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Chapter 1 Why the Vocal Folds Vibrate by Themselves: Phase Difference and Threshold Pressure

Picking up from Volume 10

Chapter 1 of Volume 10 set out the myoelastic–aerodynamic theory: muscles set the folds’ position, length and tension, but each opening and closing is a self-sustained oscillation of airflow and elastic tissue (Berg 1958); and “Bernoulli suction” alone cannot sustain it. This chapter asks the next question: what exactly makes the air do net positive work on the tissue in each cycle? Titze’s 1988 small-amplitude theory answers it and yields a formula for the phonation threshold pressure (Titze 1988).

Why a symmetric shape gains no energy

Evidence

Titze treated the cover of the vocal folds as a thin layer that can carry a surface wave: the lower margin of the fold moves outward first and the upper margin follows, so the shape of the glottis changes during the cycle. The central result of the theory is that if the glottal shape stays the same throughout the cycle (whether straight, convergent or divergent), the net work done by the airflow on the tissue is zero; only when the lower and upper margins move with a phase difference, making the glottis more convergent while opening and more divergent while closing, can the air feed net energy into the tissue in each cycle. The theory also predicts that lowering the mucosal-wave speed, bringing the folds closer together and reducing the convergence angle of the glottis all lower the threshold pressure, and that vocal-tract inertance lowers it while vocal-tract resistance raises it (Titze 1988, 1994). The last point is the subject of Chapter 2.

The result is easy to compute. Let the entry (lower) and exit (upper) half-areas of the glottis move sinusoidally with the same amplitude, the upper one lagging by a phase φ\varphi. In Titze’s formula the mean intraglottal pressure is Pg=Ps(1−a2/a1)P_g = P_s(1 – a_2/a_1) (with the pressure above the glottis taken as zero), acting on the medial surface of the folds; integrating it over the mean displacement of that surface for one cycle gives the net work done by the airflow on the tissue.

Calculation

# Net aerodynamic work per cycle on the folds in a surface-wave glottis (after Titze
# 1988). Entry (lower) and exit (upper) half-areas move sinusoidally; the exit lags by
# phi:
#   a1 = a0 + A sin(wt),  a2 = a0 + A sin(wt - phi)
# Mean intraglottal pressure (supraglottal pressure taken as zero): Pg = Ps (1 - a2 / a1).
# Work per cycle W = integral of Pg dx, x = (a1 + a2)/2 the mean medial-surface
# displacement. All values illustrative.
import math

PS = 800.0                     # Pa, subglottal pressure (about 8 cm H2O)
A0, AMP = 1.0, 0.4             # mean and amplitude of the half-areas (arbitrary units)

def work_per_cycle(phi, n=4000, tilt=0.0):
    # tilt > 0 gives a fixed convergent prephonatory shape (entry wider than exit)
    w, dt = 0.0, 2 * math.pi / n
    for i in range(n):
        t = i * dt
        a1 = A0 + tilt + AMP * math.sin(t)
        a2 = A0 - tilt + AMP * math.sin(t - phi)
        pg = PS * (1 - a2 / a1)
        dx = AMP * (math.cos(t) + math.cos(t - phi)) / 2 * dt     # dx/dt * dt
        w += pg * dx
    return w

print("phase lag of upper edge | net work per cycle (Pa x area units)")
for deg in (0, 15, 30, 60, 90, 120):
    print(f"   {deg:4d} deg             | {work_per_cycle(math.radians(deg)):+8.1f}")
print(f"   -30 deg (upper leads) | {work_per_cycle(math.radians(-30)):+8.1f}"
      "   energy flows from tissue to air")
print(f"fixed convergent shape (entry 1.2, exit 0.8), no lag: "
      f"{work_per_cycle(0.0, tilt=0.2):+.1f}  (no net work)")
best = max(range(0, 181, 5), key=lambda d: work_per_cycle(math.radians(d), 1000))
print(f"largest energy transfer in this sketch at a lag of about {best} deg")
# phase lag of upper edge | net work per cycle (Pa x area units)
#       0 deg             |     +0.0
#      15 deg             |   +108.8
#      30 deg             |   +211.1
#      60 deg             |   +371.7
#      90 deg             |   +438.8
#     120 deg             |   +388.2
#    -30 deg (upper leads) |   -211.1   energy flows from tissue to air
# fixed convergent shape (entry 1.2, exit 0.8), no lag: +0.0  (no net work)
# largest energy transfer in this sketch at a lag of about 90 deg

Three points stand out. First, with no phase lag the net work is exactly zero; even when the glottis has a fixed convergent shape (entry 1.2, exit 0.8), as long as the two margins move together the net work is still zero. This is what “a symmetric or unchanging shape gains no energy” means: the pressure is then a function of displacement alone, and its integral around a closed path must vanish. Second, when the upper margin lags, the net work is positive, largest in this sketch at a lag of about 90°; when the upper margin leads, the work is negative and energy flows from the tissue back into the air, acting as extra damping. Third, the Bernoulli effect has not disappeared, since the intraglottal pressure does change with shape, but what sets the direction of energy flow is the timing between changes of shape and motion.

Threshold pressure: checking the formula against the original

The lowest subglottal pressure at which vibration can just be sustained is the phonation threshold pressure. In Titze’s theory it is the pressure at which the “negative damping” supplied by the airflow exactly cancels the damping of the tissue.

Evidence

Titze’s 1988 general expression, as reproduced by Zhang (2010) and by Fulcher and Scherer (2011), is

Pth=2ktBcξ012T(ξ01+ξ02),P_{\text{th}} = \frac{2k_t\,B\,c\,\xi_{01}^{2}}{T\,(\xi_{01}+\xi_{02})},

where ktk_t is the transglottal pressure coefficient (about 1.1), BB is the tissue damping per unit area of the medial surface, cc is the mucosal-wave speed, TT is the thickness of the medial surface (in the inferior–superior direction), and ξ01\xi_{01} and ξ02\xi_{02} are the prephonatory half-widths of the glottis at its lower (entry) and upper (exit) margins (Zhang 2010; Fulcher and Scherer 2011). For a rectangular glottis, ξ01=ξ02=ξ0\xi_{01} = \xi_{02} = \xi_0, and the expression reduces to

Pth=ktBcξ0T.P_{\text{th}} = \frac{k_t\,B\,c\,\xi_0}{T}.

This is the form used in Volume 10 (Titze 1988). If damping is written as a total rather than per unit area, the glottal length and thickness appear in the denominator as well (as in Fulcher and Scherer’s version); the two forms are equivalent.

The framework’s Pth=2ktBcξ0/TP_{\text{th}} = 2k_tBc\xi_0/T keeps the factor 2 of the general expression but replaces ξ012/(ξ01+ξ02)\xi_{01}^2/(\xi_{01}+\xi_{02}) by ξ0\xi_0 outright; for a rectangular glottis this doubles the threshold. The program below compares the two versions with the same illustrative parameters and looks at the effect of glottal shape and tissue properties.

Calculation

# Phonation threshold pressure in Titze's (1988) small-amplitude surface-wave theory.
# General form (as reproduced by Zhang 2010; Fulcher & Scherer 2011):
#     Pth = 2 kt B c xi01^2 / [T (xi01 + xi02)]
# kt transglottal pressure coefficient (~1.1); B damping per unit medial area (N s/m^3); c
# mucosal-wave speed (m/s); T medial-surface thickness (m); xi01, xi02 prephonatory
# half-widths at entry (lower) and exit (upper). Rectangular glottis: Pth = kt B c xi0 /
# T. Parameter values illustrative, chosen to give about 3 cm H2O at baseline.
KT, B, C, T = 1.1, 800.0, 1.0, 0.003
PA_PER_CMH2O = 98.07

def pth(xi01, xi02, b=B, c=C, t=T, kt=KT):
    return 2 * kt * b * c * xi01 ** 2 / (t * (xi01 + xi02))

xi0 = 0.001                                   # 1 mm
p_rect = pth(xi0, xi0)
p_short = KT * B * C * xi0 / T                 # rectangular special case
p_author = 2 * KT * B * C * xi0 / T            # the outline's "2 kt B c xi0 / T"
print(f"rectangular glottis, general formula : {p_rect:6.1f} Pa"
      f" = {p_rect / PA_PER_CMH2O:4.2f} cm H2O")
print(f"rectangular glottis, kt B c xi0 / T  : {p_short:6.1f} Pa (identical)")
print(f"'2 kt B c xi0 / T' would give        : {p_author:6.1f} Pa (twice too high)")
print("shape at the same mean half-width of 1 mm (entry / exit, mm):")
for e, x in ((1.0, 1.0), (1.2, 0.8), (1.4, 0.6), (0.9, 1.1)):
    p = pth(e / 1000, x / 1000)
    print(f"  {e:.1f} / {x:.1f}  Pth = {p / PA_PER_CMH2O:4.2f} cm H2O"
          f"  ({p / p_rect:4.2f} x rectangular)")
print("one factor at a time from the rectangular baseline (illustrative multipliers):")
cases = (("tissue damping B x 0.85 (better hydrated?)", {"b": 0.85 * B}),
         ("tissue damping B x 1.25 (drier?)", {"b": 1.25 * B}),
         ("mucosal wave 1.3 x faster (stiffer cover)", {"c": 1.3 * C}),
         ("thinner medial surface, T x 0.7", {"t": 0.7 * T}))
for name, kw in cases:
    p = pth(xi0, xi0, **kw)
    print(f"  {name:43s} {p / PA_PER_CMH2O:4.2f} cm H2O ({p / p_rect - 1:+.0%})")
# rectangular glottis, general formula :  293.3 Pa = 2.99 cm H2O
# rectangular glottis, kt B c xi0 / T  :  293.3 Pa (identical)
# '2 kt B c xi0 / T' would give        :  586.7 Pa (twice too high)
# shape at the same mean half-width of 1 mm (entry / exit, mm):
#   1.0 / 1.0  Pth = 2.99 cm H2O  (1.00 x rectangular)
#   1.2 / 0.8  Pth = 4.31 cm H2O  (1.44 x rectangular)
#   1.4 / 0.6  Pth = 5.86 cm H2O  (1.96 x rectangular)
#   0.9 / 1.1  Pth = 2.42 cm H2O  (0.81 x rectangular)
# one factor at a time from the rectangular baseline (illustrative multipliers):
#   tissue damping B x 0.85 (better hydrated?)  2.54 cm H2O (-15%)
#   tissue damping B x 1.25 (drier?)            3.74 cm H2O (+25%)
#   mucosal wave 1.3 x faster (stiffer cover)   3.89 cm H2O (+30%)
#   thinner medial surface, T x 0.7             4.27 cm H2O (+43%)

The baseline parameters (kt=1.1k_t = 1.1, B=800B = 800 N·s/m³, c=1c = 1 m/s, ξ0=1\xi_0 = 1 mm, T=3T = 3 mm) give about 293 Pa, or about 3.0 cm H2O, the same baseline as Volume 10. For a rectangular glottis the general form and the simplified form agree exactly; “2ktBcξ0/T2k_tBc\xi_0/T” gives 587 Pa.

The effect of shape matches Titze’s prediction. Keeping the mean half-width at 1 mm, a convergent glottis with entry 1.2 mm and exit 0.8 mm raises the threshold to 1.44 times the rectangular value, and 1.4/0.6 mm raises it to 1.96 times; a slightly divergent glottis (0.9/1.1 mm) lowers it to 0.81 times. Note, though, that this is a consequence of a small-amplitude theory applied to the prephonatory shape: in a clearly divergent glottis the point where the flow separates moves in real airflow, the small-amplitude formula may no longer hold, and one cannot conclude that “the more divergent, the easier the onset”.

As for tissue properties, 25 % more damping raises the threshold by 25 % and 15 % less lowers it by 15 % (the threshold is proportional to BB); a 30 % faster mucosal wave (a stiffer cover) raises it by 30 %; and thinning the medial surface to 0.7 times raises it by 43 %, which is in the same direction as the experience that thresholds are higher at high pitch (elongated folds have thinner medial surfaces).

“Hydration lowers viscosity”: stating the evidence accurately

Singing teachers often say, “drink plenty of water; moist folds start more easily.” Real research lies behind this, but the form of the evidence needs to be stated clearly.

Evidence

Excised larynges. Finkelhor, Titze and Durham exposed the vocal folds of excised canine larynges to solutions of different osmolarity so that the tissue took up or lost water; they assumed that hydration changed the internal viscosity of the tissue and measured the threshold pressure. Lower hydration (presumed higher viscosity) raised the threshold, higher hydration lowered it, as the theory predicts (Finkelhor et al. 1988). Human experiments. Verdolini-Marston, Titze and Druker asked six adults to phonate as quietly as possible under no treatment, hydration and mild dehydration: thresholds were lowest when hydrated, with the largest reduction at high pitch, and highest when dry, with the largest increase at low pitch; thresholds at intermediate (speaking) pitches were unaffected by hydration (Verdolini-Marston et al. 1990). Verdolini, Titze and Fennell then used a double-blind, placebo-controlled design with twelve untrained adults and found the same direction: an inverse relation between hydration level and phonatory effort (threshold pressure and perceived effort), mainly for high-pitched tasks; the authors noted that direct measures of tissue viscosity were lacking (Verdolini et al. 1994). A systematic review concluded that systemic dehydration (fasting, fluid restriction) and surface drying from mouth breathing worsen several acoustic measures, and that studies of nebulised isotonic saline show lower threshold pressures (Alves et al. 2019).

So this book puts it this way: hydration affects how easily phonation starts, most clearly at high pitch; researchers explain this through tissue viscosity, but changes in viscosity have not been measured directly in people. “Damping × 0.85” or “× 1.25” in the program are only illustrations; there are no reliable figures for how much a real change in hydration changes BB. The book gives no advice on how much to drink, nor on nebulisers or medicines; consult a doctor about voice problems.

Hypothesis · not established

High-note onset hypothesis (not yet established). In trained singers, after a period of surface drying on the same day (for example, mouth breathing in low humidity), the sound pressure level of the softest sustainable tone at a high pitch (for example, C5) rises compared with before, while the change at mid pitch is smaller. Testable prediction: in a randomised crossover study with each singer as their own control, the rise in softest-tone level is significantly larger at the high pitch than at the mid pitch. If the high and mid pitches change by the same amount, or both stay within measurement error, the hypothesis should be dropped. (Step 1 of the Chapter 8 checklist uses this rough measure; it depends on microphone distance and room, is no substitute for a laboratory threshold measurement and cannot be used for diagnosis.)

Chapter summary

The energy of self-sustained vocal fold oscillation comes from the phase difference between the lower and upper margins: it makes the glottis more convergent while opening and more divergent while closing, so that the pressure “pushes at the right moment”; no unchanging or synchronously moving shape gains net energy. Checked against Titze’s 1988 general form, the threshold pressure is 2ktBcξ012/[T(ξ01+ξ02)]2k_tBc\xi_{01}^2/[T(\xi_{01}+\xi_{02})], reducing to ktBcξ0/Tk_tBc\xi_0/T for a rectangular glottis as in Volume 10; the framework’s 2ktBcξ0/T2k_tBc\xi_0/T is twice too high. The threshold rises with damping, mucosal-wave speed and convergence, and falls as the medial surface thickens. The evidence that hydration affects ease of onset comes from excised canine larynges and small human experiments, appears mainly at high pitch, and treats tissue viscosity as an explanation rather than a measurement. The next chapter turns to the last term of the theory: how the vocal tract changes the threshold in return.

References

Alves, Maxine, Esedra Kruger, Bhavani Sarveshvari Pillay, Kristiane van Lierde, and Jeannie van der Linde. 2019. “The Effect of Hydration on Voice Quality in Adults: A Systematic Review.” Journal of Voice 33 (1): 125.e13–28.
Berg, Janwillem van den. 1958. “Myoelastic-Aerodynamic Theory of Voice Production.” Journal of Speech and Hearing Research 1 (3): 227–44. https://doi.org/10.1044/jshr.0103.227.
Finkelhor, B. K., Ingo R. Titze, and P. L. Durham. 1988. “The Effect of Viscosity Changes in the Vocal Folds on the Range of Oscillation.” Journal of Voice 1 (4): 320–25. https://doi.org/10.1016/S0892-1997(88)80005-5.
Fulcher, Lewis P., and Ronald C. Scherer. 2011. “Phonation Threshold Pressure: Comparison of Calculations and Measurements Taken with Physical Models of the Vocal Fold Mucosa.” Journal of the Acoustical Society of America 130 (3): 1597–605.
Titze, Ingo R. 1988. “The Physics of Small-Amplitude Oscillation of the Vocal Folds.” Journal of the Acoustical Society of America 83 (4): 1536–52. https://doi.org/10.1121/1.395910.
Titze, Ingo R. 1994. Principles of Voice Production. Prentice Hall.
Verdolini, Katherine, Ingo R. Titze, and A. Fennell. 1994. “Dependence of Phonatory Effort on Hydration Level.” Journal of Speech and Hearing Research 37 (5): 1001–7. https://doi.org/10.1044/jshr.3705.1001.
Verdolini-Marston, Katherine, Ingo R. Titze, and D. G. Druker. 1990. “Changes in Phonation Threshold Pressure with Induced Conditions of Hydration.” Journal of Voice 4 (2): 142–51. https://doi.org/10.1016/S0892-1997(05)80139-0.
Zhang, Zhaoyan. 2010. “Dependence of Phonation Threshold Pressure and Frequency on Vocal Fold Geometry and Biomechanics.” Journal of the Acoustical Society of America 127 (4): 2554–62. https://doi.org/10.1121/1.3308410.

Fan, Y. (2026). Vocal Biomechanics, Non-Linear Source-Filter Coupling and Auditory-Motor Feedback: From Titze's Self-Sustained Vocal Fold Oscillation and Vocal-Tract Inertance to the Lombard Effect, Read Beside Classical Chinese Vocal Aesthetics [嗓音生物力学、非线性源-滤波耦合与听觉-运动反馈的数学模型] (Version 1.0.0). 5D Library. https://doi.org/10.5281/zenodo.23770084 · Licensed under Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International (CC BY-NC-ND 4.0).