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Fimbristylis sericea propagates asexually by short, thick rhizomes that produce clusters of ramets, which belong to the same genet.
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Counting individuals of clonal plants is very difficult, so we counted apparent clusters of stems as an individual (a ramet in most cases).
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.
To assess the response of S. orbiculatus to prescribed fires we used maximum ramet height, maximum ramet canopy diameter and number of live stems per ramet, and density of ramets per 100 m2 as response variables.
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.
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.
The number of ramets in each culture tank was counted after 77 78 days following settlement of each founder.
Dong et al. (2010) recently showed that the survival and growth of ramets of Alternanthera philoxeroides increased with increasing length of attached stolons.
In P. tenax, the number of ramets remained unchanged, as no new ramets were produced during the 54 days of the experiment and growth was limited to increasing size of existing ramets.
Overall for transplanted mats, more ramets died than were recruited (mean change number of ramets per mat between years = -1.38; two-sided t-test, P = 0.01).
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