I think there is some validity to both views:
It's true that the drift rate is a constant in the standard DDM, such that once it begins accumulating the rate is fixed (+gaussian noise).
But accumulation doesn't necessarily start right at stimulus onset: the non-decision time reflects a period of time for perceptual encoding before accumulation begins (and also motor execution after). So it is plausible that the animal would first perceive the stimulus during the non decision time (which is likely > 50 or 100 ms, so enough to encompass the short duration stims), requiring reliance on degraded iconic memory to accumulate after that. So then accumulation could be steeper / more efficient for stimuli that were processed more robustly (or continue to be presented after non decision time) compared to those that rely on noisy memory. And there are certainly lots of cases where higher drifts correspond to stimuli that are easier to encode (higher contrast, numerosity differences, etc).
Another possibility is that a better model would be a drift rate that accelerates with stimulus duration (sort of like the ornstein uhlenbeck model but with an acceleration instead of leak), which would require using LANs in HDDM or HSSM. But even if that would be more accurate, the DDM might still roughly approximate that with different slopes per duration. In that case you could acknowledge that the DDM is still useful for your purposes in approximating a different dynamic.
Michael J Frank, PhD | Edgar L. Marston Professor