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Phenological and reproductive shifts of plants due to climate change may have important influences on population dynamics. Climate change may also affect invasive species by changing their phenology and reproduction, but few studies have explored this possibility. Here, we investigated the impact of climate change on the phenology, reproduction and invasion potential of two alien Solidago canadensis and Bidens frondosa and one native weed, Pterocypsela laciniata, all of which are in the Asteraceae family. The three species responded to simulated climate change by increasing reproductive investments and root/leaf ratio, prolonging flowering duration, and while the two alien species also displayed a mass-flowering pattern. Moreover, our experimental results indicated that the alien invasive species may have greater phenological plasticity in response to simulated warming than that of the native species (P. laciniata). As such, climate change may enhance the invasion and accelerate the invasive process of these alien plant species.

Disanthus cercidifolius Maxim. var. longipes H. T. Chang, a plant species that only occurs in a few counties in Hunan, Jiangxi and Zhejiang Provinces and with a relatively small number of individuals, is ranked as a second Class endangered species for conservation in China. We have studied the effect of pollen and resources available to female reproduction, and the reproductive mechanism of "excess flowers with low fruit set" in Disanthus cercidifolius Maxim. var. longipes H. T. Chang was discussed. Results are as follows:Pollen from different sources has significant effects on fruit set and seed set of Disanthus cercidifolius Maxim. var. longipes H. T. Chang. The pollen source rather than pollen numbers significantly affected reproduction of this species. In wild populations, producing one fruit needs about 54.8 flowers, and one satiation seed needs about 6.60 flowers or 83.19 ovules.After fertilizing, which was propitious to flower development, the abortion rate of flower buds was decreasing, but the flowering rate was increasing. The fruit set and seed set was also significantly increasing, while abortion rate of fruit was significantly decreasing. With the increasing percentages of cutting leaves, the fruit set decreased, but the abortion rate of fruit shows no significant differentiation among treatments. After cutting branches that were puny, broken and insectinfested branches, the flower number seemed to be decreasing, but the fruit set and seed set all increased significantly. After removing some flowers, the fruit set was calculated with respect to the number of flowers remaining after the treatment increased with increasing of percentages of flower removal, whereas fruit set calculated with respect to the initial number of flowers remained constant, and the mean weights of per fruit and per seed all decreased significantly.Sufficient spatial or temporal heterogeneities in nutrient levels might allow limitation of seed set by resources and pollen in a natural population, while supplying resources may indirectly affect pollination by increasing attraction of the flowers to pollinators. There were very low fruit and seed sets in natural populations of Disanthus cercidifolius Maxim. var. longipes H. T. Chang. Different factors may have interacted to effect a low fruit set. A joint adoption of the "selection abortion hypothesis", "ovary reserve hypothesis" and "male function hypothesis" seems to be the most likely explanation for the reproductive strategy of "excess flowers with few fruit sets" in Disanthus cercidifolius Maxim. var. longipes H. T. Chang.

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