Nitrogen fertilization alters the functioning of arbuscular mycorrhizas at two semiarid grasslands

By L. Corkidi, D. Rowland, N. Johnson, E. Allen. Plant and Soil, 2002

164 citations recorded by the source corpus.

Subfields: Nature and Landscape Conservation, Plant Science, Soil Science

View Paper: https://www.semanticscholar.org/paper/e1d1b5a116fe0550d21390c4c3120c4fc5074178

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Citations in the corpus

Nitrogen enrichment alters mycorrhizal allocation at five mesic to semiarid grasslands (2003, background): “…experiments indicate that N enrichment diminishes the mutualistic functioning of communities of AM fungi at Sevilleta and Shortgrass Steppe (Corkidi et al. 2002), at Cedar Creek (Johnson 1993), and at Kellogg (N. C. Johnson, D. L. Rowland, L. Corkidi, and E. B. Allen, unpublished…”
Mycorrhiza : state of the art, genetics and molecular biology, eco-function, biotechnology, eco-physiology, structure and systematics (2008, background): “Corkidi et al. (2002) observed that enrichment with N consistently decreased root colonization by AM fungi in grasses grown in soils with high P availability, but not when they were grown under conditions of limited P availability.”
Increased N availability in grassland soils modifies their microbial communities and decreases the abundance of arbuscular mycorrhizal fungi (2006, background): “Further, changes in the soil community are very likely to influence interspecific interactions of the existing plant community (Johnson, 1993; Corkidi et al., 2002; Johnson et al., 2003a; Gustafson and Casper, 2004), and may ultimately alter its composition, productivity and/or diversity.”
Native arbuscular mycorrhizal fungal communities differentially influence the seedling performance of rare and common Pulsatilla species (2004, unknown): “The only exceptions known to us are pot experiments showing differential plant growth in the presence of natural soil or root inocula of different origin (Johnson 1993; Kiers et al . 2000; Corkidi et al . 2002; Frank et al . 2003).”
Mycorrhizal mediation of plant N acquisition and residue decomposition: Impact of mineral N inputs (2006, background): “Some studies have shown that increased N inputs negatively impact AM fungi by suppressing their abundance and functioning (Buwalda & Goh, 1982; Egerton-Warburton & Allen, 2000; Corkidi et al., 2002).”
Where, when and how plant-soil feedback matters in a changing world (2016, background): “…nutrient availabilities suggest that the outcomes are likely to be strongly species specific and depending on the proportional levels of various nutrients, changing individual plant performance and consequently community composition (Corkidi et al. 2002; Manning et al. 2008; Larios & Suding 2015).”
MYCORRHIZAL COMMUNITY DYNAMICS FOLLOWING NITROGEN FERTILIZATION: A CROSS‐SITE TEST IN FIVE GRASSLANDS (2007, background): “It follows that any changes in AMF community composition with N enrichment could have significant consequences for plant community function (Johnson 1993, Corkidi et al. 2002, Johnson et al. 2003).”
Effect of long-term nitrogen fertilization on mycorrhizal fungi associated with a dominant grass in a semiarid grassland (2007, methodology): “But at the SNWR study site, Corkidi et al. (2002) and Johnson et al. (2003) reported no significant differences in the percentage of root length colonized by AMF in N fertilized plants with respect to control plants.”
Responses of extracellular enzyme activities and microbial community in both the rhizosphere and bulk soil to long-term fertilization practices in a fluvo-aquic soil (2012, background): “…in increased or altered fungal populations (Bastida et al., 2007; Elfstrand et al., 2007), altered populations of arbuscular mycorrhizal fungi (Corkidi et al., 2002), shifts in Gram-positive and Gram-negative bacteria (Marschner, 2003; Peacock et al., 2001), and increased fungi/bacteria…”
Root-colonizing and soil-borne communities of arbuscular mycorrhizal fungi in a temperate forest understorey1 (2014, background): “1998; Klironomos 2003; Pringle and Bever 2008) and communities (Corkidi et al. 2002; Moora et al. 2004; Johnson et al. 2008; Uibopuu et al. 2009; Martinez and Johnson 2010; Williams et al. 2011; Uibopuu et al. 2012) can have differential effects on plant species growth and performance.”
Six-year fertilization modifies the biodiversity of arbuscular mycorrhizal fungi in a temperate steppe in Inner Mongolia (2014, background): “Similarly, Corkidi et al. (2002) and Johnson et al.”
A general suite of fungal endophytes dominate the roots of two dominant grasses in a semiarid grassland (2010, background): “Most research on plant-fungal interactions has focused on AMF because of the ubiquity of their symbiotic associations (Smith and Read, 1997; Treseder, 2004; van der Heijden, 2004).”
Translocation of nitrogen and carbon integrates biotic crust and grass production in desert grassland (2008, background): “The vegetation of semi-arid grassland is dominated by C 4 perennial grasses that grow in association with arbuscular mycorrhizal fungi (AMF) (Corkidi et al. 2002; Johnson et al. 2003) and other diverse fungi that are variously characterized as dark-septate endophytes, saprophytes and facultative…”
Impact of Land Use Intensity on the Species Diversity of Arbuscular Mycorrhizal Fungi in Agroecosystems of Central Europe (2003, background): “In this context, it is interesting that AMF derived from high-input agroecosystems have repeatedly been shown to be less efficient in plant growth promotion than those derived from low-input systems (10, 25, 26, 48).”
Relationships among arbuscular mycorrhizal fungi, vascular plants and environmental conditions in oak savannas (2004, background): “light, moisture, phosphorus (P) and nitrogen (N) supplies) would also affect plant and AMF communities, both directly and indirectly (Givnish, 1986; Tilman, 1988; Johnson (1992); Smith & Read, 1997; Clark & Zeto, 2000; Corkidi et al ., 2002; Facelli & Facelli, 2002; Miller et al ., 2002; Bauer et ”