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Replicate ramets were grown in a split split plot design with two levels of dissolved nutrients and four different grazer species combinations (Tozeuma carolinense alone, Pagurus maclaughlinae alone, both species together, and no grazers present).
For each clone, two ramets were randomly selected giving a total of 24 trees for measurements.
Individual ramets were identified by spatial independence based on vertical stems arising from the same root crown.
Ramets were sampled from 60 different meadows, distributed geographically between the Mediterranean basin and the Atlantic Ocean, covering the entire plant distribution [11].
The ramets were maintained in the salt-free environment for another two weeks, whereupon more samples were collected.
Survival and final size of single-node stolon fragments of A. philoxeroides were greatest when ramets were oriented in the horizontal position.
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The results show that plasticity of clonal growth forms, by which more spreading ramets are produced, is an effective strategy to avoid sedimentation stress under our experimental conditions.
We measured grazing intensity based on the amount of plant ramets being grazed in 75 plots positioned across a rangeland landscape in central Tibet.
Ramets are distinguished by colour, with ramet 1 being red and ramet 2 being blue.
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).
Epifluorescence microscopy revealed that pollen from both FS and H ramets was capable of producing functional pollen tubes (Fig. 5).
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