Brian M. Wood’s research while affiliated with University of California, Los Angeles and other places

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Publications (16)


Beyond the here and now: hunter–gatherer socio-spatial complexity and the evolution of language
  • Literature Review
  • Full-text available

September 2024

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145 Reads

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1 Citation

Brian M. Wood

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Human evolutionary ecology stands to benefit by integrating theory and methods developed in movement ecology, and in turn, to make contributions to the broader field of movement ecology by leveraging our species’ distinct attributes. In this paper, we review data and evolutionary models suggesting that major changes in socio-spatial behaviour accompanied the evolution of language. To illustrate and explore these issues, we present a comparison of GPS measures of the socio-spatial behaviour of Hadza hunter–gatherers of northern Tanzania to those of olive baboons (Papio anubis), a comparatively small-brained primate that is also savanna-adapted. While standard spatial metrics show modest differences, measures of spatial diversity, landscape exploration and spatiotemporal displacement between individuals differ markedly. Groups of Hadza foragers rapidly accumulate a vast, diverse knowledge pool about places and things over the horizon, contrasting with the baboon’s narrower and more homogeneous pool of ecological information. The larger and more complex socio-spatial world illustrated by the Hadza is one where heightened cognitive abilities for spatial and episodic memory, navigation, perspective taking and communication about things beyond the here and now all have clear value. This article is part of the theme issue ‘The spatial–social interface: a theoretical and empirical integration’.

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The region east of Lake Eyasi, Tanzania, occupied by Hadza hunter-gatherers (image courtesy of FIRMS and Google maps)
Two Hadza men walking along a grass fire that has been intentionally set (photo by BMW)
The landscape burning area of interest. Only MODIS pixels that fell within this 740 km² region were included in subsequent analyses (image courtesy of FIRMS)
Hadza (a) women’s and (b) men’s responses to the free-list question, “What are the reasons Hadza might burn the landscape?” The size of the starburst sections represents the proportion of the responses relative to respective levels. (data from ESM Tables S1a, b)
An area of dry grass was intentionally burned to control the population of dangerous snakes and promote the growth of grass shoots. The image on the left (a) depicts the height and density of grass directly adjacent to the burned area (b). (Photos by JAH)

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Hadza Landscape Burning

August 2024

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60 Reads

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1 Citation

Human Nature

We present the first published ethnographic description of landscape burning by Hadza hunter-gatherers of northern Tanzania and identify environmental, social, and cultural influences on Hadza landscape burning, thereby broadening the ethnographic record of anthropogenic burning practices described for hunter-gatherer communities. We report interview data collected in 2022 and 2023, describing their practices and attitudes regarding the causes and consequences of burning. We provide context by comparing our observations with those recorded for hunting and gathering populations in Africa, Australia, and North America. Hadza landscape burning is generally a solitary and male-dominated activity, contrary to ethnographic accounts of Indigenous landscape burning from North America and Australia. The primary goals stated by Hadza for landscape burning were improved hunting, reduced hazards from dangerous animals, and to reduce the density of livestock. Firsthand observations suggest that landscape burning has decreased over the past 20 years, and this historical trend is supported by interviews. Satellite imagery also suggests an overall decrease in burning activity in the region from 2001 to 2022. Among the Hadza, landscape burning is a culturally influenced and strongly gender-biased activity that is rapidly disappearing. Because burning can radically transform landscapes, these practices often generate or amplify conflicts of interest between groups with different land use strategies. Hadza report serious social conflict with pastoralists over landscape burning, and our study suggests this tension has constrained the practice in the past two decades.


Culturally determined interspecies communication between humans and honeyguides

December 2023

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150 Reads

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13 Citations

Science

Species interactions that vary across environments can create geographical mosaics of genetic coevolution. However, traits mediating species interactions are sometimes culturally inherited. Here we show that traditions of interspecies communication between people and wild birds vary in a culturally determined geographical mosaic. Honey hunters in different parts of Africa use different calls to communicate with greater honeyguides ( Indicator indicator ) that lead them to bees’ nests. We show experimentally that honeyguides in Tanzania and Mozambique discriminate among honey hunters’ calls, responding more readily to local than to foreign calls. This was not explained by variation in sound transmission and instead suggests that honeyguides learn local human signals. We discuss the forces stabilizing and diversifying interspecies communication traditions, and the potential for cultural coevolution between species.


Demographic and hormonal evidence for menopause in wild chimpanzees

October 2023

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118 Reads

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30 Citations

Science

Among mammals, post-reproductive life spans are currently documented only in humans and a few species of toothed whales. Here we show that a post-reproductive life span exists among wild chimpanzees in the Ngogo community of Kibale National Park, Uganda. Post-reproductive representation was 0.195, indicating that a female who reached adulthood could expect to live about one-fifth of her adult life in a post-reproductive state, around half as long as human hunter-gatherers. Post-reproductive females exhibited hormonal signatures of menopause, including sharply increasing gonadotropins after age 50. We discuss whether post-reproductive life spans in wild chimpanzees occur only rarely, as a short-term response to favorable ecological conditions, or instead are an evolved species-typical trait as well as the implications of these alternatives for our understanding of the evolution of post-reproductive life spans.


Lifestyle and patterns of physical activity in Hadza foragers

September 2023

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144 Reads

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3 Citations

American Journal of Biological Anthropology

Objectives Physically active lifestyles are associated with several health benefits. Physical activity (PA) levels are low in post‐industrial populations, but generally high throughout life in subsistence populations. The Hadza are a subsistence‐oriented foraging population in Tanzania known for being physically active, but it is unknown how recent increases in market integration may have altered their PA patterns. In this study, we examine PA patterns for Hadza women and men who engage in different amounts of traditional foraging. Materials and Methods One hundred and seventy seven Hadza participants (51% female, 19–87 years) wore an Axivity accelerometer (dominant wrist) for ~6 days during dry season months. We evaluated the effects of age, sex, and lifestyle measures on four PA measures that capture different aspects of the PA profile. Results Participants engaged in high levels of both moderate‐intensity PA and inactivity. Although PA levels were negatively associated with age, older participants were still highly active. We found no differences in PA between participants living in more traditional “bush” camps and those living in more settled “village” camps. Mobility was positively associated with step counts for female participants, and schooling was positively associated with inactive time for male participants. Conclusions The similarity in PA patterns between Hadza participants in different camp types suggests that high PA levels characterize subsistence lifestyles generally. The sex‐based difference in the effects of mobility and schooling on PA could be a reflection of the Hadza's gender‐based division of labor, or indicate that changes to subsistence‐oriented lifestyles impact women and men in different ways.


Trends over time for changes in energy expenditure components
a–c, Trends over time for males of adjusted TEE (a), adjusted BEE (b) and adjusted AEE (c). Adjustments were made for body composition (FM and FFM or BM, and age); for details, see Methods. All expenditures are in megajoules per day, and time is expressed in months since January 1982. Significant years are also indicated. Each data point is a different individual measurement of expenditure. The red lines are the fitted least squares regression fits. For regression details refer to the text and Table 1.
Trends over time for changes in energy expenditure components
a–c, Trends over time for females of adjusted TEE (a), adjusted BEE (b) and adjusted AEE (c). Adjustments were made for body composition (fat and lean mass, and age); for details, see Methods. Significant years are also indicated. All expenditures are in megajoules per day and time is expressed in months since January 1982. Each data point is a different individual measurement of expenditure. The red lines are the fitted least squares regression fits. For regression details refer to the text and Table 1.
Trend in basal metabolic rate with body mass and over time
a, Effect of logeBM on the logeBMR in a systematic review of 165 studies dating back to the early 1900s (first study, 1919). Data for males in blue and for females in red. Studies with mixed male and female data are not illustrated. b, Bubble plot showing the residual logebasal metabolism derived from a weighted regression of logeBMR against sex, age and logeBM plotted against date of measurement in the same 165 studies. Bubbles represent the sample size of the studies. The red line is the fitted weighted regression.
Effect of body weight and diet on mouse energy expenditure
a, The relationship between body weight and metabolic rate in the mice fed different diets with variable FA compositions. b, The effect of SAT intake on residual metabolic rate, corrected for body weight.
Total daily energy expenditure has declined over the past three decades due to declining basal expenditure, not reduced activity expenditure

April 2023

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1,432 Reads

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39 Citations

Nature Metabolism

Obesity is caused by a prolonged positive energy balance1,2. Whether reduced energy expenditure stemming from reduced activity levels contributes is debated3,4. Here we show that in both sexes, total energy expenditure (TEE) adjusted for body composition and age declined since the late 1980s, while adjusted activity energy expenditure increased over time. We use the International Atomic Energy Agency Doubly Labelled Water database on energy expenditure of adults in the United States and Europe (n = 4,799) to explore patterns in total (TEE: n = 4,799), basal (BEE: n = 1,432) and physical activity energy expenditure (n = 1,432) over time. In males, adjusted BEE decreased significantly, but in females this did not reach significance. A larger dataset of basal metabolic rate (equivalent to BEE) measurements of 9,912 adults across 163 studies spanning 100 years replicates the decline in BEE in both sexes. We conclude that increasing obesity in the United States/Europe has probably not been fuelled by reduced physical activity leading to lowered TEE. We identify here a decline in adjusted BEE as a previously unrecognized factor.


Fig. 2. Relationships between age and total body water (TBW) or water turnover (WT) in 3729 females (orange) and 1875 males (blue) aged 0 to 96 years with mean and SD. (A) displays WT (L/d), (B) TBW (kg), (C) WT per TBW (%), (D) TBW per body weight (%), (E) WT per total energy expenditure (TEE) (L/MJ), or (F) TEE (MJ/d). Water turnover increases with age until about 30 years and is higher in men (4.3 L/d) than women (3.4 L/d). Water turnover significantly decreases after 30 years in men and 55 years in women, reaching an average water turnover of 3.1 and 2.8 L/d in men and women aged over 70 years, respectively. The average water turnover rate as a percent of total body water is a maximum of ~25% in neonates, decreases with development, and is ~15% in 5-year-old children. At puberty, water turnover falls to ~10% and remains constant until age 40 years in men and 65 years in women, after which it decreases. The average water turnover per TEE is about 0.33 L/MJ (~1.4 ml/kcal) in adults. Note that the variation in water turnover is incredibly large -the low end for men and women is ~1-1.5 L/day while the upper end is around ~6 L/day -and the outliers lie in the 10L/d range. On average, water accounts for 60% of the body weight in infants, 50% in older adults, and only 42% in women at 60 years of age, reflecting a larger % body fat.
Fig. 3.
Fig. 4. (A) Repeated measures of 72 people (31 females and 41 males) shows water turnover (WT) was significantly higher in the summer (3.7 ± 1.0 L/d) with an average temperature of 29°C than in the spring (3.0 ± 0.7 L/d) with 18°C (P < 0.001). (B) In contrast, total energy expenditure (TEE) was not significantly different between summer and spring (P = 0.233). (C) Repeated measures of 63 pregnant women show that total water turnover was significantly higher during late pregnancy and lactation (data from Butte et al. 2005). (Pre = Before pregnancy; Post = 27 weeks postpartum).
Fig. 5.
Fig. 6. Determinants of human water turnover. Objective measures of water turnover from a large global dataset indicate that water turnover is strongly related to anthropometric, lifestyle, and environmental factors. PAL = Physical activity level (Total energy expenditure/Basal energy expenditure), HDI = Human development index.
Variation in human water turnover associated with environmental and lifestyle factors

November 2022

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1,025 Reads

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66 Citations

Science

Water is essential for survival, but one in three individuals worldwide (2.2 billion people) lacks access to safe drinking water. Water intake requirements largely reflect water turnover (WT), the water used by the body each day. We investigated the determinants of human WT in 5604 people from the ages of 8 days to 96 years from 23 countries using isotope-tracking (2H) methods. Age, body size, and composition were significantly associated with WT, as were physical activity, athletic status, pregnancy, socioeconomic status, and environmental characteristics (latitude, altitude, air temperature, and humidity). People who lived in countries with a low human development index (HDI) had higher WT than people in high-HDI countries. On the basis of this extensive dataset, we provide equations to predict human WT in relation to anthropometric, economic, and environmental factors.


Figure 3. Age-specific A) variance and B) coefficient of variance in total energy expenditure in males (circles) and females (triangles) and C) male:female variance ratio. The amount of greater male variability (GMV) remains fairly constant across age categories. Values shown are the posterior modes with 95% highest posterior density credible intervals (95% CIs) extracted from a single model that included multiple covariates and sex-specific nonlinear aging and body condition effects. Numbers shown below the symbols are the sample sizes for each category.
Figure 4. Male (circles) and female (triangles) variance for total energy expenditure disaggregated into Western countries and non-Western countries. Values shown are the posterior modes with 95% highest posterior density credible intervals (CIs) for the sex-specific residual variance estimates extracted from models that included height, fat-free mass, fat mass, age, and sex-specific nonlinear age and body composition effects, and country as a random factor. Numbers shown by the symbols are the sample sizes for each category. Variance in total energy expenditure among males is much higher in Western than non-Western countries, whereas the variance among females is similar in Western and non-Western countries; thus, the magnitude of greater male variability is decreased in non-Western countries.
Variability in energy expenditure is much greater in males than females

October 2022

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706 Reads

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22 Citations

Journal of Human Evolution

In mammals, trait variation is often reported to be greater among males than females. However, to date, mainly only morphological traits have been studied. Energy expenditure represents the metabolic costs of multiple physical, physiological, and behavioral traits. Energy expenditure could exhibit particularly high greater male variation through a cumulative effect if those traits mostly exhibit greater male variation, or a lack of greater male variation if many of them do not. Sex differences in energy expenditure variation have been little explored. We analyzed a large database on energy expenditure in adult humans (1494 males and 3108 females) to investigate whether humans have evolved sex differences in the degree of interindividual variation in energy expenditure. We found that, even when statistically comparing males and females of the same age, height, and body composition, there is much more variation in total, activity, and basal energy expenditure among males. However, with aging, variation in total energy expenditure decreases, and because this happens more rapidly in males, the magnitude of greater male variation, though still large, is attenuated in older age groups. Considerably greater male variation in both total and activity energy expenditure could be explained by greater male variation in levels of daily activity. The considerably greater male variation in basal energy expenditure is remarkable and may be explained, at least in part, by greater male variation in the size of energy-demanding organs. If energy expenditure is a trait that is of indirect interest to females when choosing a sexual partner, this would suggest that energy expenditure is under sexual selection. However, we present a novel energetics model demonstrating that it is also possible that females have been under stabilizing selection pressure for an intermediate basal energy expenditure to maximize energy available for reproduction.


Cross-cultural regularities in infant-directed vocalizations
a, We recorded examples of speech and song from 21 urban, rural or small-scale societies, in many languages. The map indicates the approximate location of each society and is colour-coded by the language family or subgroup represented by the society. b, Machine-learning classification demonstrates the stereotyped acoustics of infant-directed speech and song. We trained two LASSO models, one for speech and one for song, to classify whether recordings were infant- or adult-directed on the basis of their acoustic features. These predictors were regularized using fieldsite-wise cross-validation, such that the model optimally classified infant-directedness across all 21 societies studied. The vertical bars represent the mean classification performance across societies (n = 21 societies for both speech and song; quantified via receiver operating characteristic/AUC); the error bars represent 95% CI of the mean; the points represent the performance estimate for each fieldsite; and the horizontal dashed lines indicate chance level of 50% AUC. The horizontal bars show the six acoustic features with the largest influence in each classifier; the green and red triangles indicate the direction of the effect, for example, with median pitch having a large, positive effect on classification of infant-directed speech. The full results of the variable selection procedure are in Supplementary Table 2, with further details in Methods.
How people alter their voices when vocalizing to infants
Eleven acoustic features had a statistically significant difference between infant- and adult-directed vocalizations, within-voices, in speech, song or both. Consistent with the LASSO results (Fig. 1b and Supplementary Table 2), the acoustic features operated differently across speech and song. For example, median pitch was far higher in infant-directed speech than in adult-directed speech, whereas median pitch was comparable across both forms of song. Some features were highly consistent across fieldsites (for example, lower inharmonicity in infant-directed speech than adult-directed speech), whereas others were more variable (for example, lower roughness in infant-directed speech than in adult-directed speech). The boxplots, which are ordered approximately from largest to smallest differences between effects across speech and song, represent each acoustic feature’s median (vertical black lines) and IQR (boxes); the whiskers indicate 1.5× IQR; the notches represent the 95% CI of the medians; and the doughnut plots represent the proportion of fieldsites where the main effect repeated, based on estimates of fieldsite-wise random effects. Only comparisons that survived an exploratory–confirmatory analysis procedure are plotted; the faded boxplots denote comparisons that did not reach statistical significance in confirmatory analyses. Significance values are computed via linear combinations with two-sided tests, following multilevel mixed-effects models (n = 1,570 recordings); *P < 0.05, **P < 0.01, ***P < 0.001; no adjustments were made for multiple comparisons, given the exploratory–confirmatory approach taken. Regression results are in Supplementary Table 3 and a full report of fieldsite-level estimates is in Supplementary Table 5. Note: the model estimates are normalized jointly on speech and song data so as to enable comparisons across speech and song for each feature; as such, the absolute distance from 0 for a given feature is not directly interpretable but estimates are directly comparable across speech and song. ID, infant-directed; AD, adult-directed.
Naive listeners distinguish infant-directed vocalizations from adult-directed vocalizations across cultures
Participants listened to vocalizations drawn at random from the corpus, viewing the prompt ‘Someone is speaking or singing. Who do you think they are singing or speaking to?’ They could respond with either ‘adult’ or ‘baby’ (Extended Data Fig. 3). From these ratings (after exclusion n = 473 song recordings; n = 394 speech recordings), we computed listener sensitivity (d′\documentclass[12pt]{minimal} \usepackage{amsmath} \usepackage{wasysym} \usepackage{amsfonts} \usepackage{amssymb} \usepackage{amsbsy} \usepackage{mathrsfs} \usepackage{upgreek} \setlength{\oddsidemargin}{-69pt} \begin{document}$$d^{\prime}$$\end{document}). a, Listeners reliably detected infant-directedness in both speech and song, overall (indicated by the diamonds, with 95% CI indicated by the horizontal lines) and across many fieldsites (indicated by the black dots), although the strength of the fieldsite-wise effects varied substantially (see the distance between the vertical dashed line and the black dots; the shaded regions represent 50%, 80% and 95% CI, in increasing order of lightness). Note that one fieldsite-wise d′\documentclass[12pt]{minimal} \usepackage{amsmath} \usepackage{wasysym} \usepackage{amsfonts} \usepackage{amssymb} \usepackage{amsbsy} \usepackage{mathrsfs} \usepackage{upgreek} \setlength{\oddsidemargin}{-69pt} \begin{document}$$d^{\prime}$$\end{document} could not be estimated for song; complete statistical reporting is in Supplementary Table 5. b, The participants in the citizen-science experiment hailed from many countries; the gradients indicate the total number of vocalization ratings gathered from each country. c, The main effects held across different combinations of the linguistic backgrounds of vocalizer and listener. We split all trials from the main experiment into three groups: those where a language the listener spoke fluently was the same as the language of the vocalization (n = 82,094), those where a language the listener spoke fluently was in the same major language family as the language of the vocalization (n = 110,664) and those with neither type of relation (n = 285,378). The plot shows the estimated marginal effects of a mixed-effects model predicting d′\documentclass[12pt]{minimal} \usepackage{amsmath} \usepackage{wasysym} \usepackage{amsfonts} \usepackage{amssymb} \usepackage{amsbsy} \usepackage{mathrsfs} \usepackage{upgreek} \setlength{\oddsidemargin}{-69pt} \begin{document}$$d^{\prime}$$\end{document} values across language and music examples, after adjusting for fieldsite-level effects. The error bars represent 95% CI of the mean. In all three cases, the main effects replicated; increases in linguistic relatedness corresponded with increases in sensitivity.
Human inferences about infant-directedness are predictable from acoustic features of vocalizations
To examine the degree to which human inferences were linked to the acoustic forms of the vocalizations, we trained two LASSO models to predict the proportion of ‘baby’ responses for each non-confounded recording from the human listeners. While both models explained substantial variability in human responses, the model for speech was more accurate than the model for song, in part because the human listeners erroneously relied on acoustic features for their predictions in song that less reliably characterized infant-directed song across cultures (Figs. 1b and 2). Each point represents a recorded vocalization (after exclusions n = 528 speech recordings; n = 587 song recordings), plotted in terms of the model’s estimated infant-directedness of the model and the average ‘infant-directed’ rating from the naive listeners; the barplots depict the relative explanatory power of the top eight acoustical features in each LASSO model, showing which features were most strongly associated with human inferences (the green or red triangles indicate the directions of effects, with green higher in infant-directed vocalizations and red lower); the dashed diagonal lines represent a hypothetical perfect match between model predictions and human guesses; the solid black lines depict linear regressions (speech: F(1,526) = 773, R² = 0.59; song: F(1, 585) = 126, R² = 0.18; both P < 0.0001; P values computed using robust standard errors); and the grey ribbons represent the standard errors of the mean, from the regressions.
Acoustic regularities in infant-directed speech and song across cultures

July 2022

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487 Reads

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120 Citations

Nature Human Behaviour

When interacting with infants, humans often alter their speech and song in ways thought to support communication. Theories of human child-rearing, informed by data on vocal signalling across species, predict that such alterations should appear globally. Here, we show acoustic differences between infant-directed and adult-directed vocalizations across cultures. We collected 1,615 recordings of infant- and adult-directed speech and song produced by 410 people in 21 urban, rural and small-scale societies. Infant-directedness was reliably classified from acoustic features only, with acoustic profiles of infant-directedness differing across language and music but in consistent fashions. We then studied listener sensitivity to these acoustic features. We played the recordings to 51,065 people from 187 countries, recruited via an English-language website, who guessed whether each vocalization was infant-directed. Their intuitions were more accurate than chance, predictable in part by common sets of acoustic features and robust to the effects of linguistic relatedness between vocalizer and listener. These findings inform hypotheses of the psychological functions and evolution of human communication.


Figure 1. Associations between unadjusted total, basal, activity energy expenditure, physical activity levels, and ambient temperature (A) average temperature ( o C) vs TEE (MJ/day). (B) average temperature ( o C) vs BEE (MJ/day). (C) average temperature ( o C) vs AEE (MJ/day). (D) average temperature ( o C) vs PAL. Each data point is a different individual. The black lines are the least-squares fitted regression lines for males, and the red lines are for females.
Figure 3. Associations between (A): outdoor temperature ( o C) and (B): indoor temperature ( o C) and latitude ( o N)
Human total, basal and activity energy expenditures are independent of ambient environmental temperature

June 2022

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547 Reads

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13 Citations

iScience

Lower ambient temperature (Ta) requires greater energy expenditure to sustain body temperature. However, effects of Ta on human energetics may be buffered by environmental modification and behavioral compensation. We used the IAEA DLW database for adults in the USA (n = 3213) to determine the effect of Ta (-10 to +30°C) on TEE, basal (BEE) and activity energy expenditure (AEE) and physical activity level (PAL). There were no significant relationships (p > 0.05) between maximum, minimum and average Ta and TEE, BEE, AEE and PAL. After adjustment for fat-free mass, fat mass and age, statistically significant (p < 0.01) relationships between TEE, BEE and Ta emerged in females but the effect sizes were not biologically meaningful. Temperatures inside buildings are regulated at 18-25°C independent of latitude. Hence, adults in the US modify their environments to keep TEE constant across a wide range of external ambient temperatures.


Citations (14)


... Traditionally, subsistence relied upon men hunting and women gathering; however, ethno-tourism and agricultural immigrants have increased the prevalence of mixed economies, outsider trade, and wage labour. Despite open access to land and resources amongst Hadza, land and water tensions exist with these external groups including, increasingly, both pastoralists and farmers (Harris et al., 2024;Pollom et al., 2020). Hadza practice bilateral descent and serial monogamy (Crittenden, 2019). ...

Reference:

“Fiercely Egalitarian”: Thematic Cross-Cultural Analysis Reveals Regularities in the Maintenance of Egalitarianism Across Four Independent African Hunter-Gatherer Groups
Hadza Landscape Burning

Human Nature

... Preliminary evidence for our hypothesis may be found in a recent study of the different human cultures working with honeyguide birds who lead humans to bee nests; humans crack open and extract the honey, leaving the wax for the birds to eat. The Hadza-honeyguide and the Yao-honeyguide societies have different communicative signals, and the birds respond to their local signal at a significantly higher rateproviding evidence that these capacities are learned (Spottiswoode & Wood, 2023). ...

Culturally determined interspecies communication between humans and honeyguides
  • Citing Article
  • December 2023

Science

... The model (Kim et al. 2012) assumed a chimpanzee-like ancestral condition with age at maturity and birth intervals scaled to adult longevity as in Charnov's mammal model. Simulations began with very few females surviving as their fertility was ending, the pattern usually observed in chimpanzees , Emery Thompson et al. 2007, Hawkes and Smith 2010, Muller and Wrangham 2014, but see Wood et al. 2023). Then, assuming ecological circumstances drew some hominin ancestors to exploit resources that gave high returns to adults but were not accessible to infants and small juveniles, those few older females' productivity would subsidize dependents, allowing the infants' mothers to bear next offspring sooner. ...

Demographic and hormonal evidence for menopause in wild chimpanzees
  • Citing Article
  • October 2023

Science

... Participants in this study took, on average, 10,998 ± 2916 (s.d.) steps per day during the study period, whereas the average daily step count for adults in the United States is only 4774 (Althoff et al., 2017). In contrast, Hadza hunter-gatherers have been shown to take an average of 15,047 ± 5377 steps per day (Sayre et al., 2023) and Rar amuri subsistence farmers have been reported to take an average of 18,800 ± 4500 steps per day (Shave et al., 2019). It is possible that stronger associations between physical activity levels and foot traits exist, even among adults who habitually wear restrictive shoes, but such associations were undetectable in this study because they are non-linear, or there is some type of threshold effect, and we lacked enough especially inactive participants. ...

Lifestyle and patterns of physical activity in Hadza foragers
  • Citing Article
  • September 2023

American Journal of Biological Anthropology

... Moreover, lack of correlation between densities of fast-food restaurants and obesity prevalence has been reported [7]. Moreover, doubly labeled water studies have demonstrated that energy expenditure from physical activity has remained relatively stable since the late 1980s [8]. Furthermore, an upward trend in birth cohort body mass index throughout the 20th century has been observed, with a marked acceleration after World War II [6,9,10]. ...

Total daily energy expenditure has declined over the past three decades due to declining basal expenditure, not reduced activity expenditure

Nature Metabolism

... Higher temperatures, higher activity levels, and/or low water content diet may increase water needs. 19 Greater levels of stress and/or increased consumption of caffeine and alcohol may disturb sleep. [20][21][22] Unlike PSG, PPG technology cannot assess brain waves to record sleep stages. ...

Variation in human water turnover associated with environmental and lifestyle factors

Science

... That is, a randomly selected sample of males is believed to exhibit more variability amongst themselves in terms of, for example, their weight than is a similarly sized sample of females. This phenomenon is termed greater male variance (GMV), but the extent to which it applies across traits and taxa is far from clear [3][4][5][6], with many studies underpowered [7]. Moreover, rather than showing GMV, some traits show the reverse pattern of greater female variance (GFV) [3,6,8,9]. ...

Variability in energy expenditure is much greater in males than females

Journal of Human Evolution

... In clinical settings, such articles have used mostly biochemical parameters as indices, such as blood glucose, lipid metabolites, energy regulation hormones, or markers for inflammation and cell signaling components. [4][5][6][7] Although essential to formulating selected clinical judgments, such criteria seldom directly address the fundamental principles that drive energy balance and homeostasis, that is, physical properties critical to thermogenic regulation and thermodynamic principles. Moreover, relying on only biochemical parameters without considering the underlying physical principles can lead to conceptual and clinical misinterpretations ascribed to biological processes. ...

Human total, basal and activity energy expenditures are independent of ambient environmental temperature

iScience

... Similar to CDS, singing is a universal part of caregiving routines across the world (Mehr et al. 2019;Hilton et al. 2022) and provides a powerful means to modulate children's arousal state (Cirelli et al. 2019). In addition to their socio-emotional appeal, songs should be considered a source of native languageinput for young children. ...

Acoustic regularities in infant-directed speech and song across cultures

Nature Human Behaviour

... Earliest evidence on animal cultures came from studies of chimpanzees from more than 50 years ago [18], while fossil evidence indicates the use of stone tools in chimpanzees dating back around 4300 years [103]. Although modern science may have been slow to develop tools to recognize cultural transmission in species beyond our own, some Indigenous Peoples and local communities have long understood the transmission of knowledge between ourselves and other species, through intergenerational mutualism between a range of species from birds to killer whales [104][105][106][107]. Integrating different streams of knowledge with this depth of understanding on people and place will be an essential part of this field moving forward. ...

The ecology and evolution of human‐wildlife cooperation