Every year a little less.
Hair cells line your inner ear in a precise frequency map — high notes at the basal end of the cochlea, low notes deep in the spiral. The high-frequency cells are the first to wear out. From around twenty years old, your upper hearing limit drops steadily. Drag the age slider, run the pure-tone test below, and compare your moving boundary with the ranges other animals hear. Some live in a low sub-audible world we will never share; some hunt in an ultrasonic one we cannot enter.
Average values from ISO 7029:2017. Individual variation is large — protect-your-ears history matters more than age alone.
Use headphones or good speakers, set the volume to comfortable, then click each frequency. Where you stop hearing the tone is roughly where your personal limit lies.
The age-dependent upper limit follows the median values in ISO 7029:2017, the international standard for age-related hearing threshold distribution. The pure-tone test uses the browser's Web Audio API to synthesise sine waves locally — no sound is uploaded, your speakers determine playback quality. Animal hearing ranges come from Heffner & Heffner 2007 (Hearing Ranges of Laboratory Mammals), Au 1993 (The Sonar of Dolphins), and Payne & Webb 1971 for blue whales. The spectrum visualisation uses a logarithmic frequency axis from 1 Hz to 1 MHz — six decades — to fit infrasound, audible and ultrasound in one frame.
Four readings of one declining curve.
Why the highs go first.
Sound enters the cochlea — a fluid-filled spiral in the inner ear — and travels along the basilar membrane. The membrane is stiff and narrow at the base and flexible and wide at the apex. High-frequency vibrations resonate at the base; low frequencies travel further inward. The hair cells at the base are exposed to every loud sound that passes, every concert, every motorbike, every leaf blower. They wear out first. By the time the lower-frequency cells deeper in the spiral show damage, the basal ones are already long gone — which is why high-frequency loss is the early signature of age-related hearing loss (Hertzano et al. 2020).
The infrasound world below us.
Below 20 Hz, sound becomes physical pressure rather than recognisable pitch — for us. Blue whales communicate with calls between 10 and 40 Hz that travel thousands of kilometres through ocean SOFAR channels (Payne & Webb 1971); two whales on opposite sides of the Pacific could, in principle, hear each other. Elephants use ground-borne and air-borne infrasound around 14 Hz to coordinate family movement across kilometres of savannah, picked up through pads in their feet (O'Connell-Rodwell 2007). We feel the same frequencies — wind turbines, distant thunder, a pipe organ's lowest stops — but we don't quite hear them.
The ultrasonic world above us.
Above 20 kHz lives the world we sealed off when we became mammals with limited high-frequency range. Bats emit clicks up to 110 kHz and read returning echoes with timing precision below a microsecond — they paint a three-dimensional acoustic image of their world. Bottlenose dolphins extend even further, to 150 kHz, with sonar that can distinguish a sardine from a herring at twenty metres. And the moths the bats hunt evolved their own counter-measure: ears tuned exactly to bat echolocation frequencies (Roeder & Treat 1957), and a startle response that drops them from the sky the moment a bat closes in.
The Mosquito tone — a generation's signature.
In 2005 a British inventor commercialised a 17.4 kHz tone broadcast from small loudspeakers outside shops. Most adults could not hear it. Most teenagers could. It was sold as an anti-loitering device. Within months teenagers reverse-engineered it as a ringtone they could use in class without their teachers hearing — a frequency they owned, briefly, before age took it from them too. There is something tender in this: the upper end of our hearing is the part most quietly lost, and we usually only notice when someone younger points it out.
- ISO 7029:2017 — Acoustics. Statistical distribution of hearing thresholds related to age and gender.
- Heffner, H. E. & Heffner, R. S. (2007) — Hearing ranges of laboratory animals. Journal of the American Association for Laboratory Animal Science 46(1).
- Au, W. W. L. (1993) — The Sonar of Dolphins. Springer.
- Payne, R. & Webb, D. (1971) — Orientation by means of long range acoustic signaling in baleen whales. Annals of the New York Academy of Sciences 188.
- Roeder, K. D. & Treat, A. E. (1957) — Ultrasonic reception by the tympanic organ of noctuid moths. Journal of Experimental Zoology 134.
- Hertzano, R. et al. (2020) — Specifying the ageing cochlea. Hearing Research 386.
- O'Connell-Rodwell, C. E. (2007) — Keeping an 'ear' to the ground: seismic communication in elephants. Physiology 22.
- Cruickshanks, K. J. et al. (1998) — Prevalence of hearing loss in older adults in Beaver Dam, Wisconsin. American Journal of Epidemiology 148.
