Soil pathogens and spatial patterns of seedling mortality in a temperate tree
By A. Packer, K. Clay. Nature, 2000
905 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/b81bf42338648ccc72a7dd1ebda8730c7ad473dd
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
- W. H. van der Putten
- R. Callaway
- R. Bardgett
- David A. Wardle
- Petr Pyšek
- James D. Bever
- T. Martijn Bezemer
- A. Kulmatiski
In Nature and Landscape Conservation
- W. H. van der Putten
- R. Callaway
- David A. Wardle
- Stephen P. Hubbell
- Petr Pyšek
- R. Bardgett
- H. Muller‐Landau
- L. Gómez‐Aparicio
In Plant Science
- W. H. van der Putten
- R. Callaway
- A. Kulmatiski
- T. Martijn Bezemer
- James D. Bever
- J. Klironomos
- Kurt O. Reinhart
- R. Bardgett
Citations in the corpus
- Mycorrhizas in changing ecosystems1,2 (2014, background): “temperate arbuscular mycorrhizal tree species, shows negative feedback (Packer and Clay 2000).”
- Soil invertebrate fauna enhances grassland succession and diversity (2003, background): “More recently, symbiotic and pathogenic soil microbes have been shown to exert a profound effect on the composition of vegetatio”
- Invasive plants and their escape from root herbivory: a worldwide comparison of the root-feeding nematode communities of the dune grass Ammophila arenaria in natural and introduced ranges (2005, background): “…that soil pathogens and root herbivores play important roles in controlling plant abundance (Klironomos 2002), plant species diversity (Bever 1994; Packer and Clay 2000, 2002; De Deyn et al. 2003), and vegetation succession (Brown and Gange 1992; van der Putten et al. 1993; De Deyn et al. 2003).”
- Trophic control of grassland production and biomass by pathogens (2003, background): “…and community ecology (Burdon 1987; Dobson & Crawley 1994; Castello et al. 1995; Jarosz & Davelos 1995; Peters & Shaw 1996; Hansen & Goheen 2000; Packer & Clay 2000; Klironomos 2002; Strengbom et al. 2002), they have generally been viewed as being outside of the central framework of ecosystem…”
- When do Localized Natural Enemies Increase Species Richness (2005, background): “Hubbell et al. (2001) found strong reductions in survival of trees and saplings when conspecific density was high within 10 m. Large effects have also been reported in seedlings (Webb & Peart 1999; Packer & Clay 2000; HilleRisLambers et al. 2002), and have been shown to increase diversity during t”
- Crop rotational diversity increases disease suppressive capacity of soil microbiomes (2018, background): “Abiotic factors (e.g., salt, moisture, nutrients) can limit the strength and alter the direction of plant–soil feedbacks (Bever et al. 1997, Mills and Bever 1998, Packer and Clay 2000, Kulmatiski et al. 2008, Mavrodi et al. 2012).”
- Negative plant-soil feedback and species coexistence (2005, background): “including seed germination (Rice 1984, Li and Romane 1997), seedling survival (Packer and Clay 2000), individual growth (Miller 1996), vegetative propagation (Van der Putten et al.”
- Resilience of forests to pathogens: An evolutionary ecology perspective (2015, background): “Thus, the pathogen pressure generated by an infected mature tree, whose own seed production is not affected, may be sufficient to prevent regeneration of seedlings in its immediate vicinity (Augspurger and Kelly, 1984; Packer and Clay, 2000).”
- Plant diversity in tropical forests: a review of mechanisms of species coexistence (2017, background): “Insects and the few microbial pathogens studied to date do, however, act in a manner consistent with the Janzen-Connell hypothesis (Augspurger 1984; Gilbert et al. 1994; Gilbert and DeSteven 1996; Packer and Clay 2000).”
- Mutualisms with the wreckage of an avifauna: the status of bird pollination and fruit- dispersal in New Zealand (2010, positive): “We collated all available field data on pollen limitation in ornithophilous-flowered native plants in New Zealand, excluding data from bird sanctuaries, based on the summary in Robertson et al. (2008) but with the following changes.”
- Soil feedback and pathogen activity in Prunus serotina throughout its native range (2005, background): “To test the effect of soil-borne oomycetes on the survival of Prunus serotina seedlings in the field, recently germinated seeds were transplanted near P. serotina or non-Prunus spp. (n = 3–4 trees population−1) in Blm on 28–29 April 2004 (n = 3 populations), in Indiana Dunes National Lakeshore (IDNL”
- Seed dispersal patterns produced by white‐faced monkeys: implications for the dispersal limitation of neotropical tree species (2003, background): “1998; Packer & Clay 2000), seed predators (Howe & Primack 1975; Janzen et al .”
- Microhabitats shift rank in suitability for seedling establishment depending on habitat type and climate (2005, background): “Ecological Society, Journal of Ecology 93 , 1194‐1202 2002), seed arrival (Dalling et al . 2002; Russo & Augspurger 2004), herbivory (Ostfeld & Canham 1993; Gomez et al . 2003), pathogens (Augspurger 1983; Packer & Clay 2000 ) and competition with herbs (De Steven 1991).”
- How mycorrhizal associations drive plant population and community biology (2020, background): “Negative density dependence may arise not only from intraspecific competition but also from species-specific pathogens under their preferred hosts (5, 54, 55).”