doi.org/10.1093/sysbio/syv007openalex-snapshot
Multilocus Species Trees Show the Recent Adaptive Radiation of the Mimetic Heliconius Butterflies
inferredcites →https://doi.org/10.1098/rspb.1998.0523openalex-snapshot
Visual specialization and brain evolution in primates
inferredcites →https://doi.org/10.1098/rspb.2003.2552openalex-snapshot
Pollen feeding in the butterfly Heliconius charitonia : isotopic evidence for essential amino acid transfer from pollen to eggs
inferredcites →https://doi.org/10.1098/rspb.2007.1446openalex-snapshot
A parasitoid wasp uses landmarks while monitoring potential resources
inferredcites →https://doi.org/10.1098/rspb.2010.0269openalex-snapshot
Socially induced brain development in a facultatively eusocial sweat beeMegalopta genalis(Halictidae)
inferredcites →https://doi.org/10.1098/rspb.2010.0694openalex-snapshot
Gregarious desert locusts have substantially larger brains with altered proportions compared with the solitarious phase
inferredcites →https://doi.org/10.1098/rspb.2010.2161openalex-snapshot
Parasitoidism, not sociality, is associated with the evolution of elaborate mushroom bodies in the brains of hymenopteran insects
inferredcites →https://doi.org/10.1098/rstb.1995.0076openalex-snapshot
Evolutionary radiation of visual and olfactory brain systems in primates, bats and insectivores
inferredcites →https://doi.org/10.1101/lm.5.1.115openalex-snapshot
Experience-Expectant Plasticity in the Mushroom Bodies of the Honeybee
inferredcites →https://doi.org/10.1111/j.1095-8312.2007.00830.xopenalex-snapshot
Do pollen feeding, pupal-mating and larval gregariousness have a single origin in Heliconius butterflies? Inferences from multilocus DNA sequence data
inferredcites →https://doi.org/10.1111/j.1460-9568.2004.03527.xopenalex-snapshot
Flies lacking all synapsins are unexpectedly healthy but are impaired in complex behaviour
inferredcites →https://doi.org/10.1111/j.2041-210x.2011.00153.xopenalex-snapshot
smatr 3– an R package for estimation and inference about allometric lines
inferredcites →https://doi.org/10.1111/jeb.12119openalex-snapshot
Pollen feeding, resource allocation and the evolution of chemical defence in passion vine butterflies
inferredcites →https://doi.org/10.1126/science.171.3967.203openalex-snapshot
Euglossine Bees as Long-Distance Pollinators of Tropical Plants
inferredcites →https://doi.org/10.1126/science.176.4037.936openalex-snapshot
Natural Selection for Müllerian Mimicry in Heliconius erato in Costa Rica
inferredcites →https://doi.org/10.1126/science.197.4302.487openalex-snapshot
Ovarian Dynamics in Heliconiine Butterflies: Programmed Senescence versus Eternal Youth
inferredcites →https://doi.org/10.1146/annurev-ento-011613-162031openalex-snapshot
Organization and Functional Roles of the Central Complex in the Insect Brain
inferredcites →https://doi.org/10.1146/annurev-ento-120710-100538openalex-snapshot
Advances in Insect Phylogeny at the Dawn of the Postgenomic Era
inferredcites →https://doi.org/10.1146/annurev.en.13.010168.000555openalex-snapshot
Chemosensory Bases of Host Plant Selection
inferredcites →https://doi.org/10.1146/annurev.en.26.010181.002235openalex-snapshot
The Biology of Heliconius and Related Genera
inferredcites →https://doi.org/10.1146/annurev.en.39.010194.002113openalex-snapshot
Oviposition Behavior in Lepidoptera
inferredcites →https://doi.org/10.1146/annurev.es.12.110181.000531openalex-snapshot
Adaptation and Evolution in Heliconius: A Defense of NeoDarwinism
inferredcites →https://doi.org/10.1146/annurev.psych.50.1.651openalex-snapshot
NEUROETHOLOGY OF SPATIAL LEARNING: The Birds and the Bees
inferredcites →https://doi.org/10.1159/000113330openalex-snapshot
Microhabitat Use, Trophic Patterns, and the Evolution of Brain Structure in African Cichlids
inferredcites →https://doi.org/10.1159/000213647openalex-snapshot
Brain Size: A Global or Induced Cost of Learning?
inferredcites →https://doi.org/10.1159/000352057openalex-snapshot
Evolution of Complex Higher Brain Centers and Behaviors: Behavioral Correlates of Mushroom Body Elaboration in Insects
inferredcites →https://doi.org/10.1159/000355845openalex-snapshot
Plasticity of the Worker Bumblebee Brain in Relation to Age and Rearing Environment
inferredcites →https://doi.org/10.1242/jeb.01508openalex-snapshot
Three-dimensional antennal lobe atlas of male and female moths, Lobesia botrana (Lepidoptera: Tortricidae) and glomerular representation of plant volatiles in females
inferredcites →https://doi.org/10.1242/jeb.199.9.2011openalex-snapshot
Age-Dependent and Task-Related Morphological Changes in the Brain and The Mushroom Bodies of The Ant Camponotus Floridanus
inferredcites →https://doi.org/10.1371/journal.pgen.1003620openalex-snapshot
Female Behaviour Drives Expression and Evolution of Gustatory Receptors in Butterflies
inferredcites →https://doi.org/10.1523/jneurosci.16-10-03154.1996openalex-snapshot
Invertebrate Synapsins: A Single Gene Codes for Several Isoforms inDrosophila
inferredcites →https://doi.org/10.1523/jneurosci.21-16-06395.2001openalex-snapshot
Experience- and Age-Related Outgrowth of Intrinsic Neurons in the Mushroom Bodies of the Adult Worker Honeybee
inferredcites →https://doi.org/10.2307/2410309openalex-snapshot
Hybrid Zones and the Evolutionary Process.
inferredcites →https://doi.org/10.2307/2484318openalex-snapshot
Coevolution of Animals and Plants.
inferredcites →https://doi.org/10.2307/2989656openalex-snapshot
Population Structure and Dynamics of the Tropical Butterfly Heliconius ethilla
inferredcites →https://doi.org/10.2307/2989703openalex-snapshot
Experiments on the Demography of Tropical Butterflies. II. Longevity and Home-Range Behaviour in Heliconius erato
inferredcites →https://doi.org/10.3389/neuro.06.003.2010openalex-snapshot
3D standard brain of the red flour beetle Tribolium castaneum: a tool to study metamorphic development and adult plasticity
inferredcites →https://doi.org/10.3389/neuro.06.014.2009openalex-snapshot
Digital, three-dimensional average shaped atlas of the heliothis virescens brain with integrated gustatory and olfactory neurons
inferredcites →https://doi.org/10.7560/710313-011openalex-snapshot
Ecological consequences of a coevolved mutualism between butterflies and plants

What points at this work

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

inferred← citeshttps://doi.org/10.1038/s41598-025-92712-3openalex-snapshot
Sexual dimorphism and morphological integration in the orchid bee brain
inferred← citeshttps://doi.org/10.1093/oxfordhb/9780190456757.013.1openalex-snapshot
Recent Trends in Invertebrate Neuroscience
inferred← citeshttps://doi.org/10.1093/oxfordhb/9780190456757.013.2openalex-snapshot
The Divergent Evolution of Arthropod Brains
inferred← citeshttps://doi.org/10.1101/043182openalex-snapshot
Adaptive divergence in brain composition between ecologically distinct incipient species
inferred← citeshttps://doi.org/10.1111/jeb.12672openalex-snapshot
The diversification of Heliconius butterflies: what have we learned in 150 years?
Editorial review for independent work. ICSAC — the Institute for Complexity Science and Advanced Computing — runs a structured editorial panel for researchers publishing outside journals, and publishes on CiteStamp rails. Submission is free and goes through ORCID: icsacinstitute.org/submit.