2014
DOI: 10.15287/afr.2014.173
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Nestedness in bipartite networks of Thuja plicata, Prunus laurocerasus and Buxus sempervirens and their pathogens

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Cited by 5 publications
(6 citation statements)
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“…Few studies of T. plicata are concerned with fungi communities (Weber et al 2005;Lim et al 2007;Fodor and Hâruta 2014;Adnan et al 2018). Our analyses are the first research in Poland concerned with the communities of soil fungi associated with the western red cedar growing in forests; however, other fungi colonising the trees of this species have been checked (Dominik and Grzywacz 1998;Damszel et al 2020).…”
Section: Discussionmentioning
confidence: 99%
“…Few studies of T. plicata are concerned with fungi communities (Weber et al 2005;Lim et al 2007;Fodor and Hâruta 2014;Adnan et al 2018). Our analyses are the first research in Poland concerned with the communities of soil fungi associated with the western red cedar growing in forests; however, other fungi colonising the trees of this species have been checked (Dominik and Grzywacz 1998;Damszel et al 2020).…”
Section: Discussionmentioning
confidence: 99%
“…Interactions with both lower and higher trophic levels can have a profound impact on species niches (Fodor 2011, Arribas et al 2018). We found that variation in tree autumn phenology did not affect either of the powdery mildew species, indicating that the timing of leaf senescence is not important for the successful production and overwintering of chasmothecia.…”
Section: Discussionmentioning
confidence: 99%
“…This is a clear knowledge gap, since hyperparasites can reduce pathogen population growth, reproduction and overwintering success (Kiss et al 2004, Tollenaere et al 2014, Sun et al 2019, Zewdie et al 2021). Cryptic species may differ in hyperparasitism rates, for example due to differences in susceptibility to the hyperparasite, and this may allow for the co‐existence of fungal pathogens (Fodor 2011, van Hoesel et al 2020). Importantly, climate may not only affect the distribution of cryptic pathogen species directly, but also indirectly by shaping the distribution of their hyperparasite (Álvarez‐Loayza et al 2011, Wisz et al 2013).…”
Section: Introductionmentioning
confidence: 99%
“…These functional bipartite networks are a paleoecological counterpart, or analog, to the taxonomically based plant–insect interaction networks commonly found in the modern ecological literature (Table 1; major differences between taxonomic vs. functional bipartite networks). Examples from the modern literature include undirected network associations between woody perennial species and their pathogens, specialization in plant‐host–gall interactions, and the preference of insects for particular fern hosts (Araújo & Kollár, 2019; Fodor & Hâruṭa, 2014; Fuentes‐Jacques et al, 2021). However, for fossil data, one of these node classes, the DTs functionally serve as ecological units that have links to plant taxa and would incorporate data such as one herbivore species producing multiple DTs and multiple herbivore species producing one DT, the multidamagers and monodamagers of Carvalho et al (2014).…”
Section: Introductionmentioning
confidence: 99%