scholarly journals Male mating behaviour and mating systems of bees: an overview

Apidologie ◽  
2005 ◽  
Vol 36 (2) ◽  
pp. 145-156 ◽  
Author(s):  
Robert John Paxton

Male mammals show a diverse array of mating bonds, including obligate monogamy, unimale and group polygyny and promiscuity. These are associated with a wide variety of different forms of mate guarding, including the defence of feeding and mating territories, the defence of female groups and the defence of individual receptive females. Female mating bonds include long-term monogamy, serial monogamy, polyandry and promiscuity. Both male and female mating behaviour varies widely within species. Variation in male mating behaviour is related to the effect of male assistance in rearing young and to the defensibility of females by males. The latter is, in turn, related to female ranging behaviour and to the size and stability of female groups. Much of the variation in mammalian mating bonds and systems of mate guarding can be attributed to differences in these three variables.


2013 ◽  
Vol 61 (1) ◽  
pp. 31-41 ◽  
Author(s):  
Yukie Sato ◽  
Maurice W. Sabelis ◽  
Martijn Egas ◽  
Farid Faraji

2020 ◽  
Author(s):  
Noritaka Hirohashi ◽  
Noriyosi Sato ◽  
Yoko Iwata ◽  
Satoshi Tomano ◽  
Md Nur E Alam ◽  
...  

Male animals are not given equal mating opportunities under competitive circumstances. Small males often exhibit alternative mating behaviours and produce spermatozoa of higher quality to compensate for their lower chances of winning physical contests against larger competitors [1]. Because the reproductive benefits of these phenotypes depend on social status/agonistic ranks that can change during growth or aging [2], sperm traits should be developed/switched into fitness optima according to their prospects. However, reproductive success largely relies upon social contexts arising instantaneously from intra- and inter-sexual interactions, which deter males from developing extreme traits and instead favour behavioural plasticity. Nevertheless, the extent to which such plasticity influences developmentally regulated alternative sperm traits remains unexplored. Squids of the family Loliginidae are excellent models to investigate this, because they show sophisticated alternative reproductive tactics (ARTs) by which small males, known as “sneakers”, produce longer spermatozoa and perform extra-pair copulation to attach their sperm packages near the female seminal receptacle (SR). In contrast, large “consort” males have shorter spermatozoa and copulate via pair-bonding to insert their sperm packages near the internal female oviduct [3]. In addition, plasticity in male mating behaviour is common in some species while it is either rare or absent in others. Thus, squid ARTs display a broad spectrum of adaptive traits with a complex repertoire in behaviour, morphology and physiology [3].


Behaviour ◽  
2015 ◽  
Vol 152 (14) ◽  
pp. 1883-1910 ◽  
Author(s):  
Peter Morse ◽  
Kyall R. Zenger ◽  
Mark I. McCormick ◽  
Mark G. Meekan ◽  
Christine L. Huffard

The southern blue-ringed octopus,Hapalochlaena maculosaHoyle (1883), is a nocturnal species that exhibits a mating system in which females hold sperm from multiple males over a one to two month breeding window before laying a single egg clutch. Contrary to most studied animal mating systems where anisogamy exists, gamete package production is limited for both males and females of this species (approx. 50 spermatophores/eggs). This presents an animal model for studying aspects of sperm competition and dynamic mate choice behaviours. The present study reports on the mating behaviour ofH. maculosaobserved under laboratory conditions using infrared closed-circuit television video footage. Rates of male copulation attempts increased with male size, while female receptivity to mating attempts increased with female size, resulting in larger animals of both sexes gaining more copulations and spending more time per day in copulation. There was some evidence of female preference of larger males, but no male preference of females based on measured morphological traits. Both sexes terminated copulations in equal frequencies but male-terminated copulations were significantly shorter in duration. Males were more likely to terminate copulation early with females they had previously mated with, however were less likely to do so if the female had recently mated with a different male. Among male-terminated copulations, males mated for longer with females that had previously mated with other males in the trial. Male–male mounts were as common as male–female mounts, suggesting that maleH. maculosaare not able to discriminate the sex of conspecifics. These findings suggest male strategic allocation of spermatophores based female mating history is an important factor influencing mating behaviours of this species.


1991 ◽  
Vol 69 (3) ◽  
pp. 604-613 ◽  
Author(s):  
Kevin M. O'Neill ◽  
Howard E. Evans ◽  
Louis B. Bjostad

The behaviour of males of the bumblebees Bombus nevadensis nevadensis, B. griseocollis, and B. rufocinctus was examined at sites in Colorado and Montana, U.S.A. Males of all three species defended individual mating territories on which they scent marked plants with cephalic chemicals, which we hypothesize to be sex pheromones. Males aggressively excluded conspecific males from the vicinity of scent-marked plants for several hours each day. At times on certain B. griseocollis territories, the great number of intruding males resulted in a near breakdown of the territorial system, with repeated aggressive interactions and turnover. In preliminary chemical analyses, dichloromethane extracts of heads of B. nevadensis and B. griseocollis were each dominated by single components, while those of B. rufocinctus, in each population studied, had three major components. Extracts of plant parts scent marked by males reveal the presence of the cephalic chemicals not present on unmarked control plants. Mating is initiated on or near territories. The behavioural and morphological correlates of male mating systems in the genus Bombus and other aculeate Hymenoptera are discussed.


2009 ◽  
Vol 77 (1) ◽  
pp. 49-54 ◽  
Author(s):  
Jean-François Lemaître ◽  
Thierry Rigaud ◽  
Stéphane Cornet ◽  
Loïc Bollache

2002 ◽  
Vol 5 (1) ◽  
pp. 45-49 ◽  
Author(s):  
Andreas Niemeitz ◽  
Ralf Kreutzfeldt ◽  
Manfred Schartl ◽  
Jakob Parzefall ◽  
Ingo Schlupp

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