Helium atoms are strongly attracted to the interstitial channels within a bundle of carbon nanotubes. The strong corrugation of the axial potential within a channel can produce a lattice gas system where the weak mutual attraction between atoms in neighboring channels of a bundle induces condensation into a remarkably anisotropic phase with very low binding energy. We estimate the binding energy and critical temperature for 4 He in this novel quasi-onedimensional condensed state. At low temperatures, the specific heat of the adsorbate phase (fewer than 2% of the total number of atoms) greatly exceeds that of the host material.Low temperature research on Helium was initially stimulated by the challenge of determining the condensation temperature of bulk He [1]. In recent decades, two-dimensional He films, in which the superfluid transition differs qualitatively from that of the bulk [2], have been particularly intriguing. While once of only academic interest [3][4][5][6], Helium in one-dimensional or quasi-one-dimensional systems has received increased attention recently since the realization that such systems can be created in the laboratory. He atoms are very strongly bound within the hexagonal lattice of narrow interstitial channels between tubes within the triangular lattice of a bundle of carbon nanotubes [7][8][9][10]. Within this very narrow channel, the transverse degrees of freedom are frozen out even at relatively high temperatures of ∼50 K. The binding energy per atom, 340 K, is the highest known for He, almost twice that calculated for He within individual nanotubes [11] and 2.4 times higher than that on the basal plane of graphite [12,13]. It exceeds the ground state binding energy of bulk liquid 4 He by nearly fifty times [14].Here we describe how the strong axial confinement of the He wavefunctions within a single channel can produce a direct experimental realization of a lattice gas model, wherein the weak coupling between atoms in neighboring channels induces a finitetemperature transition into a remarkably anisotropic and extremely weakly bound condensed state. First we present a localized model wherein the Helium resides in periodic array of relatively deep potential wells; this "bumpy channel" approximation is supported by single-particle Helium band structure calculations. For comparison, we also describe a delocalized model which assumes translational invariance within each channel (a "smooth channel" approximation). The large difference between the models in 1