Symbiotic germination and development of the myco‐heterotrophic orchid Neottia nidus‐avis in nature and its requirement for locally distributed Sebacina spp.

By SL Mckendrick, J. Leake, D. Taylor, D. Read. 2002

229 citations recorded by the source corpus.

Subfields: Cell Biology, Ecology, Evolution, Behavior and Systematics

View Paper: https://www.semanticscholar.org/paper/f273f79c20cf343cdadf790584d1ed802f7b152b

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Citations in the corpus

Isolation and identification of mycorrhizal fungi associating with an achlorophyllous plant, Epipogium roseum (Orchidaceae) (2005, background): “(Taylor and Bruns 1997, 1999), Therepholaceae with Cepharanthera austinae (Taylor and Bruns 1997), and Sebacinaceae with both Neottia nidus-avis ( McKendrick et al. 2002 ) and Hexalectris spicata (Taylor et al. 2003).”
Spatial variation in below‐ground seed germination and divergent mycorrhizal associations correlate with spatial segregation of three co‐occurring orchid species (2012, background): “…seed germination often significantly declines with increasing distance from existing individuals (McKendrick, Leake & Read 2000; Batty et al. 2001; McKendrick et al. 2002; Diez 2007), which suggests that the local availability and abundance of suitable mycorrhizal fungi decline with increasing…”
Hierarchical patterns of symbiotic orchid germination linked to adult proximity and environmental gradients (2007, unknown): “Although some studies have suggested a positive association between germination and adult locations for myco-heterotrophic orchids (McKendrick et al. 2000, 2002; Leake et al. 2004), and one study with photosynthetic orchids (Batty et al. 2001), others have found no relationship between protocorm…”
Exploring structural definitions of mycorrhizas, with emphasis on nutrient-exchange interfaces (2004, background): “For example, the successful colonization of germinating seeds of Neottia nidus-avis in nature is dependent on a specific Sebacina-like fungus (McKendrick et al. 2002).”
Biological Flora of the British Isles: Fagus sylvatica (2012, background): “In the UK, Neottia nidus-avis requires the presence of the fungus Sebacina dimitica for germination and growth, which appears to persist in mycorrhizal association with F. sylvatica (McKendrick et al. 2002).”
Do mycorrhizal symbioses cause rarity in orchids? (2011, background): “Alternatively, other orchids use a small range of fungi at one site but are capable of switching to different fungi in other parts of their distribution (McKendrick et al. 2002; Martos et al. 2009).”
Variation in mycorrhizal performance in the epiphytic orchid Tolumnia variegata in vitro: the potential for natural selection (2004, background): “Recent molecular evidence suggests that orchid mycorrhizal specificity is common, although there is considerable variation (Taylor et al., 2002; McKendrick et al., 2002; Selosse et al., 2003; Otero et al., 2002, 2004).”
Asymbiotic and symbiotic seed germination of Eulophia alta (Orchidaceae)—preliminary evidence for the symbiotic culture advantage (2007, background): “This type of preference is not uncommon in the Orchidaceae and can be genus, species, or site specific (McCormick et al. 2006; McKendrick et al. 2002; Stewart and Kane 2006b, 2007; Taylor and Bruns 1997).”
Terrestrial orchid conservation in the age of extinction. (2009, background): “Fungal isolations can also be made from developing protocorms and seedlings to determine endophyte diversity and specificity (McKendrick et al., 2002; Taylor and Bruns, 2003).”
Microbial Endophytes of Orchid Roots (2006, methodology): “It has also been used on Dactylorhiza in Denmark (Kristiansen et al. 2001) and Neottia in the United Kingdom, Germany ( McKendrick et al. 2002 ) and in France (Selosse et al. 2002).”
Variation in sexual reproduction in orchids and its evolutionary consequences: a spasmodic journey to diversification (2004, background): “…by guest on 28 July 2018 © 2005 The Linnean Society of London, Biological Journal of the Linnean Society, 2005, 84, 1–54 fungal associations for germination and seedling establishment (Batty et al., 2001; McKendrick et al., 2002; Rasmussen & Whigham, 2002; Selosse et al., 2002).”
The evolutionary ecology of vegetative dormancy in mature herbaceous perennial plants (2009, background): “1), which includes non-photosynthetic, myco-heterotrophic species such as Cephalanthera austinae (Taylor & Bruns 1997) and Neottia nidus-avis (McKendrick et al. 2002), as well as many photosynthetic species in which occasional nonphotosynthetic ‘mutants’ arise (Abadie et al. 2006).”
Networks of power and influence: the role of mycorrhizal mycelium in controlling plant communities and agroecosystem functioning (2004, background): “Many orchids switch from associations with soil saprotrophs and pathogens, such as fungi in the form genus Rhizoctonia, to associate with EM fungi (Taylor et al. 2002; McKendrick et al. 2002) that are better able to supply large amounts of C over long periods of time.”