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SUMMARYMochokidae are able to produce pectoral spine stridulation sounds. During sound production, high speed videos were used to study the pectoral fin movements to identify the mechanisms involved. A call consisted of a series of pulses and occurred during a spine sweep, which was in fact made up of a series of jerky movements. The morphology of the pectoral spines and associated muscles was also observed in different species. The contractions of adductor profundus and superficial adductor allows adduction and abduction movements (sweep) of the spine, respectively. Simultaneously, the contraction of the arrector ventralis or the arrector 3 of the pectoral spine allows the pulling and pressing the ridges of the dorsal process, against the rough lateral face of the spinal fossa. This results in the rubbing of the ridges of the dorsal process, producing sounds. In Synodontis the analogy for sound production would be a brake shoe pressing against a wheel. Supplementary material available online at

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Stridulatory sound-producing behavior is widespread across catfish families, but some are silent. To understand why, we compared spine morphology and ecotype of silent and vocal clades. We determined vocal ability of laboratory specimens during disturbance behavior. Vocal families had bony (not flexible or segmented) spines, well-developed anterior and/or posterior serrations, and statistically significantly longer spines. We compared morphology of the proximal end of the pectoral spine between vocal and silent species. For vocal taxa, microscopic rounded or bladed ridges or knobs were present on the dorsal process. Most silent species had reduced processes with exclusively smooth, convoluted, or honeycombed surfaces very similar to spine-locking surfaces, or they had novel surfaces (beaded, vacuolated, cobwebbed). Most callichthyids had ridges but many were silent during disturbance. All doradid, most auchenipterid and most mochokid species were vocal and had ridges or knobs. Within the Auchenipteridae, vocal species had spines with greater weight and serration development but not length. Silent auchenipterids had thin, brittle, distally segmented spines with few microscopic serrations on only one margin and a highly reduced dorsal process lacking any known vocal morphology. Silent auchenipterids are derived and pelagic, while all vocal genera are basal and benthopelagic. This is the first phylogenetic evidence for stridulation mechanism loss within catfishes. Phylogenetic mapping of vocal ability, spine condition, and ecotype revealed the repeated presence of silence and vocal taxa, short and long spines, and ecotype shifts within clades. The appearance and loss of vocal behavior and supporting morphologies may have facilitated diversification among catfishes.