"The faculty of erecting the ears and of directing them to different points of the compass, is no doubt of the highest service to many animals, as they thus perceive the point of danger; but I have never heard of a man who possessed the least power of erecting his ears": Charles Darwin, The Descent of Man, 18711
"Unlike dogs and cats, people do not point their ears as they focus attention on novel, salient, or task-relevant stimuli. Our species may nevertheless have retained a vestigial pinna-orienting system that has persisted as a 'neural fossil' within in the brain for about 25 million years.": Strauss and colleagues, eLife, 20202
Summary
The parent article, Vestigial Structures, separates the dead claim that a vestige is useless from the live claim that it is a reduced copy of a structure that does a fuller job in related animals, and gives the live claim three steps: homology, reduction, and an ancestral explanation that fits a tree built from other characters. This article runs that test on the small muscles that tie the outer ear to the scalp and skull.
- What they are. Gray's Anatomy of 1918 names three extrinsic muscles, the auricularis anterior, superior and posterior, which move the ear as a whole, and six intrinsic muscles inside its cartilage, all supplied by the facial nerve.333 "In man, these muscles possess very little action".3 A 2022 EMG study of all nine muscles in twelve adults found every one alive, firing most during smiling and deliberate ear-wiggling.4
- What they do in other mammals. Sisson's veterinary anatomy gives the horse more than a dozen extrinsic ear muscles, driving an ear whose movements "resemble those of a ball-and-socket joint".55 A cat's pinna is served by 22 motoneuron pools6 and swings toward a sound about 25 milliseconds after it starts.7 Waller and colleagues, who lifted a macaque's whole ear by stimulating one auricular muscle,8 found the human face "little altered" from the monkey's "with the exception of the reduction in musculature around the external ear."8
- Still wired. Strauss and colleagues reported in eLife in 2020 that EMG activity is larger at the ear on the side of an attended sound, for surprise sounds and for a story listened to on purpose, and called the system a "neural fossil".2 Schroeer and colleagues found in 2025 that the superior auricular muscle works harder as listening gets harder and the posterior one fires more for sounds from behind.9 The postauricular reflex to a click, peaking at 12.5 to 15 milliseconds, is used as an objective hearing test.1011
- Who can move them. In Linder's 1949 sample of 104 men and 70 women, 54 % and 22 % could move their ears; in Barcelona in 1980, 19.9 % and 9.57 %.12 It runs in families, and it is learnable: in 1901 J. H. Bair trained twelve non-movers until each could,1313 and in 2019 six of ten learned two-ear control with electrical stimulation and biofeedback.14 Even then the movement is a few millimetres; nobody erects or points the ear.1
- The claim's history. Darwin opened his 1871 list of human rudiments with the ear muscles,1 Wiedersheim put them in the vestigial section of his 1895 conspectus,15 and Coyne in 2009 called them "silly ear muscles".16
- The creationist replies. Menton (2000, 2007), Sanders (2011) and Bergman (2000) argue that small muscles are not useless, that an unused muscle would waste away, and that a wax-clearing role is possible.1718 Menton concedes that human ear movements are "slight" and give no known hearing benefit.19 None asks whether the muscles are reduced copies of the mammalian pinna muscles, which is the only claim the modern argument makes, and no primary source supports the wax suggestion. Bergman alone has answered the attention studies, in 2020: he calls the activity body language rather than an attempt to move the ear, but the movements it measured are generally invisible.202
Verdict: the ear muscles pass steps 1 and 2 at full strength. They are the same muscles, on the same nerve, from the same embryonic arch, that orient the pinna in cats, horses and monkeys; in humans they are fewer, smaller and nearly motionless, while the circuit that drives them still fires toward the attended side. Function is real and settles nothing, because the physiologists who found it are the ones calling the system vestigial. Step 3, a mobile-eared ancestor behind the human line, is inferred from the primate tree, not from the human body, and a creationist can grant reduction within the human kind without granting that ancestor. What that reply has not yet done is say convincingly why a system designed for humans would carry an orienting reflex that cannot orient: the one attempt, Bergman's 2020 proposal that the reflex is a social signal, needs a movement other people can see, and the measured movement is one to two orders of magnitude smaller than deliberate ear-wiggling.
Part 1: What the ear muscles are and what they do in people
"The muscles of the auricula (Fig. 906) consist of two sets: (1) the extrinsic, which connect it with the skull and scalp and move the auricula as a whole; and (2) the intrinsic, which extend from one part of the auricle to another. The extrinsic muscles are the Auriculares anterior, superior, and posterior."3 The six intrinsic muscles are the helicis major and minor, tragicus, antitragicus, transversus auriculae and obliquus auriculae.3 "In man, these muscles possess very little action: the Auricularis anterior draws the auricula forward and upward; the Auricularis superior slightly raises it; and the Auricularis posterior draws it backward."3
The nerve matters: "The Auriculares anterior and superior and the intrinsic muscles on the lateral surface are supplied by the temporal branch of the facial nerve, the Auricularis posterior and the intrinsic muscles on the cranial surface by the posterior auricular branch of the same nerve."3 The facial nerve is the nerve of the second pharyngeal arch, and Gray's embryology explains why every muscle of expression hangs from it: "The facial nerve, which early enters the common facial muscle mass of the second branchial or hyoid arch, is dragged about with the muscle as it spreads over the head and face and neck, and as the muscle splits into the various muscles of expression, the nerve is correspondingly split."3 David Menton, the creationist anatomist, agrees: the auricular muscles "are typically grouped with the muscles of facial expression", and "All of the facial muscles (including the auricularis muscles) are innervated by the same cranial nerve, the facial nerve."19
What they do was measured by Hannah Rüschenschmidt and colleagues at the Jena facial-nerve centre, who recorded all nine muscles by surface EMG in 2022, starting from the standard view: "These muscles have been considered vestigial in humans, and are rarely under voluntary control."4 Every muscle gave a signal in all twelve subjects. "In general, the ear muscle EMG activity was highest during smiling and ear wiggling. The lowest activity was seen during ipsilateral or contralateral gaze. Only the obliquus auriculae and the transversus auriculae muscle showed a robust activity during the isolated lateral gaze."4 They also have a medical use unrelated to hearing: cranial nerves bypass the spinal cord, so a person paralysed from the neck down keeps them, and "such patients can learn to steer a wheelchair with ear muscle activation".4 The team that built such a device put the anatomy bluntly: "The peri-auricular muscles (PAMs) can be found in 95% of the population but do not currently serve any physiologic function".14
Part 2: What the same muscles do in other mammals
The horse is the textbook case. Sisson's Anatomy of the Domestic Animals of 1914 gives the extrinsic list two pages: "The anterior auricular muscles (Mm. auriculares orales) are four in number"; "The dorsal auricular muscles (Mm. auriculares dorsales) are two in number"; "The posterior auricular muscles (Mm. auriculares aborales) are three in number"; two deep rotators "cross each other" under the scutiform cartilage, and the strongest "is flat and is about an inch wide."5 Add the three-part scutularis, the parotido-auricularis and the tragicus. What they do is what every rider sees: "The base of the concha is rounded and rests in a pad of fat (Corpus adiposum auriculae), so that the movements of the external ear resemble those of a ball-and-socket joint." "When the ear is vertical or drawn forward ("pricked up"), the opening is usually directed forward ; conversely, when the ears are "laid back," the opening faces backward."5
The cat has been measured. Populin and Yin traced the nerve supply in 1995: "The topographical organization of the 22 motoneuron pools that innervate the pinna muscles of the cat was examined"; "All 22 pools are found in the facial nucleus".6 In 1998 they implanted search coils in the pinnae of cats trained to look at lights and sounds. "Prominent pinna movements accompany eye movements when the animal orients to either auditory or visual stimuli." To a sound the ear moved first: "The short-latency component (∼25 msec) was highly asymmetrical, being largest in the pinna ipsilateral to the stimuli."7 In a cat the facial nerve carries a fast, direction-coded command that turns the ear toward a sound before the eyes move.
Monkeys keep much of this. Waller and colleagues stimulated single facial muscles in an anaesthetised rhesus macaque in 2008 and filmed the result. "Stimulation of the superior auricularis caused the ear to elevate superiorly (supplemental material 16), but without the medial contraction seen in orbito-auricularis. Stimulation of inferior auricularis caused the ear to flatten to the head and slight lateral retraction of the scalp (supplemental material 17)."8 Their conclusion is the comparison this article turns on: "the facial muscles we see in humans appear to be little altered from the format we see in a monkey species, with the exception of the reduction in musculature around the external ear." "The most striking difference between the three species is the great potential for ear movement in the rhesus macaque, which is not seen in humans and chimpanzees."8
Strauss and colleagues assemble the primate series in their 2020 discussion. "The ability to swivel and point the pinnae seems to have been lost during the transition from the primarily nocturnal lifestyles of prosimians to the diurnal ones of New World monkeys, and then, Old World monkeys (Coleman and Ross, 2004). Mobility continued to decline as the ears became shorter and more rigid ... The musculature degenerated. For example, an inferior auricular muscle to oppose SAM still exists in lesser apes such as gibbons and siamangs (Burrows et al., 2011), but not in chimpanzees (Burrows et al., 2011) or humans (Cattaneo and Pavesi, 2014)."2 Coleman and Ross had found that "most nonanthropoids have ears that are tall and narrow, whereas monkeys and apes are characterized by ears with more equal height and width dimensions."21 One more difference matters for the reduction claim: "Although the ear muscles of Old World monkeys have spindles (Lovell et al., 1977), those of humans do not (Cattaneo and Pavesi, 2014)."2 Spindles are the stretch sensors that report a muscle's length. Their absence counts for less than it seems, because it is not peculiar to the ear. Cobo and colleagues wrote in 2017 that "The human craniofacial muscles innervated by the facial nerve typically lack muscle spindles", yet "these muscles have proprioception that participates in the coordination of facial movements."22 A 2023 survey of lip and cheek muscles across mammals by Omstead, Burrows and colleagues did find spindles, but "humans (and other primates) had the lowest number of muscle spindles", with carnivores and the horse the highest.23 The lips are aimed precisely in speech with few or none, so a spindle-free muscle can still be aimed, and the ear's lack of spindles is part of a primate-wide trait of the whole face, not a mark of the ear alone. Darwin's informants had already placed the apes with humans: the London zoo keepers assured him "that these animals never move or erect them; so that they are in an equally rudimentary condition, as far as function is concerned, as in man."1 Wiedersheim in 1895 called the human intrinsic muscles "the vestige of a primitive apparatus functional either for the opening and closing, or for the widening and narrowing of the auditory funnel and the external auditory passage".15
Part 3: The system is still wired
The finding that changed this topic is that the human brain still sends direction-specific commands to muscles that cannot carry them out. Steven Hackley's 2015 review in Psychophysiology set the thesis: "Humans and apes do not move their ears to express emotion, they do not defensively retract them when startled, and they do not point them at novel, salient, or task-relevant stimuli. Nevertheless, it is the thesis of this review that neural circuits for pinna orienting have survived in a purely vestigial state for over 25 million years."24 His evidence was the curl of the ear's edge when the eyes turn hard aside, "a weak EMG response in the muscle behind the corresponding ear" to a surprise sound from that side, and reflex bursts in a listening task that "suggested that subjects were unconsciously attempting to orient their ears toward the relevant sounds."24 The oculo-auricular effect goes back to Wilson in 1908: "shifting the gaze hard to one side elicits a 1 to 4 mm deflection of the lateral rim of both ears."2
Strauss and colleagues tested the thesis in 2020, recording the posterior, anterior, superior and transverse auricular muscles while adults read a dull text interrupted by novel sounds from four speakers, and again while they followed a story from one side and ignored a competing story from the other. "In both experiments, EMG recordings showed larger activity at the ear on the side of the attended stimulus, but with slightly different patterns."2 Their discussion opens: "These data provide compelling evidence that our brains retain, in vestigial form, circuitry for orienting the pinnae during both exogenous and endogenous modes of attention."2 They are plain about how small the effect is: "The neural drive to our ear muscles is so weak that the actual movements (see co-registered video data in the Supplementary Information) are at least one to two orders of magnitude smaller compared to those generated during biting, smiling, grimacing, or voluntary ear-wiggling."2 In 2024 the same group found that a surprise sound raises the posterior muscle on the same side and briefly suppresses the superior muscle at the same moment, "synchronized excitatory and inhibitory components in different auricular muscles" that "points toward a coordinated attempt at reflexively orienting the pinna toward a sound."25
In 2025, in Frontiers in Neuroscience, twenty young adults with normal hearing followed a podcast against distractors at three levels of difficulty, from a speaker in front or behind. "averaged PAM activity was not affected by different levels of effortful listening, but was significantly larger when stimuli were presented from the back, as opposed to the front. Averaged SAM activity, however, was significantly larger in the most difficult condition, which required the largest amount of effort". The authors "interpret the increased SAM activity to be the response of the vestigial pinna–orienting system to an effortful stream segregation task".9 In cats and dogs a large enough movement "would impact the head-related transfer function",9 but in humans "it is currently not known if they are strong enough to achieve an actual benefit",9 and the authors state the limitation the parent article flags: "Participants formed a relatively small and homogeneous group, i.e., young and normal-hearing".9
The one part of this system used every day is the postauricular muscle reflex, which O'Beirne and Patuzzi describe as "One objective electrophysiological test for deafness", "a simple bipolar compound action potential with a first peak latency of between 12.5 and 15 ms" that reaches "adult values by 12 months of age."10 Purdy and colleagues showed in 2005 that "PAMR thresholds were correlated with audiometric thresholds" in hearing-impaired adults and that at "35 dB nHL, the level widely used for infant hearing screening, most normal-hearing adults had a PAMR."11 Hackley reads this reflex as "a vestigial startle response", the remnant of the ear-flattening a startled cat performs.24
Part 4: Who can move their ears, and whether it can be learned
Darwin's 1871 paragraph has the three observations later work confirmed: the muscles are "variable in development, or at least in function";1 "most of us" could "by repeated trials recover some power of movement";1 and nobody erects the ear.1 Wiedersheim was blunter: "In most people it is entirely wanting".15
The one family study on record is Linder's, in Hereditas in 1949, summarised by the OMIM catalogue: "Linder (1949) examined 104 men and 70 women and found the ability to move the ears in 54% and 22%, respectively. The frequency of the trait among sibs of probands was 47% and among parents was 74%. However, in 5 of 24 cases both parents lacked the trait, leading Linder (1949) to suggest that the ability is inherited as a somewhat irregular dominant. In Barcelona, Hernandez (1980) found that 19.9% of men and 9.57% of women could move their ears."12 The prevalence differs twofold between samples, as expected when a trait is scored by asking people to try.
Learnability was settled in 1901, when J. H. Bair at Michigan chose the retrahens aurem for a study of how voluntary control develops because most people cannot contract it. "Of the fourteen subjects who rendered us their services, only two could move their ears at the beginning of the experiment and these only when vigorously raising their brow. The remaining twelve had no idea of the movement and could not produce it, however hard they tried."13 Electrical stimulation, a kymograph tracing the ear and practice did the rest: "All of our subjects acquired control over this muscle".13 The path ran through the facial-expression mass: "In this stage the retrahens is always contracted by biting the jaws together or vigorously raising the brow. The ear was thus first reached by innervating a group of muscles over which one has already control."13 The 2019 study by Chanthaphun and colleagues repeated this with modern tools and a wheelchair controller in view: ten adults with no visible ear movement on request "finished the facilitation phase in 3 to 9 sessions and achieved some level of voluntary auricle movement that ranged between 1 and 5 mm"; "Sixty percent of those who completed the facilitation phase were able to learn and demonstrate functional voluntary control of the vestigial PAMs", with "20% deemed Poor/Non-Learners".14 The muscle, the nerve and the cortical path are present in people who cannot use them; what is missing is a motor programme, and for most people it can be built in weeks. Nobody in either study learned to erect or aim an ear.
Part 5: The claim's history and the creationist replies
Darwin opened his survey of human rudiments with the muscles: "The extrinsic muscles which serve to move the whole external ear, and the intrinsic muscles which move the different parts, all of which belong to the system of the panniculus, are in a rudimentary condition in man".1 His explanation was disuse, with a caveat: "It may be, though I am not quite satisfied with this view, that owing to their arboreal habits and great strength they were but little exposed to danger".1 Wiedersheim's 1895 conspectus lists "Muscles of the pinna and the Musculus occipitalis" in section B, the organs "which may be rightly termed Vestigial".15 Coyne's 2009 version is a phrase: "Tiny, nonfunctional wings, a dangerous appendix, eyes that can't see, and silly ear muscles simply don't make sense if you think that species were specially created".16 Coyne also states the modern definition that makes function beside the point: "A trait can be vestigial and functional at the same time. It is vestigial not because it's functionless, but because it no longer performs the function for which it evolved."16
The creationist literature answers the adjectives. Jerry Bergman's 2000 paper opens with Asimov's two examples, the coccyx and "the small muscles around the ears (which Asimov claims are 'unworkable muscles once meant to move the ears')", and says "these conclusions are not based on empirical evidence but instead on evolutionary assumptions."26 The paper says nothing more specific about the ear. Bergman and Howe's 1990 monograph has a chapter "The Ear Muscles" on its page 58; no copy could be obtained, so the CMI reply that cites it stands in for it here.
That reply is David Menton's, written in 2003 and published by Creation Ministries International in 2007. "The auricularis muscles are a favorite example of evolutionists as vestigial muscle presumably left over from when we could move our ears (auricles) about like a rabbit. Clearly, the ability to orient the ears assists in sensing the stereo imaging of sound (location and distance)."19 Menton concedes the central fact: "The ability of humans to move the auricle in a grossly noticeable way varies from individual to individual but generally the movements are slight. Are any of these movements, when noticeable or measurable, able to improve our hearing or stereo perception? None that we know of at this time."19 His 2000 paper on the plantaris names the ear muscles first among "The muscles most frequently claimed to be vestigial in man", grants that they "give the appearance of producing little or no useful work by their weak contractions",17 and argues from atrophy: "It is unlikely that any muscle that was virtually unused for the lifetime of an individual (to say nothing of generations of individuals over millions of years) would remain as healthy muscle tissue."17 Hence "any muscle in the body that actually exists in the present, serves some function."17
Lita Sanders's 2011 CMI reply adds a proposal: "A CMI biologist suggested that one function of ear muscles could be to help remove wax from the ears. When a person is chewing, or smiling, etc. the ear muscles move the ears. This gradually moves the wax outwards, cleaning the ears. But there could be other functions also."18 The premise holds: the Jena study found the ear muscles most active during smiling. The conclusion has no source. A Europe PMC full-text search for cerumen together with the auricular or ear muscles finds no paper connecting them, and the standard clinical review of ear wax, by Guest and colleagues in 2004, says "the physiology, clinical significance and management implications of excessive and impacted cerumen remain poorly characterized."27 The wax suggestion is a conjecture and should be labelled as one.
Jerry Bergman is the one creationist who has answered the attention studies directly, in a July 2020 article for Creation-Evolution Headlines written against the Saarland press release on the eLife paper.20 He makes three claims. First, the muscles serve "as a framework supporting and stabilizing the pinna", aid blood supply in the temple, and act as "padding to protect the underlining structures in the temples."20 Second, the attention-driven activity is "not to move the ears" but "to communicate with others", which he says is what "the authors themselves note".20 Third, evolution cannot say why the ability was lost: "no one has any idea why movement of the auricle to better focus on a certain sound source, as cats and some dogs do, would be lost by evolution."20
The third point is fair. Darwin was "not quite satisfied" with his own explanation of the loss,1 and no study cited here tests why pinna orienting declined in apes. But it is a question about step 3, the ancestral explanation, not about whether the muscles are reduced. The first two points do not hold up. Bergman cites no measurement of support, circulation or padding, and the same could be said of any thin sheet of muscle. The communication claim is not in the eLife paper, whose text says nothing about communication or social signals.2 It also runs against Bergman's own summary of the study, which describes "the very small, generally invisible, movements of the pinna",20 and against the authors' measurement that attention moves the ear one to two orders of magnitude less than deliberate ear-wiggling.2 Bergman cites no study showing that anyone can see the movement. His reply is still the only creationist attempt to give the direction-coded activity itself a present job, and it is the right kind of answer, even though this version of it fails.
Menton, Sanders and Bergman's 2000 paper answer the useless claim. Menton's atrophy argument is the strongest, and the physiology confirms its premise: the muscles are used daily by the facial-expression mass, the eye-movement coupling and the postauricular reflex. But use is not at issue; the claim is that what they do is the remnant of pointing an ear, and on that claim the creationist literature has only Bergman's 2020 social-signal proposal.
Part 6: The three-step test
Step 1, homology. The human auricularis anterior, superior and posterior correspond, muscle for muscle, to the anterior, dorsal and posterior auricular groups of the horse and to the auricularis muscles Waller stimulated in the macaque. They attach in the same places, run on the same cranial nerve from the same second-arch muscle mass, and in the cat the pinna motoneurons sit in the same facial nucleus. No source on either side disputes this.
Step 2, reduction. This is measured, not assumed. The horse has more than a dozen extrinsic ear muscles and the cat 22 motoneuron pools; humans have three extrinsic muscles. Gibbons and macaques have an inferior auricular muscle; chimpanzees and humans do not. Old World monkeys' ear muscles have spindles; human ones do not, though this is weak evidence because human facial muscles in general have few or none. The macaque's superior auricularis lifts the whole ear; the human one "slightly raises it". Voluntary movement is a few millimetres, and attention-driven movement one to two orders of magnitude smaller. Variability between individuals, Darwin's diagnostic of a rudiment, is met by every survey from 1871 to 1980. The reduction is measured against living animals and depends on no fossil and no tree.
Step 3, the ancestral explanation. Nothing in the human body says that a human ancestor pointed its ears. The claim that one did is the claim that humans and Old World monkeys share an ancestor and that the reduction happened on the human side of the split. Strauss and colleagues put it in those terms: "When pinna-orienting movements became too small to modify acoustic input substantially, possibly 25 million years ago when lesser apes branched off from Old World monkeys, see Gibbs et al., 2007 as discussed in Hackley, 2015, selective environmental pressure ceased. The neural system became more-or-less 'frozen' in a form optimized for controlling taller, more flexible ears, mounted on a smaller, more spherical head."2 The 25 million years is read off the primate tree, and the "frozen" system is an interpretation of the EMG pattern, not a second measurement. A creationist who holds that the human kind was created with small ear muscles can accept every number in Parts 1 to 4 and reject this paragraph, and the parent article's Sarfati-and-Batten reply, that loss within a kind is devolution, not evolution, is available here as everywhere.
What the evidence does bear on is the shape of the leftover. The reflex that Strauss, Schroeer and Hackley measured is not a general facial-expression signal: it fires in the posterior muscle for sounds from behind, on the attended side, at about the cat's EMG latency,2 with the superior muscle briefly inhibited at the same moment. That is the pattern a pinna-orienting controller produces. In a cat it turns the ear; in a human it moves a spindle-free muscle by a distance nobody has shown to change the sound reaching the drum. A design explanation has to say what a controller of that shape is for in an animal that cannot use it. The one creationist attempt, Bergman's proposal that it is a social signal, has no evidence that the signal can be seen. The atavism evidence that helps other vestige cases, extra toes on horses or tail muscles on people, has no counterpart here: nobody has been reported who can erect an ear, and the training studies produce lift and pull-back, never pointing. So step 3 stands or falls with the primate tree, and the ear muscles add to that case one thing: a working orienting circuit in the wrong animal.
Objections and responses
The 2020 and 2025 studies found a function, so the muscles are not vestigial. The authors of those studies say the opposite in their titles. On the modern definition a structure is vestigial because it is a reduced homologue, not because it is idle; Coyne states the definition and the physiologists apply it.
Unused muscle atrophies, so the ear muscles must be doing something. They are: they contract with smiling and hard sideways gaze, and the postauricular muscle twitches to clicks. That answers the useless claim only. A muscle kept alive by co-contraction with its neighbours can still be the reduced remnant of a muscle that had a job of its own.
The ear muscles help move wax out. No primary source says so. Even if a millimetre of ear movement during chewing nudged wax, that would be a function of the reduced muscle, not a reason to deny the reduction.
Calling the muscles reduced assumes the evolutionary history. Reduction is measured against horses, cats and macaques alive today, by muscle count, spindle content, force and range, and assumes nothing about descent. What assumes descent is the next step, that the fuller condition is ancestral. Bergman's objection is right about step 3 and wrong about step 2.
Humans could have been created with small ear muscles that do exactly what they do. This is the honest form of the reply, and the anatomy cannot refute it. What it owes is an account of the orienting reflex: why a created system carries a fast, side-specific, effort-sensitive command to a muscle that cannot move the ear far enough to matter. Facial expression and hearing screening do not need direction coding. A social signal of where a person is listening would need it, which is why Bergman's 2020 proposal is the right kind of answer, but it would also need a movement others can see, and none has been shown.
The attention studies are small and come from one group. True. Strauss 2020, Schroeer 2024 and Schroeer 2025 come from one Saarland and Missouri collaboration, with 28, 10 and 20 participants; only the 2020 study included older adults.2 The postauricular reflex is established enough to serve as a hearing test, and the comparative anatomy depends on none of these studies.
Issues and unanswered questions
- Hackley's 2015 review is cited from its abstract; the full text is paywalled and was not read. Bergman and Howe's 1990 chapter was not obtainable, and Linder's 1949 abstract is cited through OMIM's summary.
- Whether the attention-driven movements alter the sound reaching the eardrum in anyone, including good ear-wigglers, has not been tested; Schroeer and colleagues call for a study of people "who are able to voluntarily move their ears".9
- The "neural fossil" reading treats the EMG pattern as a frozen controller. An alternative no study has excluded is that the auricular muscles are recruited as a side effect of the general orienting response, with no pinna-specific programme surviving. The 2024 excitation-and-inhibition result argues against that, on ten participants.
- No creationist source engages the homology or reduction steps for this structure, so the strongest reply, that reduction occurred within the human kind, is this article's reconstruction, not a quotation.
- Bergman's 2020 note in Journal of Creation 34(2), "Useless ear muscles are very useful", which his Creation-Evolution Headlines article cites for the support and padding roles, was not read, so any data it gives for those roles are not weighed here.
- The spindle comparison rests on the abstracts of Cobo 2017 and Omstead 2023. No count of spindles in human or monkey ear muscles themselves was read; the Old World monkey figure is Lovell and colleagues 1977 as reported by Strauss.
- The 25-million-year figure and the sequence prosimian, New World monkey, Old World monkey are drawn from the primate tree and are used here as the evolutionary side's own claim, not as measurements.
- The horse and cat counts come from anatomy of 1914 and 1995 and were not rechecked against modern dissections.
Verdict
The ear muscles are the clearest reduced-homologue case among the human muscles. Homology is undisputed, reduction is measured against living mammals by count, force and range, and the circuit that would point a cat's ear still fires, in the right direction and at the right latency, in people whose ears do not move. Function is real and answers only the argument that died in 1895. The ancestral step is a claim about the primate tree, and the creationist reply that the loss happened within the human kind is coherent, unfalsified by anything here, and so far unwritten. What the ear muscles contribute to the larger dispute is one exact fact that the design reading has to explain and has not yet explained, since its one attempt, a social signal, rests on movements too small to see: a direction-coded orienting reflex in a body that cannot orient.
Sources
- 1.
Darwin, Charles. The Descent of Man, and Selection in Relation to Sex. Volume 1. John Murray. 1st edition. 1871. A book by Charles Darwin, the first of its two volumes, arguing that man descended from a lower form of animal. Its first chapter gathers that evidence, including rudimentary structures and muscles. The article uses it for the first list of human rudiments to begin with the ear muscles, and for Darwin's report that he had never heard of a man who could erect his ears.
- 1a.
Page 20: “The extrinsic muscles which serve to move the whole external ear, and the intrinsic muscles which move the different parts, all of which belong to the system of the panniculus, are in a rudimentary condition in man; they are also variable in development, or at least in function. I have seen one man who could draw his ears forwards, and another who could draw them backwards;”. ↩ ↩ ↩
- 1b.
Page 21: “and from what one of these persons told me, it is probable that most of us by often touching our ears and thus directing our attention towards them, could by repeated trials recover some power of movement.” ↩
- 1c.
Page 21: “The faculty of erecting the ears and of directing them to different points of the compass, is no doubt of the highest service to many animals, as they thus perceive the point of danger; but I have never heard of a man who possessed the least power of erecting his ears”. ↩ ↩ ↩
- 1d.
Page 21: “I am assured by the keepers in the Zoological Gardens that these animals never move or erect them; so that they are in an equally rudimentary condition, as far as function is concerned, as in man. Why these animals, as well as the progenitors of man, should have lost the power of erecting their ears we cannot say. It may be, though I am not quite satisfied with this view, that owing to their arboreal habits and great strength they were but little exposed to danger, and so during a lengthened period moved their ears but little, and thus gradually lost the power of moving them.” ↩ ↩ ↩
- 1a.
- 2.
Strauss, Daniel J. et al. “Vestigial auriculomotor activity indicates the direction of auditory attention in humans.” eLife 9:e54536. Jul 3, 2020. A laboratory study that used surface electrodes on the skin to record electromyography, the electrical signal of a muscle, from the muscles around each ear while adults read or followed a story. The ear muscles were more active on the side of the sound or story the listener attended, and the authors call the system a 'neural fossil'. The article relies on it for the claim that the human brain still drives the ear muscles toward attended sounds. ↩
- 2a.
Section Abstract: “Unlike dogs and cats, people do not point their ears as they focus attention on novel, salient, or task-relevant stimuli. Our species may nevertheless have retained a vestigial pinna-orienting system that has persisted as a 'neural fossil' within in the brain for about 25 million years.” “In both experiments, EMG recordings showed larger activity at the ear on the side of the attended stimulus, but with slightly different patterns.” The printed abstract reads 'within in the brain'. ↩ ↩ ↩
- 2b.
Section Introduction: “The first was Wilson's oculo-auricular phenomenon (Wilson, 1908), in which shifting the gaze hard to one side elicits a 1 to 4 mm deflection of the lateral rim of both ears.” “Additional evidence comes from a 1987 study (Hackley et al., 1987) of the bilateral postauricular muscle (PAM) reflex (onset latency = 10 ms) to acoustic onset transients. Increased amplitudes were observed when subjects directed their attention to a stream of tones on the same side as the recorded muscle while ignoring a competing, contralateral stream.” ↩
- 2c.
Section Discussion: “These data provide compelling evidence that our brains retain, in vestigial form, circuitry for orienting the pinnae during both exogenous and endogenous modes of attention.” ↩
- 2d.
Section Discussion: “The neural drive to our ear muscles is so weak that the actual movements (see co-registered video data in the Supplementary Information) are at least one to two orders of magnitude smaller compared to those generated during biting, smiling, grimacing, or voluntary ear-wiggling.” ↩ ↩ ↩
- 2e.
Section Discussion, Vestigial Pinna-Orienting: “The ability to swivel and point the pinnae seems to have been lost during the transition from the primarily nocturnal lifestyles of prosimians to the diurnal ones of New World monkeys, and then, Old World monkeys (Coleman and Ross, 2004). Mobility continued to decline as the ears became shorter and more rigid, see Waller et al., 2008; Coleman and Ross, 2004. The musculature degenerated. For example, an inferior auricular muscle to oppose SAM still exists in lesser apes such as gibbons and siamangs (Burrows et al., 2011), but not in chimpanzees (Burrows et al., 2011) or humans (Cattaneo and Pavesi, 2014).” ↩
- 2f.
Section Discussion, Vestigial Pinna-Orienting: “Although the ear muscles of Old World monkeys have spindles (Lovell et al., 1977), those of humans do not (Cattaneo and Pavesi, 2014).” ↩
- 2g.
Section Discussion, Vestigial Pinna-Orienting: “When pinna-orienting movements became too small to modify acoustic input substantially, possibly 25 million years ago when lesser apes branched off from Old World monkeys, see Gibbs et al., 2007 as discussed in Hackley, 2015, selective environmental pressure ceased. The neural system became more-or-less 'frozen' in a form optimized for controlling taller, more flexible ears, mounted on a smaller, more spherical head.” ↩
- 2h.
Section Discussion, Potential neural mechanisms: “Using a 4-speaker set-up similar to that of the present Experiment 1, Siegmund and Santibáñez, 1982 found cats’ unconditioned pinna responses to have an EMG onset latency that averaged 78 ms, similar to our value of about 70 ms.” ↩
- 2i.
Section Materials and methods, Participants: “Both older (N = 12, mean age = 62.7 ± 5.9 y, 8 F, all right-handed) and younger adult (N = 16, mean age = 24.1 ± 3.1 y, 8 F, 15 right-handed, one left-handed) volunteers in Experiment one had age-typical, pure tone audiometric thresholds”. “Only data from the final 21 subjects were retained for Experiment 2.” ↩
- 2a.
- 3.
Gray, Henry. Anatomy of the Human Body. Lea & Febiger. 20th edition. Edited by Warren H. Lewis. 1918. A book on human anatomy. The article uses it for Gray's list of the nine ear muscles, three that move the whole ear and six inside its cartilage, all supplied by the facial nerve, and for his remark that in man these muscles "possess very little action".
- 3a.
Page 1035: “The muscles of the auricula (Fig. 906) consist of two sets: (1) the extrinsic, which connect it with the skull and scalp and move the auricula as a whole; and (2) the intrinsic, which extend from one part of the auricle to another. The extrinsic muscles are the Auriculares anterior, superior, and posterior.” ↩ ↩
- 3b.
Page 1035: “In man, these muscles possess very little action: the Auricularis anterior draws the auricula forward and upward; the Auricularis superior slightly raises it; and the Auricularis posterior draws it backward.” ↩ ↩
- 3c.
Page 1035: “The intrinsic muscles are the: Helicis major. Helicis minor. Tragicus. Antitragicus. Transversus auriculae. Obliquus auriculae.” ↩ ↩
- 3d.
Page 1035: “The Auriculares anterior and superior and the intrinsic muscles on the lateral surface are supplied by the temporal branch of the facial nerve, the Auricularis posterior and the intrinsic muscles on the cranial surface by the posterior auricular branch of the same nerve.” ↩ ↩
- 3e.
Page 372: “The facial nerve, which early enters the common facial muscle mass of the second branchial or hyoid arch, is dragged about with the muscle as it spreads over the head and face and neck, and as the muscle splits into the various muscles of expression, the nerve is correspondingly split.” ↩
- 3a.
- 4.
Rüschenschmidt, Hannah et al. “Electromyography of Extrinsic and Intrinsic Ear Muscles in Healthy Probands and Patients with Unilateral Postparalytic Facial Synkinesis.” Diagnostics 12(1):121. 2022. A study that recorded the electrical activity of the ear muscles with electrodes on the skin (surface EMG), in healthy people and in patients with unilateral postparalytic facial synkinesis, a one-sided facial condition. It covers all of the ear muscles, the extrinsic ones that move the whole ear and the intrinsic ones inside it, and reports which of them are active during smiling, ear wiggling and gaze. The article uses it to show that the ear muscles are still alive and firing.
- 4a.
Section Introduction: “The human auricle contains three extrinsic and six intrinsic muscles [1]. These muscles have been considered vestigial in humans, and are rarely under voluntary control [2]. Like the mimic muscles, all ear muscles are innervated by the facial nerve [1].” ↩
- 4b.
Section Introduction: “Finally, the ear muscles are beneficial for individuals with quadriplegia because these muscles are usually not affected by high-level spinal lesions [2]. For instance, such patients can learn to steer a wheelchair with ear muscle activation [8].” ↩
- 4c.
Section 3.3: “Surface EMG could be recorded from all ear muscles in all healthy subjects.” “In general, the ear muscle EMG activity was highest during smiling and ear wiggling. The lowest activity was seen during ipsilateral or contralateral gaze. Only the obliquus auriculae and the transversus auriculae muscle showed a robust activity during the isolated lateral gaze.” ↩ ↩
- 4a.
- 5.
Sisson, Septimus. The Anatomy of the Domestic Animals. W. B. Saunders, Philadelphia. 2nd edition. 1914. A veterinary anatomy book on domestic animals. The article uses it for the horse, its textbook case, where the extrinsic ear muscles are counted group by group and the movement of the ear is compared with a ball-and-socket joint.
- 5a.
Page 872: “The anterior auricular muscles (Mm. auriculares orales) are four in number”. “The dorsal auricular muscles (Mm. auriculares dorsales) are two in number.” Page 873: “The posterior auricular muscles (Mm. auriculares aborales) are three in number”. “The deep auricular or rotator muscles (M. auricularis profundi s. rotatores auriculae), two in number, are situated under the scutiform cartilage and the base of the concha and cross each other.” “The scutulo-auricularis profundus major is the strongest of the auricular muscles. It is flat and is about an inch wide.” ↩ ↩
- 5b.
Page 875: “The base of the concha is rounded and rests in a pad of fat (Corpus adiposum auriculae), so that the movements of the external ear resemble those of a ball-and-socket joint.” “When the ear is vertical or drawn forward ("pricked up"), the opening is usually directed forward ; conversely, when the ears are "laid back," the opening faces backward. These movements evidently result from the coordinated actions of several muscles which are very complex and cannot be discussed in detail here.” “The anterior auricular muscles in general erect the ear and turn the opening forward.” ↩ ↩
- 5a.
- 6.
Populin, Luis C., and Tom C. T. Yin. “Topographical organization of the motoneuron pools that innervate the muscles of the pinna of the cat.” Journal of Comparative Neurology 363(4):600–614. 1995. A study in cats that injected a nerve tracer into single pinna muscles and mapped the motor nerve cells that drive each one. The tracer was the B-subunit of cholera toxin linked to horseradish peroxidase, and the cells were found in the facial nucleus, arranged by what each muscle does. The article uses it for the count of 22 nerve pools that serve the cat's ear.
- 6a.
Section Abstract: “The topographical organization of the 22 motoneuron pools that innervate the pinna muscles of the cat was examined”. “All 22 pools are found in the facial nucleus, organized as rostro-caudally oriented columns, and arranged according to the action of the muscles they innervate.” ↩ ↩
- 6a.
- 7.
Populin, Luis C., and Tom C. T. Yin. “Pinna movements of the cat during sound localization.” Journal of Neuroscience 18(11):4233–4243. 1998. A research paper that reports how the outer ear moves in animals when they turn toward a sound or a light. It finds that the first, fast part of the movement comes about 25 milliseconds after a sound starts and is largest on the ear on the same side as the sound. The article uses it for the timing of the ear's first movement toward a sound.
- 7a.
Section Abstract: “Prominent pinna movements accompany eye movements when the animal orients to either auditory or visual stimuli.” “Whereas the long-latency component seemed to occur with the eye movement to the target, the short-latency component was coupled to the onset of the stimulus.” “The short-latency component (∼25 msec) was highly asymmetrical, being largest in the pinna ipsilateral to the stimuli.” ↩ ↩
- 7a.
- 8.
Waller, Bridget M. et al. “Mapping the contribution of single muscles to facial movements in the rhesus macaque.” Physiology & Behavior 95(1–2):93–100. 2008. A study that stimulated single facial muscles one at a time in a rhesus macaque, a monkey, and compared the result with humans and chimpanzees. It finds that the rhesus macaque has great potential for ear movement, which humans and chimpanzees do not show. The article uses it for the finding that the human face is little altered from the monkey's, apart from reduced muscles around the outer ear.
- 8a.
Section Results and Discussion, ear muscles: “Stimulation of the superior auricularis caused the ear to elevate superiorly (supplemental material 16), but without the medial contraction seen in orbito-auricularis. Stimulation of inferior auricularis caused the ear to flatten to the head and slight lateral retraction of the scalp (supplemental material 17).” ↩ ↩
- 8b.
Section Conclusions: “Thus, the facial muscles we see in humans appear to be little altered from the format we see in a monkey species, with the exception of the reduction in musculature around the external ear.” “The most striking difference between the three species is the great potential for ear movement in the rhesus macaque, which is not seen in humans and chimpanzees.” ↩ ↩
- 8a.
- 9.
Schroeer, Andreas et al. “Electromyographic correlates of effortful listening in the vestigial auriculomotor system.” Frontiers in Neuroscience 18:1462507. Jan 31, 2025. A laboratory study of 20 young adults with normal hearing, who followed a target podcast while distracting sound streams played at three levels of difficulty. The posterior ear muscle was more active when the sounds came from behind, and the superior ear muscle was more active in the hardest condition. The article uses it to show that the superior muscle works harder as listening gets harder.
- 9a.
Section Abstract, page 1: “Twenty participants were recruited”. “averaged PAM activity was not affected by different levels of effortful listening, but was significantly larger when stimuli were presented from the back, as opposed to the front. Averaged SAM activity, however, was significantly larger in the most difficult condition, which required the largest amount of effort”. “We interpret the increased SAM activity to be the response of the vestigial pinna–orienting system to an effortful stream segregation task.” ↩ ↩
- 9b.
Section Discussion, page 11: “If such a movement is large enough, as in many mammals such as cats and dogs, this would impact the head-related transfer function”. “If attention-driven auricular movements are purely vestigial in our own species, clues as to their original function might be discerned from other primates. Directly stimulating the 7th nerve branch to SAM in an anesthetized macaque (see the Supplementary material of Waller et al., 2008) showed that maximum contraction yields an upward, essentially rigid, translation of the pinna relative to the ear canal.” ↩
- 9c.
Section Discussion, page 12: “An interesting intermediate step would be a study which exclusively includes participants who are able to voluntarily move their ears.” ↩
- 9d.
Section Conclusion, page 13: “While increased activity of auricular muscles in response to automatic and intentional attention can lead to visible movements of the pinna (Strauss et al., 2020), it is currently not known if they are strong enough to achieve an actual benefit.” ↩
- 9e.
Section Discussion, page 13: “Participants formed a relatively small and homogeneous group, i.e., young and normal-hearing”. ↩
- 9a.
- 10.
O'Beirne, Greg A., and Robert B. Patuzzi. “Basic properties of the sound-evoked post-auricular muscle response (PAMR).” Hearing Research 138(1–2):115–132. 1999. A research paper on the electrical response recorded from the muscle behind the ear after a sudden sound. It sets out how the response is best measured, and says the response has been 'ignored by most clinicians'. The article cites it for the claim that the reflex is used as an objective hearing test.
- 10a.
Section Abstract: “One objective electrophysiological test for deafness involves presenting a brief acoustic stimulus to a subject and measuring the electrical activity evoked in the muscle located just behind the ear (the post-auricular muscle or PAM).” “The response consists of a simple bipolar compound action potential with a first peak latency of between 12.5 and 15 ms”. “The response latency and duration are longer in very young infants, but reach adult values by 12 months of age.” ↩ ↩
- 10a.
- 11.
Purdy, Suzanne C. et al. “The post-auricular muscle response: an objective electrophysiological method for evaluating hearing sensitivity.” International Journal of Audiology 44(11):625–630. 2005. A research paper that tested the post-auricular muscle response as a hearing test in sixteen adults with normal hearing and twenty adults with hearing loss, using clicks at several loudness levels. The authors found that the response tracked hearing thresholds in people with hearing loss, and that most normal-hearing adults had it at the level used for infant hearing screening. The article cites it as support for the reflex as an objective hearing test.
- 11a.
Section Abstract: “In hearing-impaired subjects, PAMR thresholds were correlated with audiometric thresholds for the eyes-turned condition.” “With eyes turned and monaural clicks at 35 dB nHL, the level widely used for infant hearing screening, most normal-hearing adults had a PAMR. Thus the PAMR is a robust response that may be a useful adjunct to ABR for objective hearing assessment.” ↩ ↩
- 11a.
- 12.
Online Mendelian Inheritance in Man. Entry 129100: Ears, Ability to Move. Johns Hopkins University. n.d. Retrieved Apr 19, 2022. “The ability to move the ears,”. A secondary source, a catalogue entry that summarises two older studies: L. Linder's 1949 study in Hereditas 35 (suppl.):620–621, and M. Hernandez's 1980 study. The article uses its figures for how many people can move their ears and how the ability runs in families. Mirror: Archive.org
- 12a.
Section Entry text: “Linder (1949) examined 104 men and 70 women and found the ability to move the ears in 54% and 22%, respectively. The frequency of the trait among sibs of probands was 47% and among parents was 74%. However, in 5 of 24 cases both parents lacked the trait, leading Linder (1949) to suggest that the ability is inherited as a somewhat irregular dominant. In Barcelona, Hernandez (1980) found that 19.9% of men and 9.57% of women could move their ears.” ↩ ↩
- 12a.
- 13.
Bair, J. H. “Development of voluntary control.” Psychological Review 8(5):474–510. 1901. A 1901 laboratory study from the University of Michigan that set out to develop control over one small ear muscle, the retrahens aurem, which most people cannot contract. It worked with fourteen subjects, only two of whom could move their ears at the start, and recorded the ear movements on a kymograph, a rotating drum that draws a trace of them. The article uses it to show that moving the ears can be learned.
- 13a.
Page 475: “Of the fourteen subjects who rendered us their services, only two could move their ears at the beginning of the experiment and these only when vigorously raising their brow. The remaining twelve had no idea of the movement and could not produce it, however hard they tried.” ↩ ↩
- 13b.
Pages 479–480: “All of our subjects acquired control over this muscle in the same way, and the introspections were also fairly uniform, so that the results, in general, of each subject corroborate those of the others.” The sentence begins under the running head of page 479 and ends after the head of page 480. The running heads read: “DEVELOPMENT OF VOLUNTARY CONTROL. 479”. “480 J. H. BAIR.” ↩ ↩
- 13c.
Page 483: “In this stage the retrahens is always contracted by biting the jaws together or vigorously raising the brow. The ear was thus first reached by innervating a group of muscles over which one has already control.” ↩
- 13a.
- 14.
Chanthaphun, Siwaphorn et al. “Development of a training paradigm for voluntary control of the peri-auricular muscles: a feasibility study.” Journal of NeuroEngineering and Rehabilitation 16:75. 2019. A feasibility study, a small first test of a training method, in which 10 people completed the protocol. The senior authors disclose that one of them owns the company whose device was tested. The article uses its finding that most people who finished the training could control these muscles.
- 14a.
Section Background: “The peri-auricular muscles (PAMs) can be found in 95% of the population but do not currently serve any physiologic function [5–8].” ↩
- 14b.
Section Abstract: “The 10 who completed the protocol, finished the facilitation phase in 3 to 9 sessions and achieved some level of voluntary auricle movement that ranged between 1 and 5 mm.” “Sixty percent of those who completed the facilitation phase were able to learn and demonstrate functional voluntary control of the vestigial PAMs.” “with 20% deemed Poor/Non-Learners and unable to complete even the most basic game following training.” ↩ ↩
- 14a.
- 15.
Wiedersheim, Robert. The Structure of Man: An Index to His Past History. Macmillan. 2nd German edition. Translated by H. Bernard and M. Bernard. 1895. A comparative anatomy textbook for medical students, written by a German professor at Freiburg and translated into English, with notes and a preface by G. B. Howes, professor of zoology at the Royal College of Science, London. It sets out the parts of the body that link man with lower animals, and its conspectus lists the organs its author calls vestigial. The article uses it for the 1895 list that puts the ear muscles among the vestigial organs, and for Wiedersheim's remark that in most people the capacity to move them is entirely wanting.
- 15a.
Page 107: “Muscles round the pinna : attrahens, retrahens, and attollens auriculam (cf. Figs. 70 and 71). The capacity for moving these muscles varies greatly in individuals. In most people it is entirely wanting ; and the retrogressive character of these muscles is due to the degeneration of the pinna”. ↩
- 15b.
Page 109: “Taking all the facts into consideration, this intrinsic musculature of the pinna, which is no longer under the control of the will, must be considered as the vestige of a primitive apparatus functional either for the opening and closing, or for the widening and narrowing of the auditory funnel and the external auditory passage”. ↩
- 15c.
Pages 200–201: Section B of the conspectus, headed on page 200: “Retrogressively modified, the Organs having become wholly or in part functionless ... For the greater part Organs which may be rightly termed Vestigial”. Page 201: “Muscles of the pinna and the Musculus occipitalis.” ↩ ↩
- 15a.
- 16.
Coyne, Jerry A. Why Evolution Is True. Viking. 2009. A book by Jerry A. Coyne, published by Viking in 2009. The article uses it for Coyne's own words on the ear muscles, which he called "silly ear muscles" while arguing that such features make no sense if species were specially created.
- 16a.
Page 58: “Evolutionary theory doesn't say that vestigial characteristics have no function. A trait can be vestigial and functional at the same time. It is vestigial not because it's functionless, but because it no longer performs the function for which it evolved.” ↩
- 16b.
Page 64: “Sometimes useful, but often not, they're exactly what we'd expect to find if natural selection gradually eliminated useless features or refashioned them into new, more adaptive ones. Tiny, nonfunctional wings, a dangerous appendix, eyes that can't see, and silly ear muscles simply don't make sense if you think that species were specially created.” ↩ ↩
- 16a.
- 17.
Menton, David N. “The plantaris and the question of vestigial muscles in man.” CEN Technical Journal 14(2):50–53. 2000. A short argument paper about the calf muscle called the plantaris, which the author says is neither vestigial nor useless. It says the plantaris serves a sense of limb position and muscle contraction, that a muscle unused for a lifetime would not stay healthy, and that any muscle still in the body is overwhelmingly likely to serve some function. The article uses it for those general arguments, that small muscles are not useless and that an unused muscle would waste away.
- 17a.
Page 50: “The muscles most frequently claimed to be vestigial in man are the auricular muscles of the ear, the erector pili muscles of hair follicles, and the plantaris muscle of the calf of the leg. All of these muscles are relatively small and give the appearance of producing little or no useful work by their weak contractions.” ↩
- 17b.
Pages 50–51: “It is unlikely that any muscle that was virtually unused for the lifetime of an individual (to say nothing of generations of individuals over millions of years) would remain as healthy muscle tissue.” ↩ ↩
- 17c.
Page 51: “It seems overwhelmingly likely that any muscle in the body that actually exists in the present, serves some function.” ↩
- 17a.
- 18.
Sanders, Lita. “Badly designed arguments: 'vestigial organs' revisited.” Creation Ministries International. Nov 25, 2011. A reply by Lita Sanders (née Cosner) for Creation Ministries International, a ministry that defends Genesis history, to a reader who asked for a rebuttal of a list of supposedly useless organs. It goes through the list and finds that not one item fits the definition of a truly vestigial organ, and it suggests that the ear muscles could help remove wax from the ears. The article uses it for that wax proposal, which it says no primary source supports.
- 18a.
Section Extrinsic ear muscles: “A CMI biologist suggested that one function of ear muscles could be to help remove wax from the ears. When a person is chewing, or smiling, etc. the ear muscles move the ears. This gradually moves the wax outwards, cleaning the ears. But there could be other functions also.” ↩ ↩
- 18a.
- 19.
Menton, David N. Ear Muscles. Creation Ministries International. Nov 6, 2007. A reply that David N. Menton wrote in 2003 to an enquirer at CMI-Australia, published as a web page by Creation Ministries International on 6 November 2007. Its only citation is "'The Ear Muscles', p.58 in "Vestigial Organs" Are Fully Functional, Bergman & Howe, 1990." The article uses it as one of the creationist replies on the ear muscles: Menton calls the movements "slight" and says no hearing benefit is known.
- 19a.
Paragraph 1: “The auricularis muscles are a favorite example of evolutionists as vestigial muscle presumably left over from when we could move our ears (auricles) about like a rabbit. Clearly, the ability to orient the ears assists in sensing the stereo imaging of sound (location and distance).” ↩
- 19b.
Paragraph 2: “The ability of humans to move the auricle in a grossly noticeable way varies from individual to individual but generally the movements are slight. Are any of these movements, when noticeable or measurable, able to improve our hearing or stereo perception? None that we know of at this time.” ↩ ↩
- 19c.
Paragraph 3: “The external auricular muscles are typically grouped with the muscles of facial expression.” “All of the facial muscles (including the auricularis muscles) are innervated by the same cranial nerve, the facial nerve.” ↩
- 19a.
- 20.
Bergman, Jerry. “Ear Muscle "Wiggle": A Vestigial-Organ Claim That We Should 'Turn a Deaf Ear To'.” Creation-Evolution Headlines. Jul 24, 2020. A young-earth creationist reply by a biologist and frequent writer on vestigial organs, aimed at the 2020 eLife attention study as reported in a university press release. It argues that the ear muscles stabilise and pad the ear and that their attention-driven activity is a form of body language, and it asks why evolution would lose a useful ability. It is the only creationist text found that answers the attention studies directly. ↩
- 20a.
Section Opening section, before the heading Evolutionary claims: “In my book Useless Organs, I described how these muscles have several very important functions, including serving as a framework supporting and stabilizing the pinna.” “Another function is to serve as padding to protect the underlining structures in the temples.” ↩
- 20b.
Section A better explanation for the auriculomotor system: “It is not to move the ears (as the vestigial-organ explanation claims) but rather—as the authors themselves note—to communicate with others. They are part of the facial response to sounds of interest and as part of the body communication system.” ↩ ↩
- 20c.
Section Evolutionary claims: “The researchers were able to record the signals that control the very small, generally invisible, movements of the pinna by surface electromyogram (EMGs) probes placed in the skin near muscles connected to the pinna.” ↩
- 20d.
Section A better explanation for the auriculomotor system: “Actually, no one has any idea why movement of the auricle to better focus on a certain sound source, as cats and some dogs do, would be lost by evolution.” ↩
- 20a.
- 21.
Coleman, Mark N., and Callum F. Ross. “Primate auditory diversity and its influence on hearing performance.” Anatomical Record Part A 281(1):1123–1137. 2004. A study that measured the outer ears of cadaver specimens from nearly every primate family and worked out a shape ratio, height against width. Primates outside the monkey and ape group have ears that are taller and narrower than those of monkeys and apes. The article uses it for the change in ear shape across the primates, from tall and narrow ears to ears of equal height and width.
- 21a.
Section Abstract: “It was found that nonanthropoids have a significantly higher ratio than anthropoids, although the actual height was not found to differ. This indicates that most nonanthropoids have ears that are tall and narrow, whereas monkeys and apes are characterized by ears with more equal height and width dimensions.” ↩
- 21a.
- 22.
Cobo, J. L. et al. “Searching for proprioceptors in human facial muscles.” Neuroscience Letters 640:1–5. 2017. A histology study of two facial muscles, the zygomatic major and the buccinator, taken from Spanish cadavers and stained for nerve fibres and two proteins linked to touch and stretch sensing. It starts from the accepted finding that facial-nerve muscles lack typical spindles and reports Ruffini-like sensory corpuscles that could stand in for them. The article uses it to show that a missing spindle is normal for human facial muscles, which are still finely controlled.
- 22a.
Section Abstract: “The human craniofacial muscles innervated by the facial nerve typically lack muscle spindles. However these muscles have proprioception that participates in the coordination of facial movements.” ↩
- 22a.
- 23.
Omstead, Kailey M. et al. “Mammalian facial muscles contain muscle spindles.” Anatomical Record 306(10):2562–2571. 2023. A comparative histology survey that counted spindles in the upper lip and cheek muscles of a broad range of mammals. It found spindles in facial muscles, fewest in humans and other primates and most in carnivores and the horse; the authors warn that the sample was small and some groups were missing. The article uses it to show that few or no facial spindles is a primate-wide trait, not a mark of the ear alone.
- 23a.
Section Abstract: “Our results indicate that mammalian facial muscles contain muscle spindles, supporting our hypothesis. Contrary to our prediction, though, humans (and other primates) had the lowest number of muscle spindles. We instead found that the carnivoran sample and the horse sample had the greatest number of spindles.” ↩
- 23a.
- 24.
Hackley, Steven A. “Evidence for a vestigial pinna-orienting system in humans.” Psychophysiology 52(10):1263–1270. 2015. A review that argues the brain's circuits for turning the ears have survived as a vestigial remnant, one that no longer does its original job. It gives three lines of evidence: a 2–3 mm curl of the ear's edge and electromyography (EMG, the electrical signal of a muscle) when the eyes turn hard aside, a weak EMG response to an unexpected sound from behind, and EMG bursts during an attention task. The article uses it for the thesis that these neural circuits still survive in humans.
- 24a.
Section Abstract: “Although some people can voluntarily move their ears, overt reflexive control of the pinnae has been lost during the course of primate evolution. Humans and apes do not move their ears to express emotion, they do not defensively retract them when startled, and they do not point them at novel, salient, or task-relevant stimuli. Nevertheless, it is the thesis of this review that neural circuits for pinna orienting have survived in a purely vestigial state for over 25 million years.” ↩
- 24b.
Section Abstract: “(1) Shifting the eyes hard to one side is accompanied by electromyographic (EMG) activity in certain ear muscles and by a barely visible (2-3 mm) curling of the dorsal edge of the pinna. (2) The capture of attention by a novel, unexpected sound emanating from behind and to one side has been found to trigger a weak EMG response in the muscle behind the corresponding ear. (3) Reflexive EMG bursts recorded during a selective attention task suggested that subjects were unconsciously attempting to orient their ears toward the relevant sounds.” ↩
- 24c.
Section Abstract: “It is suggested that the postauricular reflex to sudden, intense sounds constitutes a vestigial startle response, but that the reflex arc is dominated by a pathway that bypasses the main organizing center for startle.” ↩
- 24a.
- 25.
Schroeer, Andreas et al. “The vestigial pinna-orienting system in humans briefly suppresses superior auricular muscle activity during reflexive orienting toward auditory stimuli.” Journal of Neurophysiology 132(2):514–526. 2024. A laboratory study of 10 adults with normal hearing, who heard sudden sounds from one side in silence and during a podcast while two ear muscles were recorded by electromyography. The posterior ear muscle became more active on the side of the sound, but the superior ear muscle went briefly quieter, which the authors say points to a more complicated system than assumed. The article uses it to show that the two muscles do not simply respond together.
- 25a.
Section Abstract: “Although ipsilateral PAM activity increased in response to transient stimuli, the SAM displayed the opposite behavior, i.e., a brief, ipsilateral suppression of activity.” “the presence of synchronized excitatory and inhibitory components in different auricular muscles points toward a coordinated attempt at reflexively orienting the pinna toward a sound.” ↩
- 25a.
- 26.
Bergman, Jerry. “Do any vestigial structures exist in humans?” CEN Technical Journal 14(2):95–98. 2000. A short argument paper, not a study. It says the list of vestigial organs in humans "has shrunk from 180 in 1890 to 0 in 1999", and it rejects a "revisionistic" definition of a vestigial organ as one that has merely been reduced in size or function. The article uses it for the author's reply to Asimov's two examples, the coccyx and the ear muscles, and for his claim that Asimov's conclusions rest on evolutionary assumptions rather than evidence.
- 26a.
Page 95: “Asimov provides two examples of a vestigial organ: (1) the tiny bones posterior to the sacrum called the coccyx (which Asimov claims were 'once meant for a tail'); and (2) the small muscles around the ears (which Asimov claims are 'unworkable muscles once meant to move the ears'). As we will see, these conclusions are not based on empirical evidence but instead on evolutionary assumptions.” ↩
- 26a.
- 27.
Guest, Julian F. et al. “Impacted cerumen: composition, production, epidemiology and management.” QJM 97(8):477–488. 2004. A clinical review of impacted ear wax that covers what wax is made of, how it is produced, how common it is and how it is managed. It reports that some 2.3 million people in the UK had wax problems serious enough to need management, and that the evidence on treatments is inconsistent. The article cites it for its statement that the physiology of wax is poorly characterized.
- 27a.
Section Abstract: “Despite this, the physiology, clinical significance and management implications of excessive and impacted cerumen remain poorly characterized.” ↩
- 27a.