Influence of mating experience on mating latency and copulation duration in Drosophila melanogaste females

2009 ◽  
Vol 45 (7) ◽  
pp. 875-877 ◽  
Author(s):  
S. Pavković-Lučić ◽  
V. Kekić
2020 ◽  
Author(s):  
Julie M. Collet ◽  
Jacqueline L Sztepanacz

AbstractThe total strength of sexual selection on males depends on the relationship between various components of pre- and post-copulatory fitness. Misalignment between male and female interests creates inter-locus sexual conflict, where the fitness of one sex is increased at the expense of the other. Although rarely considered, mating behaviours can also be genetically correlated between males and females, creating intra-locus sexual conflict, where beneficial alleles in one sex are costly when expressed in the other sex. How inter- and intra-locus sexual conflicts operate on the expression of mating behaviours remains little understood. Here, we study male attractiveness, mating latency and copulation duration in two populations of the polyandrous Drosophila serrata. Univariate analyses show little genetic variance in mating latency, and that males, but not females, contribute to copulation duration genetic variance. Further, multivariate analyses revealed little covariance between the studied traits. However, analyses considering male and female contribution in a single framework supported genetic contributions from both sexes for mating behaviours and complex patterns of between sexes correlations. Finally, our study did not find any association between those mating behaviours and fitness component, specifically (i) no phenotypic covariance between male attractiveness and mating latency and, (ii) longer copulations did not result in the production of more offspring. With no detectable fitness benefits in any sexes for shorter mating latency or longer copulation duration, our results do not support the presence of inter-nor intra-locus sexual conflict for these mating traits.


2018 ◽  
Vol 24 (1) ◽  
Author(s):  
SHAMIM AKHTER CHOUDHARY

In the present study, an attempt was made to study the effect of plant extract on Sexual behaviour of Mutant Strain (Curled) of Drosophila melanogaster. The LC50 has been estimated with 1% of the food media. The virgin females and males were isolated and fed with normal food media for three days. Then sub-lethal concentrations of 0.625 μl / 100 ml food, 1.2 μl /100 ml food, 2.5μl /100 / food of nicotine were mixed in food medium and allowed in flies to feed for two days. Then appropriate combination of untreated / treated males and females were introduced into the mating chamber. Courtship latency, mating latency and copulation duration were studied. After observation of the behaviour, mated flies were allowed to produce progeny. The sexual behaviour of bachelor male and virgin female obtained in the progeny was also studied. The pooled data were analyzed by student t-test and the result indicates p-value significant at 0.05 levels. The courtship latency was affected by in treatment but it is neither dose dependent nor sex dependent.


Apidologie ◽  
2005 ◽  
Vol 36 (2) ◽  
pp. 157-167 ◽  
Author(s):  
Mark J.F. Brown ◽  
Boris Baer

2018 ◽  
Vol 10 (9) ◽  
pp. 12203
Author(s):  
Nilesh R. Thaokar ◽  
Payal R. Verma ◽  
Raymond J. Andrew

The Coromandel Damselfly Ceriagrion coromandelianum can be easily identified because of its bright yellow abdomen, greenish thorax and eyes.  In females, the abdomen is darker with light brown colouration extending to dark brown towards the terminal end.  The documentation of the reproductive behaviour of Ceriagrion coromandelianum was carried out at the botanical garden of Hislop College, Nagpur, India.  The males of C. coromandelianum arrive early in the morning by 07:00hr at the ovipositing site.  They belong to “sit and wait” type of mate-location.  While perched and waiting for the female to arrive they at times exhibit abdominal bobbing, and oviposition posture.  The territorial area of male C. coromandelianum is very small, within a range of about 45cm around his perch.  There is no precopulatory courtship display and the male move toward the arriving receptive female and directly tries to form a tandem link.  The other males of the group follow the pair.  The tandem pair flies towards the safety of the surrounding vegetation to copulate. Before copulation, the male fills his penis vesicle with sperm material by the process of “intra male sperm translocation” which lasts for 30±8 seconds.  The female curves her abdomen ventrally forward so that her gonopore which is located between the eighth and ninth sternite comes to lie before the secondary copulatory apparatus of the male and forms a strong genital link, to form the copulatory wheel.  The copulation duration can be long (34–55 min) or short (12–15 min).  Two stages of copulation depending upon the pumping movement of the couple can be differentiated.  During the first stage, the male rhythmically and forcefully depresses and stretches the first two abdominal segments, vigorously pumping the penis inside the female vagina which accounts for 72% of the copulation duration.  The second stage starts with rapid short thrusting movement which are not forceful but exhibit shallow movements of the first two abdominal segment of the male.  The tandem pairs after copulation may directly move for oviposition or settle around the surrounding foliage and exhibit “post-copulatory resting” (PCR) behaviour.  It is noted that 23.3% females immediately commence oviposition, 53.4% exhibit brief, while 23.3% display prolonged PCR behaviour.  


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