Predictability of plant and fungal species richness of old‐growth boreal forest islands

By H. Berglund, B. Jonsson. 2001

109 citations recorded by the source corpus.

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

View Paper: https://www.semanticscholar.org/paper/94f4bf84a6780efb6fe43fb9b05a0e433a9d69c9

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In Ecology, Evolution, Behavior and Systematics

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Citations in the corpus

Influence of habitat quantity, quality and isolation on the distribution and abundance of two epiphytic lichens (2003, background): “A few recent studies have examined the influence of patch size, quality and isolation on lichen species incidence, abundance, richness or composition (Kruys & Jonsson 1997; Peck & McCune 1997; Dettki & Esseen 1998; Berglund & Jonsson 2001; Gu et al .”
Specialist species of wood‐inhabiting fungi struggle while generalists thrive in fragmented boreal forests (2013, background): “…respond to fragmentation, as species richness and the occurrence of particular species have been shown to vary with forest patch isolation and size (Berglund & Jonsson 2001; Penttil€a et al. 2006; Laaksonen et al. 2008; Berglund, O’Hara & Jonsson 2009), the latter at least partly due to edge…”
Cryptogam communities on decaying deciduous wood – does tree species diversity matter? (2005, background): “On a coarser scale, Ohlson et al. (1997), Jonsson and Jonsell (1999), Berglund and Jonsson (2001) and Berg et al. (2002) found discrepancies in richness patterns among bryophytes and fungi in various nemoral and boreal forest communities.”
Wood-inhabiting macrofungi in Danish beech-forests – conflicting diversity patterns and their implications in a conservation perspective (2005, unknown): “Even in natural forests cwd amounts have been shown to be a very good predictor of fungal species richness using this approach (Ohlson et al., 1997; Berglund and Jonsson, 2001).”
Factors Influencing Bryophyte Assemblage at Different Scales in the Western Canadian Boreal Forest (2005, background): “…variation may be linked to habitat variables including microsite availability (Frisvoll & Prestø 1997; Rambo & Muir 1998); stand structure (Berglund & Jonsson 2001; Håkan & Jonsson 2001); stand integrity (time since last disturbance; Økland 2000); stand fertility (Pitkänen 2000); and…”
Wood-decaying fungi in the forest: conservation needs and management options (2007, background): “groups, whenever possible not merely involving a single functional group, but reXecting the requirements of diVerent organisms (Jonsson and Jonsell 1999; Berglund and Jonsson 2001; Roberge and Angelstam 2004; Similä et al. 2006).”
Co-variation and indicators of species diversity: Can richness of forest-dwelling species be predicted in northern boreal forests? (2006, background): “…Kerr, 1997; Prendergast and Eversham, 1997; van Jaarsveld et al., 1998; Myers et al., 2000; Summerville et al., 2004; Schmit et al., 2005) but less often in small-scale (Howard et al., 1998; Jonsson and Jonsell, 1999; Pharo et al., 1999; Berglund and Jonsson, 2001; Ranius, 2002; Kati et al., 2004).”
Consequences of forest fragmentation for polyporous fungi at two spatial scales (2006, result): “In agreement with this, the studies of Berglund and Jonsson (2005) from northern Sweden show that in recently isolated woodland key habitats there seems to be a delay in the loss of species richness of polypores and red-listed polypore and epiphytic lichen species when compared to old isolates.”
Diversity of dead wood inhabiting fungi and bryophytes in semi-natural beech forests in Europe (2006, background): “Jonsson and Jonsell (1999) and Berglund and Jonsson (2001) found that species richness of bryophytes (including also non saproxylic species) and wood inhabiting fungi was generally weakly correlated in old growth spruce forests.”
Diversity and fruiting patterns of ectomycorrhizal and saprobic fungi in an old-growth Mediterranean forest dominated by Quercus ilex L. (2004, background): “Superimposed on this complex structure, old-growth forests also harbour a high diversity of interacting plants, animals , and fungi (Berglund and Jonsson 2001).”
Species richness patterns and metapopulation processes – evidence from epiphyte communities in boreo‐nemoral forests (2006, result): “This is supported by several other studies from boreal and boreo-nemoral forests: Berglund and Jonsson (2001) found correlations of species richness only among a few plant and fungal species groups.”
Verifying an Extinction Debt among Lichens and Fungi in Northern Swedish Boreal Forests (2005, background): “The flora of cryptogams was often diverse, however, with a large number of rare and threatened species (Berglund & Jonsson 2001).”