Male accessory gland secretions: modulators of female reproductive physiology and behavior.

By C. Gillott. Annual Review of Entomology, 2003

808 citations recorded by the source corpus.

Subfields: Cellular and Molecular Neuroscience, Ecology, Evolution, Behavior and Systematics, Genetics

View Paper: https://www.semanticscholar.org/paper/9775cf8ef22542f5e1549c965a19d59e8d9c8e1e

How researchers see this paper

The researchers whose trusted networks rank it highest, strongest advocate first. Every researcher gets a different order.

In Cellular and Molecular Neuroscience

1. B. Baer
2. S. Lewis
3. M. Eberle
4. Adam South
5. A. Poiani
6. D. Damiens
7. Peter M. Kappeler
8. G. Boivin

In Ecology, Evolution, Behavior and Systematics

1. M. Eberle
2. Peter M. Kappeler
3. S. Lewis
4. Adam South
5. B. Baer
6. Tom Tregenza
7. A. Poiani
8. C. Kvarnemo

In Genetics

1. B. Baer
2. S. Lewis
3. M. Eberle
4. Tom Tregenza
5. Adam South
6. A. Poiani
7. D. Damiens
8. N. Wedell

Citations in the corpus

• Why do sperm-depleted parasitoid males continue to mate? (2006, background): “Among these adaptations, the ejaculate (sperm and/or accessory secretions), whose first function is to transfer sperm to the female, has also a role in maximizing male paternity if competition among males for mates occurs (Gillot, 2003).”
• Complexity of seminal fluid: a review (2006, background): “In this work, I review the molecular diversity and functional role of seminal fluid components in invertebrates (mainly insects, see also Gillott 2003) and vertebrates (mainly mammals) with internal fertilisation, focusing on the costs and benefits of those molecules to both males and females.”
• Bumblebees as model organisms to study male sexual selection in social insects (2003, background): “Copulation II: transfer of male accessory-gland compounds Accessory glands are widespread among insects (Gillott 1996, 2003; Simmons 2001) and their compounds are known to influence male mating success in many different and sophisticated ways (see Table 4.1 in Simmons 2001; Gillott 2003).”
• Insect Seminal Fluid Proteins: Identification and Function (2011, background): “melanogaster SP stimulates egg laying in mated females (56, 130), and the long-term persistence of this activity requires the four Acps that localize SP to sperm (114, 131, 132).”
• Behaviour and ecology of the western corn rootworm (Diabrotica virgifera virgifera LeConte) (2009, background): “…Agricultural and Forest Entomology, 11, 9–27 No claims to original US government works substances have been extensively studied in a number of insect orders ( Gillott, 2003 ), notably in Diptera where the Drosophila melanogaster sex peptide receptor has been identified ( Yapici et al. , 2007 ).”
• Sex in the dark: determinants and consequences of mixed male mating tactics in Microcebus murinus, a small solitary nocturnal primate (2004, background): “Mating plugs are known from many taxa (insects: Gillott 2003, snakes: Devine 1975, rodents: Voss 1979, primates: Dixson and Anderson 2002), and their occurrence is closely related to sperm competition.”
• The Evolution of Animal Nuptial Gifts (2012, background): “However, because various constituents of seminal fluid have been shown to exert diverse effects on both male and female fitness (Gillott, 2003; Leopold, 1976; Poiani, 2006), such inclusion seems appropriate.”
• Sexual conflict and life histories (2006, background): “In many insects, males transfer factors in the ejaculate that manipulate female reproductive physiology to increase their reproductive success (Gillott 2003).”
• The Physiological and Genomic Bases of Bumble Bee Social Behaviour (2015, background): “Mating causes extensive short- and long-term physiological as well as behavioural modifications in females (Chapman et al., 1995; Gillott, 2003; Kocher et al., 2008).”