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1. The Integrative Life History of Maternal Effects

   https://doi.org/10.1093/icb/icae117  

   Marks, Jamie_R; Lailvaux, Simon_P (July 2024, Integrative And Comparative Biology)

   Synopsis Context-dependent allocation of resources drives trade-offs among fitness-related traits and other phenotypes to which those traits are linked. In addition, the amount and type of acquired resources can also affect the phenotypes of other organisms through indirect genetic effects, as exemplified by the maternal provisioning of offspring. Despite a large literature on maternal effects, we lack a comprehensive understanding of the extent to which mothers might affect the phenotypes of their offspring, as well as the various mechanisms by which they do so, particularly with regard to many functional traits that are key determinants of survival and reproduction. Our goals in this paper are to review the various approaches to measuring and understanding maternal effects and to highlight some promising avenues for integration of maternal effects with some other key areas of evolutionary ecology. We focus especially on nutritional geometry; maternal age; and traits proximate to fitness such as whole-organism performance. Finally, we discuss the logistic and practical limits of quantifying these effects in many animal systems and emphasize the value of integrative approaches in understanding the mechanisms underlying maternal influence on offspring phenotypes. 

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2. The Pace of Life: Metabolic Energy, Biological Time, and Life History

   https://doi.org/10.1093/icb/icac058  

   Brown, James H; Burger, Joseph R; Hou, Chen; Hall, Charles A (July 2022, Integrative and Comparative Biology)

   Synopsis New biophysical theory and electronic databases raise the prospect of deriving fundamental rules of life, a conceptual framework for how the structures and functions of molecules, cells, and individual organisms give rise to emergent patterns and processes of ecology, evolution, and biodiversity. This framework is very general, applying across taxa of animals from 10–10 g protists to 108 g whales, and across environments from deserts and abyssal depths to rain forests and coral reefs. It has several hallmarks: (1) Energy is the ultimate limiting resource for organisms and the currency of biological fitness. (2) Most organisms are nearly equally fit, because in each generation at steady state they transfer an equal quantity of energy (˜22.4 kJ/g) and biomass (˜1 g/g) to surviving offspring. This is the equal fitness paradigm (EFP). (3) The enormous diversity of life histories is due largely to variation in metabolic rates (e.g., energy uptake and expenditure via assimilation, respiration, and production) and biological times (e.g., generation time). As in standard allometric and metabolic theory, most physiological and life history traits scale approximately as quarter-power functions of body mass, m (rates as ∼m–1/4 and times as ∼m1/4), and as exponential functions of temperature. (4) Time is the fourth dimension of life. Generation time is the pace of life. (5) There is, however, considerable variation not accounted for by the above scalings and existing theories. Much of this “unexplained” variation is due to natural selection on life history traits to adapt the biological times of generations to the clock times of geochronological environmental cycles. (6) Most work on biological scaling and metabolic ecology has focused on respiration rate. The emerging synthesis applies conceptual foundations of energetics and the EFP to shift the focus to production rate and generation time. 

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3. Life History Adaptations to Seasonality

   https://doi.org/10.1093/icb/icx123  

   Varpe, Øystein (October 2017, Integrative and Comparative Biology)
4. Life history and the evolutionary loss of parental care

   https://doi.org/10.1098/rspb.2022.0658  

   Udu, Isimeme N.; Bonsall, Michael B.; Klug, Hope (July 2022, Proceedings of the Royal Society B: Biological Sciences)

   Parental care has been gained and lost evolutionarily multiple times. While many studies have focused on the origin of care, few have explored the evolutionary loss of care. Understanding the loss of parental care is important as the conditions that favour its loss will not necessarily be the opposite of those that favour the evolution of care. Evolutionary hysteresis (the case in which evolution depends on the history of a system) could create a situation in which it is relatively challenging to lose care once it has evolved. Here, using a mathematical approach, we explore the evolutionary loss of parental care in relation to basic life-history conditions. Our results suggest that parental care is most likely to be lost when egg and adult death rates are low, eggs mature quickly, and the level of care provided is high. We also predict evolutionary hysteresis with respect to egg maturation rate: as egg maturation rate decreases, it becomes increasingly more costly to lose care than to gain it. This suggests that once care is present, it will be particularly challenging for it to be lost if eggs develop slowly. 

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5. Life history scaling in a tropical forest

   https://doi.org/10.1111/1365-2745.14245  

   Grady, John M.; Read, Quentin D.; Record, Sydne; Rüger, Nadja; Zarnetske, Phoebe L.; Dell, Anthony I.; Hubbell, Stephen P.; Michaletz, Sean T.; Enquist, Brian J. (January 2024, Journal of Ecology)

   Abstract Both tree size and life history variation drive forest structure and dynamics, but little is known about how life history frequency changes with size. We used a scaling framework to quantify ontogenetic size variation and assessed patterns of abundance, richness, productivity and light interception across life history strategies from >114,000 trees in a primary, neotropical forest. We classified trees along two life history axes: afast–slowaxis characterized by a growth–survival trade‐off, and astature–recruitmentaxis with tall,long‐lived pioneersat one end and short,short‐lived recruitersat the other.Relative abundance, richness, productivity and light interception follow an approximate power law, systematically shifting over an order of magnitude with tree size.Slowsaplings dominate the understorey, butslowtrees decline to parity with rapidly growingfastandlong‐lived pioneerspecies in the canopy.Like the community as a whole,slowspecies are the closest to obeying the energy equivalence rule (EER)—with equal productivity per size class—but other life histories strongly increase productivity with tree size. Productivity is fuelled by resources, and the scaling of light interception corresponds to the scaling of productivity across life history strategies, withslowandallspecies near solar energy equivalence. This points towards a resource‐use corollary to the EER: the resource equivalence rule.Fitness trade‐offs associated with tree size and life history may promote coexistence in tropical forests by limiting niche overlap and reducing fitness differences.Synthesis. Tree life history strategies describe the different ways trees grow, survive and recruit in the understorey. We show that the proportion of trees with a pioneer life history strategy increases steadily with tree size, as pioneers become relatively more abundant, productive, diverse and capture more resources towards the canopy. Fitness trade‐offs associated with size and life history strategy offer a mechanism for coexistence in tropical forests. 

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