2022
DOI: 10.3390/f13010117
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Life Stage and Neighborhood-Dependent Survival of Longleaf Pine after Prescribed Fire

Abstract: Determining mechanisms of plant establishment in ecological communities can be particularly difficult in disturbance-dominated ecosystems. Longleaf pine (Pinus palustris Mill.) and its associated plant community exemplify systems that evolved with disturbances, where frequent, widespread fires alter the population dynamics of longleaf pine within distinct life stages. We identified the primary biotic and environmental conditions that influence the survival of longleaf pine in this disturbance-dominated ecosyst… Show more

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Cited by 8 publications
(4 citation statements)
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“…Negative conspecific density dependence (CDD) can be a stabilizing mechanism for species coexistence when it is more negative than heterospecific density dependence (Adler et al, 2007;HilleRisLambers et al, 2012;Hülsmann et al, 2021Hülsmann et al, , 2024. Many studies have quantified the density-and distance-dependence effects of living conspecific trees on neighbouring seedlings and tree vital rates, yielding valuable insights into patterns of recruitment, growth and survival (e.g., Comita et al, 2010;Jevon et al, 2022;Magee et al, 2022). These analyses often evaluate survival as a function of distance-and size-weighted neighbourhood crowding indices (Comita & Hubbell, 2009;Jevon et al, 2020;Johnson et al, 2017;Smith, 2022), finding that the presence of large neighbouring trees decreases seedling, sapling and tree survival (Piao et al, 2013;Pu & Jin, 2018;Yao et al, 2020;Zhu et al, 2015).…”
Section: Introductionmentioning
confidence: 99%
“…Negative conspecific density dependence (CDD) can be a stabilizing mechanism for species coexistence when it is more negative than heterospecific density dependence (Adler et al, 2007;HilleRisLambers et al, 2012;Hülsmann et al, 2021Hülsmann et al, , 2024. Many studies have quantified the density-and distance-dependence effects of living conspecific trees on neighbouring seedlings and tree vital rates, yielding valuable insights into patterns of recruitment, growth and survival (e.g., Comita et al, 2010;Jevon et al, 2022;Magee et al, 2022). These analyses often evaluate survival as a function of distance-and size-weighted neighbourhood crowding indices (Comita & Hubbell, 2009;Jevon et al, 2020;Johnson et al, 2017;Smith, 2022), finding that the presence of large neighbouring trees decreases seedling, sapling and tree survival (Piao et al, 2013;Pu & Jin, 2018;Yao et al, 2020;Zhu et al, 2015).…”
Section: Introductionmentioning
confidence: 99%
“…Competition has been less studied in open‐canopy forests such as longleaf woodlands. There are indications that mature hardwoods may facilitate longleaf pine establishment in drought‐prone sandhills (Johnson et al, 2021; Loudermilk et al, 2016; Magee et al, 2022), but whether this phenomenon may extend to interactions among mature trees, and on more productive sites, is not known.…”
Section: Introductionmentioning
confidence: 99%
“…Generally, when the root collar diameter of a grass-stage Longleaf Pine reaches ≥2.56 cm, it will initiate rapid height growth (i.e., bottlebrush or bolt stage), which removes the terminal bud from within the flame length of most low-intensity surface fires (Brethauer et al 2021, Hatchell and Marx 1987). As the tree enters the sapling stage, bark thickness increases to prevent girdling (Eberhardt 2013, Magee et al 2022), and sexually mature individuals, ∼30 years old, start to naturally prune lower branches, and form tall (18–34 m), straight boles (Boyer and Peterson 1990).…”
Section: Introductionmentioning
confidence: 99%