Factors Influencing Realized Sex Ratios in Fig Wasps: Double Oviposition and Larval Mortalities

2011 ◽  
Vol 25 (3) ◽  
pp. 254-263 ◽  
Author(s):  
Salah Ghana ◽  
Nazia Suleman ◽  
Stephen G. Compton
Bird-Banding ◽  
1976 ◽  
Vol 47 (4) ◽  
pp. 340 ◽  
Author(s):  
Martha Hatch Balph ◽  
David F. Balph

Oikos ◽  
2019 ◽  
Vol 128 (6) ◽  
pp. 859-868 ◽  
Author(s):  
Nico Chung ◽  
Jason Pienaar ◽  
Jaco M. Greeff

2022 ◽  
Vol 19 (1) ◽  
Author(s):  
Jaco M. Greeff ◽  
Finn Kjellberg

AbstractLocal mate competition (LMC) favours female biased clutch sex ratios because it reduces competition between brothers and provides extra mating opportunities for sons. Fig wasps seem to fit LMC model assumptions and lay female-biased sex ratios as predicted. These female biased sex ratios increase fitness greatly. In line with predictions, their sex ratios become less female-biased as the number of mothers laying in the same fig increases. However, this variation results in comparatively small fitness benefits compared to just biased ratios and data suggest substantial mismatches with LMC theory. The mismatches are due to several factors. (1) Multiple foundresses typically lay too many daughters. (2) Single foundress sex ratios are explained by sequential oviposition and ladies-last models. (3) Mortality that typically exceeds 10% may decouple the link between primary sex ratios, the focus of model predictions, and secondary sex ratios of adult wasps that are counted by researchers. (4) Model assumptions are frequently violated: (a) clutch sizes are unequal, (b) oviposition may not be simultaneous (c) cryptic/multiple wasp species inhabit the same host, (d) foundress numbers are systematically undercounted, (e) inbreeding coefficient calculations are inaccurate, and (f) male wasps sometimes disperse. These data and calculations suggest that alternative explanations must be considered seriously. Substantial data show that wasps typically lay most of their male eggs first followed by mostly female eggs require a new approach. These “slope” strategies result in more accurate sex ratios that are automatically adjusted to foundress number, own and relative clutch sizes and to sequential clutches. This effect will alter sex ratios in all species once the egg capacity of a fig is crossed or when interference reduces clutch sizes. In addition to this passive response, the females of about half the studied species have a conditional response that reduces female bias under higher foundress numbers by laying more sons. Therefore, wasps seem to use a very simple strategy that increases their fitness. Natural selection could have optimized parameters of the slope strategy and possibly the existence of the slope strategy itself. Variation in the slope strategy that is the result of natural selection is adaptive. Research should therefore focus on quantifying variables of this slope strategy. Currently, it is unclear how much of the variation is adaptive as opposed to being coincidental by-products. Graphical Abstract


2015 ◽  
Author(s):  
Md. Talukder ◽  
Ubaidur Rob ◽  
Md. Hossain ◽  
Forhana Noor

2014 ◽  
Vol 57 ◽  
pp. 73-79 ◽  
Author(s):  
Finn Kjellberg ◽  
Nazia Suleman ◽  
Shazia Raja ◽  
Abelouahad Tayou ◽  
Martine Hossaert-McKey ◽  
...  

1996 ◽  
Vol 21 (3) ◽  
pp. 300-302 ◽  
Author(s):  
JACO M. GREEFF ◽  
STEPHEN G. COMPTON
Keyword(s):  

2011 ◽  
Vol 86 (4) ◽  
pp. 401-405 ◽  
Author(s):  
S. D'Ávila ◽  
E.C.A. Bessa ◽  
S. Souza-Lima ◽  
M.L.A. Rodrigues

AbstractIn the present study populations of the avian nematode species Baruscapillaria obsignata are described from Columba livia. Male and female individuals were obtained from 27 birds, fixed in alcohol/formalin/acetic acid (AFA) and preserved in 70% ethanol. Nematodes were identified and then counted under a stereoscopic microscope. Baruscapillaria obsignata were much more frequent in the anterior third of the small intestine, and females were more abundant than males in all infra populations. The prevalence was 55.6%, mean intensity was 11.8 (median 11.0; range 1–31) and abundance 6.56. In the present study, we observed an aggregated distribution of parasite infrapopulations, as demonstrated by the value of the exponent of the negative binomial distribution, K = 0.2773; by the discrepancy index, D = 0.656 and by the variance/mean ratio, 12.44. The female/male sex ratios found in all infrapopulations were always greater than 1, showing a bias in favour of female abundance. This tendency was especially marked in infrapopulations containing fewer individuals. The sizes of infrapopulations ranged from 5 to 31 individuals. The mean sex ratio observed was 2.69 ± 3.28 (median 1.83; range 0–11). In infrapopulations with 5–15 individuals, the sex ratios observed varied from 2.6 to 11, while in those with 17–31 individuals, the sex ratios were lower, ranging from 1.7 to 2.4. There was a negative correlation between the intensity of infection and the sex ratio of infrapopulations. Results are discussed in terms of possible factors influencing the processes that lead to niche restriction and biased sex ratios in parasite infrapopulations.


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