26 research outputs found

    Agent-based modeling of multilevel selection : the evolution of feeding restraint as a case study

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    Evolutionary biologists are increasingly interested in the dynamics of multilevel selection, or selection acting simultaneously at more than one level in a hierarchy of reproducing entities (e.g., gene, chromosome, organelle, cell, organism, social group, multi-species community). Systems of linear equations are the usual tool for studying evolution, but are limited in their ability to capture important dynamics of multilevel selection. Here we use an agent-based model to study the evolution of cooperation in spatially structured populations. This work addresses the long-standing controversy over the role of group selection , or natural selection between versus within groups of interacting individuals. In an ecologically plausible setting, cooperative individuals with lower rates of food consumption. The results show that changing the spatial distribution of food, and thus the distribution of the individuals seeking it, can determine whether or not cooperation evolves. In this model cooperation evolved under a fairly wide range of parameter values, even without the kinship effects and discrete mixing phase that are sometimes thought to be necessary. We suggest that integrating equation-based analysis tools into agent-based models is a powerful way to study selection in systems with complex dynamics

    Chimpanzee Politics: Sex and power among Apes : By Frans B.M. de Waal. New York: Harper and Row, 1982, 223 pp., $16.50

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    Peer Reviewedhttp://deepblue.lib.umich.edu/bitstream/2027.42/25846/1/0000409.pd

    RESPONSES TO CALF ENTANGLEMENT IN FREE-RANGING BOTTLENOSE DOLPHINS

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    Peer Reviewedhttp://deepblue.lib.umich.edu/bitstream/2027.42/74984/1/j.1748-7692.1995.tb00280.x.pd

    Reproduction in wild female olive baboons

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    The purpose of this paper is to evaluate several factors that influence female reproduction in a large troop of wild olive baboons ( Papio cynocephalus anubis ) based on 4 consecutive years of demographic data. Interbirth intervals were significantly shorter for females whose infants died before their next conception than for females whose infants survived. High-ranking mothers of surviving infants had significantly shorter birth intervals than comparable low-ranking mothers, independent of maternal age. This occurred mainly because the interval from resumption of cycling to conception was significantly shorter for high-vs. low-ranking females. Dominance rank did not influence sex ratio at birth, infant survival in the first 2 years, or adult female mortality. Age was also significantly related to interbirth intervals, with older females having shorter intervals. Primiparous females had consistently longer reproductive intervals than did multiparous females, but this difference reached statistical significance only for females whose infants died before the next conception. Primiparous females also experienced significantly higher infant mortality. Data on body size and estrous cycle length indicated no differences between high- and low-ranking females. Nutritional and stress-related mechanisms that may underlie the reproductive advantages of high rank are discussed.Peer Reviewedhttp://deepblue.lib.umich.edu/bitstream/2027.42/38425/1/1350190405_ftp.pd

    Social relationships and ritualized greetings in adult male baboons ( Papio cynocephalus anubis )

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    Greetings involving exchanges of ritualized sexual gestures are a common form of interaction among adult male baboons, although relatively little attention has been paid to them. In this study, we investigate how greetings reflect important aspects of the male's social relationships, including dominance rank, age/residence status, and cooperative tendencies. The results are based on over 600 greetings among 12 adult males recorded during a 4-month study of a troop of wild olive baboons near Gilgil, Kenya. Four of the adult males were older, lower-ranking, long-term residents, which frequently formed coalitions to take estrous females away from the eight young, higher-ranking males. Virtually all dyads greeted: greetings occurred more than twice as often as other types of male-male interactions; and nearly all greetings occurred in a neutral context, in which there was no resource at stake. The percentage of greetings completed, the frequency with which different gestures were employed, and the roles adopted by each male varied significantly across old-old, old-young, and young-young dyads. Greetings between young adult males were often interrupted or actively resisted, consistent with their unstable and ambiguous dominance relationships. Greetings between old-old dyads were usually completed and appeared consistent with their cooperative relationships. One pair of old males formed a stable, reciprocal coalition against young males, and this pair's greetings showed remarkable symmetry of roles. Greetings, we hypothesize, function to allow males to negotiate important aspects of their relationships, including cooperation.Peer Reviewedhttp://deepblue.lib.umich.edu/bitstream/2027.42/44558/1/10764_2005_Article_BF02192786.pd

    Additional conference abstracts

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    Peer Reviewedhttp://deepblue.lib.umich.edu/bitstream/2027.42/43490/1/11111_2005_Article_BF02208413.pd

    Genetic mechanisms of critical illness in COVID-19.

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    Host-mediated lung inflammation is present1, and drives mortality2, in the critical illness caused by coronavirus disease 2019 (COVID-19). Host genetic variants associated with critical illness may identify mechanistic targets for therapeutic development3. Here we report the results of the GenOMICC (Genetics Of Mortality In Critical Care) genome-wide association study in 2,244 critically ill patients with COVID-19 from 208 UK intensive care units. We have identified and replicated the following new genome-wide significant associations: on chromosome 12q24.13 (rs10735079, P = 1.65 × 10-8) in a gene cluster that encodes antiviral restriction enzyme activators (OAS1, OAS2 and OAS3); on chromosome 19p13.2 (rs74956615, P = 2.3 × 10-8) near the gene that encodes tyrosine kinase 2 (TYK2); on chromosome 19p13.3 (rs2109069, P = 3.98 ×  10-12) within the gene that encodes dipeptidyl peptidase 9 (DPP9); and on chromosome 21q22.1 (rs2236757, P = 4.99 × 10-8) in the interferon receptor gene IFNAR2. We identified potential targets for repurposing of licensed medications: using Mendelian randomization, we found evidence that low expression of IFNAR2, or high expression of TYK2, are associated with life-threatening disease; and transcriptome-wide association in lung tissue revealed that high expression of the monocyte-macrophage chemotactic receptor CCR2 is associated with severe COVID-19. Our results identify robust genetic signals relating to key host antiviral defence mechanisms and mediators of inflammatory organ damage in COVID-19. Both mechanisms may be amenable to targeted treatment with existing drugs. However, large-scale randomized clinical trials will be essential before any change to clinical practice

    Design and baseline characteristics of the finerenone in reducing cardiovascular mortality and morbidity in diabetic kidney disease trial

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    Background: Among people with diabetes, those with kidney disease have exceptionally high rates of cardiovascular (CV) morbidity and mortality and progression of their underlying kidney disease. Finerenone is a novel, nonsteroidal, selective mineralocorticoid receptor antagonist that has shown to reduce albuminuria in type 2 diabetes (T2D) patients with chronic kidney disease (CKD) while revealing only a low risk of hyperkalemia. However, the effect of finerenone on CV and renal outcomes has not yet been investigated in long-term trials. Patients and Methods: The Finerenone in Reducing CV Mortality and Morbidity in Diabetic Kidney Disease (FIGARO-DKD) trial aims to assess the efficacy and safety of finerenone compared to placebo at reducing clinically important CV and renal outcomes in T2D patients with CKD. FIGARO-DKD is a randomized, double-blind, placebo-controlled, parallel-group, event-driven trial running in 47 countries with an expected duration of approximately 6 years. FIGARO-DKD randomized 7,437 patients with an estimated glomerular filtration rate >= 25 mL/min/1.73 m(2) and albuminuria (urinary albumin-to-creatinine ratio >= 30 to <= 5,000 mg/g). The study has at least 90% power to detect a 20% reduction in the risk of the primary outcome (overall two-sided significance level alpha = 0.05), the composite of time to first occurrence of CV death, nonfatal myocardial infarction, nonfatal stroke, or hospitalization for heart failure. Conclusions: FIGARO-DKD will determine whether an optimally treated cohort of T2D patients with CKD at high risk of CV and renal events will experience cardiorenal benefits with the addition of finerenone to their treatment regimen. Trial Registration: EudraCT number: 2015-000950-39; ClinicalTrials.gov identifier: NCT02545049

    Social Bonding and Nurture Kinship: Compatibility between Cultural and Biological Approaches

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