The DOI matches its Crossref record; 36 of the 36 references it cites were found in a registry or an index.
The Role of Nourishment in Oogenesis
Abstract
Sexual receptivity is female behavior that allows or helps a male to fertilize her eggs; through this behavior, females play an active role in reproduction. Multiple signals may be used for receptivity or unreceptivity. Insect species exhibit three ontogenetic patterns of receptivity: cyclic, in which females alternately become receptive and unreceptive; brief, in which females mate during one short developmental period; and continuous. Primary (initial) receptivity may be stimulated or inhibited by diet, ovarian development, or juvenile hormone. In species with cyclic receptivity, remating may be inhibited by copulation itself, the presence of eggs, sperm stored in spermathecae, or seminal factors—usually peptides—secreted by the male accessory glands. In many species, there is substantial genetic variation for both primary receptivity and speed of remating. Several single-gene mutations reduce female receptivity; most of these mutations also impair sensory functioning.
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Cites
Wilson, E. O. (1971) · Medical Entomology and Zoology · Cited by 4,756
The Biology of Blood-Sucking in Insects
Lehane, M. J. (2005) · Cambridge University Press eBooks · doi:10.1017/cbo9780511610493 · Cited by 903
A male accessory gland peptide that regulates reproductive behavior of female D. melanogaster
Chen, P. S., Stumm-Zollinger, E., Aigaki, T., Balmer, J., Bienz, M., & Böhlen, P. (1988) · Cell · doi:10.1016/0092-8674(88)90192-4 · Cited by 671
THE EVOLUTION OF WING DIMORPHISM IN INSECTS
Roff, D. A. (1986) · Evolution · doi:10.1111/j.1558-5646.1986.tb00568.x · Cited by 629
Queen number and sociality in insects
(1994) · Choice Reviews Online · doi:10.5860/choice.32-0298 · Cited by 476
Pollen Feeding and Reproductive Biology of Heliconius Butterflies
Gilbert, L. E. (1972) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.69.6.1403 · Cited by 386
Courtship feeding increases female reproductive success in bushcrickets
Gwynne, D. T. (1984) · Nature · doi:10.1038/307361a0 · Cited by 339
Bell, W. J., & Bohm, M. K. (1975) · Biological reviews/Biological reviews of the Cambridge Philosophical Society · doi:10.1111/j.1469-185x.1975.tb01058.x · Cited by 274
Boggs, C. L., & Ross, C. L. (1993) · Ecology · doi:10.2307/1939305 · Cited by 260
Murphy, D. D., Launer, A. E., & Ehrlich, P. R. (1983) · Oecologia · doi:10.1007/bf00379699 · Cited by 258
Cited by
Guerra, P. A. (2011) · Biological Reviews · doi:10.1111/j.1469-185x.2010.00172.x · Cited by 210
Effects of food stress and density in different life stages on reproduction in a butterfly
Bauerfeind, S. S., & Fischer, K. (2005) · Oikos · doi:10.1111/j.0030-1299.2005.13888.x · Cited by 164
Allocation of larval and adult resources to reproduction in a fruit-feeding butterfly
FISCHER, K., O'BRIEN, D. M., & BOGGS, C. L. (2004) · Functional Ecology · doi:10.1111/j.0269-8463.2004.00892.x · Cited by 115
An ordination of life histories using morphological proxies: capital vs. income breeding in insects
Davis, R. B., Javoiš, J., Kaasik, A., Õunap, E., & Tammaru, T. (2016) · Ecology · doi:10.1002/ecy.1435 · Cited by 57
She Shapes Events as they Come: Plasticity in Female Insect Reproduction
Hodin, J. (2009) · Phenotypic Plasticity of Insects · doi:10.1201/b10201-12 · Cited by 28
Metadata
- Authors
- Wheeler, D.
- Venue
- Annual Review of Entomology
- Publisher
- Annual Reviews
- Published
- 1996-01
- Volume
- 41
- Issue
- 1
- Pages
- 407-431
- ISSN
- 0066-4170 (ISSN-L)
- 1545-4487
- OpenAlex
- W2179182636
- Cited by
- 513
- References
- 36
- FWCI
- 3.63
- Type
- journal article
- Language
- en
- Open access
- closed
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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.
