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Thus, some spaces were kept between the crowns of ramets.
For V. neoglutinosa, we measured the number of ramets produced by each mother-plant and the respective branching angles.
Canopy diameter and density of ramets was not affected by time since fire, but burned pastures had marginally lower densities than plots excluded from fire (P = 0.07).
For A. nudicaulis, we mapped six clonal fragments and measured the number of ramets produced by each mother-plant, rhizome length and branching angle.
Among the 40 ramets taken at each site, after removal of genet (i.e., clonal) repetitions the number of ramets available in the data set ranged from 4 to 34 per meadow.
Ramets per 100 m2 were measured by noting the total number of ramets in a plot and then converting that to 100 m2, a reflection of alterations to ramet density from fire-induced mortality.
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A detailed map of individual ramets and their corresponding rhizome network was produced and the seasonal development of ramet sprouting and rhizome growth was reconstructed.
Figure 2 Mean ± SE of ramet height (A), ramet canopy diameter (B), stems per ramet (C), and ramets per 100 m 2 (D) for Symphoricarpos orbiculatus plants exposed to three fire treatments in the Grand River Grasslands of Iowa, USA, 2011 2013.
The cover of Gnaphalium supinum was recorded at the peak of the aboveground biomass development in the three years, while the temporal dynamic of ramet density and reproductive phenophases were monitored during the 2005 growing season.
We fitted models to data that included all ramets irrespective of morpho-species to explore the overall community patterns of ramet survival, recruitment, and population change, and then modeled common morpho-species separately to look at individual morpho-species responses.
Abundance of flowering ramets of a plant species was a significant predictor of the abundance of bees found on that plant.
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