We assessed the pollen hydration, the pollen germination, and the stigma papilla penetration of Crocus vernus subsp. vernus (Iridaceae) after 2 h fumigations with O-3, NO2, and CO gases within humidified (90-100% RH) box experiments. When the pollen and the pistil were separately fumigated, the pollen retained the capacity to emit a tube which penetrated papilla, and the stigma papillae retained the receptivity; when the pistils were first pollinated and then fumigated, the capacity of pollen to hydrate was not affected, but the germination was significantly reduced. The vulnerability to gases became evident at 0.3 ppm O-3, 0.2 ppm NO2, and 0.5 ppm CO. The inhibition curves as a function of the gas concentrations were of an exponential type, and they saturated at 2 ppm NO2, 25 ppm CO, and 0.5 ppm 03, with germination percentages of 17%, 27%: and 60%, respectively. Both the pollen germination and the papilla penetration were fully restored by prolonging for 60-90min the incubation at 90-100% RH, after the cessation of fumigations. The vulnerability of the pollen-papilla system is discussed.
Reversible inhibition of the pollen germination and the stigma penetration in Crocus vernus ssp vernus (Iridaceae) following fumigations with NO2, CO, and O-3 gases
2007
Abstract
We assessed the pollen hydration, the pollen germination, and the stigma papilla penetration of Crocus vernus subsp. vernus (Iridaceae) after 2 h fumigations with O-3, NO2, and CO gases within humidified (90-100% RH) box experiments. When the pollen and the pistil were separately fumigated, the pollen retained the capacity to emit a tube which penetrated papilla, and the stigma papillae retained the receptivity; when the pistils were first pollinated and then fumigated, the capacity of pollen to hydrate was not affected, but the germination was significantly reduced. The vulnerability to gases became evident at 0.3 ppm O-3, 0.2 ppm NO2, and 0.5 ppm CO. The inhibition curves as a function of the gas concentrations were of an exponential type, and they saturated at 2 ppm NO2, 25 ppm CO, and 0.5 ppm 03, with germination percentages of 17%, 27%: and 60%, respectively. Both the pollen germination and the papilla penetration were fully restored by prolonging for 60-90min the incubation at 90-100% RH, after the cessation of fumigations. The vulnerability of the pollen-papilla system is discussed.I documenti in IRIS sono protetti da copyright e tutti i diritti sono riservati, salvo diversa indicazione.
