1982
DOI: 10.1007/bf01067849
|View full text |Cite
|
Sign up to set email alerts
|

The role of female movement in the sexual behavior ofDrosophila melanogaster

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
3
1
1

Citation Types

4
104
1

Year Published

1988
1988
2017
2017

Publication Types

Select...
10

Relationship

1
9

Authors

Journals

citations
Cited by 179 publications
(109 citation statements)
references
References 29 publications
4
104
1
Order By: Relevance
“…Since an increase in preening activity also occurs when the flies are isolated, preening behaviour may have no specifically sexual connotation but does provide some indication of the level of female reactivity. Courtship reduces the activity of receptive females and this may be partly due to odour cues (Tompkins et a!., 1982), and to the effects of acoustic stimuli generated through wing vibration by the male (Cook, 1973;von Schilcher, 1976). The amount of wing vibration appears to be relatively independent of differences in female locomotor activity, although it may not be so in situations involving females from selected lines, or for neurological mutants, which cause more extreme deviations in the expression of female mobility.…”
Section: Discussionmentioning
confidence: 93%
“…Since an increase in preening activity also occurs when the flies are isolated, preening behaviour may have no specifically sexual connotation but does provide some indication of the level of female reactivity. Courtship reduces the activity of receptive females and this may be partly due to odour cues (Tompkins et a!., 1982), and to the effects of acoustic stimuli generated through wing vibration by the male (Cook, 1973;von Schilcher, 1976). The amount of wing vibration appears to be relatively independent of differences in female locomotor activity, although it may not be so in situations involving females from selected lines, or for neurological mutants, which cause more extreme deviations in the expression of female mobility.…”
Section: Discussionmentioning
confidence: 93%
“…The mutation tipE (temperature-induced paralysis locus E) also disrupts para expression and confers temperatureinduced paralysis as a result of a decrease in sodium channel numbers (Feng et al, 1995) The sbl (smellblind) mutation, which is not temperature sensitive, is also an allele of the para gene (Lilly et al, 1994). This associates sodium channel mutations with olfactory and chemotactic defects (Lilly and Carlson, 1990) and with changes in sexual behaviour (Tompkins et al, 1982(Tompkins et al, , 1983. In another unrelated point mutation conferring resistance to the cyclodienes, a mutation in the structural gene encoding the g-aminobutyric acid receptor (rdl or resistance to dieldrin) also appears to induce reversible temperaturesensitive paralysis (Ffrench-Constant et al, 2000).…”
Section: Discussionmentioning
confidence: 99%
“…These include mutations in genes required for normal morphology [white (13,14), yellow (14), and curved (15)], as well as genes involved in learning and memory [Calcium calmodulin kinase II (16), dunce (17,18), rutabaga (19,20), turnip (19,21), and amnesiac (20,22,23)], circadian rhythm [period (18,(24)(25)(26)] and dopamine and serotonin synthesis [Dopa decarboxylase (27), pale (28,29), tan (30,31), and ebony (32)(33)(34)], sex determination [doublesex (35)(36)(37), transformer (38)(39)(40)(41)(42)(43), fruitless (44)(45)(46)(47), and sex lethal (48)], pheromone production [desaturase 2 (49)], and accessory gland-specific peptides (6-8, 50-52). a subset of loci identified by mutational analysis, or will the analysis of natural variants reveal novel loci?…”
Section: Drosophila Mating Behaviormentioning
confidence: 99%