Stern has criticized a body of work from several groups that have independently studied the so-called "Kyriacou and Hall" courtship song rhythms of male Drosophila melanogaster, claiming that these ultradian ∼60-s cycles in the interpulse interval (IPI) are statistical artifacts that are not modulated by mutations at the period (per) locus [Stern DL (2014) BMC Biol 12:38]. We have scrutinized Stern's raw data and observe that his automated song pulse-detection method identifies only ∼50% of the IPIs found by manual (visual and acoustic) monitoring. This critical error is further compounded by Stern's use of recordings with very little song, the large majority of which do not meet the minimal song intensity criteria which Kyriacou and Hall used in their studies. Consequently most of Stern's recordings only contribute noise to the analyses. Of the data presented by Stern, only per L and a small fraction of wild-type males sing vigorously, so we limited our reanalyses to these genotypes. We manually reexamined Stern's raw song recordings and analyzed IPI rhythms using several independent time-series analyses. We observe that per L songs show significantly longer song periods than wildtype songs, with values for both genotypes close to those found in previous studies. These per-dependent differences disappear when the song data are randomized. We conclude that Stern's negative findings are artifacts of his inadequate pulse-detection methodology coupled to his use of low-intensity courtship song records.D uring courtship, the Drosophila melanogaster male vibrates his wing toward the female and produces a series of pulses and hums (1). The pulses have a variable interpulse interval (IPI), which ranges from 15 to 80 ms but usually averages between 30 and 40 ms, whereas sympatric Drosophila simulans mean IPIs vary from 45 to 80 ms depending on the strain (2, 3). In 1980, in these pages, the first of a series of studies by Kyriacou, Hall, and their collaborators revealed that superimposed on these IPIs was a low-amplitude oscillation of about 60 s in D. melanogaster and 40 s in D. simulans (4-12). Furthermore, in D. melanogaster, these cycles were modulated in a predictable fashion by the circadian rhythm period (per) mutations (13): per L males with long 29-h circadian cycles also sang with long ∼80-s song cycles, whereas circadian arrhythmic per 01 males showed a corresponding song phenotype (2, 4, 9, 10). These cycles were shown to have functional significance in playback experiments in which females were shown to be most responsive to both their species-specific IPI and cycle (2, 14-16).The work of Kyriacou, Hall, and collaborators was performed in the late 1970s and 1980s using extremely laborious analog technology, so to attain any kind of throughput, IPIs were binned into consecutive 10-s intervals and a mean IPI calculated on a minimum of 10 IPIs (2, 4-6, 8). Initially, sine/cosine functions were fitted to the mean IPIs (2, 4-6, 8), and this was later complemented by spectral analyses, with both types of statisti...