When velvetleaf plants from Mississippi and Minnesota populations were maintained in growth chambers with day/night temperatures of 29/23 C and photoperiods of 11, 12, 13, 14, and 15 h, flower buds and open flowers appeared first in the 12 h photoperiod. Buds and flowers appeared 2 to 4 d later at photoperiods of 11, 13, or 14 h. Increasing the photoperiod beyond 14 h to 15 h delayed bud appearance an additional 7 d in the MN plants and 12 d in the MS plants. Open flowers appeared four to five nodes higher, 10 d later at 15 than at 14 h in the MN plants and 20 d later in the MS plants. Vegetative shoot weight and fruit weight 73 d after emergence were greater in 13 h or longer photoperiods than at 11 or 12 h. In shorter photoperiods, MN plants produced more vegetative growth than MS plants, but the reverse occurred at longer photoperiods where MS plants were taller than MN plants. These growth differences occurred because earlier shifts in allocation to reproductive growth in MN plants limited their vegetative growth, particularly in the longest photoperiods. Differences in rate of reproductive development between populations were not evident until photoperiod exceeded 13 h. Reciprocal transfer of plants of the MS population between short and long photoperiods revealed the durations of the juvenile (pre-inductive), inductive, and post-inductive phases to be 3 to 5, 7 to 8 (short day) or 30 (long day), and 10 to 11 d, respectively. Differences in competitive ability among latitudinal biotypes of photoperiodically-sensitive weeds may depend on time of emergence in the field and consequent photoperiod exposure. Weed growth simulation models to be used in development of expert systems for weed management should take photoperiodic sensitivity into account.