The ‘Thing’ from this world

Science progresses by making contrasts, and the living world is a gold mine of contrasts. Often disciplines become victims by focusing on too narrow a slice of that diversity, leading to a myopic view of how nature works. The relationships between the brain and behavior have been intensively studied in vertebrates, especially mammals, and we have become complacent in our assumptions about how behavior is constructed. As the target article by Mather (2019) shows, the relationship between the brain and behavior in octopuses forces us to reevaluate some of those assumptions

Guilty as charged

Sheep have had a bad rap with regard to their behavioral capabilities, and to a large extent, that negative view of sheep has arisen from our failure as human observers to view the world from the perspective of the sheep themselves. Studies sensitive to what sheep identify as of value in the world have revealed a different picture: sheep have cognitive, emotional and social complexity beyond our crude stereotype. Clearly, what we need to do is to evaluate non-human animals on their own terms and not as a reflection of ourselves

Targets, tactics, and cooperation in the play fighting of two genera of old world monkeys (Mandrillus and Papio): Accounting for similarities and differences

Play fighting in many species involves partners competing to bite one another while avoiding being bitten. Species can differ in the body targets that are bitten and the tactics used to attack and defend those targets. However, even closely related species that attack and defend the same body target using the same tactics can differ markedly in how much the competitiveness of such interactions is mitigated by cooperation. A degree of cooperation is necessary to ensure that some turn-taking between the roles of attacker and defender occurs, as this is critical in preventing play fighting from escalating into serious fighting. In the present study, the dyadic play fighting of captive troops of 4 closely related species of Old World monkeys, 2 each from 2 genera of Papio and Mandrillus, was analyzed. All 4 species have a comparable social organization, are large bodied with considerable sexual dimorphism, and are mostly terrestrial. In all species, the target of biting is the same – the area encompassing the upper arm, shoulder, and side of the neck – and they have the same tactics of attack and defense. However, the Papio species exhibit more cooperation in their play than do the Mandrillus species, with the former using tactics that make biting easier to attain and that facilitate close bodily contact. It is possible that species differences in how rigidly dominance relationships are maintained are expressed in the play of juveniles by altering the balance between competition and cooperation

The Goldilocks Principle: Balancing Familiarity and Novelty in the Selection of Play Partners in Groups of Juvenile Male Rats

Like many mammals, rats frequently engage in play fighting as juveniles, an activity that influences the development of socio-cognitive skills. Most studies that assess play are based on staged dyadic encounters, implying that some average quantity and quality of play are sufficient to produce these developmental effects. However, there are individual differences, with some rats not only preferring to play more, but also to have more physical contact than others. Given that rats have individual differences in play, it raises the possibility that rats might express these preferences when playing in groups. To determine whether rats form partner preferences, trials were conducted in which a focal rat was given the opportunity to play with three partners of varying familiarity. One partner was a cage mate, another was housed on the other side of a transparent and perforated divider and so familiar, but not a prior play partner, and the third was a stranger from another cage. A total of 36 focal rats, between 30-36 days of age, were tested and video recorded in 20-minute trials following 2.5 h of social isolation. Focal rats expressed a preference for neighbors over both strangers and cage mates, indicating that balancing between familiarity and novelty influences social play partner preferences. Mechanisms by which this preference might have been established, such as dominance relationships, weight differences, and congruency of play style, were investigated, but none were correlated with the preferences expressed. This group dynamics perspective provides a novel approach to studying play, and more generally, provides insights into social exploration and decision-making

The development of strain typical defensive patterns in the play fighting of laboratory rats

Open access article. Creative Commons Attribution 4.0 International License (CC BY 4.0) appliesDuring play fighting, rats attack and defend the nape, which if contacted is nuzzled with the snout. While all strains of rats use the same suite of defensive tactics to protect the nape, different strains use some tactics more frequently. This study tests two hypotheses for this strain difference: (1) each strain has a preference for using particular tactics and (2) strain differences in defense are a byproduct of strain differences in patterns of nape attack. Juvenile Long-Evans (LE) and Sprague-Dawley (SD) males, raised in same strain quads from shortly after weaning to the early juvenile period (i.e., 24-31 days), were tested with unfamiliar same-strain and different-strain partners (Experiment 1) and LE and SD males raised in mixed LE-SD quads were tested with both familiar (Experiment 2) and unfamiliar same-strain and different-strain partners. If hypothesis (1) were true, they would maintain strain-typical defense patterns irrespective of the strain of the attacking partner, whereas if hypothesis (2) were true, it would vary with the strain of the attacking partner. Hypothesis (1) was supported in the first experiment; all the rats maintained their strain-typical patterns regardless of the partner’s strain. However, Experiments 2 and 3 supported neither hypothesis, as each animal displayed strain-divergent behavior when playing with partners of either strain. Given that in Experiments 2 and 3, subjects were reared in mixed-strain groups, it is possible that, during the early juvenile period, play fighting experiences shape strain-typical patterns of use of defensive tactics.Ye

Toward a Theory of the Evolution of Fair Play

Juvenile animals of many species engage in social play, but its functional significance is not well understood. This is especially true for a type of social play called fair play (Fp). Social play often involves behavioral patterns similar to adult behaviors (e.g., fighting, mating, and predatory activities), but young animals often engage in Fp behaviors such as role-reversals and self-handicapping, which raises the evolutionary problem of why Fp exists. A long-held working hypothesis, tracing back to the 19th century, is that social play provides contexts in which adult social skills needed for adulthood can be learned or, at least, refined. On this hypothesis, Fp may have evolved for adults to acquire skills for behaving fairly in the sense of equitable distribution of resources or treatment of others. We investigated the evolution of Fp using an evolutionary agent-based model of populations of social agents that learn adult fair behavior (Fb) by engaging in Fp as juveniles. In our model, adults produce offspring by accumulating resources over time through foraging. Adults can either behave selfishly by keeping the resources they forage or they can pool them, subsequently dividing the pooled resources after each round of foraging. We found that fairness as equitability was beneficial especially when resources were large but difficult to obtain and led to the evolution of Fp. We conclude by discussing the implications of this model, for developing more rigorous theory on the evolution of social play, and future directions for theory development by modeling the evolution of play

Specific 50-kHv vocalizations are tightly linked to particular types of behavior in juvenile rats anticipating play

Sherpa Romeo green journal. Open access article. Creative Commons Attribution 4.0 International License (CC BY 4.0) appliesRat ultrasonic vocalizations have been suggested to be either a byproduct of physical movement or, in the case of 50-kHz calls, a means to communicate positive affect. Yet there are up to 14 distinct types of 50-kHz calls, raising issues for both explanations. To discriminate between these theories and address the purpose for the numerous 50-kHz call types, we studied single juvenile rats that were waiting to play with a partner, a situation associated with a high number of 50-kHz calls. We used a Monte-Carlo shuffling procedure to identify vocalization-behavior correlations that were statistically different from chance. We found that certain call types (“split”, “composite” and “multi-step”) were strongly associated with running and jumping while other call types (those involving “trills”) were more common during slower movements. Further, non-locomotor states such as resting and rearing were strongly predictive of a lack of vocalizations. We also found that the various sub-types of USVs can be clustered into 3–4 categories based on similarities in the way they are used. We did not find a one-to-one relationship between any movements and specific vocalizations, casting doubt on the motion byproduct theory. On the other hand, the use of specific calls during specific behaviors is problematic for the affect communication hypothesis. Based on our results, we suggest that ultrasonic calls may serve to coordinate moment-to-moment social interactionsYe

The development of juvenile-typical patterns of play fighting in juvenile rats does not depend on peer-peer play experience in the peri-weaning period

Open access article. Creative Commons Attribution 4.0 International License (CC BY 4.0) appliesPlay fighting in rats involves attack and defense of the nape. To protect the nape, rats use a variety of defensive tactics, with different strains having specific preferences. Targeting of the nape is established before weaning and defense matures over the course of the week preceding and the week proceeding weaning. Thus, it is possible that experience from engaging in immature forms of play is needed to consolidate the nape as the playful target and for the development of the juvenile-typical pattern of defense. Two experiments were conducted to evaluate this possibility. For the first experiment, male rats were reared over the week post-weaning in either pairs or alone, and their play tested with unfamiliar partners when juveniles (31-34 days). For the second experiment, during the week preceding weaning, male and female rats were placed into one of three conditions: (1) with the mother and no peers, (2) with same-sex siblings but no mother, or (3) with both the mother and same-sex siblings. The subjects were tested in same-sex, samecondition pairs when juveniles (31-34 days). Rats from all conditions, in both experiments, attacked the nape during play fighting and developed the same juvenile-typical patterns of playful defense. This suggests that the experience of peer-peer play in the peri-weaning period is not necessary for the development of the attack and defense components of juvenile-typical play.Ye

Pinning in the play fighting of rats: a comparative perspective with methodological recommendations

Open access article. Creative Commons Attribution 4.0 International LIcense (CC BY 4.0) appliesDuring play fighting, rats attack and defend the nape of the neck and during the course of this competitive interaction, they may adopt a configuration in which one animal stands over its supine partner (i.e., pin). Because the pin configuration is typically frequent and relatively easy to identify, it has been widely used as a marker to detect the effects of experimental treatments. In the present study, the frequency of pinning during standardized, 10-min trials in three strains of rats, Long Evans hooded (LE), Sprague-Dawley (SD) and wild (WWCPS), was compared. LE and SD had higher rates than WWCPS rats (#/min: 6.5, 5.5, 1.5, respectively). When adjusted for strain differences in the frequency of attacks, SD as well as WWCPS rats had lower rates of pinning compared to LE rats. Both SD and WWCPS rats were less likely to use tactics of defense that promote pinning. Moreover, while the majority of the pins achieved in LE rats arose from the defender actively rolling over onto its back, the majority of pins in WWCPS rats arose because one partner pushed the other onto its back. SD rats were intermediate in this regard. Finally, once they do adopt the pin configuration, SD rats are less likely to remain supine than LE and WWCPS rats. That is, both SD and WWCPS rats have significantly fewer pins than LE rats, but a different combination of factors account for this. These data highlight the need to use a battery of measures for ascertaining the effects of experimental manipulations on play. Some suggested guidelines are provided.Ye

Children with Moderate Acute Malnutrition with No Access to Supplementary Feeding Programmes Experience High Rates of Deterioration and No Improvement: Results from a Prospective Cohort Study in Rural Ethiopia

Background: Children with moderate acute malnutrition (MAM) have an increased risk of mortality, infections and impaired physical and cognitive development compared to well-nourished children. In parts of Ethiopia not considered chronically food insecure there are no supplementary feeding programmes (SFPs) for treating MAM. The short-term outcomes of children who have MAM in such areas are not currently described, and there remains an urgent need for evidence-based policy recommendations. Methods: We defined MAM as mid-upper arm circumference (MUAC) of ≥11.0cm and <12.5cm with no bilateral pitting oedema to include Ethiopian government and World Health Organisation cut-offs. We prospectively surveyed 884 children aged 6–59 months living with MAM in a rural area of Ethiopia not eligible for a supplementary feeding programme. Weekly home visits were made for seven months (28 weeks), covering the end of peak malnutrition through to the post-harvest period (the most food secure window), collecting anthropometric, socio-demographic and food security data. Results: By the end of the study follow up, 32.5% (287/884) remained with MAM, 9.3% (82/884) experienced at least one episode of SAM (MUAC <11cm and/or bilateral pitting oedema), and 0.9% (8/884) died. Only 54.2% of the children recovered with no episode of SAM by the end of the study. Of those who developed SAM half still had MAM at the end of the follow up period. The median (interquartile range) time to recovery was 9 (4–15) weeks. Children with the lowest MUAC at enrolment had a significantly higher risk of remaining with MAM and a lower chance of recovering. Conclusions: Children with MAM during the post-harvest season in an area not eligible for SFP experience an extremely high incidence of SAM and a low recovery rate. Not having a targeted nutrition-specific intervention to address MAM in this context places children with MAM at excessive risk of adverse outcomes. Further preventive and curative approaches should urgently be considered