Spatial occurrence and colonisations in patch‐tracking metapopulations: local conditions versus dispersal

By Tord Snäll, Paulo Justiniano Ribeiro Jr., H. Rydin. 2003

212 citations recorded by the source corpus.

Subfields: Ecology, Evolution, Behavior and Systematics, Plant Science

View Paper: https://www.semanticscholar.org/paper/6fa7cb8307cee4d52bfb5ca154cb6cca23ebb5b4

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In Ecology, Evolution, Behavior and Systematics

In Plant Science

Citations in the corpus

Lichen diversity and red-listed lichen species relationships with tree species and diameter in wooded meadows (2010, background): “In terms of colonization rates, the time that the tree has been available for colonization (tree age, as reflected by tree diameter) may be equally important as the area effect itself (Snäll et al. 2003).”
How far and how fast do bryophytes travel at the landscape scale? (2008, background): “Individuals of most species indeed tend to be spatially aggregated rather than uniformly distributed (Snäll et al ., 2003, 2004a, 2005; Löbel et al ., 2006).”
The effects of stand structure on ground-floor bryophyte assemblages in temperate mixed forests (2009, background): “For epiphytic species the presence of large trees is favourable, because of the increase in the number of microhabitats (McGee and Kimmerer 2002), the changes in bark structure (Gustaffson and Eriksson 1995) and elongation in colonization time (Snall et al. 2003; Löbel et al. 2006).”
Bryophytes in a changing landscape: The hierarchical effects of habitat fragmentation on ecological and evolutionary processes (2007, background): “Snail et al. (2003) found that while dispersal distance between aspen trees was important in explaining recent colonisations of Orthotrichum, it was not quite as important as the sum of the local effects, with shading being particularly influential.”
Colonization-extinction dynamics of an epiphyte metapopulation in a dynamic landscape (2005, methodology): “In many other species, even the short-term extinction rate is potentially determined by patch destruction (Snäll et al. 2003).”
Species richness patterns and metapopulation processes – evidence from epiphyte communities in boreo‐nemoral forests (2006, methodology): “The ''neutral'' perspective, highlighting the importance of stochastic metapopulation processes for community species richness, may be of relatively little importance in the epiphyte community (e.g. Snäll et al. 2003).”
Colonization and extinction patterns of wood‐decaying fungi in a boreal old‐growth Picea abies forest (2008, methodology): “The parameter α should not be considered as an actual average dispersal distance, but can be used when biological estimates of dispersal patterns are lacking (Hanski, 1999; Snäll et al. 2003, 2005a; Oksanen 2004).”
The influence of tree age and microhabitat quality on the occurrence of crustose lichens associated with old oaks (2008, background): “This is because at least three different interrelated factors are involved (cf. Snäll et al. 2003; Kantvilas & Jarman 2004; Johansson et al. 2007).”
The effect of stand structure and tree species composition on epiphytic bryophytes in mixed deciduous-coniferous forests of Western Hungary (2010, background): “It is supposed that dispersal limitation of the species influences their spatial distribution in the studied region less than in more fragmented landscapes of Western and Northern Europe (Löbel et al., 2006; Snäll et al., 2003, 2004; Rose, 1992).”