Attachment and life history strategy

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.

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.


2016 ◽  
Vol 31 (2) ◽  
pp. 5-16 ◽  
Author(s):  
Curtis S. Dunkel ◽  
Paul R. Gladden ◽  
Eugene W. Mathes

Author(s):  
Martin Brüne

Human life-history patterns are characterized by slow maturation, long parental dependency, longevity, and low number of offspring. These developmental peculiarities determine the amount of parental investment in offspring and mating effort, and assign an adaptive role to postmenopausal women. Hence evolution has produced specific adaptations pertaining to the relationship of human infants with their primary caregivers, subsumed under the term ‘attachment’. The way attachment patterns or ‘styles’ develop during early infancy coin the child’s view of the world in terms of the emotional availability and trustworthiness of others. Harsh environmental conditions during infancy promote insecure attachment styles and a ‘faster’ life-history strategy, including earlier sexual maturation and sexual activity and less parental investment in own offspring. The opposite is more likely to emerge when children grow up in secure conditions with responsive and emotionally available caregivers. These developmental trajectories have profound implications for social interaction and stress-regulation abilities.


2021 ◽  
Vol 15 (1) ◽  
pp. 10-26 ◽  
Author(s):  
Aurelio José Figueredo ◽  
Steven C. Hertler ◽  
Mateo Peñaherrera-Aguirre

2019 ◽  
Author(s):  
Gretchen F. Wagner ◽  
Emeline Mourocq ◽  
Michael Griesser

Biparental care systems are a valuable model to examine conflict, cooperation, and coordination between unrelated individuals, as the product of the interactions between the parents influences the fitness of both individuals. A common experimental technique for testing coordinated responses to changes in the costs of parental care is to temporarily handicap one parent, inducing a higher cost of providing care. However, dissimilarity in experimental designs of these studies has hindered interspecific comparisons of the patterns of cost distribution between parents and offspring. Here we apply a comparative experimental approach by handicapping a parent at nests of five bird species using the same experimental treatment. In some species, a decrease in care by a handicapped parent was compensated by its partner, while in others the increased costs of care were shunted to the offspring. Parental responses to an increased cost of care primarily depended on the total duration of care that offspring require. However, life history pace (i.e., adult survival and fecundity) did not influence parental decisions when faced with a higher cost of caring. Our study highlights that a greater attention to intergenerational trade-offs is warranted, particularly in species with a large burden of parental care. Moreover, we demonstrate that parental care decisions may be weighed more against physiological workload constraints than against future prospects of reproduction, supporting evidence that avian species may devote comparable amounts of energy into survival, regardless of life history strategy.


Author(s):  
Abraham P. Buunk ◽  
Karlijn Massar ◽  
Pieternel Dijkstra ◽  
Ana María Fernández

This chapter discusses sex differences in intersexual competition and describes particularly the consequences of such competition for conflict between the sexes, as well as for sex differences in mate guarding and, relatedly, in the types of infidelity that evoke jealousy, including online infidelity. It also discusses individual differences in jealousy as related to attachment styles and describes the effects of height, hormones, and the menstrual cycle on jealousy. Next, the chapter moves on to intrasexual competition and discusses, among other topics, intrasexual competition among men and among women, the role of sex differences in rival characteristics in evoking jealousy, the role of attachment styles and hormones, and individual differences in intrasexual competitiveness.


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