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‘Who’s a good boy?!’ Dogs prefer naturalistic dog-directed speech

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Infant-directed speech (IDS) is a special speech register thought to aid language acquisition and improve affiliation in human infants. Although IDS shares some of its properties with dog-directed speech (DDS), it is unclear whether the production of DDS is functional, or simply an overgeneralisation of IDS within Western cultures. One recent study found that, while puppies attended more to a script read with DDS compared with adult-directed speech (ADS), adult dogs displayed no preference. In contrast, using naturalistic speech and a more ecologically valid set-up, we found that adult dogs attended to and showed more affiliative behaviour towards a speaker of DDS than of ADS. To explore whether this preference for DDS was modulated by the dog-specific words typically used in DDS, the acoustic features (prosody) of DDS or a combination of the two, we conducted a second experiment. Here the stimuli from experiment 1 were produced with reversed prosody, meaning the prosody and content of ADS and DDS were mismatched. The results revealed no significant effect of speech type, or content, suggesting that it is maybe the combination of the acoustic properties and the dog-related content of DDS that modulates the preference shown for naturalistic DDS. Overall, the results of this study suggest that naturalistic DDS, comprising of both dog-directed prosody and dog-relevant content words, improves dogs’ attention and may strengthen the affiliative bond between humans and their pets. Electronic supplementary material The online version of this article (10.1007/s10071-018-1172-4) contains supplementary material, which is available to authorized users.
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Animal Cognition (2018) 21:353–364
https://doi.org/10.1007/s10071-018-1172-4
ORIGINAL PAPER
‘Who’s agood boy?!’ Dogs prefer naturalistic dog‑directed speech
AlexBenjamin1· KatieSlocombe1
Received: 29 August 2017 / Revised: 22 February 2018 / Accepted: 23 February 2018 / Published online: 2 March 2018
© The Author(s) 2018. This article is an open access publication
Abstract
Infant-directed speech (IDS) is aspecial speech register thought to aid language acquisition and improve affiliation in human
infants. Although IDS shares some of its properties with dog-directed speech (DDS), it is unclear whether the production
of DDS is functional, or simply an overgeneralisation of IDS within Western cultures. One recent study found that, while
puppies attended more to a script read with DDS compared with adult-directed speech (ADS), adult dogs displayed no
preference. In contrast, using naturalistic speech and a more ecologically valid set-up, we found that adult dogs attended to
and showed more affiliative behaviour towards a speaker of DDS than of ADS. To explore whether this preference for DDS
was modulated by the dog-specific words typically used in DDS, the acoustic features (prosody) of DDS or a combination
of the two, we conducted a second experiment. Here the stimuli from experiment 1 were produced with reversed prosody,
meaning the prosody and content of ADS and DDS were mismatched. The results revealed no significant effect of speech
type, or content, suggesting that it is maybe the combination of the acoustic properties and the dog-related content of DDS
that modulates the preference shown for naturalistic DDS. Overall, the results of this study suggest that naturalistic DDS,
comprising of both dog-directed prosody and dog-relevant content words, improves dogs’ attention and may strengthen the
affiliative bond between humans and their pets.
Keywords Dog-directed speech· Human–dog communication· Infant-directed speech· Dog cognition· Affiliative
behaviour· Dog attention
Introduction
When talking to an infant, adults use a special speech regis-
ter characterised by elevated fundamental frequency (pitch),
exaggerated intonation contours and high affect (Burnham
etal. 2002). This phenomenon is evident across languages
including English, Russian, Swedish and Japanese (Kuhl
etal. 1997; Andruski etal. 1999). It is thought that infant-
directed speech (IDS) facilitates infants’ linguistic develop-
ment by amplifying the phonetic characteristics of native
language vowels (Kuhl etal. 1997), allows infants’ to select
appropriate social partners (Schachner and Hannon 2011)
and increases social bonding between infant and caregiver
(Kaplan etal. 1995).
In the same way that IDS is produced automatically when
talking to infants, humans in Western cultures also produce
a special speech register when talking to their pets. This
pet-directed speech (PDS) shares some of the acoustic fea-
tures of IDS including elevated pitch and exaggerated affect
compared to adult-directed speech (ADS) (Burnham etal.
1998). It is possible that pitch is elevated in IDS and PDS
in order to attract the listener’s attention, while affect is ele-
vated to meet listener’s emotional needs, possibly motivating
affiliative interaction with the speaker. One crucial feature
not shared between IDS and PDS and only found in IDS
is the hyperarticulation of vowels (Burnham etal. 1998).
Hyperarticulation of vowels may be the aspect of IDS that
assists spoken language acquisition (Kuhl etal. 1997) and
the speaker’s hyperarticulation may be mediated by the per-
ceived linguistic capacity of the receiver; evidence that sup-
ports this view is provided by a study that compared speech
produced to dogs, parrots and infants. Speakers seem to
hyperarticulate their vowels most with prelinguistic human
Electronic supplementary material The online version of this
article (https ://doi.org/10.1007/s1007 1-018-1172-4) contains
supplementary material, which is available to authorized users.
* Katie Slocombe
Ks553@york.ac.uk
1 Department ofPsychology, The University ofYork, York,
UK
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354 Animal Cognition (2018) 21:353–364
1 3
infants, followed by parrots, with little evidence of this when
addressing dogs, who in contrast to parrots have no ability
to produce speech (Xu etal. 2013).
It is evident that speakers are sensitive to their audience in
terms of acoustic preference, emotional needs and linguistic
potential; however, in order to understand the function of
special speech registers, it is crucial to understand how they
affect the receiver. Human infants show a preference for IDS
from a very early age (Kaplan etal. 1995), with Cooper and
Aslin (1990) finding preferences for IDS over ADS in 2-day-
old infants. Werker and McLeod (1989) measured affective
responsiveness to ADS and IDS in 4–5- and 7–9-month-old
infants. Two trained raters judged the affective responsive-
ness of infants, comprising of how much they thought the
infant was trying to interact with the speaker, how interested
they appeared and the valence of the infant’s emotional state.
They found that infants of both age groups showed greater
affective responsiveness to IDS than to ADS. They also
found that when presented with video recordings of infants
listening to speech, unfamiliar observers rated the infants
more ‘appealing’ when the infants were listening to IDS
than when they were listening to ADS. This indicates that
the use of IDS may facilitate the development of an emo-
tional bond between adults and infants. In contrast to IDS,
there has been very little research into the effect of PDS on
receivers, meaning that it is currently unclear whether PDS
is a non-functional overgeneralisation of IDS in Western cul-
tures where pets often have the status of infants or whether it
functions to gain pets’ attention and strengthen the affiliative
bond between humans and their pets.
Ben-Aderet etal. (2017) were the first to investigate
both the production of dog-directed speech (DDS) and the
behavioural response to DDS in puppies, adult dogs and
older dogs. Acoustic analysis of DDS confirmed previ-
ous descriptions of the acoustic structure of this speech
register, where DDS was higher in pitch, with more pitch
variation over time, and higher harmonicity than ADS.
They also showed that human adults produced DDS to
dogs of all ages. Crucially, Ben-Aderet etal. (2017) then
conducted playback experiments using the DDS and
ADS recorded in the first part of the study to test dog
responses to these types of speech. Stimuli consisted of
repetitions of the phrase ‘Hi! Hello cutie! Who’s a good
boy? Come here! Good Boy! Yes! Come here sweetie pie!
What a good boy!’ in dog- and adult-directed prosody.
Speech was played from a loudspeaker in the corner of
the room, with no human near the source of the sound and
various measures of dogs’ attention to and approach of
the loudspeaker were combined into a composite behav-
ioural response measure. They found that puppies showed
a higher behavioural response to DDS than for ADS,
but this preference decreased as a function of age. The
authors conclude that puppies are highly reactive to DDS
and that pitch is a key feature in modulating this prefer-
ence, but that adult dogs do not react differentially to DDS
and ADS. They argue that DDS may have a functional
value in puppies, but not adult dogs, and therefore, the
use of DDS with adult dogs may simply be a ‘spontaneous
attempt to facilitate interactions with non-verbal listeners
(Ben-Aderet etal. 2017, p. 1). It is, however, possible that
alternative explanations of the null result with adult dogs
exist. As Ben-Aderet etal. discuss, adult dogs may need
additional cues (e.g. gestures) to respond to unfamiliar
speakers. If DDS functions to facilitate social communi-
cation and interaction, it may only be relevant to attend
to it when it comes from a human that can be attended
to and socialised with. It is possible that if no human
experimenter is present, adult dogs realise that there is
no social benefit to reacting preferentially to any speech.
Puppies, with little experience of the world, may not rec-
ognise this and therefore still responded to DDS in the
absence of a feasible producer. While it is clear that pup-
pies are more reactive to the prosody of DDS than adult
dogs, further testing with a human speaker present during
stimulus presentation is required in order to rigorously
test whether adult dogs really are insensitive to DDS. We
therefore aimed to test the possible function of DDS with
adult dogs in a more ecologically valid setting where atten-
tion and affiliation towards the individuals who produced
DDS could be directly measured. Dogs were presented
with two experimenters with audio speakers on their laps
that played naturalistic DDS or ADS (differing in both
prosody and content), and we measured the dogs’ atten-
tion to each individual during speech and then proximity
to the experimenters once dogs were given the opportunity
to approach them after the speech finished. We predicted
that if DDS is functional for adult dogs, in experiment
1 they should attend more to DDS than ADS, and when
given the opportunity to approach the experimenters,
they should choose to spend more time in proximity to
the individual who produced DDS. We then ran a second
experiment to investigate whether content or prosody was
driving any preferences for naturalistic DDS. Here we
presented content-mismatched stimuli (e.g. adult content
with dog prosody and vice versa) and predicted that if the
content of naturalistic DDS was driving preferences, dogs
should attend to and spend more time near the individual
producing dog-relevant content. If, on the other hand, the
prosody of DDS was driving preferences, as was the case
for the puppies studied by Ben-Aderet etal. (2017), dogs
should attend to and spend more time near the individual
producing dog-directed prosody. Finally if preferences for
naturalistic DDS are driven by both content and prosody,
or result from the combination of dog-relevant content and
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355Animal Cognition (2018) 21:353–364
1 3
DDS prosody, we expect to find no significant preference
for either of the mismatched stimuli.
Experiment 1
As we were interested in naturalistic dog- and adult-directed
speech, the stimuli used in this experiment varied in both
content and prosody. The stimuli were ‘matched’ in prosody
and content such that DDS consisted of dog-relevant con-
tent and dog-directed prosody, and ADS consisted of adult-
relevant content and adult-directed prosody.
Methods
Study site andparticipants
Dogs were recruited from Redhouse Boarding Kennels,
York, with permission from the kennel owner. In experi-
ment 1, 37 dogs took part (17 females and 20 males; mean
age 6years ± 3.86) in this study between January and May
2014. See supplementary material for more detailed age,
gender and breed information (TableS1). Where dogs have
been removed from various parts of the analysis due to inter-
ruptions, equipment failures or safety reasons, the details
and N for each analysis are given.
Stimuli
Stimuli were recorded as uncompressed WAV files using a
Marantz PMD661 solid-state recorder from the two human
female experimenters (aged 20–21). The recordings from
experimenter A were always presented through experimenter
A’s speaker (and the same for experimenter B), ensuring con-
gruency of speech with physical characteristics. Although
only presenting speech from the experimenters meant that
multiple dogs heard the same recordings, it ensured that the
stimuli were congruous with the physical characteristics of
the experimenters (age, gender, height), thus maximising
ecological validity and removing the possibility of looking
time measures being affected by incongruity of the stimuli.
DDS was chosen from a sample of recorded naturalistic
interactions with a friendly dog (irish setter). ADS was cho-
sen from a sample of naturalistic adult–adult interactions
that occurred between the experimenters (see supplementary
material for transcripts).
Two different segments of DDS and ADS for each experi-
menter were selected from the continuous speech recordings
(one 10-s segment and one 15-s segment). The amplitude of
the speech in each segment was modified using Raven Pro
(version 1.4), so that the mean RMS amplitude of each seg-
ment was equalised at approximately 3000. For each trial,
the DDS track of one experimenter was paired with the ADS
track of another. Figure1 illustrates the stimulus timeline.
Design
This experiment used a within-subject design, where all
dogs heard both DDS and ADS. All dogs heard simultane-
ous speech first, followed by DDS only and ADS only. The
order of DDS and ADS only segments was counterbalanced
across trials. Simultaneous was played again at the end, to
eliminate the possibility that dogs would approach the indi-
vidual who spoke last. We also counterbalanced the identity
of the DDS speaker (experimenter 1 or 2) and the location
from which DDS was played (left/right) across trials.
Procedure
Equipment was set up as illustrated in Fig.2. The speakers
were equalised to 70dB at 1m away with white noise using
a sound pressure meter, to ensure that that speech broadcast
from each speaker would be equal in volume. Experimenters
1 and 2 then left the room via door 2. The third experimenter
Fig. 1 A diagram illustrating the stimulus timeline. ADS only and
DDS only segments were counterbalanced such that half the dogs
heard ADS only first and half heard DDS only first. Each track was
played simultaneously (DDS from one speaker, ADS from another
speaker) from an iPod paired with an Anchor speaker. The same 10-s
segment was used in simultaneous 1 and 2 for each speaker, though
these segments differed from the 15-s segments in ADS and DDS
only phases
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356 Animal Cognition (2018) 21:353–364
1 3
(handler) retrieved the dog from its kennel and entered the
experimental room through door 1. The dog was allowed to
explore the experimental room for 1min (to habituate to the
environment in order to reduce distraction during the trial),
before being put back on a lead and taken into a waiting
room via door 3. Experimenters 1 and 2 entered through
door 2 and sat in the chairs. The handler entered with the
dog. Once the dog was in position, the stimulus was played.
For the duration of the stimulus, the experimenters sat
still to ensure the dogs were not exposed to any body lan-
guage cues. The experimenters did not attempt to move their
mouths simulating the speech. Instead, the experimenters
placed one hand covering their mouths so that the dog could
not see their lips. They also maintained neutral expressions
with eyes directed towards the dog to ensure the dog did not
receive differential facial cues from the experimenters.
While the stimulus played, the dog was kept on a short
lead to ensure it remained within camera visibility, while
still allowing the dog to move around within 1m of the han-
dler. The handler did not interact with the dog and looked at
the ground throughout. At the end of the stimulus phase, the
lead was removed and the dog was allowed to explore freely
for 1min and approach experimenters 1 and 2 if they wished.
The dog received no interaction from any experimenter.
Video coding
Video recordings of each session were analysed, and during
the stimulus presentation, time spent looking towards DDS
and ADS was recorded as measured by head direction. Dur-
ing the 1-min off-lead period following the stimulus pres-
entation, time spent in proximity to DDS and ADS speakers
was recorded, as measured by the position of the dog’s head
in the 1.1m2 area surrounding the speaker (see Fig.2).
The period after the dog entered the room, but before
the stimulus began was used as a control period (mean
duration 4.56 ± 2.14s). Looking times during this phase
were recorded in order to establish whether the dog dis-
played any preference for one experimenter in particular, or
one location (left or right) that may have influenced looking
times in the experiment.
Interobserver reliability
The primary observer (AB) coded 100% of videos. For
experiment 1, two trained observers each coded 30% of
videos (N = 24/36 trials total) and measured looking time
at each speaker in each section of the stimulus (control
silence, simultaneous 1, DDS only, ADS only, simultane-
ous 2; N = 10 measurements) and time in proximity to each
speaker in the minute post-stimulus presentation (N = 2
measurements). The primary coder had high agreement with
the two secondary coders, and there was also high agreement
between the two secondary coders across all measurements
(Spearman’s R > 0.90, p < 0.001 for all comparisons), indi-
cating the videos had been coded reliably.
A third observer, who was blind to the hypotheses of the
experiment, also coded 22% of the videos (N = 8/36 trials
total) with the sound turned off so that they were unaware
which speech type was heard by the dog. There was high
agreement with the primary coder for looking time (R = 0.86,
p < 0.001) and for proximity preference (R = 0.96, p < 0.001).
Statistical analysis
All data were analysed using IBM SPSS (version 24) with
the significance level set at p < .050. Attentive and affilia-
tive preference was evaluated using mixed ANOVAs with
the fixed within-subject factor speech prosody (DDS/ADS),
between-subject factors DDS identity (experimenter 1/exper-
imenter 2) and DDS location (right/left). A single mixed
ANOVA was conducted on the proximity to speakers in the
Fig. 2 Diagram of experimental
set-up at Redhouse Boarding
Kennels in York. Position of
dog marked with a cross. Cam-
eras were positioned behind
and to the right of the dog, and
behind the speakers. Doors to
other areas are marked. Dotted
lines represent edges of areas
in which proximity to speaker
was recorded. Experimenters
with speakers on their laps were
seated on chairs in the centre of
each area
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357Animal Cognition (2018) 21:353–364
1 3
minute post-stimulus presentation. For looking time, after
the ANOVA on the total looking time had been completed
(Table1), separate ANOVAs were then run for each sec-
tion of the stimulus (simultaneous; ASD only; DDS only).
We applied a more conservative Bonferroni-corrected alpha
level to the separate section analyses (p = 0.01) to correct for
family-wise error that might have arisen from running mul-
tiple tests on the same data set. Finally, we ran an ANOVA
with between-subject factors DDS identity (experimenter 1/
experimenter 2) and DDS location (right/left) on proportion
of looking times in the control period. All assumptions of
these parametric tests were tested and met.
Results
Looking preference
For this analysis, four subjects were removed due to equip-
ment failure (N = 33). During control silence, there was no
significant main effect of Identity or Location, indicating
that dogs did not display any preference for one particular
experimenter or speaker location (Table1). Dogs displayed a
significant preference for DDS across the whole trial (Fig.3;
Table1) and during each phase that contained DDS (Fig.3;
TableS3). Dogs tended to look more towards ADS when
this was the only stimulus available; however, this prefer-
ence was non-significant (Fig.3). No significant interactions
with speaker identity or location were found for total time
(Table1) or separate segments of the stimuli (simultaneous,
DDS only, ADS only) (Supplementary Material: TableS3).
Proximity preference
For this analysis, three dogs were removed from the data
set due to equipment failure or because the dog had to be
kept on a lead, resulting in an N = 34. A mixed ANOVA
revealed that after hearing content-matched stimuli, dogs
spent significantly more time in close proximity to the
DDS speaker than the ADS speaker (F (1, 30) = 5.54,
Table 1 Results of a between-subject ANOVA (df = 1, 29) on looking proportions in the control period and a mixed ANOVA (df = 1, 29) com-
paring main effects and interactions for looking times towards content-matched DDS and ADS
Bold value denotes a significant finding
Significant results are marked, where *** denotes p < 0.005
Within-subject effects F(p) Between-subject effects F(p)
Speech type Speech type *iden-
tity
Speech type * loca-
tion
Speech type *
identity * loca-
tion
Identity Location Identity * location
Control silence 0.38 (.543) 0.59 (.448) 0.85 (.364)
Total looking 40.51 (< .001)*** 0.15 (.704) 1.61 (.215) 0.24 (.627) 0.20 (.656) 1.37 (.251) 0.43 (.517)
Fig. 3 Time spent looking towards content-matched DDS and ADS
where error bars represent 1 standard error of the mean. ***refers
to significant differences (p < 0.005) and n.s denotes non-significant
comparisons as revealed by mixed ANOVAs (total: Table1; other
time segments TableS3)
Fig. 4 A graph to show the mean time spent in proximity to each
experimenter (seconds), in the minute after the speech stimuli ended,
when the dogs heard content-matched DDS and ADS. Error bars rep-
resent one standard error of the mean. (*) denotes a significant main
effect of speech type (p < 0.050) based on the results of ANOVA pre-
sented in Table2
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358 Animal Cognition (2018) 21:353–364
1 3
p = 0.025; Fig.4). No significant interactions with loca-
tion or speaker identity were found (Table2).
Discussion
This experiment showed that dogs display a behavioural
preference for naturalistic DDS (matched in prosody and
content) compared with ADS when presented in the pres-
ence of an associated human. Dogs, on average, spent
more time looking towards a speaker of DDS compared
with a speaker of ADS in all segments of the stimulus
containing DDS and across the trial as a whole. We also
found that when given the subsequent opportunity to inter-
act with the speakers, dogs chose to spend more time in
proximity with the DDS speaker, than the ADS speaker.
Although the absolute differences in looking and prox-
imity time were small and therefore their functional rel-
evance may be questioned, we feel the substantial effect
sizes obtained and the convergence of results across our
behavioural measures indicates we have detected function-
ally relevant differences in behaviour. Overall, our results
support the hypothesis that dogs display attentive and
affiliative preferences for naturalistic DDS over ADS.
The results from the control period show no signifi-
cant preference for a specific location, or speaker iden-
tity, indicating that the dogs had no a priori preference for
looking at one experimenter or location. In line with this,
no significant main effects of location or speaker identity,
or interactions of identity, location and speech type were
found.
Although our results show a robust preference for natural-
istic DDS over ADS, as the stimuli in this experiment differed
in both content and prosody, it is not possible to determine
whether this effect is driven by dog-directed prosody or con-
tent, as these factors did not vary independently. Therefore,
although this experiment clearly shows that dogs discriminate
between and show a behavioural preference for naturalistic
DDS over ADS, further investigation is required to deter-
mine the extent to which prosody and content are driving this
preference.
Experiment 2
Experiment 2 was designed in order to examine whether
content alone or prosody alone was sufficient for driving
the preference found in experiment 1. In experiment 2, the
content from experiment 1 was reproduced but with reversed
prosody such that the dog-related content was spoken with
the prosody of ADS and vice versa. For simplicity, in all
cases, DDS refers to stimuli with dog-directed prosody
(with either dog- or adult-related content) and ADS refers
to stimuli with adult-directed prosody (with either adult- or
dog-related content). In experiment 2, we presented dogs
with content-mismatched DDS (dog-directed prosody with
adult-related content) and content-mismatched ADS (adult-
directed prosody with dog-related content).
Methods
Study site andparticipants
In experiment 2, 32 dogs from Redhouse Boarding Ken-
nels in York took part (16 females and 16 males; mean age
6years ± 3.75). Data collection for this experiment was con-
ducted 2years after the first experiment (2016).
Stimuli
For experiment 2, uncompressed WAV files were recorded
from two new female experimenters (age 20 and 21). The
experimenters repeated the transcripts from experiment 1
with the opposing prosody, in order to produce content-mis-
matched DDS and ADS. All stimuli were still directed to an
appropriate live audience (e.g. adult script was produced
with dog prosody to a live dog; Irish setter) and processed
as described in experiment 1.
For the stimuli used in experiment 2, some dog content
was repeated in ADS, and some adult content was removed
in DDS. This was in order to account for differences in word
rate between naturalistic DDS and ADS. These alterations
Table 2 Results of a mixed ANOVA with degrees of freedom (1, 30) comparing the time spent near DDS and ADS speakers for content-
matched speech
Bold value denotes a significant finding
Significant results indicated, where * denotes p < 0.050
Within-subject effects F(p) Between-subject effects F(p)
Speech type Speech type *identity Speech type * location Speech type * identity *
location
Identity Location Identity * location
Proximity
prefer-
ence
5.54 (.025)* 1.64 (.210) 0.29 (.592) 0.05 (.833) 1.13 (.552) 0.36 (.552) 0.62 (.438)
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359Animal Cognition (2018) 21:353–364
1 3
are indicated in Supplementary material. The amplitude of
the speech segments was again equalised, and tracks were
built as in experiment 1 (see Fig.1).
Acoustic analysis ofstimuli
To ensure the prosody of the content-mismatched DDS and
ADS for experiment 2 was convincing, we compared the
acoustic properties of these stimuli with the stimuli used in
experiment 1. Mean, minimum and maximum pitch (FO)
was measured (Table3) in PRAAT (version 6.0.05). Pitch
settings were 75-1200Hz and continuous segments of speech
with a continuous visible pitch line were selected, and the
mean, min and max pitch in the segment was extracted using
the ‘get pitch’ function. Pitch modulation was calculated as
maxF0-minF0. Word rate was calculated as the number of
words divided by the duration from the start of the first word
to the end of the last word in a stimulus.
Generalised linear mixed models (GLMMs) were used to
assess the effect of prosody (dog-directed/adult-directed);
content (dog/adult) and content–prosody matching (matched
(experiment 1)/mismatched (experiment 2)) on the acoustic
measurements of stimuli in experiments 1 and 2. These fac-
tors were entered as fixed factors in models with (1) mean
pitch and (2) pitch modulation as DVs. In order to ensure
we were comparing the pitch-related measures of the same
words or phrases, for mean pitch and pitch modulation,
measurements of each continuous segment of speech with
a continuous visible pitch line that were available in both
experiments were entered into the analyses. Each speech
segment was numbered and included as a random factor
along with speaker identity, in order to control for repeated
sampling at these two levels (Warmelink etal. 2013). For
word rate, the rate of each 10- or 15-s stimulus produced
by each speaker was entered into analyses, with speaker
identity entered as a random factor to control for repeated
sampling of each speaker. As we only had a small number of
data points for this GLMM (N = 16), we ran three separate
models, each with a single fixed factor (prosody, content or
prosody–content matching) to avoid overfitting the models.
GLMMs revealed that the content-matched (experiment
1) and content-mismatched stimuli (experiment 2) did not
significantly differ in pitch, pitch modulation or word rate
(Tables3, 4), indicating that the content-mismatched stim-
uli were produced with prosody representative of natural
dog-directed and adult-directed speech. In line with previ-
ous descriptions of the prosody of DDS, the pitch was sig-
nificantly higher, the pitch modulation significantly greater
and word rate significantly slower for stimuli produced with
dog-directed prosody compared to adult-directed prosody
(Burnham etal. 1998; Ben-Aderet etal. 2017; Tables3, 4).
Content did not significantly affect pitch modulation or word
rate, but dog content was significantly higher pitched than
adult content (Tables3, 4).
Design
As in experiment 1, this experiment used a within-sub-
ject design with all dogs hearing both DDS and ADS.
Table 3 Acoustic measurements
of the different types of speech
produced by each experimenter
Mean values from the 10- and 15-s segments are reported in each row
Speaker ID Prosody Content Mean pitch Pitch modulation Word rate
Experimenter 1 DDS Dog 598.88 240.26 172.85
ADS Adult 452.68 170.02 216.01
Experimenter 2 DDS Dog 794.51 207.49 195.37
ADS Adult 413.47 62.97 242.40
Experimenter 3 DDS Adult 684.58 285.92 138.97
ADS Dog 487.00 87.45 270.53
Experimenter 4 DDS Adult 535.02 172.18 128.95
ADS Dog 472.75 83.26 278.71
Table 4 Results of GLMMs
exploring the effect of prosody,
content and content–prosody
matching on pitch, pitch
modulation and word rate
Bold value denotes a significant finding
Significant results are indicated where *** denotes p < 0.005
df Prosody F(p) Content F(p) Content–pros-
ody matching
F(p)
Mean pitch 1, 328 245.86 (< .001)*** 13.97 (< .001)*** 0.58 (.447)
Pitch modulation 1, 328 49.13 (< .001)*** 0.07 (.792) 0.20 (.653)
Word rate 1, 6 34.22 (< 001)*** 3.24 (.094) < 0.01 (.937)
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360 Animal Cognition (2018) 21:353–364
1 3
Between-subject factors such as DDS speaker, DDS loca-
tion and stimulus order were counterbalanced across trials.
Procedure
The procedure for this experiment was identical to that of
experiment 1.
Interobserver Reliability
The primary observer (AB) coded 100% of videos. Two
trained observers each coded 50% of the videos (N = 32/32
trials total). The primary observer had high agreement with
both secondary coders, who also had high agreement with
each other across all measurements (Spearman’s R > 0.90,
p < 0.001 for all comparisons).
A third observer, who was blind to the hypotheses of
the experiment, also coded 22% of the videos (N = 7/32
trials total) with the sound turned off so that they were
unaware which speech type was heard by the dog. There
was high agreement with the primary coder for looking
time (R = 0.93, p < 0.001) and for proximity preference
(R = 0.88, p < 0.001).
Statistical analysis
As above, attentive and affiliative preference was evaluated
using mixed ANOVAs with the fixed within-subject factor
speech prosody (DDS/ADS), between-subject factors DDS
identity (e.g. experimenter 1/experimenter 2) and DDS loca-
tion (right/left). All assumptions were tested and met.
Experiment 2: results
Looking preference
For content-mismatched DDS, 3 trials were removed due
to equipment failure and the following analysis is based
on n = 29. A mixed ANOVA revealed there was no sig-
nificant preference for DDS when content was incongruent
with prosody (Fig.5; Table5). During the control period,
there was a main effect of identity, with dogs preferring to
look towards experimenter 3 compared to experimenter 4
(Table5). There was also an interaction of speech type and
identity for total looking time. To explore the nature of the
interaction between speech type and identity, four inde-
pendent samples t tests with Bonferroni-corrected alpha
(p < 0.0125) were conducted. Firstly, at the level of DDS,
there was a significant main effect of speaker identity, with
dogs preferring the speech of experimenter 3 over experi-
menter 4 (t (27) = 3.08, p = 0.005). However, at the level of
ADS, there was no significant effect of speaker identity (t
(27) = 0.82, p = 0.419). At the level of each speaker, there
was no preference for the DDS of experimenter 3 compared
with her ADS (t (27) = 0.77, p = 0.450), and the same was
true for experimenter 4 (t (27) = −1.50, p = 0.146).
Proximity preference
This analysis is based on N = 30 following equipment fail-
ures. For content-mismatched stimuli, dogs spent more time,
on average, in proximity to the ADS location as illustrated in
Fig.6. However, a mixed ANOVA revealed that this result
was non-significant (see Table6).
To explore whether the failure to find a significant
preference for either type of speech was likely due to
reduced power associated with the slightly smaller sample
size in experiment 2 compared to experiment 1, we con-
sidered effect sizes and conducted power analyses using
G*Power (version 3.1.9.2). The preference for attending
to DDS in experiment 1 was associated with a large effect
size (η2 = 0.563), yet the same comparison in experiment
2 yielded a very small effect size (η2 < 0.001). An a priori
power analysis for looking time in experiment 2 indicated
that to find a similar effect size based on partial η2 of
0.56, with power of 0.80 and an alpha level of 0.05 for the
within-subject comparison of speech type, 6 participants
would have been needed, which we exceeded with our
29 participants in experiment 2. The proximity prefer-
ence for the DDS speaker in experiment 1 was associ-
ated with a medium effect size (η2 < 0.156), yet the same
comparison in experiment 2 yielded a small effect size
(η2 = 0.038). An a priori power analysis for proximity
duration in experiment 2 indicated that to find a similar
Fig. 5 Time spent looking towards content-mismatched DDS and
ADS during each phase, where error bars represent 1 standard error
of the mean. n.s denotes non-significant comparisons as revealed by
mixed ANOVAs (total: Table5: other time segments: TableS4)
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361Animal Cognition (2018) 21:353–364
1 3
effect size based on partial η2 of 0.16, with power of 0.80
and an alpha level of 0.05 for the within-subject com-
parison of speech type, 24 participants would have been
needed, which we exceeded with our 30 participants in
experiment 2. Together the effect sizes and power analy-
sis indicate that experiment 2 had sufficient power to find
differences similar to those found in experiment 1, had
they existed, and therefore, we can be relatively confident
in this null result.
Discussion
The results from experiment 2 suggest that there is no sig-
nificant difference in dogs’ attention or proximity preference
to speakers of DDS or ADS where content and prosody did
not match. This suggests that neither content, nor prosody,
is solely responsible for the preference for DDS shown in
experiment 1. As the same scripts were used in both experi-
ments, this result also highlights that the preference shown
in experiment 1 could not be explained by the use of specific
words in the content of the original stimuli, such as ‘walk’
or ‘dog’, for example. If this were the case, we would have
observed a preference for content-mismatched ADS, which
not only contained the specific dog-related words used in
experiment 1, but more repetitions of them (see methods).
In order to explore alternative explanations for these null
results we first considered if the difficulty of producing these
content-mismatched stimuli had resulted in poor examples
of DDS and ADS prosody being produced. The acoustic
analysis of the stimuli, however, illustrates that the content-
mismatched stimuli followed the same patterns of acoustic
properties as the naturalistic DDS of experiment 1. This
supports the use of these stimuli and highlights that the null
result found in this experiment is unlikely to be due to fail-
ures in producing authentic DDS or ADS when the content
is reversed. Second, although a broadly comparable number
of subjects were used in experiments 1 and 2, it is possible
that the slightly smaller N available in experiment 2 (33
vs 29 Looking duration; 34 vs 30 proximity duration), left
experiment 2 with slightly less power to detect differences
Table 5 Results of between-subject ANOVA (1,25) for the control silence and a mixed ANOVA with degrees of freedom (1,25) comparing main
effects and interactions for looking times towards content-mismatched DDS and ADS
Bold value denotes a significant finding
Significant results are marked, where * indicates p < 0.050
Within-subject effects F(p) Between-subject effects F(p)
Speech type Speech type *identity Speech type * location Speech type *
identity * loca-
tion
Identity Location Identity * location
Control silence 4.24 (.048)*1.44 (.242) 1.02 (.322)
Total looking < 0.01 (.985) 5.75 (.024)* 2.03 (.167) 1.00 (.328) 2.58 (.121) 0.99 (.330) 0.34 (.560)
Fig. 6 A graph to show mean time spent in proximity with each
speaker (seconds), for content-mismatched DDS and ADS. Error bars
represent one standard error of the mean
Table 6 Results of a mixed ANOVA with degrees of freedom (1,26) comparing the time spent near DDS and ADS speakers for content-mis-
matched speech
Within-subject effects F(p) Between-subject effects F(p)
Speech type Speech type *identity Speech type * location Speech type * identity *
location
Identity Location Identity * location
Proximity
prefer-
ence
1.03 (.319) 0.85 (.365) 0.01 (.992) 0.02 (.894) 1.20 (.283) 0.59 (.448) 0.52 (.477)
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362 Animal Cognition (2018) 21:353–364
1 3
compared to experiment 1. However, examination of effect
sizes indicates that while the naturalistic speech in experiment
1 elicited large effect size (η2 = 0.563), effect sizes obtained
with the reversed stimuli were extremely small (η2 < 0.001).
Power analyses confirmed that we had sufficient sample sizes
in experiment 2 to detect differences similar to those found in
experiment 1. We are therefore confident that the null result
in experiment 2 was not due to lack of power.
In experiment 2 a significant interaction between speech
type and experimenter revealed that experimenter 3’s DDS
was more effective at eliciting attention than experimenter
4’s DDS. This effect is likely mediated by what seemed to
be an a priori preference for experimenter 1, which resulted
in dogs looking significantly longer at this experimenter in
the control period before any speech was produced. It is not
clear whether visual or scent characteristics drove this pref-
erence, although scent seems unlikely as the preference did
not remain in the post-stimulus proximity to experimenters
where an attractive scent could have been actively explored.
It is interesting that dogs seemed to have an immediate pref-
erence for one experimenter and this may have enhanced
the efficacy of an experimenter’s dog-directed prosody. It is,
however, important to note that the preferred experimenter’s
DDS was still not significantly more effective in attracting
dogs’ attention than her ADS. Indeed post hoc analyses of
the interaction term at the level of each speaker confirmed
the main findings that the different types of speech did not
elicit significantly different behaviour from the dogs.
General discussion
The results provide evidence that in an ecologically valid
setting, dogs attended more towards naturalistic DDS, where
prosody and content were matched, compared with ADS.
We also show for the first time that dogs subsequently spend
more time in proximity to an experimenter who has recently
produced naturalistic DDS than one who has recently pro-
duced ADS. This novel finding suggests that DDS may
fulfil a dual function of improving attention and increasing
social bonding. This fits with the current understanding of
infant research, which suggests not only that IDS serves to
facilitate language acquisition, but that it is also crucial for
developing meaningful social relationships with caregivers.
The second experiment was designed to investigate
whether prosody or content alone was driving this pref-
erence for naturalistic DDS; however, when content and
prosody were mismatched, we found there was no differ-
ence in the amount of time spent in proximity to the experi-
menters and there was no significant attentive preference for
DDS or ADS in any part of the trial, or across the session
as a whole. This suggests that neither content, nor prosody
alone was driving the preference observed in experiment
1. Instead, it is clear that both content and prosody matter
to dogs. Future research should aim to disentangle whether
dog-related prosody and content independently affect dog
behaviour, or whether they have to be combined congruently
in order to affect dog preferences. This study is unable to
distinguish between these possibilities; however, the results
from Ben-Aderet etal. (2017), who found that adult dogs did
not prefer dog-relevant content produced with dog-directed
prosody over adult-directed prosody, indicate that it may
be the congruent combination of dog-directed content and
prosody that underpins the preference for naturalistic DDS.
Further experiments, with large sample sizes, which manipu-
late both prosody and content independently, are required to
understand this relationship more fully.
Interestingly, Ben-Aderet etal. did find a significant
preference for DDS prosody in puppies, showing that pup-
pies are more sensitive to prosodic differences compared
to adult dogs. Puppies may be more sensitive to acoustic
differences than adult dogs in the same way that human
babies are most sensitive to IDS early in life (Newman
and Hussain 2006). Puppies also have less experience of
human language and time to form associations between
specific words and positive experience (e.g. walk) and
thus should be less sensitive to content. Therefore, while
puppies may rely wholly on prosodic information, adult
dogs seem to take both content and prosody into account,
and only when these two things are relevant to them, they
do display a behavioural preference. While preference for
dog-related content needs experience of human interaction
to develop, the origins of the preference for dog-directed
prosody are less clear: they may be routed in an innate
preference for higher pitched, tonal sounds, the domestica-
tion process or be a product of early learning environment.
If preferences for DDS prosody are based on preferences
for high pithed tonal sound, which across mammalian spe-
cies is associated with affiliation and submission rather
than aggression (Morton 1977), then other mammalian
species should show a preference for DDS over ADS.
Future research could test this possibility. Alternatively,
preference for DDS prosody may have arisen through
various routes during the domestication process. Firstly,
early in the domestication process, DDS may have pro-
vided dogs with a reliable cue that indicates safe social
partners at a time when joining human groups may have
been dangerous, and identifying those who would not be
hostile would have been important for a dog’s survival.
Secondly, as dogs are able to engage with humans in
joint attention (Miklósi etal. 2003) and can cooperate to
achieve goal-directed actions (Range and Virányi 2014),
it is possible that humans selected dogs for characteris-
tics that promoted social communication during domes-
tication, including attentive and affiliative preference for
DDS. It is, however, also possible that dogs kept as pets
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363Animal Cognition (2018) 21:353–364
1 3
are conditioned over their individual lifetimes to respond
positively to DDS as this type of speech is often paired
with positive events (e.g. food treat, toy, walk or affection).
Although Ben-Aderet etal. found a clear preference for
DDS in young dogs (2–5months), it is possible that such
associations could be formed in that time. Future research
with young puppies raised with extremely minimal human
contact would enable us to test whether environmental
input is needed to shape this preference or whether it is
an innate preference, as it seems to be in human infants
(Cooper and Aslin 1990).
Although the use of real people to deliver the speech to
the dogs increased the ecological validity of our experimen-
tal set-up, it did have potential drawbacks. First, the impor-
tance of providing speech from each experimenter (exact
match with characteristics including gender, height and size)
to ensure it was physically congruous meant that the same
stimuli were heard by multiple dogs. Although acoustic anal-
ysis confirmed the structure of these stimuli were representa-
tive of DDS and ADS reported in other studies, it is unclear
whether these findings would generalise to a wider sample
of DDS and our findings suggest that there may be indi-
vidual variation in the efficacy of DDS. Thus, further studies
without pseudoreplication at the level of the stimulus are
required to confirm the generalisability of our findings. Dif-
ferential a priori interest in the experimenters, as we found
in experiment 2, is a further complication associated with
the use of live models in these experiments, which highlights
the need for rigorous counterbalancing and a control period
where such a priori biases can be measured. In addition,
our results illustrate the interesting possibility that a priori
preferences for individuals may influence the effectiveness
of and sensitivity to other cues including speech register.
In conclusion, the results from this study support the
hypothesis that dogs pay more attention to naturalistic DDS
than to ADS. It also revealed that dogs spent more time
near someone who had just produced DDS rather than ADS,
indicating for the first time that DDS may not just modulate
attentive behaviour, but also play a role in the development
of affiliative preferences. This preference for naturalistic
DDS was not driven by preference for dog-directed content
or prosody alone, as no attentive or affiliative preferences
were shown when dogs were presented with content- and
prosody-mismatched stimuli. This study concludes that natu-
ralistic DDS elicits more attention from dogs than ADS and
has the potential to strengthen the affiliative bond a human
has with a dog.
Acknowledgements We would like to extend our thanks to Alyse and
all the staff at Redhouse Boarding Kennels in York for allowing us to
conduct our research study at the Pooches Paradise. We would par-
ticularly like to thank Lucy whose friendly and helpful advice was
extremely valuable during our visits. We are grateful to the dog owners
of Newton-upon-Derwent, whose dogs provided valuable pilot data
which helped inform our final study design. Thanks also to the under-
graduate research students, Kate Dibb, Emma Curran, Amy Wilson and
Charlotte Le Bourgeois, who provided the stimuli and helped collect
and code the data. Finally, thank you Poppy, for many hours of patience
during the production of the stimuli for this study.
Compliance with ethical standards
Conflicts of interest There are no conflicts of interest to disclose.
Ethical approval All applicable international, national and/or institu-
tional guidelines for the care and use of animals were followed. All
procedures performed in studies involving human participants were
in accordance with the ethical standards of the institutional and/or
national research committee and with the 1964 Helsinki Declaration
and its later amendments or comparable ethical standards.
Informed consent Informed consent was obtained from the kennel
owner for the use of resident dogs in this study. Experimenters provided
informed consent for the use of their voices.
Open Access This article is distributed under the terms of the Crea-
tive Commons Attribution 4.0 International License (http://creat iveco
mmons .org/licen ses/by/4.0/), which permits unrestricted use, distribu-
tion, and reproduction in any medium, provided you give appropriate
credit to the original author(s) and the source, provide a link to the
Creative Commons license, and indicate if changes were made.
References
Andruski JE, Kuhl PK, Hayashi A (1999) Point vowels in Japa-
nese mothers’ speech to infants and adults. J Acoust Soc Am
105(2):1095. https ://doi.org/10.1121/1.42513 5
Ben-Aderet T, Gallego-Abenza M, Reby D, Mathevon N (2017) Dog-
directed speech: why do we use it and do dogs pay attention to it?
Proc R Soc Lond B Biol Sci 284(1846):20162429
Burnham D, Francis E, Vollmer-Conna U (1998) Are you my little
pussy-cat? acoustic, phonetic and affective qualities of infant-and
pet-directed speech. ICSLP. http://www.isca-speec h.org/archi ve/
archi ve_paper s/icslp _1998/i98_0916.pdf
Burnham D, Kitamura C, Vollmer-Conna U (2002) What’s new, pus-
sycat? On talking to babies and animals. Science 296(5572):1435.
https ://doi.org/10.1126/scien ce.10695 87
Cooper RP, Aslin RN (1990) Preference for infant-directed speech in
the first month after birth. Child Dev 61(5):1584–1595. https ://
doi.org/10.1111/j.1467-8624.1990.tb028 85.x
Kaplan PS, Goldstein MH, Huckeby ER, Owren MJ, Cooper RP (1995)
Dishabituation of visual attention by infant- versus adult-directed
speech: effects of frequency modulation and spectral composition.
Infant Behav Dev 18(2):209–223. https ://doi.org/10.1016/0163-
6383(95)90050 -0
Kuhl PK, Andruski JE, Chistovich IA, Chistovich LA, Kozhevnikova EV,
Ryskin VL, Stolyarova EI, Sundberg U, Lacerda F (1997) Cross-lan-
guage analysis of phonetic units in language. Science 227:684–686
Miklósi Á, Kubinyi E, Topál J, Gácsi M, Virányi Z, Csányi V (2003)
A simple reason for a big difference: wolves do not look back at
humans, but dogs do. Curr Biol. https ://doi.org/10.1016/S0960
-9822(03)00263 -X
Morton ES (1977) On the occurrence and significance of motiva-
tion-structural rules in some bird and mammal sounds. Am Nat
111:855–869
Content courtesy of Springer Nature, terms of use apply. Rights reserved.
364 Animal Cognition (2018) 21:353–364
1 3
Newman RS, Hussain I (2006) Changes in preference for infant-
directed speech in low and moderate noise by 4.5- to 13-month-
olds. Infancy 10(1):61–76. https ://doi.org/10.1207/s1532 7078i
n1001 _4
Range F, Virányi Z (2014) Wolves are better imitators of conspecifics
than dogs. PLoS ONE 9(1):e86559. https ://doi.org/10.1371/journ
al.pone.00865 59
Schachner A, Hannon EE (2011) Infant-directed speech drives social
preferences in 5-month-old infants. Dev Psychol 47(1):19–25
Waller BM, Warmelink L, Liebal K, Micheletta J, Slocombe KE
(2013) Pseudoreplication: a widespread problem in primate
communication research. Anim Behav 86(2):483–488. https ://
doi.org/10.1016/j.anbeh av.2013.05.038
Werker JF, McLeod PJ (1989) Infant preference for both male and
female infant-directed talk: a developmental study of attentional
and affective responsiveness. Can J Psychol/Revue Canadienne
de Psychologie 43(2):230–246. https ://doi.org/10.1037/h0084 224
Xu N, Burnham D, Kitamura C, Vollmer-Conna U (2013) Vowel hyper-
articulation in parrot-, dog- and infant-directed speech. Anthro-
zoos Multidiscip J Interact People Animals 26(3):373–380. https
://doi.org/10.2752/17530 3713X 13697 42946 3592
Content courtesy of Springer Nature, terms of use apply. Rights reserved.
1.
2.
3.
4.
5.
6.
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Supplementary resource (1)

... Almost thirty years ago, Levinson (1982) suggested that more empirical research needed to be directed at the study of linguistic interactions with animals. He was well advised, as it is now increasingly documented that people, in Western cultures, use a special speech register when talking to their pets, qualified as Pet-directed Speech, or PDS (Ben-Aderet et al., 2017;Benjamin and Slocombe, 2018;Burnham et al., 2002;Jeannin et al., 2017a;b;Lesch et al., 2019;Mitchell, 2001Mitchell, , 2004Ringrose, 2015;Xu et al., 2013). In the same way, it is rather well described that when talking to infants, human adults use a special speech register characterised, from an acoustic point of view, by an elevated fundamental frequency (pitch), exaggerated intonation contours and high affect -qualified as infant-directed Speech, or IDS (Kaplan et al., 1995). ...
... Another issue with studies on pet-directed speech is how the speech itself is elicited. Some experiments used photos of animals or robotic avatars (Acevedo, 2017;Ben-Aderet et al., 2017;Sinatra et al., 2012), others used live human-animal interactions (Benjamin and Slocombe, 2018;Burnham et al., 2002;Gergely et al., 2017Gergely et al., , 2021Hirsh-Pasek and Treiman, 1982;Jeannin et al., 2017a;b;Koda, 2001;Lesch et al., 2019;Mitchell, 2001Mitchell, , 2004Mitchell and Edmonson, 1999;Prato-Previde et al., 2006;Ringrose, 2015;Sims and Chin, 2002;Sinatra et al., 2012;Xu et al., 2013). The former method is obviously simpler than the latter and allows for a better control of the experimental parameters, but it has the disadvantage of being less ecological, which could lead to less relevant results. ...
... Indeed, it is thought that infant directed speech (IDS) increases social bonding between infant and caregiver (Kaplan et al., 1995). Benjamin and Slocombe (2018) suggested that dog directed speech (DDS) may fulfil a dual function of strengthening the affiliative bond and improving the listener's attention. This hypothesis is consistent with earlier findings by Jeannin and co-workers (2017a), who reported that DDS draws dogs' attention more efficiently than ADS. ...
Article
In Western cultures, humans tend to use a specific kind of speech when talking to their pets, characterised, from an acoustical point of view, by elevated pitch and greater pitch modulation. Pet-directed speech (PDS), which has been mainly studied in dogs, shares some acoustic features with infant-directed speech (IDS), used when talking to young children. The purpose of this study was to test the hypothesis that adult humans also modify characteristics of their voice when talking to a cat. We compared acoustic parameters of speech directed to cats (CDS) and speech directed to adult humans (ADS). In a first experiment, we compared ADS and CDS utterances of male and female participants, addressing cats through video recordings, under controlled laboratory conditions. Both men and women used a higher pitch (mean fundamental frequency, or mean F0) in CDS vs. ADS. The second experiment was conducted under conditions allowing direct cat-human interactions, in a cohort of women. Once again, mean F0 was significantly higher in CDS vs. ADS. Overall, these data confirm our hypothesis that humans change the way they speak when addressing a cat, mainly by increasing the pitch of their voice. Further research is needed to fully investigate specificities of this speech.
... Horses are also sensitive to the way we talk to them, especially to a kind of speech used to speak to companion animals, called pet-directed speech (PDS). PDS resembles the type of speech used with infants ("baby-talk", "parentese" or "infant-directed speech"-IDS) 16 and has similar characteristics, namely, a high and varying pitch, wide pitch range, slow rate of speech, simple syntax and semantics and more repeated words, compared to adult-directed speech (ADS) [16][17][18][19][20][21] . Moreover, IDS is an emotional form of speech and a multimodal communication style 16 , which includes visual modalities such as facial expressions, particularly smiles. ...
... In infant rhesus macaques, IDS has been shown to influence long-term memory 24 . Moreover, dogs looked longer at and preferred to spend time close to a loudspeaker or person broadcasting PDS rather than ADS 17,18 , and they were more attentive when spoken to in PDS rather than ADS 19 . In horses, we showed in a recent experiment that PDS induced a different way of interacting with an experimenter compared to ADS. ...
... First, PDS could attract horses' attention and arouse them. Indeed, IDS is arousing for infants 16,25 , and PDS attracts attention in dogs [17][18][19] . This hypothesis could explain why horses looked more www.nature.com/scientificreports/ at the experimenter during grooming and their better performance in finding hidden food due to greater attention given to experimenter cues. ...
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In a recent experiment, we showed that horses are sensitive to pet-directed speech (PDS), a kind of speech used to talk to companion animals that is characterized by high pitch and wide pitch variations. When talked to in PDS rather than adult-directed speech (ADS), horses reacted more favorably during grooming and in a pointing task. However, the mechanism behind their response remains unclear: does PDS draw horses’ attention and arouse them, or does it make their emotional state more positive? In this study, we used an innovative paradigm in which female horses watched videos of humans speaking in PDS or ADS to better understand this phenomenon. Horses reacted diferently to the videos of PDS and ADS: they were signifcantly more attentive and their heart rates increased signifcantly more during PDS than during ADS. We found no diference in the expressions of negative or positive emotional states during PDS and ADS videos. Thus, we confrm that horses’ perception of humans can be studied by means of video projections, and we conclude that PDS attracts attention and has an arousing efect in horses, with consequences on the use of PDS in daily interactions with them.
... It is no longer a standing secret that, in contemporary western cultures, most humans talk to their pet companions (Burnham et al. 1998(Burnham et al. , 2002Lesch et al. 2019;Mitchell 2001Mitchell , 2004Xu et al. 2013). It has been reported that humans use a particular kind of speech register when addressing dogs (Ben-Aderet et al. 2017;Benjamin and Slocombe 2018;Gergely et al. 2017;Hirsh-Pasek and Treiman 1982;Jeannin et al. 2017a, b;Ringrose 2015), horses (Lansade et al. 2021) and cats (Schötz 2019, de Mouzon et al. submitted). The speech register addressed to companion animals shares common features with speech addressed to young children, or Infant-directed speech (IDS), (Kaplan et al. 1995), including: hyperarticulation, shorter utterances, more repetitions, elevated pitch and increased pitch variation. ...
... Additionally, Ben-Aderet et al. (2017) reported that puppies showed a higher behavioural response to DDS than to ADS, even though in their study cohort dog's response seemed to decrease with age. Benjamin and Slocombe (2018) investigated the possible function of DDS with adult dogs in a more ecological setting, where attention and affiliation towards the individuals who produced DDS was directly measured. Their results suggest that naturalistic DDS, comprising of both dog-directed prosody and dog-relevant content words, improves dogs' attention. ...
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In contemporary western cultures, most humans talk to their pet companions. Speech register addressed to companion animals shares common features with speech addressed to young children, which are distinct from the typical adult-directed speech (ADS). The way dogs respond to dog-directed speech (DDS) has raised scientists’ interest. In contrast, much less is known about how cats perceive and respond to cat-directed speech (CDS). The primary aim of this study was to evaluate whether cats are more responsive to CDS than ADS. Secondarily, we seek to examine if the cats’ responses to human vocal stimuli would differ when it was elicited by their owner or by a stranger. We performed playback experiments and tested a cohort of 16 companion cats in a habituation–dishabituation paradigm, which allows for the measurement of subjects’ reactions without extensive training. Here, we report new findings that cats can discriminate speech specifically addressed to them from speech addressed to adult humans, when sentences are uttered by their owners. When hearing sentences uttered by strangers, cats did not appear to discriminate between ADS and CDS. These findings bring a new dimension to the consideration of human–cat relationship, as they imply the development of a particular communication into human–cat dyads, that relies upon experience. We discuss these new findings in the light of recent literature investigating cats’ sociocognitive abilities and human–cat attachment. Our results highlight the importance of one-to-one relationships for cats, reinforcing recent literature regarding the ability for cats and humans to form strong bonds.
... Dogdirected speech is higher pitched and more variable in pitch than adult-directed speech (Ben-Aderet et al. 2017). As a result of these changes, dogs attend significantly more to dog-directed speech than adult-directed speech (Benjamin and Slocombe 2018); this would suggest instead that dogs would learn best from speech directed to them, rather than adult-directed overheard speech. Yet if dogs can learn from ambient speech in their environment, including speech that is not dog-directed, this would presumably provide them with more opportunities to learn. ...
... There were no significant main effects, suggesting that the different stimuli in general were roughly similar in terms of dog listening times (e.g., one type of stimuli was not listened to longer by a significant portion of the dogs). While some studies have found that dogs prefer to listen to dog-directed speech over adult-directed speech (Benjamin and Slocombe 2018), other studies have found that adult dogs fail to show this preference (Ben-Aderet et al. 2017)) This study, too, failed to show a preference for DDS over ADS in adult dogs. ...
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Studies have shown that both cotton-top tamarins as well as rats can discriminate between two languages based on rhythmic cues. This is similar to the capabilities of young infants, who also rely on rhythmic cues to differentiate between languages. However, the animals in these studies did not have long-term language exposure, so these studies did not specifically assess the role of language experience. In this study, we used companion dogs, who have prolonged exposure to human language in their home environment. These dogs came from homes where either English or Spanish was primarily spoken. The dogs were then presented with speech in English and in Spanish in a Headturn Preference Procedure paradigm to examine their language discrimination abilities as well as their language preferences. Dogs successfully discriminated between the two languages. In addition, dogs showed a novelty effect with their language preference such that Spanish-hearing dogs listened longer to English, and English-hearing dogs listened longer to Spanish. It is unclear what particular cue dogs are utilizing to discriminate between the two languages; future studies should explore dogs’ utilization of phonological and rhythmic cues for language discrimination.
... Similar results have been obtained for dogs (Ben-Aderet, Gallego-Abenza, Reby, & Mathevon, 2017). However, even though dog-directed speech is used for dogs of all ages, only puppies seem to prefer this form of communication (Ben-Aderet et al., 2017;Benjamin & Slocombe, 2018). ...
... Interestingly, there seems to exist a "dog-directed speech, " which is the type of "language" addressed to dogs that parallels the "child-directed speech" or "motherese" which plays an important role in language acquisition by the child. Both puppies and adult dogs seem to attend to, and show more affiliative behavior toward people using dog-directed speech, with this effect resulting from a combination of the acoustic properties and the contents of the specific words encompassing this type of speech (Benjamin and Slocombe, 2018). It also happens that bonding with dogs also results in increased verbal communication attempts toward other nonhuman animals (Epley et al., 2008). ...
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Thesis
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Pet-directed speech is strikingly similar to infant-directed speech, a peculiar speaking pattern with higher pitch and slower tempo known to engage infants' attention and promote language learning. Here, we report the first investigation of potential factors modulating the use of dog-directed speech, as well as its immediate impact on dogs' behaviour. We recorded adult participants speaking in front of pictures of puppies, adult and old dogs, and analysed the quality of their speech. We then performed playback experiments to assess dogs' reaction to dog-directed speech compared with normal speech. We found that human speakers used dog-directed speech with dogs of all ages and that the acoustic structure of dog-directed speech was mostly independent of dog age, except for sound pitch which was relatively higher when communicating with puppies. Playback demonstrated that, in the absence of other non-auditory cues, puppies were highly reactive to dog-directed speech, and that the pitch was a key factor modulating their behaviour, suggesting that this specific speech register has a functional value in young dogs. Conversely, older dogs did not react differentially to dog-directed speech compared with normal speech. The fact that speakers continue to use dog-directed with older dogs therefore suggests that this speech pattern may mainly be a spontaneous attempt to facilitate interactions with non-verbal listeners.
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Vowel triangle area is a phonetic measure of the clarity of vowel articulation. Compared with speech to adults, people hyperarticulate vowels in speech to infants and foreigners but not to pets, despite other similarities in infant- and pet-directed-speech. This suggests that vowel hyperarticulation has a didactic function positively related to the actual, or even the expected, degree of linguistic competence of the audience. Parrots have some degree of linguistic competence yet no studies have examined vowel hyperarticulation in speech to parrots. Here, we compared the speech of 11 adults to another adult, a dog, a parrot, and an infant. A significant linear increase in vowel triangle area was found across the four conditions, showing that the degree of vowel hyperarticulation increased from adult- and dog-directed speech to parrot-directed speech, then to infant-directed speech. This suggests that the degree of vowel hyperarticulation is related to the audience's actual or expected linguistic competence. The results are discussed in terms of the relative roles of speakers' expectations versus listeners' feedback in the production of vowel hyperarticulation; and suggestions for further studies, manipulating speaker expectation and listener feedback, are provided.
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Although a large literature discusses infants' preference for infant-directed speech (IDS), few studies have examined how this preference might change over time or across listening situations. The work reported here compares infants' preference for IDS while listening in a quiet versus a noisy environment, and across 3 points in development: 4.5 months of age, 9 months of age, and 13 months of age. Several studies have suggested that IDS might help infants to pick out speech in the context of noise (Colombo, Frick, Ryther, Coldren, & Mitchell, 1995; Fernald, 1984; Newman, 2003); this might suggest that infants' preference for IDS would increase in these settings. However, this was not found to be the case; at all 3 ages, infants showed similar advantage (or lack thereof) for IDS as compared to adult-directed speech when presented in noise versus silence. There was, however, a significant interaction across ages: Infants aged 4.5 months showed an overall preference for IDS, whereas older infants did not, despite listening to the same stimuli. The lack of an effect with older infants replicates and extends recent findings by Hayashi, Tamekawa, and Kiritani (2001), suggesting that the variations in fundamental frequency and affect are not sufficient cues to IDS for older infants.
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This paper describes a concept, not altogether new but largely neglected, that should lead to a greater understanding of the information contained in certain classes of vocal communication signals of birds and mammals. The concept is based on empirical data, first pointed out by Collias (1960, p. 382), showing that natural selection has resulted in the structural convergence of many animal sounds used in "hostile" and "friendly" contexts. Simply stated, birds and mammals use harsh, relatively low-frequency sounds when hostile and higherfrequency, more pure tonelike sounds when frightened, appeasing, or approaching in a friendly manner. Thus, there appears to be a general relationship between the physical structures of sounds and the motivation underlying their use. I hope to develop the idea that this relationship has had a far greater influence on the evolution of animal communication systems than has hitherto been discussed. I will discuss the idea that there exist motivation-structural rules (MS) governing the physical structure of close contact sounds in animal communication systems. The greatest value of the MS concept is that it provides the opportunity to compare the evolution of vocal communication in any species against an abstract concept. The adaptive nature of communication systems against varying backgrounds of environment, social system, and competition will appear in clear relief.
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2 experiments examined behavioral preferences for infant-directed (ID) speech over adult-directed (AD) speech in young infants. Using a modification of the visual-fixation-based auditory-preference procedure, Experiments 1 and 2 examined whether 12 1-month-old and 16 2-day-old infants looked longer at a visual stimulus when looking produced ID as opposed to AD speech. The results showed that both 1-month-olds and newborns preferrred ID over AD speech. Although the absolute magnitude of the ID speech preference was significantly greater, with the older infants showing longer looking durations than the younger infants, subsequent analyses showed no significant difference in the relative magnitude of this effect. Differences in overall looking times between the 2 groups apparently reflect task variables rather than differences in speech processing. These results suggest that infants' preference for the exaggerated prosodic features of ID speech is present from birth and may not depend on any specific postnatal experience. However, the possible role of prenatal auditory experience with speech is considered.
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