Early-life adversity shapes the relationship between growth and reproduction in free-ranging female rhesus macaques

R Rachel M. Petersen (Department of Biological Sciences, Vanderbilt University, Nashville, TN, USA.) S Sam K. Patterson (Department of Anthropology, New York University, New York, NY, USA.) A Anja Widdig (Department of Primate Behavioral Ecology, Institute of Biology, Leipzig University) C Cassandra M. Turcotte (Department of Cell Biology and Anatomy, Cumming School of Medicine, University of Calgary) S Susan C. Antón S Scott A. Williams (Department of Anthropology, New York University) A Ashly N. Romero (Basic Medical Sciences, College of Medicine-Phoenix, University of Arizona) S Samuel E. Bauman Surratt (Caribbean Primate Research Center, University of Puerto Rico, Punta Santiago, Puerto Rico.) A Angelina Ruiz-Lambides (Cayo Santiago Field Station, Caribbean Primate Research Center, University of Puerto Rico) M Michael J. Montague (Department of Neuroscience, University of Pennsylvania, Philadelphia, PA, USA.) N Noah Snyder-Mackler (School of Life Sciences, Arizona State University, Tempe, AZ, USA.) L Lauren J. N. Brent (Centre for Research in Animal Behaviour, University of Exeter, Exeter, UK.) J James P. Higham (Department of Anthropology, New York University, New York, NY, USA.) A Amanda J. Lea (Department of Biological Sciences, Vanderbilt University, Nashville, TN, USA.)

Abstract

Life history theory predicts that organisms allocate resources across physiological processes to maximize fitness. Under this framework, early-life adversity (ELA) which limits energetic capital could shape investment in growth and reproduction, ultimately contributing to evolutionary fitness. Integrating 64 y of long-term demographic information with cross-sectional behavioral and physiological data from female rhesus macaques ( Macaca mulatta ; n = 163 to 2,105 females depending on the analysis), we tested whether naturally occurring ELA influences investment in the competing physiological demands of growth and reproduction. By analyzing ELA, growth, and reproduction in the same individuals, we also assessed whether adversity intensifies constraints and induces trade-offs between life history domains. Similar to cohort effects described in other species, we found that ELA was associated with modified growth, delayed reproductive maturity, and small adult body size. These effects largely reflected generalized constraints: females that experienced growth limitations also exhibited reproductive concessions, with ELA linked to reduced investment in both. Interestingly, however, two types of adversity were associated with shifts in growth–reproduction trade-offs, such that ELA-exposed females invested relatively more in reproduction at the expense of growth. Finally, we examined how traits modified by ELA related to lifetime reproductive success, addressing understudied links between ELA, life history, and fitness. Across the population, starting reproduction earlier and maintaining a moderate reproductive rate conferred the greatest number of surviving offspring. These findings suggest that ELA impacts key life history traits as well as the relationships between them, and can constrain individuals from adopting the most optimal reproductive strategy.

Article Details

Volume / Issue Vol. 123, Issue 19
Published May 12, 2026
ISSN 0027-8424
Publisher National Academy of Sciences

Authors (14)

R

Rachel M. Petersen

Department of Biological Sciences, Vanderbilt University, Nashville, TN, USA.

S

Sam K. Patterson

Department of Anthropology, New York University, New York, NY, USA.

A

Anja Widdig

Department of Primate Behavioral Ecology, Institute of Biology, Leipzig University

C

Cassandra M. Turcotte

Department of Cell Biology and Anatomy, Cumming School of Medicine, University of Calgary

S

Susan C. Antón

S

Scott A. Williams

Department of Anthropology, New York University

A

Ashly N. Romero

Basic Medical Sciences, College of Medicine-Phoenix, University of Arizona

S

Samuel E. Bauman Surratt

Caribbean Primate Research Center, University of Puerto Rico, Punta Santiago, Puerto Rico.

A

Angelina Ruiz-Lambides

Cayo Santiago Field Station, Caribbean Primate Research Center, University of Puerto Rico

M

Michael J. Montague

Department of Neuroscience, University of Pennsylvania, Philadelphia, PA, USA.

N

Noah Snyder-Mackler

School of Life Sciences, Arizona State University, Tempe, AZ, USA.

L

Lauren J. N. Brent

Centre for Research in Animal Behaviour, University of Exeter, Exeter, UK.

J

James P. Higham

Department of Anthropology, New York University, New York, NY, USA.

A

Amanda J. Lea

Department of Biological Sciences, Vanderbilt University, Nashville, TN, USA.