1989
DOI: 10.2307/2260816
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Density-Dependent Regulation of Ramet Populations Within the Bunchgrass Schizachyrium Scoparium: Interclonal Versus Intraclonal Interference

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Cited by 72 publications
(62 citation statements)
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“…Furthermore, k was higher in low-than in high-density populations, with the exception of R. discolor over the 1999-2000 transition. This pattern of population growth is similar to that of other clonal plant species (Barkham 1980;Cook 1985;Briske and Butler 1989) as well as that of the invasive, but non-clonal, Cytisus scoparius (Parker 2000), in response to increasing population density. The LTRE showed that for R. ursinus, the effect of density on k was due to a reduction in cane v survival with increasing population density, while in R. discolor, the difference was due to a reduction in cane v production.…”
Section: Population Growth and Invasivenesssupporting
confidence: 76%
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“…Furthermore, k was higher in low-than in high-density populations, with the exception of R. discolor over the 1999-2000 transition. This pattern of population growth is similar to that of other clonal plant species (Barkham 1980;Cook 1985;Briske and Butler 1989) as well as that of the invasive, but non-clonal, Cytisus scoparius (Parker 2000), in response to increasing population density. The LTRE showed that for R. ursinus, the effect of density on k was due to a reduction in cane v survival with increasing population density, while in R. discolor, the difference was due to a reduction in cane v production.…”
Section: Population Growth and Invasivenesssupporting
confidence: 76%
“…The LTRE showed that for R. ursinus, the effect of density on k was due to a reduction in cane v survival with increasing population density, while in R. discolor, the difference was due to a reduction in cane v production. Reduced cane v production, rather than increased mortality, is a more commonly observed response to increased population density in other clonal plant species (Cook 1985;Briske and Butler 1989), perhaps because cane v mortality generates a resource cost for the entire clone. The mortality of cane v in R. ursinus was particularly pronounced over the 2000-2001 transition interval, along with mortality of other life-history stages, and may have arisen due to the colder than normal conditions during the winter and much drier than normal spring.…”
Section: Population Growth and Invasivenessmentioning
confidence: 99%
“…Understanding tiller dynamics is critical in developing appropriate grazing strategies for rangelands (Cullan et al 1999). Most perennial grasses have bimodal recruitment patterns with flushes of new tillers emerging during the spring and fall (Langer 1956, Briske and Butler 1989, Briske and Richards 1995 ) , o n l y produced 1 annual cohort. These established patterns of tiller recruitment may be affected by defoliation which extends the recruitment period (Butler and Briske 1988), promotes additional tiller cohorts (Olson and Richards 1988a), and changes the timing of peak recruitment (Bullock et al 1994).…”
Section: Introductionmentioning
confidence: 99%
“…2d). The ability of the grass life form at our site to exhibit a rapid, positive response to warmer conditions and to extend the season of growth is likely the result of (1) the existence of a large leaf area at the time of treatment application, (2) the inherent physiological capacity of grasses to alter patterns of resource allocation (Welker et al, 1985(Welker et al, , 1987Welker & Briske, 1992), (3) their morphological and demographic capacity to elongate fall tillers (Briske & Butler, 1989), and (4) the ability to grow when environmental constraints are temporally removed (Sala et al, 1992). Grasses at other tundra sites have also exhibited an ability to respond rapidly to simulated changes in climate as exemplified by Calamagrostis biomass increases in the sub-arctic at Abisko, Sweden under warmer conditions .…”
Section: Resultsmentioning
confidence: 99%