Phytochrome-mediated photocontrol of the germination of the scentless mayweed, Matricaria inodora L., and its sensitization by nitrate and temperature

The emergence of Matricaria inodora (M. perforata) may poorly respond to modified light exposure during tillage. Therefore, the influence of light, nitrate and temperature on the germination of M. inodora has been studied under laboratory conditions. Germination of a native seed batch levels off around 77% after 7 to 9 days at 20°C, if sown in 0.01 M KNO₃ or NaNO₃ with a daily photoperiod of 14 h weak white light. In 0.01 M NaCl or in bidistilled water germination reaches 48 ± 5%. One saturating red-light pulse, applied 12 h after imbibition in 0.01 M KNO₃, gives only 12 ± 3% germination after 7 days, but 5 daily repeated red-pulses produce 75% germination. Ten twofold daily repeated red-light pulses are equivalently efficient, and if all immediately followed by a saturating far-red pulse, perfect reversibility down to the far-red level of 7 ± 3% germination is found. The dark germination was 1.7 ± 0.7%.

A fluence-response curve, elaborated for 10 red-pulses, gives an exponential pattern with half-saturating pulse fluence around 35 J m^?2, as indicative of phytochrome photoconversion. The influence of additional temperature pretreatment in darkness was tested, followed by half-saturating red-light pulses every 12 or 24 h. Chilling at 2 °C was ineffective up to 6 days, but slightly sensitizing after 21 days, giving around 30% and 46% germination, respectively. Preincubation for 6 days between 20 and 36 °C was more efficient and led to 58–68% germination at 20 °C. A thermoperiodic pretreatment with daily 12 h at 10 °C and 12 h at 30 °C was most efficient, giving 73 ± 4% germination. For all these pretreatments dark germination never exceeded 3%.

Elevated dark germination occurred when water-imbibed achenes, being exposed and dried in red-light of 1 W m^?2, have been reimbibed in darkness. If drying in red-light was for 6 h to a water content of 20% and reimbibition was in water or 0.01 M KNO₃, dark germination increased to 22 ± 5% or 40 ± 6%, respectively. This dark germination was far-red reversible down to 5 ± 2% with half-escape time around 5 h. If drying in red-light was for 24 h to reach the storing content of water around 11%, the dark germination after reimbibition in water or 0.01 M KNO₃ was only 4 ± 2% and 13 ± 2%, respectively. All corresponding controls for drying and reimbibition in darkness, for both water and nitrate, never exceeded 1% germination. This means that drying of seed in light — but not in darkness — increases emergence after the next rainfall and that the nitrate ion acts as a sensitizer for preformed P_fr and facilitates phytochrome-mediated germination.

Thus, for maximum germination of surface exposed M. inodora a thermoperiodic pretreatment, daily repeated light exposures and nitrate are needed. This is typical of the shallow germinating ancestor occurring in coastal ranges, the Sea Mayweed, Tripleurospermum maritimum, and may explain why the emergence of M. inodora is scarcely reduced after lightless tillage.