scholarly journals Dimorphic sperm-transfer strategies and alternative mating tactics in loliginid squid

2014 ◽  
Vol 81 (1) ◽  
pp. 147-151 ◽  
Author(s):  
Y. Iwata ◽  
Y. Sakurai ◽  
P. Shaw
1996 ◽  
Vol 7 (3) ◽  
pp. 334-340 ◽  
Author(s):  
Paula Stockley ◽  
Jeremy B. Searle ◽  
David W. Macdonald ◽  
Catherine S. Jones

2021 ◽  
Vol 18 (1) ◽  
Author(s):  
Lenka Sentenská ◽  
Aileen Neumann ◽  
Yael Lubin ◽  
Gabriele Uhl

Abstract Background Mating generally occurs after individuals reach adulthood. In many arthropods including spiders, the adult stage is marked by a final moult after which the genitalia are fully developed and functional. In several widow spider species (genus Latrodectus), however, immature females may mate a few days before they moult to adulthood, i.e. in their late-subadult stage. While the “adult” mating typically results in cannibalism, males survive the “immature” mating. During both “immature” and “adult” matings, males leave parts of their paired copulatory organs within female genitalia, which may act as mating plugs. To study potential costs and benefits of the two mating tactics, we investigated female genital morphology of the brown widow spider, L. geometricus. Light microscopy, histology and micro-computed tomography of early-subadult, late-subadult and adult females were conducted to determine the overall pattern of genital maturation. We compared genitalia of mated late-subadult and adult females to reveal potential differences in the genitalic details that might indicate differential success in sperm transfer and different environments for sperm storage and sperm competition. Results We found that the paired sperm storage organs (spermathecae) and copulatory ducts are developed already in late-subadult females and host sperm after immature mating. However, the thickness of the spermathecal cuticle and the staining of the secretions inside differ significantly between the late-subadult and adult females. In late-subadult females mating plugs were found with higher probability in both spermathecae compared to adult females. Conclusions Sperm transfer in matings with late-subadult females follows the same route as in matings with adult females. The observed differences in the secretions inside the spermathecae of adult and late-subadult females likely reflect different storage conditions for the transferred sperm which may lead to a disadvantage under sperm competition if the subadult female later re-mates with another male. However, since males mating with late-subadult females typically transfer sperm to both spermathecae they might benefit from numerical sperm competition as well as from monopolizing access to the female sperm storage organs. The assessment of re-mating probability and relative paternity will clarify the costs and benefits of the two mating tactics in light of these findings.


2008 ◽  
Vol 20 (1) ◽  
pp. 153-159 ◽  
Author(s):  
Craig A. Walling ◽  
Clare E. Stamper ◽  
Claire L. Salisbury ◽  
Allen J. Moore

2020 ◽  
pp. 27-62
Author(s):  
John M. McNamara ◽  
Olof Leimar

Standard examples in biological game theory are introduced. The degree of cooperation at evolutionary stability is analysed in models that deal with situations such as the Prisoner’s Dilemma, the Tragedy of the Commons and the conflict of interest between parents over care of their common young. Several models of aggressive interactions are treated in this book. In this chapter the Hawk–Dove game, which is the simplest of these models, is analysed. Further models in the chapter deal with the situation in which individuals vary in their fighting ability and the situation in which information about the opponent is available before an individual decides whether to be aggressive. The problem of the allocation of resources to sons versus daughters has played a central role in biological game theory. This chapter introduces the basic theory, as well as a model in which the environmental temperature affects the development of the sexes differentially, so that at evolutionary stability the sex of offspring is determined by this temperature. Coordination games, alternative mating tactics, dispersal to avoid kin competition, and the idea that signals can evolve from cues are also introduced.


2003 ◽  
Vol 81 (6) ◽  
pp. 1025-1033 ◽  
Author(s):  
Damian C Lidgard ◽  
Daryl J Boness ◽  
W Don Bowen ◽  
Jim I McMillan

We examined the diving behaviour of breeding male grey seals (Halichoerus grypus) at Sable Island, Nova Scotia, from 1997 to 2001. The proportion of time spent at sea varied between 0 and 78% (N = 30). Males engaged in deep (43.4 ± 3.3 m (mean ± SE), N = 27) diving, and these dives were clustered into bouts, which mostly occurred during long trips (62.2 ± 14.7 h). We suggest that males spent time foraging during deep dives. Shallow diving (5.9 ± 0.1 m, N = 27) accounted for 40.8% of dives, which were also clustered into bouts that mostly occurred during short trips (2.1 ± 0.37 h). We suggest that shallow diving comprised a suite of behaviours, but included little foraging behaviour. Phenotypic traits had little influence on diving behaviour. Further work is required to understand the extent to which foraging behaviour enhances reproductive success, and whether shallow diving is a component of the mating tactics of male grey seals at Sable Island.


2009 ◽  
Vol 87 (8) ◽  
pp. 684-688 ◽  
Author(s):  
Tero Toivanen ◽  
Markus J. Rantala ◽  
Jukka Suhonen

Alternative mating tactics are a widespread feature in insects. A typical form of alternative mating behaviour is being a sneaker in the vicinity of a territorial male. Such nonterritorial males have lower mating success, but they may benefit from lower energetic costs and decreased predation risk. In this study, we examined whether nonterritorial male damselflies Calopteryx virgo (L., 1758) are subject to lower predation risk than territorial males. To distinguish predation from other sources of mortality, we used models. The experiment consisted of dried male damselflies settled into the typical perching positions of territorial and nonterritorial males. Also the spatiotemporal patterns of predation risk were studied. The survival of nonterritorial male models was consistently higher than that of territorial male models, which can be attributed to different predation risk. Survival of the models was lower in the presence of avian predators and in large populations. Survival rates were affected by habitat type but did not change during the season. We conclude that nonterritorial male damselflies are less vulnerable to predation and that there may be a trade-off which could potentially make the fitness of sneakers equal to that of territorial males.


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