Motion-receptive fields are known to be center–surround antagonistic (e.g., Allman, Miezin, & McGuinness,
1985; Eifuku & Wurtz,
1998; Jones, Grieve, Wang, & Sillito,
2001; Nakayama & Loomis,
1972; Raiguel, van Hulle, Xiao, Marcar, & Orban,
1995; Tadin, Lappin, Gilroy, & Blake,
2003). At least in the motion extrastriate MT+ complex and the equivalent human cortical area hMT+ (Eifuku & Wurtz,
1998; Moutsiana et al.,
2011; Takemura et al.,
2012)—but also, though not systematically, in V1 (Heeger, Boynton, Demb, Seidemann, & Newsome,
1999; Jones et al.,
2001)—neurons' response to their preferred motion direction in the center of their receptive fields increases when the surround motion is in the opposite direction to that in the center and decreases when surround motion is in the same direction as that in the center. Moreover, the hMT+ response to a central moving patch encroached by a moving surround correlates with subjects' perceived speed of the central patch rather than with its physical speed relative to that of the surround (Takemura et al.,
2012). Taken together with such findings, the present perceived speed results suggest that the observed perceived duration dependency on perceived speed is mediated by the response strength (or, equivalently, by the amount of energy used to encode a stimulus; Eagleman,
2008; Pariyadath & Eagleman,
2007; Mayo & Sommer,
2012) of neural mechanisms at the hMT+ motion processing stage. The “amount of energy” account of duration perception belongs to the class of “intrinsic” (as opposed to “dedicated”) models of time perception, with some physiological support (see Eagleman,
2008; Ivry & Schlerf,
2008; Mayo & Sommer,
2012). The present findings comply with this view. Nonetheless, as noted by many (e.g., Eagleman,
2008; Gorea,
2011; Grondin,
2010; Ivry & Schlerf,
2008; van Wassenhove,
2009), the amount of energy cannot be the only substrate of our perception of short durations. For example, it cannot account for our capability of timing empty intervals (e.g., Grondin,
1993; Rammsayer,
2010), nor for a number of within- (e.g., Westheimer,
1999) and cross-modal (e.g., Roberts,
1982; van Wassenhove, Buonomano, Shimojo, & Shams,
2008) transfers of learned temporal estimation capabilities. In conjunction with the relevant physiological literature, the present report of duration modulation by perceived rather than by physical speed does, however, emphasize the significant contribution of early sensory mechanisms to our perception of time, at least partly indexed to their response strength.