Supplementary Info. Brazeau and Ahlberg MS-2005-05-06098A 1 Panderichthys sp. LDM 60/123 The specimen consists of a single individual from the tip of the snout to approximately the mid-trunk in ventral view. The ventral half of the specimen is missing, exposing the braincase (Ahlberg et al. 1996), dorsal hyoid arch, palatal surface in ventral view and the internal surfaces of the dorsal operco-gular series and squamation. The posterior part of the (anatomical) left lower jaw ramus is preserved in articulation with the quadrate. The right quadrate is missing. The specimen is well-preserved, but is substantially fractured as the bone and surrounding matrix is quite brittle. It is preserved in a light-coloured clay matrix, resulting in a low visual contrast with the bone that makes it difficult to distinguish the two in photographs. However, all structures described are well represented in the actual specimen and detailed in the specimen drawings. The specimen has been slightly flattened dorsoventrally. This has compacted the suspensorium and forced the quadrates laterally. However, the orientation, position, and connectivity of elements does not appear to be greatly affected. All elements appear to have approximate positional correspondence with their homologues in Eusthenopteron (Jarvik 1980). One significant difference from the description by Ahlberg et al. (1996) is the interpretation of the hyomandibula. The previous work was conducted prior to more complete preparation in the region of the suspensorium, which revealed that the “hyomandibula” of Ahlberg et al. was in fact a pair of epibranchials (1 and 2) that partly concealed the real hyomandibula. Ahlberg et al. (1996) mistakenly concluded the hyomandibula to be generally like that of Eusthenopteron, in spite of some significant Supplementary Info. Brazeau and Ahlberg MS-2005-05-06098A 2 differences pointed out by Vorobyeva and Schultze (1991). Our interpretation, however, differs from both these accounts in demonstrating a modified relationship to the opercular bone and the epipterygoid region of the palatoquadrate. On the anatomical left side of the specimen, the distal tip of the hyomandibula rests at the position of the opercular facet. The hyomandibula measures approximately 40 mm long (however the ends appear to have been unossified). This corresponds to the approximate distance between the opercular facet and the lateral commissure. In the reconstructed skull (main text Fig. 3) The measurements do not greatly alter given that the reorientation of the opercular is commensurate with the restoration of the quadrates to a more ventromedial position. We conclude that the hyomandibular ossification terminates at the position of the opercular facet, representing the location of the ligamentous attachment between the two. References Ahlberg, P. E., J. A. Clack, et al. (1996). "Rapid braincase evolution between Panderichthys and the earliest tetrapods." Nature 381: 61-64. Jarvik, E. (1980). Basic Structure and Evolution of Vertebrates. London, Academic Press. Vorobyeva, E. and H.-P. Schultze (1991). Description of panderichthyid fishes with comments on their relationship to tetrapods. Origins of the Higher Groups of Tetrapods: Controversy and Consensus. H.-P. Schultze and L. Trueb. Ithaca, NY, Cornell University Press (Canstock): 68-109.