scholarly journals Sex Differences in Moral Reasoning: The Role of Intelligence and Life History Strategy

2016 ◽  
Vol 31 (2) ◽  
pp. 5-16 ◽  
Author(s):  
Curtis S. Dunkel ◽  
Paul R. Gladden ◽  
Eugene W. Mathes
2016 ◽  
Vol 17 (2) ◽  
pp. 552 ◽  
Author(s):  
A. GRAU ◽  
F. SABORIDO-REY ◽  
E. PASTOR ◽  
M. PALMER ◽  
E. MASSUTÍ-PASCUAL ◽  
...  

Common dentex Dentex dentex is an iconic endangered species in the Mediterranean where is a sought after target species for small-scale, recreational and spearfishing fisheries. The reproductive biology of D. dentex in the natural environment is poorly known; therefore the reproductive strategy of the species was assessed by combining reproductive traits with the growth characteristics (estimated from length-at-age data), the size/age of sexual maturity and the energetic dynamics. A total of 358 wild fish were sampled on Mallorca Island (W Mediterranean) from March 1996 to June 1999 with a 19 to 84.7 cm total length (LT) range. The sex ratio was skewed towards females (1.361) albeit the length composition was not different between sexes (p = 0.551). Three young immature individuals (< 28 cm LT, 0.8% individuals) were rudimentary hermaphrodites supporting the late gonochoristic species classification. The age composition determined from sagitta otolith interpretation ranged from 0 to 26 years (yr). Concerning growth, between sex differences in von Bertalanffy parameters were not relevant, even after accounting for potential between-year differences. The most noticeable difference was found for L∞ (64.7 cm for females versus 61.6 for males) but even in this case, the bayesian credibility interval of between-sex differences included zero.  Maturity ogives at size and age showed that females achieved 50% maturity at 34.9 cm LT and 3.3 years, while males did at 33.8 cm LT and 2.5 years. The onset of gonad developing phase took place in December, while it progresses until April. The spawning peak was in April and May for both sexes. A generalized linear model showed that female size didn’t affect significantly the spawning season, whilst there was a strong seasonality in the spawning. Most of the evidences showed that fecundity is likely determinate, with an asynchronous oocyte development before spawning and a clear ovarian bimodal organization after the onset of spawning. Female weight explained 84% of the observed variance for fecundity. The gonadosomatic, hepatosomatic and condition indexes varied significantly with the reproductive season for females and only the gonadosomatic index for males. Storage in muscle seemed to be the primary source of energy for reproduction, although liver appeared to play a short-term role in egg production, suggesting a combination of capital and income breeding. The results indicate that the life history strategy of common dentex possess consist on maturing well before reaching maximum size, investing in growth after maturation, and therefore the reproductive effort is distributed through a longer lifespan and related with the size attained after maturation. At present no management measures are directed to D. dentex; given its life history strategy we suggest that a slot limit should be implemented, i.e. a minimum and a maximum landing size, with a minimum size of 35 cm. The upper threshold, to protect the higher reproductive potential of older and larger fish, should still be defined.


2020 ◽  
Vol 16 (1) ◽  
pp. 20190727 ◽  
Author(s):  
Joshua S. Madin ◽  
Andrew H. Baird ◽  
Marissa L. Baskett ◽  
Sean R. Connolly ◽  
Maria A. Dornelas

Body size is a trait that broadly influences the demography and ecology of organisms. In unitary organisms, body size tends to increase with age. In modular organisms, body size can either increase or decrease with age, with size changes being the net difference between modules added through growth and modules lost through partial mortality. Rates of colony extension are independent of body size, but net growth is allometric, suggesting a significant role of size-dependent mortality. In this study, we develop a generalizable model of partitioned growth and partial mortality and apply it to data from 11 species of reef-building coral. We show that corals generally grow at constant radial increments that are size independent, and that partial mortality acts more strongly on small colonies. We also show a clear life-history trade-off between growth and partial mortality that is governed by growth form. This decomposition of net growth can provide mechanistic insights into the relative demographic effects of the intrinsic factors (e.g. acquisition of food and life-history strategy), which tend to affect growth, and extrinsic factors (e.g. physical damage, and predation), which tend to affect mortality.


2009 ◽  
Vol 32 (1) ◽  
pp. 26-27 ◽  
Author(s):  
Aurelio José Figueredo ◽  
Jon A. Sefcek ◽  
Sally G. Olderbak

AbstractDel Giudice addresses a complex and pertinent theoretical issue: the evolutionary adaptiveness of sex differences in attachment styles in relation to life history strategy. Although we applaud Del Giudice for calling attention to the problem, we regret that he does not sufficiently specify how attachment styles serve as an integral part of a coordinate life history strategy for either sex.


2021 ◽  
Vol 30 (1) ◽  
pp. 31-56
Author(s):  
Asmir Gračanin ◽  
Kevin Kutnjak ◽  
Igor Kardum

Previous research (Laeng et al., 2007) conducted on Norwegian samples showed that blue-eyed men rate blue-eyed women as more attractive, while brown-eyed men and all the women show no differences in attractiveness assessments with respect to eye colour. Correspondingly, positive assortative mating was found for blue, but not brown eyes, and it most often occurred in blue-eyed men. We aimed to replicate this blue-like-blue effect in the Croatian population, which differs in the ratio of eye colour phenotypes (blue eye colour is the most prevalent in Norway while brown is the most prevalent in Croatia). Additionally, we examined whether this effect is moderated by life history strategies and sociosexuality. Our hypothesis was that the effect would be larger in those blue-eyed men who exert a slower life history strategy and who are sociosexually restrictive. One hundred and twenty-eight participants assessed the attractiveness of blue-eyed and brown-eyed models, whose eye colours were experimentally manipulated in such a way that participants were shown models with natural or artificially changed eye colours. The blue-like-blue effect was replicated in the context of preferences, although it was smaller than in the original study. However, unlike the original study, in a sample of 138 participants no assortative pairing by eye colour was found between participants and their romantic partners. Finally, the hypothesis about the moderation was supported for life history strategies, but not for sociosexuality. In addition to the rationale for the blue-like-blue effect based on the paternity uncertainty account, which was offered by the authors of the original study, we discussed other accounts of this phenomenon.


2021 ◽  
Vol 15 (1) ◽  
pp. 27-41
Author(s):  
Curtis S. Dunkel ◽  
Jonathan J. Hammersley ◽  
Micheal L. Waters ◽  
Dimitri van der Linden ◽  
Laureon A. Merrie ◽  
...  

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