Register      Login
Australian Journal of Botany Australian Journal of Botany Society
Southern hemisphere botanical ecosystems
RESEARCH ARTICLE

Consequences of season of prescribed burning on two spring-flowering terrestrial orchids and their endophytic fungi

N. U. Jasinge A , T. Huynh A B and A. C. Lawrie A
+ Author Affiliations
- Author Affiliations

A ASchool of Science, RMIT University (Bundoora West Campus), PO Box 71, Bundoora, Vic. 3083, Australia.

B BCorresponding author. Email: tien.huynh@rmit.edu.au

Australian Journal of Botany 66(4) 298-312 https://doi.org/10.1071/BT17179
Submitted: 24 September 2017  Accepted: 17 May 2018   Published: 10 July 2018

Abstract

Prescribed burning is mandated in seasonally dry regions of the world to reduce fuel load and fire risk. This study investigated the effects of prescribed burning at different seasons on two Australian terrestrial orchids (Glossodia major R.Br. and Thelymitra pauciflora R.Br.) and their orchid mycorrhizal fungi (OMF) to find the least damaging season for a burn. Burns were conducted mid-season in autumn, winter, spring and summer. Orchids were enumerated and measured and their OMF isolated during their flowering seasons. The OMF were grouped and identified using their internal transcribed spacer (ITS) regions and tested for sensitivity to smoke water. Orchid numbers decreased by up to 100% after autumn and winter burns but not spring and summer burns. Plant height, leaf and flower dimensions decreased between the two years. Fire reduced success in the isolation of OMF. The relative frequencies of ITS sequences of Serendipita Roberts from G. major (but not of Tulasnella asymmetrica Warcup and P.H.B. Talbot from Th. pauciflora) changed after burns. OMF from G. major were up to 100% inhibited by smoke water, twice the inhibition of the OMF from Th. pauciflora. Prescribed burning during active orchid growth damaged both the orchids and their OMF. The least damaging practical season for a prescribed burn was in late spring, soon after seed dispersal.

Additional keywords: fire, fungus, mycorrhiza, orchid, season, smoke, symbiosis.


References

Australian Government Bureau of Meteorology (2017) Climate data online. Available at http://www.bom.gov.au/climate/data. [Verified 19 September 2017]

Australian Government Department of the Environment and Energy (2018) Species profile and threats database. Available at http://www.environment.gov.au/cgi-bin/sprat/public/publicthreatenedlist.pl?wanted=flora. [Verified 21 February 2018]

Baar J, Horton TR, Kretzer A, Bruns TD (1999) Mycorrhizal colonization of Pinus muricata from resistant propagules after a stand‐replacing wildfire. New Phytologist 143, 409–418.
Mycorrhizal colonization of Pinus muricata from resistant propagules after a stand‐replacing wildfire.Crossref | GoogleScholarGoogle Scholar |

Bååth E, Frostegard Å, Pennanen T, Fritze H (1995) Microbial community structure and pH response in relation to soil organic matter quality in wood-ash fertilized, clear-cut or burned coniferous forest soils. Soil Biology & Biochemistry 27, 229–240.
Microbial community structure and pH response in relation to soil organic matter quality in wood-ash fertilized, clear-cut or burned coniferous forest soils.Crossref | GoogleScholarGoogle Scholar |

Backhouse G, Cameron D (2005) Application of the IUCN 2001 Red List categories for determining the conservation status of the native orchids of Victoria, Australia. Selbyana 26, 58–74.

Backhouse GN, Jeanes J (1995) ‘Orchids of Victoria.’ (The Miegunyah Press at Melbourne University Press: Carlton, Vic., Australia)

Basiewicz M, Weiß M, Kogel KH, Langen G, Zorn H, Zuccaro A (2012) Molecular and phenotypic characterization of Sebacina vermifera strains associated with orchids, and the description of Piriformopora williamsii sp. nov. Fungal Biology 116, 204–213.
Molecular and phenotypic characterization of Sebacina vermifera strains associated with orchids, and the description of Piriformopora williamsii sp. nov.Crossref | GoogleScholarGoogle Scholar |

Batty AL, Dixon KW, Brundrett M, Sivasithamparam K (2001) Constraints to symbiotic germination of terrestrial orchid seed in a Mediterranean bushland. New Phytologist 152, 511–520.
Constraints to symbiotic germination of terrestrial orchid seed in a Mediterranean bushland.Crossref | GoogleScholarGoogle Scholar |

Bergner B, Johnstone J, Treseder KK (2004) Experimental warming and burn severity alter soil CO2 flux and soil functional groups in a recently burned boreal forest. Global Change Biology 10, 1996–2004.
Experimental warming and burn severity alter soil CO2 flux and soil functional groups in a recently burned boreal forest.Crossref | GoogleScholarGoogle Scholar |

Bond WJ, van Wilgen BW (1996) Fire and plants. (Chapman and Hall: London, UK)

Bougoure J, Ludwig M, Brundrett M, Grierson P (2009) Identity and specificity of the fungi forming mycorrhizas with the rare mycoheterotrophic orchid Rhizanthella gardneri. Mycological Research 113, 1097–1106.
Identity and specificity of the fungi forming mycorrhizas with the rare mycoheterotrophic orchid Rhizanthella gardneri.Crossref | GoogleScholarGoogle Scholar |

Buscardo E, Rodriguez-Echeverria S, Freitas H, De Angelis P, Pereira JS, Muller LAH (2015) Contrasting soil fungal communities in Mediterranean pine forests subjected to different wildfire frequencies. Fungal Diversity 70, 85–99.
Contrasting soil fungal communities in Mediterranean pine forests subjected to different wildfire frequencies.Crossref | GoogleScholarGoogle Scholar |

Chumpookam J, Lin HL, Shiesh CC, Ku KL (2012) Effect of smoke water on seed germination and resistance to Rhizoctonia solani inciting papaya damping-off. Horticulture NCHU 37, 13–29.

Ciafardini G, Zullo BA (2003) Antimicrobial activity of oil-mill waste water polyphenols on the phytopathogen Xanthomonas campestris spp. Annals of Microbiology 53, 283–290.

Clements MA, Muir H, Cribb PJ (1986) A preliminary report on the symbiotic germination of European terrestrial orchids. Kew Bulletin 41, 437–445.
A preliminary report on the symbiotic germination of European terrestrial orchids.Crossref | GoogleScholarGoogle Scholar |

Coates F, Duncan M (2009) Demographic variation between populations of Caladenia orientalis – a fire-managed threatened orchid. Australian Journal of Botany 57, 326–339.
Demographic variation between populations of Caladenia orientalis – a fire-managed threatened orchid.Crossref | GoogleScholarGoogle Scholar |

Coates F, Lunt ID, Tremblay RL (2006) Effects of disturbance on population dynamics of the threatened orchid Prasophyllum correctum D.L.Jones and implications for grassland management in south-eastern Australia. Biological Conservation 129, 59–69.
Effects of disturbance on population dynamics of the threatened orchid Prasophyllum correctum D.L.Jones and implications for grassland management in south-eastern Australia.Crossref | GoogleScholarGoogle Scholar |

Cruz D, Suárez JP, Kottke I, Piepenbring M (2014) Cryptic species revealed by molecular phylogenetic analysis of sequences obtained from basidiomata of Tulasnella. Mycologia 106, 708–722.
Cryptic species revealed by molecular phylogenetic analysis of sequences obtained from basidiomata of Tulasnella.Crossref | GoogleScholarGoogle Scholar |

Cruz D, Suárez JP, Piepenbring M (2016) Morphological revision of Tulasnellaceae, with two new species of Tulasnella and new records of Tulasnella spp. for Ecuador. Nova Hedwigia 102, 279–338.
Morphological revision of Tulasnellaceae, with two new species of Tulasnella and new records of Tulasnella spp. for Ecuador.Crossref | GoogleScholarGoogle Scholar |

Davis BJ, Phillips RD, Wright M, Linde CC, Dixon KW (2015) Continent-wide distribution in mycorrhizal fungi: implications for the biogeography of specialized orchids. Annals of Botany 116, 413–421.
Continent-wide distribution in mycorrhizal fungi: implications for the biogeography of specialized orchids.Crossref | GoogleScholarGoogle Scholar |

Dearnaley JDW (2007) Further advances in orchid mycorrhizal research. Mycorrhiza 17, 475–486.
Further advances in orchid mycorrhizal research.Crossref | GoogleScholarGoogle Scholar |

Dearnaley JDW, Martos F, Selosse MA (2012) Orchid mycorrhizas: molecular ecology, physiology, evolution and conservation aspects. In ‘Fungal associations’. (2nd edn) (Ed. B Hock) pp. 207–230. (Springer: Berlin)

DeBano LF, Neary DG, Ffolliott PF (1998) ‘Fire’s effects on ecosystems.’ (John Wiley & Sons: Hoboken, NJ, USA)

DELWP (Department of Environment, Land, Water and Planning Victoria) (2017a) NatureKit (biodiversity interactive map). Available at http://maps.biodiversity.vic.gov.au/viewer/?viewer=NatureKit. [Verified 19 September 2017]

DELWP (Department of Environment, Land, Water and Planning Victoria) (2017b) ‘Forest fire management Victoria: past bushfires 1851–2013. Available at https://www.ffm.vic.gov.au/history-and-incidents/past-bushfires. [Verified 19 September 2017]

Dixon K, Barrett R (2003) Defining the role of fire in south-west Western Australian plants. In ‘Fire in ecosystems of south-west Western Australia: impacts and management’. (Eds I Abbott, N Burrows) pp. 205–223. (Backhuys Publishers: Leiden, The Netherlands)

Duncan M (2012) ‘Response of orchids to bushfire. Black Saturday Victoria 2009. Natural values fire recovery program.’ (Department of Sustainability and Environment: Heidelberg, Vic., Australia)

Dunn PH, Barro SC, Poth M (1985) Soil moisture affects survival of microorganisms in heated chaparral soil. Soil Biology & Biochemistry 17, 143–148.
Soil moisture affects survival of microorganisms in heated chaparral soil.Crossref | GoogleScholarGoogle Scholar |

Fiddler W, Daerr RC, Wasserman AE, Salay JM (1966) Composition of hickory sawdust smoke. Furans and phenols. Journal of Agricultural and Food Chemistry 14, 659–662.
Composition of hickory sawdust smoke. Furans and phenols.Crossref | GoogleScholarGoogle Scholar |

Flematti GR, Ghisalberti EL, Dixon KW, Trengove RD (2004) A compound from smoke that promotes seed germination. Science 305, 977–977.
A compound from smoke that promotes seed germination.Crossref | GoogleScholarGoogle Scholar |

Fuller WH, Shannon S, Burgess PS (1955) Effect of burning on certain forest soils of northern Arizona. Forest Science 1, 44–50.

Gill MA, Groves RH, Noble IR (Eds) (1981) ‘Fire and the Australian biota.’ (Australian Academy of Science: Canberra)

Haines TK, Martinez J, Cleaves DA (1998) Influences on prescribed burning activity in the United States National Forest System. International Forest Fire News 19, 43–46.

Hart SC, DeLuca TH, Newman GS, MacKenzie MD, Boyle SI (2005) Post-fire vegetative dynamics as drivers of microbial community structure and function in forest soils. Forest Ecology and Management 220, 166–184.
Post-fire vegetative dynamics as drivers of microbial community structure and function in forest soils.Crossref | GoogleScholarGoogle Scholar |

Huynh TT, Thomson R, McLean CB, Lawrie AC (2009) Functional and genetic diversity of mycorrhizal fungi from single plants of Caladenia formosa (Orchidaceae). Annals of Botany 104, 757–765.
Functional and genetic diversity of mycorrhizal fungi from single plants of Caladenia formosa (Orchidaceae).Crossref | GoogleScholarGoogle Scholar |

Jain AK, Ravichandran V, Sisodiya M, Agrawal R (2010) Synthesis and antibacterial evaluation of 2–substituted-4,5-diphenyl-N-alkyl imidazole derivatives. Asian Pacific Journal of Tropical Medicine 3, 471–474.
Synthesis and antibacterial evaluation of 2–substituted-4,5-diphenyl-N-alkyl imidazole derivatives.Crossref | GoogleScholarGoogle Scholar |

Jasinge NU, Huynh T, Lawrie AC (2018) Changes in orchid populations and endophytic fungi with rainfall and prescribed burning in Pterostylis revoluta in Victoria, Australia. Annals of Botany 121, 321–334.
Changes in orchid populations and endophytic fungi with rainfall and prescribed burning in Pterostylis revoluta in Victoria, Australia.Crossref | GoogleScholarGoogle Scholar |

Jones DL (2006) ‘A complete guide to native orchids of Australia, including the island territories.’ (Reed New Holland: Sydney, NSW, Australia)

Jones MB, Laude HM (1960) Relationships between sprouting in chamise and the physiological condition of the plant. Journal of Range Management 13, 210–214.
Relationships between sprouting in chamise and the physiological condition of the plant.Crossref | GoogleScholarGoogle Scholar |

Kaarik A (1965) ‘The identification of the mycelia of wood-decay fungi by their oxidation reactions with phenolic compounds. Studia Forestalia Suecica 31.’ (Skogshögskolan: Stockholm)

Keith D (1996) Fire-driven extinction of plant populations: a synthesis of theory and review of evidence from Australian vegetation. Proceedings of the Linnean Society of New South Wales 116, 37–78.

Kéry M, Gregg KB (2004) Demographic analysis of dormancy and survival in the terrestrial orchid Cypripedium reginae. Journal of Ecology 92, 686–695.
Demographic analysis of dormancy and survival in the terrestrial orchid Cypripedium reginae.Crossref | GoogleScholarGoogle Scholar |

Klopatek CC, DeBano LF, Klopatek JM (1988) Effects of simulated fire on vesicular-arbuscular mycorrhizae in pinyon-juniper woodland soil. Plant and Soil 109, 245–249.
Effects of simulated fire on vesicular-arbuscular mycorrhizae in pinyon-juniper woodland soil.Crossref | GoogleScholarGoogle Scholar |

Klopatek CC Freise CF Allen MF Klopatek JM 1994 Comparisons of laboratory and field burning experiments on mycorrhizae distribution, density and diversity. Journal of Forestry 94 762 776

Kohler A, Kuo A, Nagy LG, Morin E, Barry KW, Buscot F, Canbäck B, Choi C, Cichocki N, Clum A, Colpaert J, et al (2015) Convergent losses of decay mechanisms and rapid turnover of symbiosis genes in mycorrhizal mutualists. Nature Genetics 47, 410–415.
Convergent losses of decay mechanisms and rapid turnover of symbiosis genes in mycorrhizal mutualists.Crossref | GoogleScholarGoogle Scholar |

Korb JE, Johnson NC, Covington WW (2003) Arbuscular mycorrhizal propagule densities respond rapidly to ponderosa pine restoration treatments. Journal of Applied Ecology 40, 101–110.
Arbuscular mycorrhizal propagule densities respond rapidly to ponderosa pine restoration treatments.Crossref | GoogleScholarGoogle Scholar |

Kubiak PJ (2009) Some fire responses of bushland plants after the January 1994 wildfires in northern Sydney. Cunninghamia 11, 131–165.

Kuga Y, Sakamoto N, Yurimoto H (2014) Stable isotope cellular imaging reveals that both live and degenerating fungal pelotons transfer carbon and nitrogen to orchid protocorms. New Phytologist 202, 594–605.
Stable isotope cellular imaging reveals that both live and degenerating fungal pelotons transfer carbon and nitrogen to orchid protocorms.Crossref | GoogleScholarGoogle Scholar |

Kumar S, Stecher G, Tamura K (2016) MEGA7: Molecular Evolutionary Genetics Analysis ver. 7.0 for bigger datasets. Molecular Biology and Evolution 33, 1870–1874.
MEGA7: Molecular Evolutionary Genetics Analysis ver. 7.0 for bigger datasets.Crossref | GoogleScholarGoogle Scholar |

Le Maitre DC, Brown PJ (1992) Life cycles and fire-stimulated flowering in geophytes. In ‘Fire in South African mountain fynbos’. (Eds BW van Wilgen, DM Richardson, FJ Kruger, HJ van Hensbergen) pp. 145–160. (Springer: Berlin)

Light ME, Kulkarni MG, Ascough GD, van Staden J (2007) Improved flowering of a South African Watsonia with smoke treatments. South African Journal of Botany 73, 298–298.
Improved flowering of a South African Watsonia with smoke treatments.Crossref | GoogleScholarGoogle Scholar |

Lin H-L, Chumpookam J, Shiesh C-C, Chung W-H (2012) Smoke-water controls Pythium damping-off in papaya seedling. HortScience 47, 1453–1456.

Linde CC, May TW, Phillips RD, Ruibal M, Smith LM, Peakall R (2017) New species of Tulasnella associated with terrestrial orchids in Australia. IMA Fungus 8, 28–48.
New species of Tulasnella associated with terrestrial orchids in Australia.Crossref | GoogleScholarGoogle Scholar |

Linder HP, Kurzweil H (1999) ‘Orchids of southern Africa.’ (AA Balkema: Rotterdam, The Netherlands)

McCormick MK, Taylor DL, Whigham DF, Burnett RK (2016) Germination patterns in three terrestrial orchids relate to abundance of mycorrhizal fungi. Journal of Ecology 104, 744–754.
Germination patterns in three terrestrial orchids relate to abundance of mycorrhizal fungi.Crossref | GoogleScholarGoogle Scholar |

Mehra S, Morrison PD, Coates F, Lawrie AC (2017) Differences in carbon source utilisation by orchid mycorrhizal fungi from common and endangered species of Caladenia (Orchidaceae). Mycorrhiza 27, 95–108.
Differences in carbon source utilisation by orchid mycorrhizal fungi from common and endangered species of Caladenia (Orchidaceae).Crossref | GoogleScholarGoogle Scholar |

Moore RT (1987) The genera of Rhizoctonia-like fungi – Ascorhizoctonia, Ceratorhiza gen. nov., Epulorhiza gen. nov., Moniliopsis, and Rhizoctonia. Mycotaxon 29, 91–99.

Morgan JW (1999) Defining grassland fire events and the response of perennial plants to annual fire in temperate grasslands of south-eastern Australia. Plant Ecology 144, 127–144.
Defining grassland fire events and the response of perennial plants to annual fire in temperate grasslands of south-eastern Australia.Crossref | GoogleScholarGoogle Scholar |

Morrison LW, Haack-Gaynor JL, Young CC, DeBacker MD (2015) A 20-year record of the Western Prairie Fringed Orchid (Platanthera praeclara): population dynamics and modelling of precipitation effects. Natural Areas Journal 35, 246–255.
A 20-year record of the Western Prairie Fringed Orchid (Platanthera praeclara): population dynamics and modelling of precipitation effects.Crossref | GoogleScholarGoogle Scholar |

Muñoz-Roias M, Erickson TE, Martini D, Dixon KW, Merritt DJ (2016) Soil physicochemical and microbiological indicators of short, medium and long term post-fire recovery in semi-arid ecosystems. Ecological Indicators 63, 14–22.
Soil physicochemical and microbiological indicators of short, medium and long term post-fire recovery in semi-arid ecosystems.Crossref | GoogleScholarGoogle Scholar |

Neary DG, Klopatek CC, DeBano LF, Ffolliott PF (1999) Fire effects on belowground sustainability: a review and synthesis. Forest Ecology and Management 122, 51–71.
Fire effects on belowground sustainability: a review and synthesis.Crossref | GoogleScholarGoogle Scholar |

O’Brien HE, Parrent JL, Jackson JA, Moncalvo J-M, Vilgalys R (2005) Fungal community analysis by large-scale sequencing of environmental samples. Applied and Environmental Management 71, 5544–5550.
Fungal community analysis by large-scale sequencing of environmental samples.Crossref | GoogleScholarGoogle Scholar |

Palese AM, Giovannini G, Lucchesi S, Dumontet S, Perucci P (2004) Effect of fire on soil C, N and microbial biomass. Agronomie 24, 47–53.
Effect of fire on soil C, N and microbial biomass.Crossref | GoogleScholarGoogle Scholar |

Parmeter J, Uhrenholdt B (1975) Some effects of pine-needle or grass smoke on fungi. Phytopathology 65, 28–31.
Some effects of pine-needle or grass smoke on fungi.Crossref | GoogleScholarGoogle Scholar |

Peppe DJ, Royer DL, Cariglino B, Oliver SY, Newman S, Leight E, Enikolopov G, Fernandez‐Burgos M, Herrera F, Adams JA, Correa E (2011) Sensitivity of leaf size and shape to climate: global patterns and paleoclimatic applications. New Phytologist 190, 724–739.
Sensitivity of leaf size and shape to climate: global patterns and paleoclimatic applications.Crossref | GoogleScholarGoogle Scholar |

Perkins AJ, Masuhara G, McGee PA (1995) Specificity of the associations between Microtis parviflora (Orchidaceae) and its mycorrhizal fungi. Australian Journal of Botany 43, 85–91.
Specificity of the associations between Microtis parviflora (Orchidaceae) and its mycorrhizal fungi.Crossref | GoogleScholarGoogle Scholar |

Phillips RD, Barrett MD, Dixon KW, Hopper SD (2011) So mycorrhizal symbioses cause rarity in orchids? Journal of Ecology 99, 858–869.
So mycorrhizal symbioses cause rarity in orchids?Crossref | GoogleScholarGoogle Scholar |

Phillips RD, Barrett MD, Dalziell EL, Dixon KW, Swarts ND (2016) Geographical range and host breadth of Sebacina orchid mycorrhizal fungi associating with Caladenia in south-western Australia. Botanical Journal of the Linnean Society 182, 140–151.
Geographical range and host breadth of Sebacina orchid mycorrhizal fungi associating with Caladenia in south-western Australia.Crossref | GoogleScholarGoogle Scholar |

Prendergast-Miller MT, de Menezes AB, Macdonald LM, Toscas P, Bissett A, Baker G, Farrell M, Richardson AE, Wark T, Thrall PH (2017) Wildfire impact: natural experiment reveals differential short-term changes in soil microbial communities. Soil Biology & Biochemistry 109, 1–13.
Wildfire impact: natural experiment reveals differential short-term changes in soil microbial communities.Crossref | GoogleScholarGoogle Scholar |

Quarmby JP (2010) ‘Recovery plan for twelve threatened orchids in the Lofty Block Region of South Australia 2010.’ (Department of Environment and Natural Resources: Adelaide, SA, Australia)

Raison RJ (1979) Modification of the soil environment by vegetation fires, with particular reference to nitrogen transformations - review. Plant and Soil 51, 73–108.
Modification of the soil environment by vegetation fires, with particular reference to nitrogen transformations - review.Crossref | GoogleScholarGoogle Scholar |

Ramsay RR, Dixon KW, Sivasithamparam K (1986) Patterns of infection and endophytes associated with Western Australian orchids. Lindleyana 1, 203–214.

Rasmussen HN (1995) ‘Terrestrial orchids: from seed to mycotrophic plant.’ (Cambridge University Press: Cambridge, UK)

Reddell P, Malajczuk N (1984) Formation of mycorrhizae by jarrah (Eucalyptus marginata Donn ex Smith) in litter and soil. Australian Journal of Botany 32, 511–520.
Formation of mycorrhizae by jarrah (Eucalyptus marginata Donn ex Smith) in litter and soil.Crossref | GoogleScholarGoogle Scholar |

Riess K, Oberwinkler F, Bauer R, Garnica S (2014) Communities of endophytic Sebacinales associated with roots of herbaceous plants in agricultural and grassland ecosystems are dominated by Serendipita herbamans sp. nov. PLoS One 9, e94676
Communities of endophytic Sebacinales associated with roots of herbaceous plants in agricultural and grassland ecosystems are dominated by Serendipita herbamans sp. nov.Crossref | GoogleScholarGoogle Scholar |

Roche SA, Carter RJ, Peakall R, Smith LM, Whitehead MR, Linde CC (2010) A group of monophyletic Tulasnella (Tulasnellaceae) symbiont lineages are associated with multiple species of Chiloglottis (Orchidaceae): implications for orchid diversity. American Journal of Botany 97, 1313–1327.
A group of monophyletic Tulasnella (Tulasnellaceae) symbiont lineages are associated with multiple species of Chiloglottis (Orchidaceae): implications for orchid diversity.Crossref | GoogleScholarGoogle Scholar |

Sanglard D, Ischer F, Monod M, Bille J (1996) Susceptibilities of Candida albicans multidrug transporter mutants to various antifungal agents and other metabolic inhibitors. Antimicrobial Agents and Chemotherapy 40, 2300–2305.

Saravanan V, Santhi R, Kumar P, Kalaiselvi T, Vennila S (2013) Effect of forest fire on microbial diversity of the degraded shola forest ecosystem of Nilgiris Eastern Slope Range. Research Journal of Agriculture and Forestry Sciences 1, 5–8.

Sieg CH, King RM (1995) Influence of environmental factors and preliminary demographic analyses of a threatened orchid, Platanthera praeclara. American Midland Naturalist 134, 307–323.
Influence of environmental factors and preliminary demographic analyses of a threatened orchid, Platanthera praeclara.Crossref | GoogleScholarGoogle Scholar |

Smith SE, Read DJ (2008) ‘Mycorrhizal symbiosis.’ (Academic Press: San Diego, CA, USA)

Smith ZF, James EA, McLean CB (2010) Mycorrhizal specificity of Diuris fragrantissima (Orchidaceae) and persistence in a reintroduced population. Australian Journal of Botany 58, 97–106.
Mycorrhizal specificity of Diuris fragrantissima (Orchidaceae) and persistence in a reintroduced population.Crossref | GoogleScholarGoogle Scholar |

Sommer J, Pausch J, Brundrett MC, Dixon KW, Bidartondo MI, Gebauer G (2012) Limited carbon and mineral nutrient gain from mycorrhizal fungi by adult Australian orchids. American Journal of Botany 99, 1133–1145.
Limited carbon and mineral nutrient gain from mycorrhizal fungi by adult Australian orchids.Crossref | GoogleScholarGoogle Scholar |

Sugihara NG, van Wagtendonk J, Shaffer KE, Fites-Kauffman J, Thode AE, Agee JK (Eds) (2006) ‘Fire in California’s ecosystems.’ (University of California Press: Berkeley, CA, USA)

Sullivan AL, Ellis PF, Knight IK (2003) A review of radiant heat flux models used in bushfire applications. International Journal of Wildland Fire 12, 101–110.
A review of radiant heat flux models used in bushfire applications.Crossref | GoogleScholarGoogle Scholar |

Tamura K, Nei M (1993) Estimation of the number of nucleotide substitutions in the control region of mitochondrial DNA in humans and chimpanzees. Molecular Biology and Evolution 10, 512–526.

Thompson JD, Higgins DG, Gibson TJ (1994) ClustalW: improving the sensitivity of progressive multiple sequence alignment through sequence weighting, position-specific gap penalties and weight matrix choice. Nucleic Acids Research 22, 4673–4680.
ClustalW: improving the sensitivity of progressive multiple sequence alignment through sequence weighting, position-specific gap penalties and weight matrix choice.Crossref | GoogleScholarGoogle Scholar |

Threatened Species Section (2006) ‘Flora recovery plan: Tasmanian threatened orchids 2006–2010.’ (Department of Primary Industry, Water and Environment: Hobart, Tas., Australia)

Vázquez FJ, Acea MJ, Carballas T (1993) Soil microbial populations after wildfire. FEMS Microbiology Ecology 13, 93–103.
Soil microbial populations after wildfire.Crossref | GoogleScholarGoogle Scholar |

Visser S (1995) Ectomycorrhizal fungal succession in jack pine stands following wildfire. New Phytologist 129, 389–401.
Ectomycorrhizal fungal succession in jack pine stands following wildfire.Crossref | GoogleScholarGoogle Scholar |

Wade DD, Lunsford JD, Dixon MJ, Mobley HE (1989) A guide for prescribed fire in southern forests. Technical Publication R8-TP 11. US Department of Agriculture, Forest Service, Southern Region.

Warcup JH (1973) Symbiotic germination of some Australian terrestrial orchids. New Phytologist 72, 387–392.
Symbiotic germination of some Australian terrestrial orchids.Crossref | GoogleScholarGoogle Scholar |

Warcup JH (1981) The mycorrhizal relationships of Australian orchids. New Phytologist 87, 371–381.
The mycorrhizal relationships of Australian orchids.Crossref | GoogleScholarGoogle Scholar |

Warcup JH, Talbot PHB (1967) Perfect states of rhizoctonias associated with orchids. New Phytologist 66, 631–641.

Weiß M, Selosse M-A, Rexer KH, Urban A, Oberwinkler F (2004) Sebacinales: a hitherto overlooked cosm of heterobasidiomycetes with a broad mycorrhizal potential. Mycological Research 108, 1003–1010.
Sebacinales: a hitherto overlooked cosm of heterobasidiomycetes with a broad mycorrhizal potential.Crossref | GoogleScholarGoogle Scholar |

Weiß M, Waller F, Zuccaro A, Selosse M-A (2016) Sebacinales − one thousand and one interactions with land plants. New Phytologist 211, 20–40.
Sebacinales − one thousand and one interactions with land plants.Crossref | GoogleScholarGoogle Scholar |

Wells TCE, Rothery P, Cox R, Bamford S (1998) Flowering dynamics of Orchis morio L. and Herminium monorchis (L.) R.Br. at two sites in eastern England. Botanical Journal of the Linnean Society 126, 39–48.

Weston PH, Perkins AJ, Entwisle TJ (2005) More than symbioses: orchid ecology, with examples from the Sydney Region. Cunninghamia 9, 1–15.

Whelan RJ (1995)’ The ecology of fire.’ (Cambridge University Press: Cambridge, UK)

Whigham DF (1990) The effect of experimental defoliation on the growth and reproduction of a woodland orchid, Tipularia discolor. Canadian Journal of Botany 68, 1812–1816.
The effect of experimental defoliation on the growth and reproduction of a woodland orchid, Tipularia discolor.Crossref | GoogleScholarGoogle Scholar |

White JJ, Bruns TD, Lee S, Taylor JJ (1990) Amplification and direct sequencing of fungal ribosomal RNA genes for phylogenetics. In ‘PCR protocols – a guide to methods and applications’. (Eds MA Gelfand, JJ Sninsky, J White) pp. 315–322 (Academic Press: New York)

Whitehead MR, Catullo RA, Ruibal M, Dixon KW, Peakall R, Linde CC (2017) Evaluating multilocus Bayesian species delimitation for discovery of cryptic mycorrhizal diversity. Fungal Ecology 26, 74–84.
Evaluating multilocus Bayesian species delimitation for discovery of cryptic mycorrhizal diversity.Crossref | GoogleScholarGoogle Scholar |

Wilkinson KG, Dixon KW, Sivasithamparam K (1989) Interaction of soil bacteria, mycorrhizal fungi and orchid seed in relation to germination of Australian orchids. New Phytologist 112, 429–435.
Interaction of soil bacteria, mycorrhizal fungi and orchid seed in relation to germination of Australian orchids.Crossref | GoogleScholarGoogle Scholar |

Willming MM, Lilavois CR, Barron MG, Mace G, Raimondo S (2016) Acute toxicity prediction to threatened and endangered species using interspecies correlation estimation (ICE) models. Environmental Science & Technology 50, 10700–10707.
Acute toxicity prediction to threatened and endangered species using interspecies correlation estimation (ICE) models.Crossref | GoogleScholarGoogle Scholar |

Wong PY, Kitts DD (2006) Studies on the dual antioxidant and antibacterial properties of parsley Petroselinum crispum and cilantro Coriandrum sativum extracts. Food Chemistry 97, 505–515.
Studies on the dual antioxidant and antibacterial properties of parsley Petroselinum crispum and cilantro Coriandrum sativum extracts.Crossref | GoogleScholarGoogle Scholar |

Wright E, Tarrant RF (1957) Microbiological soil properties after logging and slash burning. Research Note No. 157. US Department of Agriculture, Forest Service, Pacific NW Forest and Ranges Experimental Station.

Zagory D, Parmeter JR (1984) Fungitoxicity of smoke. Phytopathology 74, 1027–1031.
Fungitoxicity of smoke.Crossref | GoogleScholarGoogle Scholar |

Zelmer CD, Cuthbertson L, Currah RS (1996) Fungi associated with terrestrial orchid mycorrhizas, seeds and protocorms. Mycoscience 37, 439–448.
Fungi associated with terrestrial orchid mycorrhizas, seeds and protocorms.Crossref | GoogleScholarGoogle Scholar |