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Identify ornamental plantings, cultivars sold by nurseries, and/or wild coastal populations of Cortaderia that are sources of recent invasions into inland habitats.
Quantify sex ratios of C. selloana in ornamental plantings and wild populations, and evaluate the effect of population sex ratio on the fitness of female and hermaphroditic plants.
Our studies of jubata grass indicated that all invasive plants sampled in California consisted of a single clone. The clone is likely to have come from southern Ecuador and is identical to invasive jubata grass found in Hawaii and New Zealand. Widespread geographic distribution of a single clone is consistent with a single genetic origin and the lack of sexual reproduction reported for this species. The genetic uniformity of invasive jubata grass in California suggests that classical biological control of the species could be successful. A lack of genetic diversity simplifies identification of native source populations to search for natural enemies, as well as reduces the variability in establishment and effectiveness of biological control agents that is often associated with genetic variation in the host plant.
Results indicate high levels of differentiation among pampas grass populations, consistent with colonization of new areas with a small number of colonists. Based on microsatellite markers, cultivated varieties clustered into cultivars clonally propagated by nurseries, varieties 'Pink' and 'White' from mail-order and online vendors propagated by seed, ornamental plantings, and unnamed generic pampas grass sold by nurseries.
The majority of wild populations appear to be derived from ornamental plantings and unnamed pampas grass sold by nurseries. In contrast, all jubata grass populations in California appear to consist of a single clone. This single clonal genotype is identical to that of 28 jubata grass samples obtained from Maui, Hawaii, indicating the same clone is invasive in both California and Hawaii. Initial evaluations of population sex ratios in pampas grass populations indicate plants can be female, male, or hemaphrodite. Further, we observe continuous morphological variation between maleness and hermaphroditism with varying degrees of female functionality/nonfunctionality.
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