Wednesday, February 7, 2018

"The phylogenetic roots of human lethal violence" (2016), and comments on the paper

The phylogenetic roots of human lethal violence. José María Gómez et al. Nature volume 538, pages 233–237 (October 13 2016), https://www.nature.com/articles/nature19758

The psychological, sociological and evolutionary roots of conspecific violence in humans are still debated, despite attracting the attention of intellectuals for over two millennia. Here we propose a conceptual approach towards understanding these roots based on the assumption that aggression in mammals, including humans, has a significant phylogenetic component. By compiling sources of mortality from a comprehensive sample of mammals, we assessed the percentage of deaths due to conspecifics and, using phylogenetic comparative tools, predicted this value for humans. The proportion of human deaths phylogenetically predicted to be caused by interpersonal violence stood at 2%. This value was similar to the one phylogenetically inferred for the evolutionary ancestor of primates and apes, indicating that a certain level of lethal violence arises owing to our position within the phylogeny of mammals. It was also similar to the percentage seen in prehistoric bands and tribes, indicating that we were as lethally violent then as common mammalian evolutionary history would predict. However, the level of lethal violence has changed through human history and can be associated with changes in the socio-political organization of human populations. Our study provides a detailed phylogenetic and historical context against which to compare levels of lethal violence observed throughout our history.



---
Comment on this paper: https://www.theatlantic.com/science/archive/2016/09/humans-are-unusually-violent-mammals-but-averagely-violent-primates/501935


Check also Genetic background of extreme violent behavior. J Tiihonen, M-R Rautiainen, H M Ollila, E Repo-Tiihonen, M Virkkunen, A Palotie, O Pietiläinen, K Kristiansson, M Joukamaa, H Lauerma, J Saarela, S Tyni, H Vartiainen, J Paananen, D Goldman & T Paunio. Molecular Psychiatry volume 20, pages 786–792 (2015). https://www.nature.com/articles/mp2014130


---
Suricata suricatta, violence, violent, meerkat, puma

Machiavellians likely use intimidation impression management tactics when they perceive threat; fairness serves as a cue for them to employ aggressive tactics to regain control, such as intimidation

When do Machiavellians feel threatened? An investigation into fair situations. Rebecca L. Badawy, Robyn L. Brouer, Elizabeth A. Fabrizio. Journal of Research in Personality, https://doi.org/10.1016/j.jrp.2018.02.004

Highlights
•    Machs perceive threat in fair environments.
•    Machs likely use intimidation impression management tactics when they perceive threat.
•    Fairness serves as a cue for Machs to employ aggressive tactics to regain control, such as intimidation.
•    Machs perceive a lower level of threat in unfair situations, suggesting that unfair situations may appeal to Machs because they are more easily able to rely on strategic manipulation.

Abstract: The Machiavellian (Mach) personality trait describes individuals who rely on manipulative strategies to achieve their goals, which are primarily extrinsic (money, success, power), often at the cost of interpersonal relationships. However, little is known about the environmental conditions that cue Machs to act in deviant ways. We explore the impact of fair environments on Machs’ perceptions of threat. Tested in an experimental study (N = 311), our results provide preliminary evidence that, contrary to normative responses to fairness, Machs have negative cognitive (experience threat) and behavioral intention (intimidation tactics) reactions to fair situations, and thus might actually function more normatively in unfair environments.

If nonhuman animals can suicide, why don’t they? On Peña-Guzman (2017) on Animal Suicide

Soper, C. A. and Shackelford, Todd K. (2018) If nonhuman animals can suicide, why don’t they?. Animal Sentience 20(14). http://animalstudiesrepository.org/animsent/vol2/iss20/14/

Abstract: An evolutionary analysis suggests that selection is unlikely to have tolerated the capacity for intentional self-killing in nonhuman animals. The potential to escape pain by suicide would have presented a recurrent and severe adaptive problem for an animal with a reproductive future to protect. If the potential for suicide arose in the evolutionary past, anti-suicide mechanisms may have co-evolved, as we believe they have in adult humans. Peña-Guzmán’s (2017) argument that some nonhuman animals can suicide is incomplete without an account of the defences that result in the vast majority opting not to.

---
Peña-Guzman (2017) questions whether only humans suicide. (We use “suicide” as a verb, to
bypass the morally loaded “commit.”) He argues that nonhuman animals might, if not kill
themselves intentionally, behave on a continuum of suicidality. Peña-Guzmán advances this
position with evidence from three domains: First, aspects of emotional states and pathologies
associated with human suicidality are also found in other species. Second, nonhumans
sometimes die as a consequence of self-neglect or self-injury (and there are anecdotal reports
of apparently intentional self-killings among diverse fauna). Third, the use of laboratory
animals to model neurological and behavioural correlates of human suicidality implies an
acceptance that these animals provide valid homologues. Challenging what he views as a
premature consensus that suicide is uniquely human, Peña-Guzmán synthesises disparate
research sources, and raises important ethical questions for animal welfare.

Peña-Guzmán does not convince us that animals can suicide, for three reasons. First,
his definition of suicide – specifically including nonhumans and embracing incidental deaths
that arise from risk-taking rather than the intentional self-killing that characterises suicide
(Fairbairn, 2003; WHO, 2014) – sets up a circular track to Peña-Guzmán’s “continuist” conclusion. His argument illustrates Baechler's (1975/1979) point that an entire theory of
suicide is sometimes contained in the definition of suicide proposed by its author.
Second, although there is not space here for an itemized critique, much of the
empirical substance of Peña-Guzmán’s position is flawed. For example, he refers to child
suicide as if it is a unitary phenomenon, overlooking the emergence of suicide risk in normal
development: completed suicide among children under the age of ten years is rare, and under
five years virtually unknown (Nock et al., 2013). Peña-Guzmán refers in passing to suicide
among people with “severe cognitive disabilities” as if this were well-documented and
uncontroversial; yet, although mild to moderate intellectual disability (ID) is linked with
suicidality, there is little evidence of suicide among those with severe ID (Merrick, Merrick,
Lunsky, & Kandel, 2006).

There is no robust evidence of nonhuman suicides, notwithstanding countless
opportunities for such self-killings, if they occurred, to be documented by the world’s farmers,
animal breeders, naturalists, and scientists (Preti, 2007). We are left with anecdote and fable,
including the scorpion’s self-sting, proffered by Peña-Guzmán as an example of animal suicide
despite clear evidence that scorpions cannot sting themselves to death (Andreotti & Sabatier,
2013).

Scorpions are immune to their own venom, presumably because selection has
eliminated the germ lines of scorpions that were not so protected. The ubiquity of such
specific, self-preserving adaptations connects to a third, theoretical, problem with animal
suicide: the absence of a coherent explanation as to how selection could favour and maintain
such a capability. Many organisms sacrifice their soma according to algorithms of inclusive
fitness: non-breeding siblings in eusocial colonies – hymenopteran insects, for example – often
die defending the colony; other organisms that breed only once have nothing to lose by dying
once their reproductive work is done. But neither of these behaviours constitutes suicide in a
meaningful sense of the word – and neither reproductive strategy characterises dolphins,
scorpions, or most of the other candidates for animal suicide suggested by Peña-Guzmán.
Most animals have reproductive futures to defend, and hence have good genetic reason to
remain alive.

Suicide is not observed in nonhumans for a straightforward evolutionary reason: any
genes that permitted suicide would have been eliminated along with the suicides’ bodies. Any
animal that, in the absence of restraints, was capable of escaping its pain and suffering by selfkilling
would be expected to seize the opportunity, because some pain is unavoidable in the
Malthusian theatre in which selection plays out, and because pain is designed to motivate
action to escape. A suicidal animal, if it appeared, would face a predictable and severe
adaptive problem – the kind of problem that selection would expectably and powerfully have
addressed in the evolutionary past.

The most parsimonious explanation for the apparent absence of suicide among
younger children, the severely cognitively impaired, and nonhuman animals, is that these
populations lack the cognitive wherewithal to conceive and enact it (Baechler, 1975/1979).
Peña-Guzmán (2017) may be right that the difference in the cognitive abilities of humans
compared to other animals is a matter of degree, not kind, but this continuity does not
preclude a threshold effect: Humans alone cross a cognitive floor for suicide (Perry, 2014) as
the brain matures, usually around puberty. That most adolescent and adult humans can and
do endure misery without resorting to suicide points to the existence of powerful anti-suicide
defences, evolved mechanisms that emerge in normal mature humans. The possible nature of
these defences is the subject of a forthcoming book-length discussion (Soper, 2018). The point to make here is that Peña-Guzmán’s argument that nonhuman animals occasionally suicide to
end their suffering is incomplete without an account of the evolved protections that thwart
the vast majority from exploiting this supposedly available means of escape.

 [References in link above.]

Sexual arousal by dominance and submissiveness was long considered as pathology; surprisingly, approximately half of respondents were excited by their partner’s submission or their own submission

Sexual Arousal by Dominance and Submissiveness in the General Population: How Many, How Strongly, and Why? Eva Jozifkova. Deviant Behavior, https://doi.org/10.1080/01639625.2017.1410607

ABSTRACT: Sexual arousal by dominance and submissiveness was long considered as pathology. Surprisingly, approximately half of respondents (n = 673) were excited by their partner’s submission or their own submission. A strong preference was found in 8.2% of respondents. Respondents of 6.1% were not even excited by equality, but only by disparity. The respondents differed in the type of disparity that they prefer, and how strongly they preferred this disparity. We suggest that sexual arousal by dominance and submissiveness is related to a common mating strategy.

Closed-loop stimulation of temporal cortex rescues functional networks and improves memory

Closed-loop stimulation of temporal cortex rescues functional networks and improves memory. Youssef Ezzyat et al. Nature Communications, volume 9, Article number: 365 (2018), doi:10.1038/s41467-017-02753-0

Abstract: Memory failures are frustrating and often the result of ineffective encoding. One approach to improving memory outcomes is through direct modulation of brain activity with electrical stimulation. Previous efforts, however, have reported inconsistent effects when using open-loop stimulation and often target the hippocampus and medial temporal lobes. Here we use a closed-loop system to monitor and decode neural activity from direct brain recordings in humans. We apply targeted stimulation to lateral temporal cortex and report that this stimulation rescues periods of poor memory encoding. This system also improves later recall, revealing that the lateral temporal cortex is a reliable target for memory enhancement. Taken together, our results suggest that such systems may provide a therapeutic approach for treating memory dysfunction.