Male-biased sex ratio in Argulus canadensis Wilson, 1916 (Crustacea: Branchiura) ectoparasitic on sticklebacks

1989 ◽  
Vol 67 (8) ◽  
pp. 2078-2080 ◽  
Author(s):  
Robert Poulin ◽  
Gerard J. FitzGerald

Females of the ectoparasitic crustacean Argulus canadensis must leave their fish hosts at least temporarily to deposit their eggs on the substrate. To test the hypothesis that this difference in reproductive behaviour between the two sexes could result in male-biased sex ratios on their stickleback hosts, we sampled sticklebacks in tide pools of a Quebec salt marsh from early July to early September 1986. During this period, fish harboured significantly more male than female A. canadensis. Laboratory experiments were done to test two alternative hypotheses offered to explain this biased sex ratio. The first hypothesis was that male A. canadensis were more successful than females in attacking their stickleback hosts; however, we found no differences in attack success on their hosts between the two parasite sexes. The second hypothesis was that sticklebacks ate more female than male A. canadensis. Although males were less vulnerable to fish predation than females, the difference was not significant. We conclude that sexual differences in reproductive behaviour, i.e., egg deposition behaviour of females, can account for the male-biased sex ratio of A. canadensis on sticklebacks.

2016 ◽  
Author(s):  
Yaqiang Wang ◽  
Ruiwu Wang ◽  
Yaotang Li ◽  
Zhanshan (Sam) Ma

There are three sex ratio strategies (SRS) in nature—male-biased sex ratio, female-biased sex ratio and, equal sex ratio depending on the proportion of male offspring being greater than, less than, or equal to ½. The problem was already noted in Darwin’s (1859) “Origin of Species,” and it was R. A. Fisher (1930) who first explained why most species in nature display a sex ratio of ½. Consequent SRS theories such as Hamilton’s (1967) local mate competition (LMC) and Clark’s (1978) local resource competition (LRC) separately explained the observed deviations from the seemingly universal 1:1 ratio. However, to the best of our knowledge, there is not yet a unified theory that accounts for the mechanisms of the three SRS. Here, we introduce the price elasticity theory in economics to define sex ratio elasticity (SRE), and present an analytical model that derives three SRSs based on the following assumption: simultaneously existing competitions for both resources and mates influence the level of SRE in both sexes differently. Consequently, it is the difference (between two sexes) in the level of their sex ratio elasticity that leads to three different SRS. Our analytical results demonstrate that the elasticity-based model not only reveals a highly plausible mechanism that explains the evolution of SRS in nature, but also offers a novel framework for unifying two major classical theories (i.e., LMC & LRC) in the field of SRS research.


Behaviour ◽  
2015 ◽  
Vol 152 (5) ◽  
pp. 653-666 ◽  
Author(s):  
Clint D. Kelly

The duration of mate guarding by males is predicted to vary in accordance with the risk of sperm competition or mate encounter rate. Mate guarding is predicted to be prolonged under a male-biased sex ratio because the risk of sperm competition is high or the mate encounter rate is low. A consistently male-biased sex ratio should thus select for greater mate fidelity, and reduced plasticity in guarding behaviour, by males. Micrarchus hystriculeus Westwood (Phasmatodea) is a sexually size dimorphic stick insect in which males form prolonged post-insemination associations with their mates and whose populations have a consistently male-biased sex ratio. My laboratory experiments showed, as predicted, little plasticity by males in the duration of their post-insemination association. Although mate guarding duration is similar under male- and female-biased sex ratios, males clasped the genitalia of their mates significantly more often under a male-biased sex ratio, suggesting that males intensify their guarding with increasing risk of sperm competition.


2010 ◽  
Vol 142 (6) ◽  
pp. 589-595 ◽  
Author(s):  
Hanae Yamashita ◽  
Katsumi Togashi ◽  
Keizi Kiritani

AbstractCarabid beetles can escape from pitfall traps. To determine whether or not a female-biased sex ratio for catches of Carabus lewisianus Breuning from pitfall traps could be explained by sexual differences in the rates of capture by and escape from traps, we performed two laboratory experiments to estimate these rates using mathematical models. The results indicated that the two sexes dropped into the pitfall traps at almost equal rates (0.0456/min for females and 0.0366/min for males) and that males escaped from the traps at rates of 0.0591 and 0.0889/min, but no females managed to escape. The bias of escape rates in the field is shown by the higher captures of female C. lewisianus by pitfall traps. Calibration of capture and escape rates suggested similar activity densities of the two sexes in the field. Development of more accurate measures of the number of the relevant sex on the soil surface, and of the methodology for estimating the values of parameters in the field is discussed.


2016 ◽  
Author(s):  
Yaqiang Wang ◽  
Ruiwu Wang ◽  
Yaotang Li ◽  
Zhanshan (Sam) Ma

There are three sex ratio strategies (SRS) in nature—male-biased sex ratio, female-biased sex ratio and, equal sex ratio depending on the proportion of male offspring being greater than, less than, or equal to ½. The problem was already noted in Darwin’s (1859) “Origin of Species,” and it was R. A. Fisher (1930) who first explained why most species in nature display a sex ratio of ½. Consequent SRS theories such as Hamilton’s (1967) local mate competition (LMC) and Clark’s (1978) local resource competition (LRC) separately explained the observed deviations from the seemingly universal 1:1 ratio. However, to the best of our knowledge, there is not yet a unified theory that accounts for the mechanisms of the three SRS. Here, we introduce the price elasticity theory in economics to define sex ratio elasticity (SRE), and present an analytical model that derives three SRSs based on the following assumption: simultaneously existing competitions for both resources and mates influence the level of SRE in both sexes differently. Consequently, it is the difference (between two sexes) in the level of their sex ratio elasticity that leads to three different SRS. Our analytical results demonstrate that the elasticity-based model not only reveals a highly plausible mechanism that explains the evolution of SRS in nature, but also offers a novel framework for unifying two major classical theories (i.e., LMC & LRC) in the field of SRS research.


Author(s):  
Massimiliano Di Ventra

This chapter expands on the previous one on the role of experiments in Science. It explains the difference between observations of phenomena and controlled laboratory experiments.


Author(s):  
Ester Premate ◽  
Špela Borko ◽  
Simona Kralj‐Fišer ◽  
Michael Jennions ◽  
Žiga Fišer ◽  
...  
Keyword(s):  

2013 ◽  
Vol 9 (2) ◽  
pp. 20130027 ◽  
Author(s):  
A. Chipman ◽  
E. Morrison

Human mating and reproductive behaviour can vary depending on various mechanisms, including the local sex ratio. Previous research shows that as sex ratios become female-biased, women from economically deprived areas are less likely to delay reproductive opportunities to wait for a high-investing mate but instead begin their reproductive careers sooner. Here, we show that the local sex ratio also has an impact on female fertility schedules. At young ages, a female-biased ratio is associated with higher birth rates in the poorest areas, whereas the opposite is true for the richest areas. At older ages, a female-biased ratio is associated with higher birth rates in the richest, but not the poorest areas. These patterns suggest that female–female competition encourages poorer women to adopt a fast life-history strategy and give birth early, and richer women to adopt a slow life-history strategy and delay reproduction.


The Auk ◽  
1990 ◽  
Vol 107 (4) ◽  
pp. 765-771 ◽  
Author(s):  
J. David Ligon ◽  
Sandra H. Ligon
Keyword(s):  

Oecologia ◽  
1999 ◽  
Vol 118 (1) ◽  
pp. 16-22 ◽  
Author(s):  
Roxana Torres ◽  
Hugh Drummond

1991 ◽  
Vol 69 (1) ◽  
pp. 208-212 ◽  
Author(s):  
Dan L. Johnson ◽  
Heather C. Proctor

The effect of predator presence on the adult sex ratio of a spider mite (Panonychus ulmi) was examined in a field experiment. Phytoseiid predators (chiefly Typhlodromus occidentalis) were removed from 32 trees harboring P. ulmi populations, and allowed to remain at natural levels on 32 other trees. Both total population density and proportion of males in the prey population were significantly higher in predator-free trees. Mechanisms that could explain the increase in the proportion of males are examined. The most probable is that greater male activity results in a higher encounter rate between predator and prey, and that subsequent higher male mortality when predators are present exaggerates the female-biased sex ratio. The theoretical effects of sex-biased predation on diplo-diploid and haplo-diploid organisms are discussed.


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