2003
DOI: 10.2458/azu_jrm_v56i6_hirata
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Responses of bahiagrass to nitrogen and defoliation

Abstract: Pensacola bahiagrass (Paspalum notatum Flugge) swards pretreated with fertilizer nitrogen rates of 0 and 66-99 kg N ha1 year-1 were exposed to repeated, severe defoliation (i.e., removal of all laminae) of every day (Dl), every 2 days (D2), and every 4 days (D4). Responses of the grass were monitored in terms of tiller survival, lamina production and changes in the mass of the stubble-stolon-root system, in an effort to investigate the effects of nitrogen rate and defoliation frequency on defoliation tolerance… Show more

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Cited by 3 publications
(4 citation statements)
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“…The main mechanism related to this adaptation and to tolerance to grazing is the capacity to store energy in reserve tissues of underground structures, a crucial feature to predominate in this environment (Strauss & Agrawal, 1999; Stowe et al, 2000). Previous work on Paspalum notatum demonstrate an increase in tillering rate, stolon length and number of primary roots in response to lower cutting heights (2 cm), in comparation to plants cut at taller heights (Hirata & Pakiding, 2003). Therefore, the great root:shoot relationship shown in our experiment for the species prevalent in the overgrazed area (prostrate and rosette growth habit) could be a strategy to “escape” from grazing and invest in underground tissues.…”
Section: Discussionmentioning
confidence: 83%
“…The main mechanism related to this adaptation and to tolerance to grazing is the capacity to store energy in reserve tissues of underground structures, a crucial feature to predominate in this environment (Strauss & Agrawal, 1999; Stowe et al, 2000). Previous work on Paspalum notatum demonstrate an increase in tillering rate, stolon length and number of primary roots in response to lower cutting heights (2 cm), in comparation to plants cut at taller heights (Hirata & Pakiding, 2003). Therefore, the great root:shoot relationship shown in our experiment for the species prevalent in the overgrazed area (prostrate and rosette growth habit) could be a strategy to “escape” from grazing and invest in underground tissues.…”
Section: Discussionmentioning
confidence: 83%
“…These relationships were supported by both the correlation and PCA and likely result from the plant's partitioning of energy. Because plant growth increases with increased N, the plant is likely allocating more energy from its rhizomes into shoot production, thereby reducing rhizome size (Hirata and Pakiding, 2003). The N effects in the three remaining morphological traits were not as clear.…”
Section: Discussionmentioning
confidence: 99%
“…1984; Lemaire and Chapman 1996; Bélanger 1998). Depletion of carbohydrate is also suggested to enhance death of shoots (Hirata and Pakiding 2003). Although defoliation of M. sinensis by animals was not very intense (degree of utilization, 25–50%; Table 3), frequent removal of young leaves having high nitrogen concentrations and high photosynthetic rates is considered to be a factor contributing to low carbohydrate and nitrogen concentrations in this defoliation‐susceptible grass.…”
Section: Discussionmentioning
confidence: 99%
“…It is reported that low carbohydrate and nitrogen concentrations restrict generation and/or development of new shoots and leaves in grasses, though the response of leaf generation to nitrogen may vary with species (Vine 1983;Coughenour et al 1984;Lemaire and Chapman 1996;Bélanger 1998). Depletion of carbohydrate is also suggested to enhance death of shoots (Hirata and Pakiding 2003). Although defoliation of M. sinensis by animals was not very intense (degree of utilization, 25-50%; Table 3), frequent removal of young leaves having high nitrogen concentrations and high photosynthetic rates is considered to be a factor contributing to low carbohydrate and nitrogen concentrations in this defoliation-susceptible grass.…”
Section: Mechanisms Behind the Decline Of M Sinensis Under Grazingmentioning
confidence: 99%