LOCAL SPECIALIZATION AND LANDSCAPE-LEVEL INFLUENCE ON HOST USE IN AN HERBIVOROUS INSECT
By M. Kuussaari, M. Singer, Ilkka Hanski. 2000
146 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/014e797b061233994d0378d3a2a830be32de1efc
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In Ecology, Evolution, Behavior and Systematics
- T. Tscharntke
- I. Steffan‐Dewenter
- Carsten Thies
- R. Brandl
- A. Kruess
- Alexandra-Maria Klein
- M. Saastamoinen
- A. Battisti
In Nature and Landscape Conservation
- T. Tscharntke
- I. Steffan‐Dewenter
- Carsten Thies
- R. Brandl
- M. Saastamoinen
- M. Nieminen
- Ilkka Hanski
- A. Kruess
In Plant Science
- T. Tscharntke
- I. Steffan‐Dewenter
- R. Brandl
- Carsten Thies
- M. Saastamoinen
- Ilkka Hanski
- N. Wahlberg
- S. Larsson
Citations in the corpus
- Insect communities and biotic interactions on fragmented calcareous grasslands - a mini review (2002, background): “Life history traits such as oviposition preference may change as an evolutionary consequence of increased habitat fragmentation (Mopper and Strauss, 1998; Thomas et al., 1998; Kuussaari et al., 2000).”
- The effects of Pleistocene glaciations on the phylogeography of Melitaea cinxia (Lepidoptera: Nymphalidae) (2007, background): “In contrast to the highly mobile Aglais urticae (Vandewoestijne et al., 2004), this variation is shown to have a strong phylogeographic signal, consistent with short-range dispersal (Hanski et al., 1994; Hanski, 1999) and host plant specificity (Kuussaari et al., 2000) in M. cinxia.”
- Life‐history, genotypic, and environmental correlates of clutch size in the Glanville fritillary butterfly (2007, methodology): “In these species, larvae typically live gregariously at least during the early larval instars and in some cases until pupation ( Fitzgerald, 1993; Kuussaari et al. , 2004 ).”
- Host‐plant use in the range expansion of the pine processionary moth, Thaumetopoea pityocampa (2006, background): “…by females (e.g. Larsson & Ekbom, 1995 ), or additional factors, such as adult performance (e.g. Scheirs et al ., 2000 ), host plant abundance (e.g. Kuussaari et al ., 2000 ), habitat suitability (e.g. Rausher, 1979 ), sequestration of secondary metabolites (e.g. Björkman et al ., 1997 ), and…”
- Population history and life history influence the migration rate of female Glanville fritillary butterflies (2002, methodology): “Females in source region 1 in A land (Eckero ¨ ) also prefer Veronica to Plantago but much less strongly so than do the Estonian females ( Kuussaari et al. 2000 ).”
- Characteristics of insect populations on habitat fragments: A mini review (2002, background): “Spatial variation in heritable traits of plant and insect populations may further shape regionally specific plant-insect assemblages (Mopper & Strauss 1998; Kuussaari et al. 2000; Thomas et al. 2001).”
- Plant-insect interactions in fragmented landscapes. (2004, background): “Trophic interactions will also dramatically change over the geographic range of a species for a wealth of reasons, including genetic changes in plant and insect traits, in insect responses to plant resources, and in complex interactions between plant resistance and insect virulence (9, 25, 93).”