The DOI matches its Crossref record; 48 of the 48 references it cites were found in a registry or an index.
Experience-Expectant Plasticity in the Mushroom Bodies of the Honeybee
Abstract
Worker honeybees (Apis mellifera) were reared in social isolation in complete darkness to assess the effects of experience on growth of the neuropil of the mushroom bodies (MBs) during adult life. Comparison of the volume of the MBs of 1-day-old and 7-day-old bees showed that a significant increase in volume in the MB neuropil occurred during the first week of life in bees reared under these highly deprived conditions. All regions of the MB neuropil experienced a significant increase in volume with the exception of the basal ring. Measurement of titers of juvenile hormone (JH) in a subset of bees indicated that, as in previous studies, these rearing conditions induced in some bees the endocrine state of high JH associated with foraging, but there was no correlation between JH titer and volume of MB neuropil. Treatment of another subset of dark-reared bees with the JH analog, methoprene, also had no effect of the growth of the MB neuropil. These results demonstrate that there is a phase of MB neuropil growth early in the adult life of bees that occurs independent of light or any form of social interaction. Together with previous findings showing that an increase in MB neuropil volume begins around the time that orientation flights occur and then continues throughout the phase of life devoted to foraging, these results suggest that growth of the MB neuropil in adult bees may have both experience-expectant and experience-dependent components.
Overview
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Integrity signals
Registry
Cites
Statistics
Verification
Claims the paper makes
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Claims other papers make about this one
Each is checked against this paper’s own text: does it say what the citing paper says it does?
In the citing paper
“Developmental processes thus triggered by bGRNs may result in NN rewiring and growth (69) or changes of cell type proportions in the brain (70), serving as a major mechanism for feedback from bGRN to NN, and thus to future behavior.”
From Behavior-related gene regulatory networks: A new level of organization in the brain (2020) · cites this paper as [70]
Self-check
Percentages, sums and reported differences re-computed from the paper’s own numbers.
The self-check needs the paper’s full text.
Citations
Cites
Comprehensive insect physiology, biochemistry and pharmacology
(1985) · Journal of Insect Physiology · doi:10.1016/0022-1910(85)90117-9 · Cited by 4,810
The efficiency of systematic sampling in stereology and its prediction*
Gundersen, H. J. G., & Jensen, E. B. V. (1987) · Journal of Microscopy · doi:10.1111/j.1365-2818.1987.tb02837.x · Cited by 3,519
Gundersen, H. J. G., Bagger, P. V., Bendtsen, T. F., Evans, S. M., Korbo, L., Marcussen, N., Møller, A., Nielsen, K. N., Nyengaard, J. R., Pakkenberg, B., et al. (1988) · Apmis · doi:10.1111/j.1699-0463.1988.tb00954.x · Cited by 2,480
Winston, M. L. (1987) · Cited by 2,071
A Method for the Combined Staining of Cells and Fibers in the Nervous System
Klüver, H., & Barrera, E. (1953) · Journal of Neuropathology & Experimental Neurology · doi:10.1097/00005072-195312040-00008 · Cited by 1,724
Black, J. E., Isaacs, K. R., Anderson, B. J., Alcantara, A. A., & Greenough, W. T. (1990) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.87.14.5568 · Cited by 1,161
Regulation of Division of Labor in Insect Societies
Robinson, G. E. (1992) · Annual Review of Entomology · doi:10.1146/annurev.en.37.010192.003225 · Cited by 1,106
Self-citationNew stereological methods for counting neurons
West, M. J. (1993) · Neurobiology of Aging · doi:10.1016/0197-4580(93)90112-o · Cited by 940
Regulation Of Division Of Labor In Insect Societies
Robinson, G. E. (1992) · Annual Review of Entomology · doi:10.1146/annurev.ento.37.1.637 · Cited by 886
Self-citationAssociative Odor Learning in Drosophila Abolished by Chemical Ablation of Mushroom Bodies
de Belle, J. S., & Heisenberg, M. (1994) · Science · doi:10.1126/science.8303280 · Cited by 788
Chemical and Anatomical Plasticity of Brain
Bennett, E. L., Diamond, M. C., Krech, D., & Rosenzweig, M. R. (1964) · Science · doi:10.1126/science.146.3644.610 · Cited by 769
Learning and memory in the honeybee
Hammer, M., & Menzel, R. (1995) · The Journal of Neuroscience · doi:10.1523/jneurosci.15-03-01617.1995 · Cited by 733
Drosophila Mushroom Body Mutants are Deficient in Olfactory Learning: Research Papers
Heisenberg, M., Borst, A., Wagner, S., & Byers, D. (1985) · Journal of Neurogenetics · doi:10.3109/01677068509100140 · Cited by 695
Mobbs, P. G. (1982) · Philosophical transactions of the Royal Society of London. Series B, Biological sciences · doi:10.1098/rstb.1982.0086 · Cited by 505
Michel, R. P., & Cruz‐Orive, L. M. (1988) · Journal of Microscopy · doi:10.1111/j.1365-2818.1988.tb04603.x · Cited by 431
Selective neuroanatomical plasticity and division of labour in the honeybee
Withers, G. S., Fahrbach, S. E., & Robinson, G. E. (1993) · Nature · doi:10.1038/364238a0 · Cited by 417
Self-citationLocalization of short‐term memory in the brain of the bee, Apis mellifera
ERBER, J., MASUHR, T., & MENZEL, R. (1980) · Physiological Entomology · doi:10.1111/j.1365-3032.1980.tb00244.x · Cited by 411
Mushroom bodies and drosophila learning
Davis, R. L. (1993) · Neuron · doi:10.1016/0896-6273(93)90266-t · Cited by 402
Huang, Z., & Robinson, G. E. (1992) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.89.24.11726 · Cited by 331
Self-citationHormonal and Genetic Control of Behavioral Integration in Honey Bee Colonies
Robinson, G. E., Page, R. E., Strambi, C., & Strambi, A. (1989) · Science · doi:10.1126/science.246.4926.109 · Cited by 310
Self-citationSexual dimorphism in the vertebrate nervous system
Breedlove, S. (1992) · The Journal of Neuroscience · doi:10.1523/jneurosci.12-11-04133.1992 · Cited by 304
Structural plasticity in the Drosophila brain
Heisenberg, M., Heusipp, M., & Wanke, C. (1995) · Journal of Neuroscience · doi:10.1523/jneurosci.15-03-01951.1995 · Cited by 265
Kenyon, F. (1896) · The Journal of Comparative Neurology · doi:10.1002/cne.910060302 · Cited by 259
Development and experience lead to increased volume of subcompartments of the honeybee mushroom body
Durst, C., Eichmüller, S. B., & Menzel, R. (1994) · Behavioral and Neural Biology · doi:10.1016/s0163-1047(05)80025-1 · Cited by 237
Physiological correlates of division of labor among similarly aged honey bees
Huang, Z., Robinson, G. E., & Borst, D. W. (1994) · Journal of Comparative Physiology A · doi:10.1007/bf00192722 · Cited by 236
Self-citationGronenberg, W., Heeren, S., & Hölldobler, B. (1996) · Journal of Experimental Biology · doi:10.1242/jeb.199.9.2011 · Cited by 224
Colour receptors in the bee eye ? Morphology and spectral sensitivity
Menzel, R., & Blakers, M. (1976) · Journal of Comparative Physiology A · doi:10.1007/bf00625437 · Cited by 223
Robinson, G. E. (1987) · Journal of Comparative Physiology A · doi:10.1007/bf00611934 · Cited by 179
Self-citationEffects of experience and juvenile hormone on the organization of the mushroom bodies of honey bees
Withers, G. S., Fahrbach, S. E., & Robinson, G. E. (1995) · Journal of Neurobiology · doi:10.1002/neu.480260111 · Cited by 175
Self-citationLi, Y., & Strausfeld, N. J. (1997) · The Journal of Comparative Neurology · doi:10.1002/(sici)1096-9861(19971103)387:4<631::aid-cne9>3.0.co;2-3 · Cited by 165
Learning and Memory in the Honeybee
Menzel, R., Erber, J., & Masuhr, T. (1974) · Springer eBooks · doi:10.1007/978-3-642-86666-1_14 · Cited by 161
Experience-Dependent Developmental Plasticity in the Optic Lobe ofDrosophila melanogaster
Barth, M., Hirsch, H. V. B., Meinertzhagen, I. A., & Heisenberg, M. (1997) · Journal of Neuroscience · doi:10.1523/jneurosci.17-04-01493.1997 · Cited by 141
Processing of antennal information in extrinsic mushroom body neurons of the bee brain
Homberg, U. (1984) · Journal of Comparative Physiology A · doi:10.1007/bf00610683 · Cited by 137
Plasticity of Synapse Structure and Pattern in the Cerebral Cortex
Greenough, W. T., & Chang, F. (1988) · Cerebral cortex · doi:10.1007/978-1-4615-6619-9_11 · Cited by 136
Neural networks in the mushroom bodies of the honeybee
Mobbs, P. G. (1984) · Journal of Insect Physiology · doi:10.1016/0022-1910(84)90107-0 · Cited by 133
Vision affects mushroom bodies and central complex in Drosophila melanogaster.Preprint
Barth, M., & Heisenberg, M. (1997) · Learning & Memory · doi:10.1101/lm.4.2.219 · Cited by 114
Volume Changes in the Mushroom Bodies of Adult Honey Bee Queens
Fahrbach, S. E., Giray, T., & Robinson, G. E. (1995) · Neurobiology of Learning and Memory · doi:10.1006/nlme.1995.1019 · Cited by 109
Self-citationEfficient estimation of cell volume and number using the nucleator and the disector
Møller, A., Strange, P., & Gundersen, H. J. G. (1990) · Journal of Microscopy · doi:10.1111/j.1365-2818.1990.tb03019.x · Cited by 105
Giray, T., & Robinson, G. E. (1996) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.93.21.11718 · Cited by 90
Self-citationA new role for the insect mushroom bodies: place memory and motor control
Mizunami, M., Weibrecht, J. M., & Strausfeld, N. J. (1993) · Cited by 75
Circadian locomotor rhythms in individual honeybees
Moore, D., & Rankin, M. A. (1985) · Physiological Entomology · doi:10.1111/j.1365-3032.1985.tb00034.x · Cited by 73
Self-citationGronenberg, W. (1986) · Journal of Insect Physiology · doi:10.1016/0022-1910(86)90111-3 · Cited by 61
Fahrbach, S. E., Giray, T., Farris, S. M., & Robinson, G. E. (1997) · Neuroscience Letters · doi:10.1016/s0304-3940(97)00772-6 · Cited by 60
Self-citationFull sisters and super sisters: a terminological paradigm
Page, R. E., & Laidlaw, H. H. (1988) · Animal Behaviour · doi:10.1016/s0003-3472(88)80181-7 · Cited by 55
Biochemistry of insect learning: Lessons from bees and flies
Meller, V. H., & Davis, R. L. (1996) · Insect Biochemistry and Molecular Biology · doi:10.1016/0965-1748(95)00100-x · Cited by 48
Regulation of Age Polyethism in Bees and Wasps by Juvenile Hormone
Fahrbach, S. E. (1997) · Advances in the study of behavior · doi:10.1016/s0065-3454(08)60382-4 · Cited by 44
Self-citationInterocular Transfer, Brain Lesions, and Maze Learning in the Wood Ant, Formica rufa
Vowles, D. M. (1967) · Springer eBooks · doi:10.1007/978-1-4899-6565-3_26 · Cited by 17
Gregory, G. E., Greenway, A. R., & Lord, K. A. (1980) · Stain Technology · doi:10.3109/10520298009067230 · Cited by 17
Research works printed but not linked: 2
- Hunnicutt, 1989, A chiral specific antiserum for juvenile hormone., Am. Zool., 29, 48A
- Laidlaw H.H. (1977) Instrumental insemination of honey bee queens. (Dadant and Sons Press, Hamilton, IL).
Cited by
Farris, S. M., Robinson, G. E., & Fahrbach, S. E. (2001) · The Journal of Neuroscience · doi:10.1523/jneurosci.21-16-06395.2001 · Cited by 272
Self-citationAn exploration of the social brain hypothesis in insects.
Lihoreau, M., Latty, T., & Chittka, L. (2012) · Frontiers in Physiology · doi:10.3389/fphys.2012.00442 · Cited by 118
On Being Small: Brain Allometry in Ants
Wehner, R., Fukushi, T., & Isler, K. (2007) · Brain, Behavior and Evolution · doi:10.1159/000097057 · Cited by 89
Behavior-related gene regulatory networks: A new level of organization in the brain
Sinha, S., Jones, B. M., Traniello, I. M., Bukhari, S. A., Halfon, M. S., Hofmann, H. A., Huang, S., Katz, P. S., Keagy, J., Lynch, V. J., et al. (2020) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1921625117 · Cited by 85
Self-citationSocial complexity influences brain investment and neural operation costs in ants
Kamhi, J. F., Gronenberg, W., Robson, S. K. A., & Traniello, J. F. A. (2016) · Proceedings of the Royal Society B Biological Sciences · doi:10.1098/rspb.2016.1949 · Cited by 56
Metadata
- Authors
- Fahrbach, S. E., Moore, D., Capaldi, E. A., Farris, S. M., & Robinson, G. E.
- Venue
- Learning & Memory
- Publisher
- Cold Spring Harbor Laboratory
- Published
- 1998-05-01
- Volume
- 5
- Issue
- 1
- Pages
- 115-123
- ISSN
- 1072-0502
- 1549-5485
- Cited by
- 135
- References
- 48
- Language
- en
About these checks
Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.
Statistics and arithmetic are recomputed, not judged.
Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.
What counts as a claim ›How we measure confidence ›How we check this ›
Are you an author, or do you see a problem with this page? Request a review
Data sources
Bibliographic data: Semantic Scholar, OpenAlex, Crossref.
Contains information from the Semantic Scholar Academic Graph Datasets, made available under the ODC Attribution License (ODC-BY 1.0).
Semantic Scholar’s data is described in: Kinney, R., et al. (2023). The Semantic Scholar Open Data Platform. arXiv:2301.10140.