DISPERSAL LIMITATION AND PATCH OCCUPANCY IN FOREST HERBS

By J. Ehrlén, O. Eriksson. 2000

424 citations recorded by the source corpus.

Subfields: Ecology, Evolution, Behavior and Systematics, Nature and Landscape Conservation, Plant Science

View Paper: https://www.semanticscholar.org/paper/a95df751a11181d7c4cb4bef058386ada315e9b3

How researchers see this paper

The researchers whose trusted networks rank it highest, strongest advocate first. Every researcher gets a different order.

In Ecology, Evolution, Behavior and Systematics

1. Z. Münzbergová
2. Martin Hermy
3. A. Helm
4. K. Verheyen
5. M. Diekmann
6. M. Pärtel
7. A. Kolb
8. I. Kühn

In Nature and Landscape Conservation

1. Z. Münzbergová
2. Martin Hermy
3. A. Helm
4. K. Verheyen
5. M. Pärtel
6. Risto Heikkinen
7. I. Kühn
8. A. Kolb

In Plant Science

1. Z. Münzbergová
2. Martin Hermy
3. A. Kolb
4. K. Verheyen
5. M. Diekmann
6. I. Kühn
7. A. Helm
8. M. Pärtel

Citations in the corpus

• Identification of suitable unoccupied habitats in metapopulation studies using co-occurrence of species (2004, methodology): “Measuring all of them is very laborious and time consuming so suitability estimation using this approach is of limited use (Ehrlén and Eriksson 2000).”
• Context and connectivity in plant metapopulations and landscape mosaics: does the matrix matter? (2004, background): “Assessment of ‘empty’ but suitable patches is even more difficult, and there are still only a few studies that have used experiments to estimate occupancy in plants (Ehrlén and Eriksson 2000).”
• Long‐term assessment of seed limitation in plants: results from an 11‐year experiment (2006, methodology): “In a previous 3-year study (Ehrlén & Eriksson 2000), we performed seed-sowing experiments at 48 different patches and showed that the availability of seeds was limiting recruitment in six of seven deciduous forest herbs.”
• Seed predation, not seed dispersal, explains the landscape‐level abundance of an early‐successional plant (2006, background): “Both may also play an important role in the landscape-dependent patterns of plant establishment that have been repeatedly noted (e.g. Quintana-Ascencio & Menges 1996; Ehrlén & Eriksson 2000; Dupré & Ehrlén 2002).”
• Life‐history traits are correlated with geographical distribution patterns of western European forest herb species (2007, background): “Nevertheless, considerable evidence indicates that many plant species are dispersal-limited at local to regional scales (Primack & Miao, 1992; Ehrlén & Eriksson, 2000; Jakobsson & Eriksson, 2000; Turnbull et al., 2000; Ozinga et al., 2005), and studies investigating the colonization of…”
• Low recruitment across life stages partly accounts for the slow colonization of forest herbs (2009, background): “If seed sowing in previously unoccupied sites results in successful seedling emergence, one can conclude that the site is actually suitable for recruitment and the absence of the sown species can be attributed to seed limitation (Ehrlén & Eriksson 2000).”
• History or abiotic filter: which is more important in determining the species composition of calcareous grasslands? (2009, background): “The absence of ancient forest indicators in recent forests is attributed to either their dispersal limitation (Ehrlén & Eriksson 2000, Graae & Sunde 2000) or the lack of dispersal processes in the current landscape (Poschlod & Bonn 1998).”
• Understory succession in post-agricultural oak forests: Habitat fragmentation affects forest specialists and generalists differently (2011, background): “Generally, the development of understory diversity and composition in new plantations is controlled by a combination of niche-based processes at local scale, and dispersal-based processes operating at both local and landscape scale (Ehrlén and Eriksson, 2000; Ozinga et al., 2005).”
• Can plantations develop understory biological and physical attributes of naturally regenerated forests (2008, background): “Dispersal is known to limit the establishment of many forest herbs, especially those with short distance dispersal such as spring-flowering herbs that are dispersed by ants (Ehrlen and Eriksson, 2000; Flinn and Vellend, 2005).”
• Habitat configuration, species traits and plant distributions (2002, background): “1996; Tilman 1997; Ehrlén & Eriksson 2000; Turnbull et al .”
• Long‐term spatial dynamics of Succisa pratensis in a changing rural landscape: linking dynamical modelling with historical maps (2006, neutral): “Many species are dispersal-limited (e.g. Primack & Miao 1992; Eriksson 1998; Ehrlén & Eriksson 2000; Turnbull et al .”