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. 2015 Mar;11(3):20140978. doi: 10.1098/rsbl.2014.0978

Reported maternal tendencies predict the reward value of infant facial cuteness, but not cuteness detection

Amanda C Hahn 1,, Lisa M DeBruine 1, Benedict C Jones 1
PMCID: PMC4387492  PMID: 25740842

Abstract

The factors that contribute to individual differences in the reward value of cute infant facial characteristics are poorly understood. Here we show that the effect of cuteness on a behavioural measure of the reward value of infant faces is greater among women reporting strong maternal tendencies. By contrast, maternal tendencies did not predict women's subjective ratings of the cuteness of these infant faces. These results show, for the first time, that the reward value of infant facial cuteness is greater among women who report being more interested in interacting with infants, implicating maternal tendencies in individual differences in the reward value of infant cuteness. Moreover, our results indicate that the relationship between maternal tendencies and the reward value of infant facial cuteness is not due to individual differences in women's ability to detect infant cuteness. This latter result suggests that individual differences in the reward value of infant cuteness are not simply a by-product of low-cost, functionless biases in the visual system.

Keywords: incentive salience, motivational salience, baby, parental behaviour, maternal desire

1. Introduction

Facial cuteness can have important effects on adult responses to infants. Adults report being more likely to care for, protect and form close bonds with infants displaying cute facial characteristics [14]. Similar patterns of results have been observed in studies of the actual care provided for infants [5]. Furthermore, neuroimaging [6] and behavioural [7,8] studies suggest that cute infant facial characteristics are rewarding. Similar results have also been reported for responses to infants with and without cleft lips [912] or displaying positive and negative emotional expressions [13].

Some studies report that the effects of infant facial cuteness on perceptual judgements and the reward value of infant faces (the latter assessed via behavioural key-press tasks similar to those used to study the motivational salience of stimuli in non-humans) are greater among women than men [7,8,14,15]. Although it has been suggested that this pattern of results occurs because women's interest in caring for infants is, on average, greater than men's [7,14,15], there have been no direct tests for links between individual differences in women's interest in caring for infants and their responses to infant facial cuteness. Indeed, some studies have not observed stronger responses to infants in women than men [1619], further calling into question the presumed link between interest in caring for infants and women's responses to infant facial cuteness.

In light of the above, we investigated how nulliparous women's reported interest in caring for infants (i.e. what some researchers have called reported maternal tendencies [20,21]) relates to their responses to experimentally manipulated infant facial cuteness in two tasks: a perceptual cuteness rating task and a behavioural key-press task. Because responses on perceptual rating and behavioural key-press tasks are thought to measure different constructs (subjective appraisal or ‘liking’ and ‘wanting’ or motivational salience, respectively [22]), maternal tendencies need not necessarily relate to responses on both tasks in the same way.

2. Material and methods

(a). Participants

Two hundred heterosexual nulliparous women (mean age = 21.93 years, s.d. = 4.58), recruited by following links from social bookmarking websites (e.g. StumbleUpon.com), participated in this online study. Participants were not compensated for their participation. All procedures were approved by the University of Glasgow Psychology Ethics Review Board.

(b). Stimuli

We used computer-graphic techniques [23] to create high-cuteness and low-cuteness prototypes. These possessed the average shape information of the 20 infant faces that received the highest and lowest cuteness ratings, respectively, in a previous study [15]. We then created high-cuteness versions of 10 different infant face images by adding 50% of the linear differences in two-dimensional shape between the high-cuteness and low-cuteness infant prototypes to each of the 10 infant face images (figure 1). Low-cuteness versions of the 10 infant face images were created by subtracting 50% of the linear differences in two-dimensional shape between the high- and low-cuteness infant prototypes from each of the 10 infant face images (figure 1). Mouth shape was held constant [14].

Figure 1.

Figure 1.

High-cuteness (left) and low-cuteness (right) versions of faces used in our study. (Online version in colour.)

(c). Procedure

Half of our participants completed a key-press task used to assess the reward value of infant facial cuteness in previous studies, e.g. [7]. The other half completed a rating task used to assess the effect of morphological cues on infant facial cuteness, e.g. [14]. Participants were randomly allocated to either the key-press or rating task to ensure that possible differences in findings for these tasks could not be due to systematic differences in the characteristics of the two groups of women. See the electronic supporting material for instructions. All participants completed a maternal tendencies questionnaire. The order in which participants completed their face rating/key-press task and the questionnaire was randomized.

(i). Key-press task

All 20 images were presented in a fully randomized order. Participants controlled the viewing duration of each face image by repeatedly pressing designated keys on their keyboard after initiating each trial by pressing the space bar. Participants could either increase the length of time a given face was displayed by alternately pressing the 7 and 8 keys or decrease the length of time a given face was displayed by alternately pressing the 1 and 2 keys. Each key press increased or decreased the viewing duration by 100 ms. The default viewing duration for each image (i.e. the length of time a face remained onscreen if no keys were pressed) was 4 s. All participants key pressed at least once during the task. Participants completed a block of practice trials at the start of the key-press task. Responses to faces assessed using key-press tasks are good predictors of neural measures of the reward value of faces [24].

Key-press scores for each face were calculated by subtracting the number of key presses made to decrease viewing time from those made to increase viewing time. These key-press scores were then used to calculate each participant's cuteness reward score by subtracting the mean key-press score for the low-cuteness versions of infant faces from that for the high-cuteness versions (M = 5.91, s.d. = 10.41). Higher scores indicate a greater effect of cuteness on reward value.

(ii). Rating task

All 20 infant face images were presented in a fully randomized order and were rated for cuteness on a 1 (not cute) to 7 (very cute) scale. We calculated each participant's cuteness perception score by subtracting the mean rating they gave to the low-cuteness versions of infant faces from that they gave to the high-cuteness versions (M = 0.36, s.d. = 0.52). Higher scores indicate that cuteness had a greater effect on ratings.

(iii). Maternal tendencies questionnaire

Participants completed a version of Ahrons' [25] Parental Involvement Scale, in which they were asked to rate on a 1 (not at all) to 5 (very much) scale how involved they would like to be in 10 aspects of child raising (e.g. dressing and grooming your child, taking them for recreational activities). Maternal tendencies were also assessed by asking participants to rate, using a 1 (much less than average) to 7 (much more than average) scale, and relative to others of their age and sex, how much they enjoy interacting with children, how maternal they consider themselves to be, and how strongly they want to have children. These additional questions have been used to assess maternal tendencies in prior work on individual differences in nulliparous women's maternal tendencies [20,21]. Factor analysis of women's average scores on the Parental Involvement Scale and scores on each of the additional questions produced a single maternal tendencies factor with which scores on the three additional questions were highly correlated (all r > 0.88) and with which the Parental Involvement Scale score was moderately correlated (r = 0.47). Scores on the maternal tendencies factor and participant age were not correlated (r = –0.08, p = 0.26).

3. Results

In all analyses, N = 100. We used non-parametric tests for all analyses because some scores were more than three standard deviations from the mean (i.e. were potential outliers). Alternative analyses using t-tests and Pearson's correlations showed identical patterns of results, however.

A Wilcoxon signed-rank test comparing cuteness reward scores with chance (i.e. zero) showed that women looked longer at high-cuteness versions than low-cuteness versions (Z = 6.33, p < 0.001, M = 5.91, s.e.m. = 1.04, d = 0.57). There was also a significant positive correlation between cuteness reward scores and scores on the maternal tendencies factor (ρ = 0.35, p < 0.001, figure 2), indicating cuteness had a greater positive effect on the reward value of infant faces among women reporting greater maternal tendencies. Cuteness reward scores were also positively and significantly correlated with each of the individual measures of maternal tendencies (all p < 0.012).

Figure 2.

Figure 2.

Correlation between cuteness reward scores and scores on the maternal tendencies factor.

A Wilcoxon signed-rank test comparing cuteness perception scores with chance (i.e. zero) showed high-cuteness versions were rated significantly higher than low-cuteness versions (Z = 5.96, p < 0.001, M = 0.36, s.e.m. = 0.05, d = 0.69). However, there was no significant correlation between cuteness perception scores and scores on the maternal tendencies factor (ρ = –0.15, p = 0.14). The correlation between cuteness reward scores and scores on the maternal tendencies factor was significantly stronger than that between cuteness perception scores and scores on the maternal tendencies factor (Z = 3.60, p < 0.001).

4. Discussion

In common with previous work [14,15], women perceived high-cuteness versions of infant faces to be more cute than low-cuteness versions. Also in common with previous work [7,8], responses on the key-press task indicated that high-cuteness versions of infant faces were more rewarding than low-cuteness versions. Importantly, however, reported maternal tendencies were positively correlated with the reward value of infant facial cuteness, but not with perceptions of infant cuteness. These results suggest that (i) maternal tendencies are more closely linked to the reward value of infant facial cuteness than to perceptual judgements of infant cuteness and (ii) the relationship between maternal tendencies and the reward value of infant facial cuteness is not simply due to individual differences in women's ability to detect infant cuteness. This latter result is noteworthy, as it suggests that the relationship between maternal tendencies and the reward value of infant facial cuteness is not simply a by-product of low-cost functionless biases in the visual system. Because we investigated this issue in nulliparous women only, further work is needed to investigate whether motherhood has additional effects on the relationship between reported maternal tendencies and responses to infant cuteness.

That the relationship between maternal tendencies and responses to infant facial cuteness appears to be task-specific (i.e. was evident in responses on the key-press task, but not perceptual ratings) is consistent with prior research suggesting that key-pressing and perceptual judgements measure different components of approach responses: ‘wanting’ or motivational salience and subjective appraisal or ‘liking’, respectively [22]. For example, heterosexual men's subjective ratings distinguish physically attractive from unattractive faces regardless of their sex, but responses on the key-press task distinguish physically attractive from unattractive faces for female stimuli only [24]. Our data extend this distinction between reward value and subjective ratings by demonstrating that only individual differences in the reward value of infant cuteness are related to nulliparous women's reported maternal tendencies.

Supplementary Material

Hahn_supplementary_materials
rsbl20140978supp1.doc (23.5KB, doc)

Supplementary Material

Hahn_data
rsbl20140978supp2.csv (7.4KB, csv)

Ethics statement

All procedures were approved by the local Ethics Review Board at the University of Glasgow and all participants provided informed consent prior to beginning the study.

Data accessibility

The data are available as electronic supplementary material.

Author contributions

A.C.H., B.C.J. and L.M.D. designed the study; A.C.H. and B.C.J. carried out statistical analyses; A.C.H., B.C.J. and L.M.D. wrote the manuscript; all authors gave final approval for publication.

Funding statement

Funded by ERC Starting grant 282655 and ESRC grant ES/1031022/1.

Conflict of interest

The authors state that they have no competing interests.

References

  • 1.Alley TR. 1981. Head shape and the perception of cuteness. Dev. Psychol. 17, 650–654. ( 10.1037/0012-1649.17.5.650) [DOI] [Google Scholar]
  • 2.Alley TR. 1983. Infantile head shape as an elicitor of adult protection. Merrill-Palmer Q. 29, 411–427. [Google Scholar]
  • 3.Glocker ML, Langleben DD, Ruparel K, Loughead JW, Gur RC, Sachser N. 2008. Baby schema in infant faces induces cuteness perception and motivation for caretaking in adults. Ethology 115, 257–263. ( 10.1111/j.1439-0310.2008.01603.x) [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 4.Langlois JH, Ritter JM, Casey RJ, Sawin DB. 1995. Infant face attractiveness affects maternal behaviours. Dev. Psychol. 31, 464–472. ( 10.1037/0012-1649.31.3.464) [DOI] [Google Scholar]
  • 5.Badr-Zahr LK, Abdallah B. 2001. Physical attractiveness of premature infants affects outcome at discharge from the NICU. Infant Behav. Dev. 24, 129–133. ( 10.1016/S0163-6383(01)00068-6) [DOI] [Google Scholar]
  • 6.Glocker ML, Langleben DD, Ruparel K, Loughead JW, Valdez JN, Griffin MD, Sachser N, Gur RC. 2009. Baby schema modulates the brain reward system in nulliparous women. Proc. Natl Acad. Sci. USA 106, 9115–9119. ( 10.1073/pnas.0811620106) [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 7.Hahn AC, Xiao D, Sprengelmeyer R, Perrett DI. 2013. Gender differences in the incentive salience of adult and infant faces. Q. J. Exp. Psychol. 66, 200–208. ( 10.1080/17470218.2012.705860) [DOI] [PubMed] [Google Scholar]
  • 8.Yamamoto R, Ariely D, Chi W, Langleben DD, Elman I. 2009. Gender differences in the motivational processing of babies are determined by their facial attractiveness. PLoS ONE 4, e6042 ( 10.1371/journal.pone.0006042) [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 9.Montirosso R, Fedeli C, Murray L, Morandi F, Brusati R, Perego GG, Borgatti R. 2012. The role of negative maternal affective states and infant temperament in early interactions between infants with cleft lip and their mothers. J. Pediatr. Psychol. 37, 241–250. ( 10.1093/jpepsy/jsr089) [DOI] [PubMed] [Google Scholar]
  • 10.Parsons CE, et al. 2011. The effect of cleft lip on adults’ responses to faces: cross-species findings. PLoS ONE 6, e25897 ( 10.1371/journal.pone.0025897) [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 11.Parsons CE, et al. 2013. Minor structural abnormalities in the infant face disrupt neural processing: a unique window into early caregiving responses. Soc. Neurosci. 8, 268–274. ( 10.1080/17470919.2013.795189) [DOI] [PubMed] [Google Scholar]
  • 12.Murray L, Hentges F, Hill J, Karpf J, Mistry B, Kreutz M, Woodall P, Moss T, Goodacre T. 2008. The effect of cleft lip and palate, and the timing of lip repair on mother–infant interactions and infant development. J. Child Psychol. Psychiatry 49, 115–123. ( 10.1111/j.1469-7610.2007.01833.x) [DOI] [PubMed] [Google Scholar]
  • 13.Parsons CE, Young KS, Bhandari R, van Ijzendoorn MH, Bakermans-Kranenburg MJ, Stein A, Kringelbach ML. 2014. The bonnie baby: experimentally manipulated temperament affects perceived cuteness and motivation to view infant faces. Dev. Sci. 17, 257–269. ( 10.1111/desc.12112) [DOI] [PubMed] [Google Scholar]
  • 14.Lobmaier JS, Sprengelmeyer RH, Wiffen B, Perrett DI. 2010. Female and male responses to cuteness, age and emotion in infant faces. Evol. Hum. Behav. 31, 16–21. ( 10.1016/j.evolhumbehav.2009.05.004) [DOI] [Google Scholar]
  • 15.Sprengelmeyer RH, et al. 2009. The cutest little baby face, a hormonal link to sensitivity to cuteness in infant faces. Psychol. Sci. 20, 149–154. ( 10.1111/j.1467-9280.2009.02272.x) [DOI] [PubMed] [Google Scholar]
  • 16.Borgi M, Cogliati-Dezza I, Brelsford V, Meints K, Cirulli F. 2014. Baby schema in human and animal faces induces cuteness perception and gaze allocation in children. Front. Psychol. 5, 411 ( 10.3389/fpsyg.2014.00411) [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 17.Little AC. 2012. Manipulation of infant-like traits affects perceived cuteness of infant, adult and cat faces. Ethology 118, 775–782. ( 10.1111/j.1439-0310.2012.02068.x) [DOI] [Google Scholar]
  • 18.Parsons CE, Young KS, Kumari N, Stein A, Kringelbach M. 2011. The motivational salience of infant faces is similar for men and women. PLoS ONE 6, e20632 ( 10.1371/journal.pone.0020632) [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 19.Weisman O, Feldman R, Goldstein A. 2012. Parental and romantic attachment shape brain processing of infant cues. Biol. Psychol. 89, 533–538. ( 10.1016/j.biopsycho.2011.11.008) [DOI] [PubMed] [Google Scholar]
  • 20.Deady DK, Law Smith MJ. 2006. Height in adult females predicts maternal tendencies and career orientation. Pers. Individual Differ. 40, 17–25. ( 10.1016/j.paid.2005.06.014) [DOI] [Google Scholar]
  • 21.Deady DK, Law Smith MJ, Sharp MA, Al-Dujaili EAS. 2006. Maternal personality and reproductive ambition in women is associated with salivary testosterone levels. Biol. Psychol. 71, 29–32. ( 10.1016/j.biopsycho.2005.01.009) [DOI] [PubMed] [Google Scholar]
  • 22.Berridge KC, Robinson TE. 2003. Parsing reward. Trends Neurosci. 26, 507–513. ( 10.1016/S0166-2236(03)00233-9) [DOI] [PubMed] [Google Scholar]
  • 23.Tiddeman BP, Burt DM, Perrett DI. 2001. Prototyping and transforming facial textures for perception research. IEEE Comput. Graph. 21, 42–50. ( 10.1109/38.946630) [DOI] [Google Scholar]
  • 24.Aharon I, Etcoff N, Ariely D, Chabris CF, O'Connor E, Breiter HC. 2001. Beautiful faces have variable reward value: fMRI and behavioral evidence. Neuron 32, 537–551. ( 10.1016/S0896-6273(01)00491-3) [DOI] [PubMed] [Google Scholar]
  • 25.Ahron CR. 1983. Predictors of paternal involvement postdivorce: mothers’ and fathers’ perceptions. J. Divorce 6, 55–69. ( 10.1300/J279v06n03_05) [DOI] [Google Scholar]

Associated Data

This section collects any data citations, data availability statements, or supplementary materials included in this article.

Supplementary Materials

Hahn_supplementary_materials
rsbl20140978supp1.doc (23.5KB, doc)
Hahn_data
rsbl20140978supp2.csv (7.4KB, csv)

Data Availability Statement

The data are available as electronic supplementary material.


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