Despite the quintessential role that music plays in human societies by enabling us to release and share emotions with others, traces of its evolutionary origins in other species remain scarce. Drumming like humans whilst producing music is practically unheard of in our most closely related species, the great apes. Although beating on tree roots and body parts does occur in these species, it has, musically speaking, little in common with human drumming. Researchers suggest that for manual beating in great apes to be compared to human drumming, it should at least be structurally even, a necessary quality to elicit entrainment (beat induction in others). Here we report an episode of spontaneous drumming by a captive chimpanzee that approaches the structural and contextual characteristics usually found in musical drumming. This drumming differs from most beating episodes reported in this species by its unusual duration, the lack of any obvious context and rhythmical properties that include long-lasting and dynamically changing rhythms, but also evenness and leisureliness. This performance is probably the first evidence that our capacity to drum is shared with our closest relatives.
Producing music, performing, singing and dancing along with others is a universal part of human behaviour1. Scientists generally agree that several features are common to most human musical production2, including intentionality, decontextualisation, formality (evenness, isochrony) and joint coordination. To address the evolutionary origins of our musical skills, anthropologists, biologists and musicologists have examined the similarities between human performances and sound production in non-human animals3 and most agree that several features of our musical abilities are found in other species4,5,6. Bird or whale songs are considered analogous to music, because like many human songs they are complex vocalizations with a potential for cultural evolution, i.e they can be learned from others7,8. In great apes, manual beating is considered homologous to human drumming, because this shared capacity may reflect a common ancestral predisposition to produce music4.
However, manual beating by great apes generally lacks an essential characteristic of human drumming, namely evenness9. Isochrony, the fact of beating at regularly spaced time intervals makes the occurrence of the next beat(s) predictable and gives a formal quality to the performance. The evenness together with leisureliness facilitates temporal coordination from others and more generally entrainment. This remarkable feature of human music is far from being widespread in our closest relatives. Beating on tree buttresses, cans, body parts or objects, as wild chimpanzees, bonobos and gorillas do10,11,12,13,14,15, may be the sign of a link between body movement and vocal production1 and is sometimes called “drumming”4,10. In essence, however, it is more a spectacular noise-making display than a structurally isochronous performance9. These behaviors therefore have little in common with the structural and contextual characteristics found in the musical human drumming9. Here, we report an unusual performance of a chimpanzee named Barney. Barney was observed beating repeatedly and spontaneously on an upturned bucket for several sequences within a period of few minutes (Supplementary Audio file and Fig. 1). We evaluated his performance to establish which features fit with the type of characteristics generally associated with human drumming2, i.e. intentionality, decontextualisation and formality and explored if and how this particular event differed from previously reported manual beating displays by apes.
Assessing intentionality in non-verbalizing beings is a complex task. While means can be found to investigate it within non-human social interactions16, it is more difficult to pinpoint in solitary acts without an objective method of investigation. Yet in this particular drumming, Barney produced more than 685 drumbeats spread over 11 sequences for over four minutes (Fig. 1 and Supplementary Fig. S1). He remained in a seated position with the bucket between his feet, sometimes using his mouth to keep it in place (Fig. 2). The focus he showed during beating indicates that it was more than just a short, uncontrolled noise-making display. In this respect, it differs from most of the drumming episodes described in chimpanzees, who generally produce intense beating bouts of only few seconds12.
Human drumming does not necessarily have a particular purpose or context. This decontextualisation is not seen in great apes, whose manual beating is generally associated with play15, aggressive display, sexual arousal12 or travel11. In contrast, Barney had isolated himself from the others in his outside enclosure. He did not show any facial expression or postures typical of play (play face, excitement), nor did he move or exhibit aggressive display (body hair was not raised). One short but remarkable sequence (sequence 3) exhibited a change in the beating pattern and was punctuated by a bark, which could indicate a display context, but this explanation is not likely as no pilo-erection was observed. Barney did not move from his seated position and resumed drumming after a few seconds of silence for another long sequence. This situation supports the notion that the performance was indeed decontextualized.
In measured music, drumming has a formal quality2 where sounds are produced in organized patterns such as periodicity or rhythm. Isochrony of the inter-beat intervals is one way to achieve evenness, a necessary quality to allow entrainment. In the drumming we recorded, 10 of the 11 recorded sequences were long enough to be analyzed for their rhythmical properties, with an average inter-beat duration of 245 ms (Table 1). Recorded sequences were considered as time series in which lag denotes the range between the equally spaced instants of measurement. Here our instants of measurement are the beats and the measure is the inter-beat duration. First, we performed a portmanteau test for each recorded sequence, i.e. a Ljung-Box test, to detect potential non-random patterns in the time series. Five sequences showed non-random patterns (Supplementary Fig. S2). In four of them, these patterns were still detectable over at least 15 consecutive lags, indicating a long-lasting dependency over the course of the sequence (for sequences 1, 4, 9 and 11). In the last sequence (sequence 6), patterns occurred over the next lag, thus changing more frequently. We then ran an autocorrelation procedure for the sequences where non-random patterns were detected, in order to test the linear dependency between each consecutive inter-beat duration (Supplementary Fig. S3). Dependency up to lag 3, for example, indicates that whatever the position in the sequence, the duration of the next three lags can be predicted. Significant dependencies were found in the five sequences, ranging from dependency between one inter-beat duration and the next (sequence 6) to dependency between 12 consecutive inter-beat durations (sequence 4). This shows that the beating in these 5 sequences was not only regular, but was even extremely so on occasions, with an average tempo of 257 beats per minute (bpm). This pace is close to human tempo for rhythmic music17. Given that this pattern is probably due to a bimanual beating, it can therefore be argued that the basic tempo averages 128 bpm, a tempo typical of rhythmic popular dance music in many humans17. Remarkably, there is an alternation of positive and negative correlations in sequence 4, meaning that a long inter-beat duration was followed by a short inter-beat duration, or vice-versa. Given the unexpected regularity of this pattern, we provide a musical notation for this sequence, which illustrates a binary rhythm that musicians can now replicate (Fig. 3). Finally, a fluctuation analysis tested for linear trends (acceleration or deceleration) in the dynamic of each sequence. Changes in dynamics, i.e a deceleration, were observed in sequences 1, 9 and 11. Thus, the rhythm varied from one sequence to the next, which counters the possibility that the rhythm may simply result from endogenous synchronization or from a “motoric ceiling effect” in the frequency of slapping to maximize the noise output9. On the contrary, Barney demonstrated evenness at leisurely, spaced time intervals. This is a novel finding, as these two characteristics are not generally associated with typical manual beating by chimpanzees.
Patterns in periodicity or rhythm such as those described above may help other musicians or the audience to “join in” during communal music making. We have no evidence that Barney’s drumming could have elicited any joining from others, or was even designed to do so, as he performed at a distance from the rest of his group. His performance nevertheless shares many of the characteristics of human drumming. Within other animal species, joint coordination is found in sound-mimicking birds like cockatoos18 and parrots19,20, but also in sea lions21, which can be trained to bob their head in rhythm to a song. Most studies suggest that it is difficult for monkeys to even perceive a beat, let alone synchronize their movements with it22,23. The great apes may be capable of synchrony, as seen when the chimpanzee Ai spontaneously pressed two keys in time to a 600 ms inter-beat interval auditory stimulus without previous training24. We do know that in the wild, chimpanzees can show loose behavioral coordination when rain dancing25, chorusing (when the call of one aroused individual elicits joining from others) or engaging in carnival displays26,27, but we have no evidence that these behaviors could be beat-based rather than simply due to emotional contagion28,29. They cannot therefore be directly compared to the type of “on-the-beat” synchrony shown by humans when they play music1. In comparison, human children can synchronize to external drumming from around the age of three onwards with an accuracy that increases as they grow older30.
It is rare for animal sound production to simultaneously possess more than one of the previously cited characteristics found in human music2. In this respect, Barney’s drumming is exceptional. It was not only decontextualised and showed formality, but also appears to be intentional. Barney’s drumming is a rare example, as other reported musical drumming in great apes, although suggestive, did not address each of this features separately. Musical drumming has been reported in a language-trained bonobo called Kanzi31, but published data are lacking. A recent report describes how two young chimpanzees14 repeatedly hit a nearby clay pot and appeared to be attracted by the sound it made, hitting it 199 times, but no analysis of its rhythmical pattern has been provided. Barney’s performance confirms that the chimpanzee, our closest relative, could indeed be capable of drumming like a human.
According to Mithen5, music played a crucial role in our evolution before the existence of articulated language and improved communication between humans. By conveying emotions and thus meaning, it is thought to have further bonded human groups, improving coordination and cohesion. Some authors have suggested a similar cohesive outcome in the drumming of great apes11. Other researchers also suggest that synchronized beating and chants by groups of individuals would have made the performance louder and more likely to be heard by travelling females, the dispersing gender in humans and chimpanzees1. Although there is very little fossil evidence regarding the birth of our musical abilities, our data are probably the first strong evidence of an evolutionary link between wild beating in chimpanzees and our own musical origins.
Subject & procedure
At the time of our study, Barney was a captive-born, 24-year-old male belonging to a group of 5 adult male chimpanzees raised at the Biomedical Primate Research Centre in the Netherlands. Barney was a rather low-ranking male but was not particularly withdrawn from the group and had not be seen to display stereotypical behaviors. All members of this group often noisily manipulated plastic bottles, buckets and branches while performing display (VD, personal observations). Environmental noises included road traffic and construction building noises close by. The chimpanzees also sometimes had a radio playing in the building. The drumming was spontaneous (not artificially elicited or encouraged by human presence) and occurred in January 2005 in the outside part of their enclosure. The observer (VD) was nearby at the start of the drumming and quietly approached Barney’s enclosure to record it on a voice recorder (type Sony M527V). No camera was available within reach to film this episode. The barrel used for the drumming was part of the objects available at all time in the enclosure and was neither new, nor newly introduced to the chimpanzee. We delimited sequences as follow: first, after a pause of two seconds, we considered the following beats to be the beginning of the next sequence. Second, if sound pollution occurred (caused by wind or when the noise of the beat was covered by background noise), the inaudible part of the sequence was not analyzed and we considered the following audible part as a new sequence. For example, because the first few beats of Sequence 6 were difficult to extract from the background noise, we started the analysis at the 6th beat. The recording of Sequence 6 was interrupted by the wind. The following beats were treated separately as Sequence 7. Additionally, the analysis started from beat 3 in Sequence 4 due to a discontinuity between the second and the third beats (a one second pause). To analyze rhythmical patterns, we selected sequences with more than 20 beats (thus discarding sequence 5). Note also that the recording was stopped after the end of sequence 2, as the observer thought that the bout was over. It was immediately restarted when Barney began drumming again a few seconds later, but the first few beats of sequence 3 are missing.
The analysis was conducted using Reaper software. We used the transient detection settings tool (threshold detection was set at −24 dB and sensitivity at 25%, 60% and 75%) to measure the inter-beat durations in each sequence. For each sequence, data were analyzed using R32. P level of significance was set at 0.05.
The study was conducted in accordance with the approved scientific reports guidelines. Due to the observational nature of this study (the audio recording of a spontaneous behavioral sequence initiated by the chimpanzee), this study does not classify as an experiment as assessed by the Biomedical Primate Research Centre Animal welfare officer. Thus no additional permission from the institutes animal experiment committee was required. The study was conducted in accordance with relevant Dutch laws and in agreement with international and scientific standards and guidelines.
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The authors are grateful to K. Zuberbuhler, Z. Clay, C. Crockford, S. Kosky, K. Slocombe and H. Honing, for early comments on parts of the recording. Data are available on request to the corresponding author.
The authors declare no competing financial interests.
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Dufour, V., Poulin, N., Charlotte Curé et al. Chimpanzee drumming: a spontaneous performance with characteristics of human musical drumming. Sci Rep 5, 11320 (2015). https://doi.org/10.1038/srep11320
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