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Durham Research Online Durham Research Online Deposited in DRO: 28 August 2015 Version of attached le: Published Version Peer-review status of attached le: Peer-reviewed Citation for published item: Hogg, R. and Godfrey, L. and Schwartz, G. and Dirks, W. and Bromage, T. (2015) 'Lemur biorhythms and life history evolution.', PLoS ONE., 10 (8). e0134210. Further information on publisher's website: http://dx.doi.org/10.1371/journal.pone.0134210 Publisher's copyright statement: Copyright: c 2015 Hogg et al. This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. Additional information: Use policy The full-text may be used and/or reproduced, and given to third parties in any format or medium, without prior permission or charge, for personal research or study, educational, or not-for-prot purposes provided that: • a full bibliographic reference is made to the original source • a link is made to the metadata record in DRO • the full-text is not changed in any way The full-text must not be sold in any format or medium without the formal permission of the copyright holders. Please consult the full DRO policy for further details. Durham University Library, Stockton Road, Durham DH1 3LY, United Kingdom Tel : +44 (0)191 334 3042 | Fax : +44 (0)191 334 2971 https://dro.dur.ac.uk RESEARCH ARTICLE Lemur Biorhythms and Life History Evolution Russell T. Hogg1*, Laurie R. Godfrey2, Gary T. Schwartz3, Wendy Dirks4, Timothy G. Bromage5 1 Department of Rehabilitation Sciences, Florida Gulf Coast University, Fort Myers, Florida, United States of America, 2 Department of Anthropology, University of Massachusetts at Amherst, Amherst, Massachusetts, United States of America, 3 Institute of Human Origins and School of Human Evolution and Social Change, Arizona State University, Tempe, Arizona, United States of America, 4 Department of Anthropology, Durham University, Durham, United Kingdom, 5 Department of Biomaterials and Biomimetics, and Department of Basic Science and Craniofacial Biology, New York University College of Dentistry, New York, New York, United States of America a11111 * [email protected] Abstract Skeletal histology supports the hypothesis that primate life histories are regulated by a neu- OPEN ACCESS roendocrine rhythm, the Havers-Halberg Oscillation (HHO). Interestingly, subfossil lemurs are outliers in HHO scaling relationships that have been discovered for haplorhine primates Citation: Hogg RT, Godfrey LR, Schwartz GT, Dirks W, Bromage TG (2015) Lemur Biorhythms and Life and other mammals. We present new data to determine whether these species represent History Evolution. PLoS ONE 10(8): e0134210. the general lemur or strepsirrhine condition and to inform models about neuroendocrine- doi:10.1371/journal.pone.0134210 mediated life history evolution. We gathered the largest sample to date of HHO data from Editor: Alistair Robert Evans, Monash University, histological sections of primate teeth (including the subfossil lemurs) to assess the relation- AUSTRALIA ship of these chronobiological measures with life history-related variables including body Received: September 24, 2014 mass, brain size, age at first female reproduction, and activity level. For anthropoids, these Accepted: July 7, 2015 variables show strong correlations with HHO conforming to predictions, though body mass and endocranial volume are strongly correlated with HHO periodicity in this group. However, Published: August 12, 2015 lemurs (possibly excepting Daubentonia) do not follow this pattern and show markedly less Copyright: © 2015 Hogg et al. This is an open variability in HHO periodicity and lower correlation coefficients and slopes. Moreover, body access article distributed under the terms of the Creative Commons Attribution License, which permits mass is uncorrelated, and brain size and activity levels are more strongly correlated with unrestricted use, distribution, and reproduction in any HHO periodicity in these animals. We argue that lemurs evolved this pattern due to selec- medium, provided the original author and source are tion for risk-averse life histories driven by the unpredictability of the environment in Mada- credited. gascar. These results reinforce the idea that HHO influences life history evolution differently Data Availability Statement: All data incorporated in in response to specific ecological selection regimes. this study are available in the supplemental information, specifically S2 Table. Funding: This work was supported by National Science Foundation (http://www.nsf.gov) grants BCS- 0622479 (RTH), BCS-0237338, BCS-0503988 (LRG Introduction and GTS), and BCS-1062680 (TGB); The Natural History Collections at the University of Massachusetts Growth, metabolism, and reproductive physiology all have a role to play in the allocation of (http://bcrc.bio.umass.edu/ummnh/) (LRG); The resources over individual lifespans, and have all been implicated in multiple explanatory mod- Royal Society of London (http://www.royalsociety.org) els of life history evolution (e.g. [1–6]). While many of the effects of ecology on life history (WD); The Institute of Human Origins (https://iho.asu. edu) (GTS); and the Max Planck Research Award have been understood for some time, the manner in which the evolution of physiological sys- (http://www.mpg.de/en), which is endowed by the tems is coordinated to achieve particular life history outcomes remains unclear. Recently, German Federal Ministry of Education and Research Bromage et al. [2,3,7] used histological evidence from primate dental and osseous tissues to PLOS ONE | DOI:10.1371/journal.pone.0134210 August 12, 2015 1 / 17 Lemur Biorhythms and Life History Evolution to the Max Planck Society and the Alexander von address this question. Using vitally labeled bone to assess the chronology between growth Humboldt Foundation in respect of the Hard Tissue increments in bones (lamellae), they showed that lamellae are laid down with a specific period- Research Program in Human Paleobiomics (TGB). icity, which ranged from 1 day in rats to 8 days in humans. Moreover, they demonstrated that The funders had no role in study design, data collection and analysis, decision to publish, or the lamellar periodicity matches that of long-period growth increments in tooth enamel, preparation of the manuscript. known as striae of Retzius. This periodicity occurs as a multiple of whole days and is variable among and within some taxa, but not within individuals. Mammalian periodicities range Competing Interests: The authors have declared that no competing interests exist. between 1 and 14 days [8,9], and manifest as daily increments between adjacent striae of Retzius, known as cross striations. While dental incremental growth lines have long been rec- ognized as periodic structures [10], the recognition that lamellae are periodic is new. Although bones and teeth are both mineralized tissues, they have different cellular and developmental origins; dental tissues, in fact, have origins from both ectoderm-derived epithe- lium (enamel) and mesenchyme (dentine), and both express long-period growth lines (called Andresen lines in dentine, while von Ebner lines between them are daily) [7]. The synchroniza- tion of enamel, dentine, and bone suggests a central mechanism operating systemically to regu- late tooth and bone development as well as the growth of other organ and tissue systems. Bromage et al. term this common biorhythm the Havers-Halberg Oscillation (HHO), and argue that it is controlled centrally by the hypothalamus via oscillations in sympathetic nervous output [2,3]. These oscillations are hypothesized to control cell proliferation and thus growth rates, metabolic rates, and body mass. If this is the case we would expect the HHO to have an expression in soft tissues as well as mineralized tissues, and several studies have provided evi- dence that this is the case. For example, in 2007 Brown et al. [11] demonstrated that mammal fibroblasts from different species lose the allometric scaling of their metabolism when removed from the physiological context of their host organism, and begin to behave similarly to one another; in other words, metabolic rates of in situ fibroblasts scale with body mass across spe- cies, whereas metabolic rates of explanted fibroblasts from the same species do not scale. This suggests that a central physiological mechanism is responsible for coordinating metabolic func- tion among the cells that make up an organism. It has also been demonstrated that all primate tissue and organ masses necessarily covary with body mass, and thus also scale with HHO peri- odicity in a manner similar to one another [12]; this indicates the HHO's general applicability to most of the body's cellular milieu. Bromage et al. [3] have also assessed HHO with regard to temporal life history variables and have shown a link between HHO periodicity and estrous cycling in anthropoids, and have noted several potential physiological pathways through which the HHO can affect metabolism, growth, and reproduction. Accordingly, the HHO would act as a metronome around which life history physiology is organized. Following this model, high-frequency HHO oscillations (e.g. 2–3 days) will foster more rapid cell proliferation and faster overall life histories linked to smaller body size, while low-frequency HHO oscillations (e.g., 8–9 days) will have the opposite effect. A more detailed discussion
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