Temperature affects both the timing and outcome of animal development, but the detailed effects of temperature on the progress of early development have been poorly characterized. To determine the impact of temperature on the order and timing of events duringDrosophila melanogasterembryogenesis, we used time-lapse imaging to track the progress of embryos from shortly after egg laying through hatching at seven precisely maintained temperatures between 17.5°C and 32.5°C. We employed a combination of automated and manual annotation to determine when 36 milestones occurred in each embryo.D. melanogasterembryogenesis takes 33 hours at 17.5°C, and accelerates with increasing temperature to a low of 16 hours at 27.5°C, above which embryogenesis slows slightly. Remarkably, while the total time of embryogenesis varies over two fold, the relative timing of events from cellularization through hatching is constant across temperatures. To further explore the relationship between temperature and embryogenesis, we expanded our analysis to cover ten additionalDrosophilaspecies of varying climatic origins. Six of these species, likeD. melanogaster, are of tropical origin, and embryogenesis time at different temperatures was similar for them all.D. mojavensis, a sub-tropical fly, develops slower than the tropical species at lower temperatures, whileD. virilis, a temperate fly, exhibits slower development at all temperatures. The alpine sister speciesD. persimilisandD. pseudoobscuradevelop as rapidly as tropical flies at cooler temperatures, but exhibit diminished acceleration above 22.5°C and have drastically slowed development by 30°C. Despite ranging from 13 hours forD. erectaat 30°C to 46 hours forD. virilisat 17.5°C, the relative timing of events from cellularization through hatching is constant across all of the species and temperatures examined here, suggesting the existence of a previously unrecognized timer controlling the progress of embryogenesis that has been tuned by natural selection in response to the thermal environment in which each species lives.