Field violet germination occurred during May to early July and again during September to November in Nova Scotia (N.S.), Canada. Germination occurred from October until early April in the North Carolina (NC) piedmont. Germination was stimulated by tillage. Seed collected in N.S. and in NC germinated optimally in the dark under a temperature regime of 15/5 C, on an 8/16 h thermoperiod. Germination at constant temperatures decreased with increasing temperatures, from 5 to 25 C. Seed collected in NC was capable of germinating at a higher constant temperature of 25 C than seed collected in N.S. Germination of seed collected in NC was partially inhibited by constant irradiance with a photosynthetic photon flux density of 100 μM m−2 s−1 (400 to 700 nm). Seed did not germinate when exposed to constant red or far-red irradiance.

The effects of temperature and light on the dormancy of velvetleaf, common waterhemp, and giant foxtail seeds were studied under controlled growth chamber conditions. Seeds were either kept chilled at 4 C for 12 wk under wet conditions or nonchilled at 4 C in dry storage. Then, seeds were germinated under increasing and decreasing temperatures and under continuous red light (R) and far-red light (FR). In addition, chilled and nonchilled seeds were germinated in the dark after being exposed to alternating R and FR flashes. Velvetleaf germination was increased by exposure to high temperatures (36 C) immediately after exposure to low temperatures (4 C), but light had no effect. Chilling increased common waterhemp seed germination and sensitivity to light and temperature. R promoted common waterhemp seed germination, whereas FR inhibited germination and maintained dormancy. In addition, the effect of light was reversible. Therefore, common waterhemp dormancy was phytochrome regulated. However, high temperatures (36 C) promoted the germination of chilled seeds, even when exposed to FR. The germination of chilled giant foxtail seeds was reduced by FR. Giant foxtail seed dormancy was partially phytochrome regulated, but dormancy regulation was more dependent on mean temperature.

Knowledge of the germination requirements of wild radish will help in determining the favorable conditions for germination and emergence and allow better management of this weed. Experiments were conducted during 2005 to 2006 and 2006 to 2007 to evaluate wild radish temperature and light requirements over a 12-mo period beginning in July on seeds placed on the soil surface and at a 10-cm depth. Germination response was influenced by temperature, light, duration of burial, and burial depth. Freshly harvested seeds (July) had no more than 18% germination whereas seeds allowed to after-ripen in the field for 3 to 6 mo (October to January) had up to 40% germination. The germination of wild radish retrieved from the soil surface was 1.2 to 1.5 times greater at alternating temperatures (2.5/17.5, 7.5/22.5, and 12.5/27.5 C) than at constant temperatures (10, 15, and 20 C) at 0, 3, and 6 mo after maturation. The light requirement for germination varied by time of year with no differences in germination between light and dark conditions for freshly harvested seeds. Far-red light inhibited germination of wild radish, indicating that wild radish may become sensitive to light following an after-ripening period.

Neurophysiological recordings have shown that activity of magnocellular neurons may be reduced by red backgrounds. This has led some researchers to use red light, or red filters, in attempts to determine the magnocellular contribution to psychophysical tasks. This requires that red light not affect parvocellular neurons, or at least that it is possible to control for the effect on the parvocellular system by using other colors. The present report investigates these assumptions by calculating the effect of red, green, and blue filters on the three cone pigments and on the four parvocellular color-opponent cell mechanisms. It is found that a red filter has a large effect on the long- and middle-wavelength cone pigments and on the red–green color-opponent mechanisms. A green filter, on the other hand, has little effect. A blue filter has a fairly pronounced effect but this effect is distinctly different from that of the red filter. These results indicate that one ought not rely upon red light to isolate magnocellular activity in psychological experiments. The results also indicate that it is difficult to use colors other than red to control for the effect of this color on the parvocellular system.