Research ArticleEVOLUTIONARY BIOLOGY

Same father, same face: Deep learning reveals selection for signaling kinship in a wild primate

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Science Advances  27 May 2020:
Vol. 6, no. 22, eaba3274
DOI: 10.1126/sciadv.aba3274

Abstract

Many animals rely on facial traits to recognize their kin; however, whether these traits have been selected specifically for this function remains unknown. Using deep learning for face recognition, we present the first evidence that interindividual facial resemblance has been selected to signal paternal kinship. Mandrills (Mandrillus sphinx) live in matrilineal societies, in which females spend their entire lives not only with maternal half-sisters (MHS) but also with paternal half-sisters (PHS). We show that PHS have more differentiated social relationships compared to nonkin, suggesting the existence of kin recognition mechanisms. We further demonstrate that facial resemblance increases with genetic relatedness. However, PHS resemble each other visually more than MHS do, despite both kin categories sharing similar degrees of genetic relatedness. This paternally derived facial resemblance among PHS indicates selection to facilitate kin recognition. This study also highlights the potential of artificial intelligence to study phenotypic evolution.

INTRODUCTION

Kin selection, the process by which traits are favored because of their beneficial effects on the survival of relatives (1, 2), is a major evolutionary force shaping cooperative interactions in animal societies (1, 3). Kin selection often implies kin recognition, which, in many species, is mediated by facial traits (4). In humans, facial traits are both the most morphologically variable and the most singular and recognizable features of the physical appearance (5). They are also highly heritable, some showing more than 90% of heritability (6, 7), resulting in elevated facial resemblance among relatives and across generations. Consequently, both human and nonhuman primate subjects are able to infer genetic relatedness from faces, in conspecifics (810) and in members of other species (11, 12). However, whether kin-biased facial resemblance merely reflects genetic ancestry or results from selection to facilitate kin recognition remains unknown. Here, we test whether interindividual facial resemblance among paternal relatives has been kin-selected, using a state-of-the-art artificial intelligence approach based on deep neural networks (DNNs) and long-term data obtained from a natural population of primates.

As many other mammals, some nonhuman primates live in multimale-multifemale groups structured around maternally related females (matrilines) and are characterized by male-biased dispersal. In these societies, reproduction is often skewed toward a few high-ranking males, whose dominance rank is frequently turned over (13). This pattern also characterizes mandrills (Mandrillus sphinx), an Old World primate inhabiting the rain forests of Central Africa. In this species, reproduction is seasonal and male-male competition is fierce, resulting in an alpha male’s monopolization of about 70% of the annual reproductive events in captivity (14) and probably also in the wild (see Supplementary Results). As a consequence of this high reproductive skew, most newborn infants of a given cohort are related through the paternal line but are born into different matrilines. While maternal half-siblings are necessarily familiar with each other from birth onward because they are raised together in the same social environment, paternal half-siblings should be less familiar with each other because they grow up in different families. Yet, there is some evidence from studies on captive mandrills that juvenile paternal half-siblings have differentiated social relationships (15), suggesting that they do recognize each other as kin.

Paternal half-siblings are often close in age because an alpha male’s tenure generally lasts for a short period of time (14). Kin recognition may therefore rely on cues of age proximity, as found in female yellow baboons [Papio cynocephalus (16)] and rhesus macaques [Macaca mulatta (17); see also (18)]. In mandrills, as in other primate species [e.g., in female blue monkeys Cercopithecus mitis (19)], however, paternal half-siblings recognize each other even when they are not close in age (15). In these species, kin recognition is probably mediated by phenotype-matching mechanisms, when interaction patterns reflect a correlation between phenotypic and genetic resemblances (18). In this study, we investigate whether facial traits act as a signal of kinship in mandrills, a primate species with a matrilineal social organization characterized by the presence of numerous paternal half-siblings.

We investigated the only free-ranging population of habituated but unprovisioned mandrills (ca. 220 individuals) on which detailed individual-based data on life history, behavior, and demography have been collected since 2012. On the basis of patterns of reproduction in this population (see Supplementary Results), we estimated that females, the philopatric sex, encounter, on average, 2.1 times more paternal half-sisters (PHS) than maternal half-sisters (MHS) in their group during the course of their lifetime. As predicted by kin selection theory (1), these numerous PHS represent a pool of potential social partners who may contribute to an increase in an individual’s inclusive fitness. We therefore expect strong selection on phenotypic traits facilitating PHS recognition in this species. In addition, the variance in the number of PHS in females is 12.8 times higher than that of MHS in the studied population (see Supplementary Results; table S1). This difference is a direct consequence of the high male reproductive skew because the alpha males’ daughters have many PHS, whereas the daughters of subordinate males only have a few PHS. The high variance in the number of PHS should select for an efficient (i.e., error-free) system of kin recognition and signaling. Thus, in such a matrilineal society, individuals should recognize MHS using cues from their matrilineal social environment, but they should also recognize PHS by relying on other cues.

We hypothesize that facial traits are under strong selection to facilitate kin recognition among PHS. We first predict that, all else being equal, PHS show more differentiated social relationships than nonkin (NK): They should, for example, associate and affiliate more with each other. Second, we predict that facial traits are under kin selection: PHS should resemble each other more than expected given their genetic resemblance. Thus, they should resemble each other more than NK do but, more importantly, also more than MHS do, even though PHS and MHS share, on average, the same degree of genetic relatedness (r = 0.25). For the past 8 years, we have collated a photobank of about 16,000 facial pictures on a total of 276 individuals, some of which are represented with regular portraits from birth to adulthood. This unique long-term resource allowed us to control for confounding effects of age difference (MHS are necessarily at least 1 year apart whereas PHS are generally age mates) on mandrill’s faces.

We used DNNs to measure the resemblance between female faces. DNNs have revolutionized the computational study of facial resemblance over the last 5 years, now outperforming human capabilities in recognizing people by their face from a photograph (20). DNNs use a cascade of multiple layers of interconnected neurons that build representations of faces with different levels of abstraction and complexity. The deeper layers ultimately represent entire faces in an informative and low-dimensional space, the so-called deep feature space (DFS). The DFS is informative because it is insensitive to variations that are irrelevant for the task the DNN has been trained on. For example, for face recognition, a DNN learns to identify individuals independently of lighting, head orientation, haircut, and accessories. In a DFS, two portrait images that differ only by these irrelevant variations are located at the same place, and, thus, the distance between images in that space reliably estimates resemblance between individuals (21). Here, we embedded portrait images into a DFS shaped specifically to represent the identity of female mandrills. To our knowledge, this is the first study that uses a DFS to quantify phenotypic resemblance in wild animals.

RESULTS

Kinship and sociality

PHS exhibit differentiated social relationships: They are spatially closer and share more grooming and more aggression compared to NK (Table 1 and Fig. 1). Restricting our datasets to pairs close in age (<2 years apart) yielded qualitatively similar results (table S2). Although MHS generally show the highest frequencies of association and interactions, the average social phenotypes of PHS and MHS are statistically similar. This result suggests that adult PHS recognize each other as kin.

Table 1 Kinship and social behavior.

Statistics obtained from generalized linear mixed models (proc GENMOD, SAS Studio) with a negative binomial distribution performed to study the relationships between social behavior (grooming and aggression) or spatial association recorded across 45 adult females and a set of explanatory variables, including kinship. Rank difference stands for the distance in rank in females from the studied pairs (see Materials and Methods); for example, “0” indicates females of equal rank and “1” indicates pairs composed of a low- and a mid-ranking female or pairs composed of a high- and a mid-ranking female.

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Fig. 1 Kinship and social behavior.

Mean frequencies (and SEM) of social behavior and spatial association across kin categories in 45 adult females over 8 years (2012 to 2019). The figure is based on raw data: time spent grooming per hour, number of aggressive interactions observed per hour, and frequency of spatial association. Pairwise differences in least square means (LSMEANS statement; SAS Studio) were calculated across kin categories for grooming and aggression. For spatial association, the effect of kinship was found in interaction with females’ age difference (Table 1). However, a closer examination of the data revealed that the same general pattern as the one depicted in the figure was observed across pairs of various age differences. We chose to present the simple effect of kinship for the sake of clarity. Sample sizes (pairs of females) are provided in parentheses.

Deep feature space to estimate facial resemblance

We estimated facial resemblance between female mandrills through the distance of their portrait images in a DFS (“face distance” hereafter). We used a two-step pipeline that performs a face identification task followed by a face verification task. For the face identification task, we used a DNN pretrained to identify human faces, which we retrained with mandrill images (different individuals from the ones used in this study; table S3). The newly trained DNN could recognize individuals (N = 202) with up to 91.9% of correct identification (table S4). This high performance indicates that our DNN is able to build a DFS that informatively represents mandrills’ faces. In the face verification task, a distance metric was learned such that the distance between same-individual pictures in the DFS was minimized. When evaluated with the studied females, the face verification model could identify whether two pictures represented the same individual with an accuracy of 83% for the adult females (table S5) and 90% for the juvenile females (table S6) despite the fact that the model was totally naïve to these individuals. This model was used to measure the average facial resemblance between all pairs of adult females and all pairs of juvenile females from the studied population. These phenotypic data were then compared to genetic data.

Genetic and facial resemblance

We studied the relationship between genetic relatedness, obtained from a well-resolved pedigree based on genetic analyses, and face distance across 38,515 pairs of pictures collected on 38 adult females (703 different pairs in total). While controlling for the identity of female pairs (random effect) and the difference in age between females within pairs, we demonstrate a negative relationship between genetic relatedness and face distance (general linear mixed models; estimate = −2.33; F = 43.09; P < 0.0001): Related females look more alike than unrelated females (Fig. 2). For example, compared to the average distance between faces of the same individual, the average face distance increases by 26% for pairs with a coefficient of relatedness r = 0.5, corresponding to, e.g., mother-offspring pairs, and by 36% for pairs with an r = 0.0625, corresponding to, e.g., first cousins.

Fig. 2 Genetic relatedness and face distance.

Mean raw face distances (±SD) across the different values of relatedness observed across 38 adult females. For scaling, we represented the averaged face distance obtained from pictures taken on the same females (i.e., intraindividual resemblance, open diamond). For the sake of clarity and for illustrative purposes, we depicted a regression line based on these averaged relatedness values. SDs are provided rather than SEM to depict the full range of variation of face distances.

Kinship, facial resemblance, and female development

We explored whether kinship was detectable from faces and, if so, when this occurred during females’ development. We treated kinship as a discrete variable and restricted our analyses to MHS and PHS with an equivalent degree of genetic relatedness (r ~ 0.25) that we compared to NK pairs. Analyzing 6992 pairs of portrait images corresponding to 45 adult females (159 pairs in total), we show that face distances differ significantly across kin categories in interaction with the difference in age between the portraits of pairs of females (Table 2). A closer examination of various classes of age differences (e.g., 0 to 1 year, 1 to 2 years, 2 to 3 years, and so on) reveals that the interaction between kinship and age difference disappears when splitting pairs of portraits of females aged less than 2 years apart from those aged more than 2 years apart. Across pairs aged less than 2 years apart, PHS show the lowest face distance; i.e., they resemble each other more than either NK or MHS do (Table 2A and Fig. 3). Across pairs aged more than 2 years apart, kinship only marginally explains face distances (Table 2A), with NK being the most dissimilar, compared to the other two kin categories (Fig. 3). In juvenile females, we observe a similar effect of the interaction between kinship and age difference on face distances. Again, this interaction disappears when splitting pictures of juveniles aged less than a year apart from those aged more than a year apart (Table 2B). PHS aged less than a year apart resemble each other more than MHS or NK do. Unexpectedly, MHS and NK do not differ significantly from each other in these young females. This pattern holds true when considering pairs aged more than a year apart, although kinship does not significantly affect face distances overall, probably because of a restricted sample size (Table 2B and Fig. 3).

Table 2 Kinship and face distance.

Statistics obtained from general linear mixed models (proc GLIMMIX, SAS Studio) performed to study the relationships between face distances and a set of explanatory variables, including kinship, in (A) all adult female-female pairs of pictures, pairs aged less than 2 years apart, and pairs aged more than 2 years apart; and in (B) all juvenile female-female pairs, pairs aged less than a year apart, and pairs aged more than a year apart.

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Fig. 3 Kinship and face distance.

Mean raw face distances (and SEM) across kin categories for pictures taken on 45 adult and 16 juvenile females at two age differences. Pairwise differences in least square means (LSMEANS statement; SAS Studio) were calculated across kin-age classes. Sample sizes (pairs of pictures) are provided inside bars. An example of a set of pictures involving one female focal and her three categories of kin is provided. Numbers below the pictures represent the averaged face distance across pictures of the focal female with herself, her PHS, her MHS, and her NK. Photo credits: Jade Meric de Bellefon and Benjamin Laubi, Projet Mandrillus, SODEPAL.

DISCUSSION

In this study, we asked whether facial traits may facilitate kin recognition. We investigated a species in which the intensity of selection to recognize relatives should be different between two kin categories, PHS and MHS, even though both categories share, on average, the same degree of genetic relatedness. As predicted, we found the highest facial resemblance among those kin probably under the strongest selection for kin recognition. This result indicates that facial resemblance among relatives may be adaptive because it goes beyond merely reflecting genetic resemblance.

In mandrills, PHS exhibit differentiated social relationships: They are spatially closer and association affords more opportunities for social interactions. This first result is remarkable for a matrilineal society where maternal relatedness profoundly influences female social relationships (22). In captive mandrills, juveniles also show elevated affiliation toward both their adult PHS and their adult MHS; however, they affiliate more with their juvenile MHS than with their juvenile PHS, probably because their social relationships are mitigated by their common mother at these young ages (15).

If individuals tend to interact more with paternal than maternal relatives, the kinship theory of genomic imprinting, which invokes a mechanism based on epigenetic processes, predicts a differential expression of patrigenic versus matrigenic alleles because of different consequences for their respective inclusive fitness (23). In humans, genomic imprinting has been proposed to account for the temporary greater mother-infant facial resemblance compared to fathers through pleiotropic effects. Indeed, maternal genes are expressed preferentially to control resource allocation during fetal development (24). Mother-child early facial resemblance would then be a by-product of genomic imprinting during fetal life, explaining why resemblance to mothers decreases between birth and 1 year of age (25).

We propose that genomic imprinting may also underlie increased facial resemblance among PHS in mandrills. Indeed, facial resemblance among PHS not only is higher at early ages but also lasts until adulthood and long after their father’s secondary dispersal. This difference between humans and mandrills (maternal resemblance versus paternal resemblance, respectively) may originate from the distinct social organization of mandrills compared to humans. Female mandrills may have many PHS in their group throughout their life; however, most PHS live in different maternal families. This social setting has probably generated intense selection on communicative traits related to the paternal line, allowing paternal kin recognition and subsequent nepotistic behaviors. In line with this idea, we recently showed that genetic relatedness is also encoded in mandrills’ voice (26). These phenotypic cues of relatedness produced differentiated behavioral responses: Captive mandrills are able to discriminate unfamiliar relatives on the basis of either acoustic (26) or visual cues (8) alone, although we did not test the impact of parental ancestry (paternal versus maternal lineage) as we do in the present study.

High facial resemblance among PHS may also be a by-product of high resemblance to a common father that may have evolved to facilitate paternal care. In a polygynous human population, for example, paternal investment is positively correlated to father-child facial resemblance (27). We think, however, that this explanation does not apply to mandrills because (i) they are highly dimorphic and an adult male does not resemble any other mandrill, (ii) males are only temporary resident in the social group of their offspring, and (iii) evidence of true paternal care is limited in this species (15). Other selective pressures, such as infanticide or incest avoidance, may also have shaped facial resemblance among PHS as a by-product of resemblance to the father (infanticide) or among mixed-sex pairs of paternal half-siblings (incest avoidance). In primates, however, infanticide is usually mitigated through strategies of paternity confusion (28). We would therefore expect infanticide avoidance to result in lower facial resemblance among PHS. Regarding incest avoidance, natal male mandrills generally disperse before entering into the competitive reproductive arena (29), making this an equally unlikely explanation. Even though we cannot exclude paternal care or incest avoidance completely as alternative or additional selection forces, we think that nepotism among philopatric females is the most likely explanation for selection for high facial resemblance among PHS in mandrills. The benefits of differentiated social relationships, such as increased affiliation or proximity, can affect health, reproduction, and survival in multiple species, including humans (30), nonhuman primates (31), and other vertebrates (32). For example, female baboons that are socially better integrated enjoy improved offspring survival (31, 33) and live longer (34). These effects appear to be mediated by affiliative interactions, such as grooming, which, in addition to hygienic functions (35), decreases cortisol levels of both groomers and groomees (36). Grooming PHS preferentially would therefore increase both the direct component of individual fitness (although also true for grooming a random groupmate) and the indirect component, as predicted by kin selection.

These results leave us with an open question about the ability of female mandrills to evaluate their own facial resemblance to others [“self-referent phenotype matching” (37)]. Although there is evidence for self-referent phenotype matching in animals (18) and some primates know what they look like (38), a more plausible explanation is that association and behavioral biases among PHS in mandrills are mediated by third parties, such as mothers. If mothers evaluate the facial resemblance of their offspring during juvenescence and, as a consequence, behave differentially with juveniles and/or their mothers, then behavioral biases may persist in these juveniles until adulthood. The fact that the difference in facial resemblance between MHS and PHS is the highest in juvenile females and that MHS are indistinguishable from NK at these young ages supports this view. Collecting detailed behavioral data on associations among mothers will allow one to test this prediction.

Last, this study highlights the potential of deep learning for the quantitative investigation of complex animal phenotypes. Faces are a typical example of such phenotypes: They can be described in multiple ways, emphasizing either details such as skin texture or the specific position of a mole or more global features such as the contour roundness. Describing faces has been therefore a historical challenge for both computer scientists and psychologists (39). The explosive popularity of DNNs in face recognition studies originates from their unprecedented capacity to extract the necessary but sufficient information to describe faces (39). However, beyond faces, DNNs can informatively describe any kind of complex phenotypes. Very recently, this approach has been leveraged to study phenotypic evolution from images of collected specimens [e.g., (40)]. With our study, we highlight that DNNs further allow the investigation of phenotypes in field conditions, where standardizing animal’s position for photographs is impossible, thereby opening new research opportunities in evolutionary biology with long-lived or endangered species.

MATERIALS AND METHODS

Studied population

Since April 2012, we have been monitoring the only habituated social group of free-ranging, not provisioned mandrills inhabiting the Lékédi Park in Southern Gabon (Bakoumba) within the framework of the “Mandrillus Project” (www.projetmandrillus.com). This group originates from 65 captive-born mandrills housed at the CIRMF (Centre International de Recherches Médicales de Franceville, Gabon) and released into the park on two occasions [36 individuals released in 2002 and 29 in 2006; see (41) for details]. At the end of this study (June 2019), the group included ca. 220 individuals of both sexes and all ages, about 160 of them being individually known and daily monitored (42). The studied population is vulnerable to predators and pathogens and, since 2012, has not been manipulated except during trappings that occurred occasionally [see (42) for details]. During everyday observations, we typically record detailed data on group living and composition as well as on social behavior. For the purpose of this study, we considered a total of 50 different females including 16 juveniles (aged 1.3 to 3.8) who contributed to the juvenile dataset of portrait images and 45 adults (aged 4.1 to 26.4) who contributed to the adult datasets of portrait images and social behaviors (some juveniles were also included in the adult data set). Dates of birth were either known to a few days thanks to daily monitoring (28 females) or approximated from general condition and patterns of tooth wear (22 females). For most of these later females (70%), the error made in age estimation was less than a year. Removing from our analyses the few females for which the error made was estimated to be more than a year did not change our results (not shown).

Genetic relatedness and kinship

DNA from the 50 studied females was extracted from either blood (46 females) or fecal (4 females) samples. Blood was collected during annual trappings that occurred from 2012 to 2015 [see (8) for details]. Fecal samples were collected on each occasion. DNA extractions either from the buffy coat or from fresh fecal pellets were performed using either QIAamp DNA Blood or Stool Mini Kits (Hilden, Germany), respectively. Microsatellite genotyping was carried out using 12 to 36 primer pairs (14, 43). Paternity analyses were performed with Cervus 3.0 software using previously described procedures (14). We reconstructed the full pedigree of the 16 females born in captivity going back as far as the generation of unrelated founder animals (14). We genetically determined both parents for 25 individuals out of the 34 females born into the wild. Pairwise genetic relatedness was calculated from the pedigree only for those females with at least the four parents unambiguously known using ENDOG version 4.8 (44). In addition, only these pairs of females with the four parents known served as possible NK. For the remaining nine females, we knew only the mother’s identity (eight females) or the father’s identity (one female) because the genetic sample did not match any adult male or female of the genetic database. We used these nine females to determine PHS or MHS pairs because none of these resulting pairs may have been full siblings (we did not use them when studying the relationship between genetic relatedness and facial resemblance). In addition to PHS (sharing the same father) and MHS (sharing the same mother) pairs, we considered as NK these females that shared less than r ≤ 0.0325. We excluded the few full siblings from our datasets and all other more distant kin categories because of our main research question.

Behavioral observations

Since August 2012, trained observers, blind to the research question, have performed behavioral observations on 45 adult females (≥4 years) using 5-min focal sampling (totalizing 1776 hours of focal observations; mean per female ± SD: 39.5 ± 41.8). During these focal observations, all social interactions between these females, including time spent grooming and aggressive behavior (grasp, bite, chase, lunge, ground slap, and head bob) considered as bouts, were recorded. In addition to grooming and aggression, we considered spatial associations: Three times during each focal observation, we scanned and recorded all studied females located less than 5 m away from the focal female. We pooled all the behavioral data over the entire study period to improve our statistical models (see below). For these behavioral analyses, we considered 48 pairs of PHS, 23 pairs of MHS, and 64 pairs of NK for which the age difference was ≤6.5 years because, in this dataset, there was no PHS more different in age than this threshold.

Female dominance rank was evaluated using the outcomes of approach-avoidance interactions collected during focal observations or ad libitum observations and calculated using normalized David’s score [as per (42)]. We divided adult females into three classes of rank of similar size across the entire study period (high ranking, medium ranking, and low ranking).

Measuring facial resemblance

Image datasets. Our complete database includes ~16,000 portrait images of 276 different mandrills. This database was split into a learning set and a test set, which are different for the adult female and juvenile female analyses (Fig. 4; see the Supplementary Materials). For the adult female analysis, the learning set included pictures of semicaptive and captive males and females of all age classes (obtained from captive groups), as well as wild individuals from the studied population, except adult females. For the juvenile analysis, the learning set was the same as above, but it included adult females from the studied population but excluded juveniles from this population. Because the face of a given individual varies considerably between its different age classes (results not shown), we trained the algorithm to recognize ind-age classes (i.e., individual at a given age class) rather than individual classes. The learning sets were, in turn, split into a validation set (two images per class) and a training set (other images). The validation set was used to compare the accuracy of identification between different parameter settings; however, for measuring resemblance in the test set, we used a DNN trained on the entire learning set. We compared training sets with different levels of image quality and number of images per class (see the Supplementary Materials). The test set included either adult or juvenile females from the study population. All portraits were downsized to 224 × 224 before analyses.

Fig. 4 Pipeline for measuring facial resemblance.

The pipeline contains two main steps. During the face identification step, a deep neural network previously trained for human face recognition (VGG-Face) is retrained to identify mandrill faces. The newly trained network is then used in a face verification task, first to learn a distance metric using a support vector machine (SVM) trained to detect whether two faces represented by their feature activation vectors (i.e., coordinates in the DFS) represent the same individual or not, and then to compute the resemblance (i.e., the distance in the DFS) between pairs of portrait images for the studied population.

Embedding portrait images into a DFS. We used the popular VGG16 architecture to recognize mandrills individually (Fig. 4). Rather than training the algorithm from scratch (i.e., initializing it with random weights), we used VGG-Face (20) as a starting point and retrained this network with mandrill portraits. This procedure, called “transfer learning,” allows one to reach high model performance even with relatively small datasets (45). VGG-Face is a VGG16 that previously learned to recognize 2600 different humans from a total of 2.6 million portrait pictures. As typical with DNNs, VGG-Face builds representations of faces hierarchically: first, shallow layers represent very simple and local features, for example, skin color and texture; the medium layers combine these features to represent more complex shapes and color patterns such as a pupil; the deeper layers combine previous features to represent an entire face; and the very last layer eventually classifies face images into different ind-age classes (39). Transfer learning exploits the fact that features of shallow layers usually describe universal properties of images and, thus, need no or minimal tuning when used for a new task or with a new dataset (45), contrary to deep features that are task and image specific. For fine-tuning VGG-Face with mandrill images, we thus set a very small (10−5) learning rate for shallow and medium layers and a slightly larger learning rate for deep layers (10−3 decreasing down to 10−5 at the end of training), and we entirely replaced the last classification layer. Training stopped after approximately 15 epochs (see the Supplementary Materials) to produce our new DNN: VGG-Mandrill (Fig. 4). All image analyses were performed using MATLAB.

Distance metric learning. Facial resemblance can be estimated by simply measuring the distance between images embedded in the DFS. However, not all features defining the DFS are similarly good for estimating facial resemblance. Following a method developed earlier (21), we learned a resemblance metric that calculates the weights of features that optimize a face verification task. We first extracted the feature activation vector (i.e., the coordinates in the DFS) of all images of the training set in the DFS of VGG-Mandrill. Next, we randomly selected 15,000 pairs of images representing different individuals and 15,000 pairs representing the same individuals, and for each of pair, we calculated the χ2 difference (f1[i] − f2[i])2/(f1[i] + f2[i]), where f1 and f2 are the feature activation vectors of the two images and i is the feature index (the χ2 difference has the same dimensionality as feature activation vectors). Then, we run a linear support vector machine (SVM) with the χ2 difference vectors in explanatory variables and 0 (different-individual pairs) or 1 (same-individual pairs) as a response variable. This SVM output feature weights ωi, which were used to calculate a weighted χ2 distance as χ2(f1,f2) = Riωi(f1[i] − f2[i])2/(f1[i] + f2[i]). We calculated the weighted χ2 distance between all pairs of images in the test sets.

Studied pairs and validation. To study facial resemblance in adult females, we considered 50 pairs of PHS, 30 pairs of MHS, and 79 pairs of NK for which the age difference was ≤9.3 years because, in this dataset, there was no PHS more different in age than this threshold. In juvenile females, we studied 16 pairs of PHS, 5 pairs of MHS, and 27 pairs of NK for which the age difference was ≤1.8 years for the same reason. We checked that intraindividual facial resemblance (identical female with photographs taken at various ages) was greater than any other pairs analyzed (table S7).

Statistical analyses

Kinship and sociality. To study the relationship between kinship and social behavior, we summarized 8 years of data collected on a monthly basis. Each month, from August 2012 to June 2019, we considered all possible pairs among the 45 studied adult females when we had collected at least one focal sample (for grooming and aggression) or recorded at least one spatial association for each female of the pair (for association). The final monthly dataset contained a large majority of zeros; we therefore pooled these data across the years and for each studied pair to improve our statistical models. We used generalized linear models (proc GENMOD, SAS Studio) with a negative binomial distribution to study the relationships between time spent grooming (in seconds), number of aggression, and number of associations along with a set of explanatory variables. We considered as an offset the log-transformed total time of observation or the log-transformed total number of scans performed during the study period on each female of the pair, to adjust for variation in sampling effort. We considered the following as explanatory variables: the difference in social rank between the two females of the pair (class variable with three modalities: no rank difference; rank difference of one, corresponding to the difference between low- and mid-ranking females or between high- and mid-ranking females; and rank difference of two, corresponding to the difference between low- and high-ranking females) and the absolute difference in age between the two females of the pair (continuous variable) and their kinship (class variable with three modalities: PHS, MHS, and NK). We further considered the interaction between difference in age and kinship to control for possible combined effects. We kept full models as final models excluding only the interaction when not significant.

Genetic and facial resemblance. To study the relationship between genetic relatedness and facial resemblance (considered as a distance) calculated from pairs of photographs taken on 38 adult females with at least both parents known, we used general linear mixed models (proc GLIMMIX, SAS Studio) with face distance as a response variable and the following explanatory variables. We considered the genetic relatedness of each pair (continuous variable ranging from 0.016 and 0.656) and the absolute difference in age between the two females of the pair (continuous variable). We further considered the interaction between difference in age and genetic relatedness to control for possible combined effects. The identity of the pair was considered as a random factor to control for the possible non-independency of the data. We kept the full model as the final model excluding only the interaction when not significant.

Kinship and facial resemblance. To study the relationship between kinship and facial resemblance (considered as a distance) calculated from pairs of photographs taken on 45 adult and on 16 juvenile females, we used general linear mixed models (proc GLIMMIX, SAS Studio) with face distance as a response variable and the following explanatory variables. We considered the kinship of each pair (class variable with three modalities: PHS, MHS, and NK) and the absolute difference in age between the two females of the pair (continuous variable). We further considered the interaction between difference in age and kinship to control for possible combined effects. Because we found a significant effect of this interaction on face distances in both adult and juvenile females, we repeated our analyses across different age differences to determine when this interaction is no longer significant (see Results). The identity of the pair was considered as a random factor to control for the possible non-independency of the data. We kept the full models as final models excluding only the interaction when not significant.

SUPPLEMENTARY MATERIALS

Supplementary material for this article is available at http://advances.sciencemag.org/cgi/content/full/6/22/eaba3274/DC1

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REFERENCES AND NOTES

Acknowledgments: We are grateful to past and present field assistants of the Mandrillus Project who collect daily behavioral data on the study population; to the Wildlife Reserves of Singapore, the Zoo of Granby, and the Primatological Centre at CIRMF (Gabon) for providing pictures of their mandrills; and to the SODEPAL-COMILOG society (ERAMET group) for their long-term logistical support and contribution to the Mandrillus Project. This is a Project Mandrillus publication number 22 and ISEM 2020-044-SUD. Funding: This study was funded by several grants that allowed long-term collection of data: Deutsche Forschungsgemeinschaft (DFG, KA 1082-20-1) to P.M.K. and M.J.E.C., SEEG Lékédi (INEE-CNRS) to M.J.E.C., and Agence Nationale de la Recherche (ANR SLEEP 17-CE02-0002) to M.J.E.C. This study was approved by an authorization from the CENAREST institute (permit number, AR0060/18/MESRS/CENAREST/CG/CST/CSAR). Author contributions: M.J.E.C. and J.P.R. designed the study and wrote the first version of the manuscript; J.M.d.B., B.L., M.H., C.P., and P.M.K. collected behavioral and photographic data; M.H. and M.J.E.C. performed genetic analyses; J.P.R. performed deep neural network analyses; and M.J.E.C. performed the statistical analyses. All authors contributed to writing the article. Competing interests: The authors declare that they have no competing interests. Data and materials availability: All data needed to evaluate the conclusions in the paper are present in the paper and/or the Supplementary Materials. Additional data related to this paper may be requested from the authors. The Mandrillus Face Database and the computer codes that support the findings of this study are available on request from the corresponding author.
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