Aluminum and iron targets were irradiated by intense (I # 10 15 W͞cm 2 ), 120 fs laser pulses with sufficiently high contrast such that the surface expanded no more than the peak electron quiver amplitude during excitation. Under these experimentally verified conditions, obliquely incident, p-polarized pulses uniquely experienced anomalous absorption, proportional to ͑Il 2 ͒ 0.64 , and as high as 20%. This extra absorption was distinguished from competing pump-induced linear mechanisms by fs-time-resolved reflectivity, and agreed quantitatively with essential features of Brunel's "vacuum heating," in which light is absorbed by drawing electrons into the vacuum and sending them back into the plasma with approximately the quiver velocity. [S0031-9007 (99)09116-4] PACS numbers: 52.50.Jm, 78.20.Ci, 78.47. + p Amplified, high contrast femtosecond laser pulses [1] have opened a new regime of laser-solid interactions in which intense light is deposited into a solid faster than the target surface can hydrodynamically expand [2]. While numerous experiments have used a single pulse to both excite and probe such sharply bound solid density fluids [3], they have not individually identified the many competing collisional and collisionless absorption mechanisms unique to this regime which an extensive theoretical literature [4-10] has enumerated. For example, Brunel [4] proposed over ten years ago that a moderately intense, p-polarized light pulse incident obliquely on an atomically abrupt metal surface could be strongly absorbed by pulling electrons into the vacuum during an optical cycle, then returning them to the surface with approximately the quiver velocity. Later simulations [5] predicted that, with a slight surface expansion of scale length L ϵ ͑≠ lnn e ͞≠z͒ 21 , the optical field would pull more electrons into the vacuum, and thus be even more strongly absorbed, as long as L did not significantly exceed the electron quiver amplitude x osc eE͞mv 2 . While this "vacuum heating" (VH) mechanism has been incorporated into laser-plasma codes [6], and may influence surface x-ray [11] and high harmonic [12] generation, and intense laser interaction with nanoclusters [13] and hollow capillaries [14]-and although a microscopically similar mechanism underlies high harmonic generation and above-threshold ionization in gases [15]-quantitative experimental identification of VH at metal surfaces is completely lacking.Two important barriers to such identification have been the production and verification of Brunel's condition L & x osc , and distinction of VH from competing linear mechanisms [7] such as inverse bremsstrahlung (IB), anomalous skin effect (ASE) [8], sheath inverse bremsstrahlung (SIB) [9], sheath transit absorption (STA) [10], and resonance absorption (RA) [16]. For example, 120 fs pulsed excitation at l 0.62 mm and peak intensity I 10 15 W͞cm 2 heats Al targets to a peak electron temperature of kT e ϳ 100 eV [3,7], resulting in a collision frequency n ϳ 5 3 10 15 s 21 [7]. For L 0, IB dominates under these conditions...