From: Fire Reduces Fungal Species Richness and In Situ Mycorrhizal Colonization: A Meta-Analysis
Reference | Guild studieda | Unit of measurementb | Fire typec | Repeat burn? | Years since fire | Biomed | Location | n c | x c | n e | x e | ln[R] | Change in richness (%) |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|
Barker et al. 2013 | ECM | morphotyping + molecular ID | W | 3 | TF | British Columbia, Canada | 15 | 8 | 15 | 6.3 | −0.2389 | −21.3 | |
ECM | morphotyping + molecular ID | W | 3 | TF | British Columbia, Canada | 15 | 8 | 15 | 4 | −0.6932 | −50.0 | ||
Bartoli et al. 1991 | microfungi | culture morphology | W | 0.01644 | TF | Italy | 5 | 21.2 | 5 | 3.2 | −1.8909 | −84.9 | |
Buscardo et al. 2010 | ECM† | morphotyping + molecular ID | W | 5 | TF | Portugal | 12 | 2.5 | 12 | 3.1 | 0.2119 | 23.6 | |
ECM† | morphotyping + molecular ID | W | 2 consecutive | 5 | TF | Portugal | 12 | 2.5 | 12 | 2.6 | 0.0276 | 2.8 | |
ECM† | morphotyping + molecular ID | W | 2 consecutive | 5 | TF | Portugal | 12 | 2.5 | 12 | 2.2 | −0.1188 | −11.2 | |
ECM† | morphotyping + molecular ID | W | 5 | TF | Portugal | 11 | 2.6 | 11 | 1.9 | −0.3032 | −26.2 | ||
ECM† | morphotyping + molecular ID | W | 2 consecutive | 5 | TF | Portugal | 11 | 2.6 | 11 | 2 | −0.2624 | −23.1 | |
ECM† | morphotyping + molecular ID | W | 2 consecutive | 5 | TF | Portugal | 11 | 2.6 | 11 | 1.6 | −0.4608 | −36.9 | |
Dahlberg et al. 2001 | ECM | morphotyping + molecular ID | P | 0.3 | BF | Sweden | 5 | 1.4 | 5 | 0.9 | −0.5272 | −41.0 | |
ECM | morphotyping + molecular ID | P | 0.3 | BF | Sweden | 5 | 2 | 5 | 0 | NA | NA | ||
Eom et al. 1999 | AM (spore) | spore morphology | P | 1 | TG | Kansas, USA | 4 | 5.3 | 4 | 3.8 | −0.3365 | −28.6 | |
Glassman et al. 2015 | ECM† | morphotyping + molecular ID | W | 1 | TF | California, USA | 25 | 30.5 | 25 | 20 | −0.4220 | −34.4 | |
Goberna et al. 2012 | All fungi | DGGE | P | 0.00274 | TG | Spain | 10 | 23.53 | 10 | 26.55 | 0.1208 | 12.8 | |
Grishkan 2016 | microfungi | culture morphology | W | 1.5 | TF | Israel | 3 | 36 | 3 | 23 | −0.4480 | −36.1 | |
microfungi | culture morphology | W | 0.5 | TF | Israel | 3 | 30 | 3 | 20 | −0.4055 | −33.3 | ||
Hernández-Rodríguez et al. 2013 | All fungi | sporocarp survey | W | 1 | TG | Spain | 6 | 22.1 | 6 | 6.1 | −1.2827 | −72.3 | |
Holden et al. 2013 | All fungi | NGS | W | 0 | BF | Alaska, USA | 2 | 122.3 | 2 | 121.2 | −0.0090 | −0.90 | |
All fungi | NGS | W | 6 | BF | Alaska, USA | 2 | 122.3 | 2 | 142.1 | 0.1501 | 16.2 | ||
All fungi | NGS | W | 11 | BF | Alaska, USA | 2 | 122.3 | 2 | 134.4 | 0.0943 | 9.9 | ||
All fungi | NGS | W | 23 | BF | Alaska, USA | 2 | 122.3 | 2 | 117.6 | −0.0392 | −3.8 | ||
All fungi | NGS | W | 54 | BF | Alaska, USA | 2 | 122.3 | 2 | 108.2 | −0.1225 | −11.5 | ||
All fungi | NGS | W | 90 | BF | Alaska, USA | 2 | 122.3 | 2 | 99.8 | −0.2033 | −18.4 | ||
Jonsson et al. 1999 | ECM | morphotyping + molecular ID | W | 62 | BF | Sweden | 2 | 22.5 | 2 | 20 | −0.1178 | −11.1 | |
Junninen et al. 2008 | WIF | sporocarp survey | P | 1 | BF | Finland | 3 | 18.42 | 3 | 18.68 | 0.0140 | 1.4 | |
Kipfer et al. 2011 | ECM | morphotyping + molecular ID | W | 3.5 | TF | Switzerland | 5 | 21.2 | 5 | 11.6 | −0.6030 | −45.3 | |
ECM | morphotyping + molecular ID | W | 15.5 | TF | Switzerland | 7 | 21.2 | 7 | 19.5 | −0.0836 | −8.0 | ||
Kurth et al. 2013 | WIF | NGS | W | 4 | TF | Arizona, USA | 6 | 3.5 | 6 | 1.8 | −0.6621 | −48.4 | |
WIF | NGS | W | 9 | TF | Arizona, USA | 6 | 3.7 | 6 | 4.3 | 0.1526 | 16.5 | ||
WIF | NGS | W | 13 | TF | Arizona, USA | 6 | 4.8 | 6 | 4.5 | −0.0728 | −7.0 | ||
WIF | NGS | W | 25 | TF | Arizona, USA | 6 | 2.7 | 6 | 5.3 | 0.6782 | 97.0 | ||
WIF | NGS | W | 32 | TF | Arizona, USA | 6 | 3.8 | 6 | 3.8 | 0.0000 | 0.0 | ||
Longo et al. 2014 | AM (spore) | spore morphology | W | 0.5 | TF | Argentina | 10 | 7.5 | 10 | 4.6 | −0.4850 | −38.4 | |
AM (spore) | spore morphology | W | 0.5 | TF | Argentina | 10 | 7.7 | 10 | 4.1 | −0.6477 | −47.7 | ||
AM (spore) | spore morphology | W | 0.5 | TF | Argentina | 10 | 6.9 | 10 | 4.3 | −0.4723 | −37.7 | ||
AM (spore) | spore morphology | W | 0.5 | TF | Argentina | 10 | 8.4 | 10 | 4.9 | −0.5371 | −41.6 | ||
AM (spore) | spore morphology | W | 0.5 | TF | Argentina | 10 | 7.7 | 10 | 4.8 | −0.4883 | −38.6 | ||
Mardji 2014 | ECM | sporocarp survey | W | 2 consecutive | 14 | TrF | India | 4 | 8.75 | 4 | 3.25 | −0.9904 | −62.9 |
Martín-Pinto et al. 2006 | All fungi | sporocarp survey | W | 1 | TF | Spain | 3 | 22.1 | 3 | 8.8 | −0.9257 | −60.4 | |
All fungi | sporocarp survey | W | 1 | TF | Spain | 3 | 16.9 | 3 | 6.3 | −0.9799 | −62.5 | ||
All fungi | sporocarp survey | W | 1 | TS | Spain | 3 | 26 | 3 | 11.7 | −0.7978 | −55.0 | ||
All fungi | sporocarp survey | W | 1 | TS | Spain | 3 | 26.1 | 3 | 3.8 | −1.9158 | −85.3 | ||
Motiejūnaitė et al. 2014 | All fungi | sporocarp survey | W | 1 | TF | Lithuania | 3 | 71.2 | 3 | 23.9 | −1.0930 | −66.5 | |
All fungi | sporocarp survey | W | 1 | TF | Lithuania | 3 | 70.7 | 3 | 42.2 | −0.5161 | −40.3 | ||
Oliver et al. 2015 | All fungi | NGS | P | every 2 yr (winter) | 3 | TF | Georgia, USA | 4 | 668 | 4 | 656.5 | −0.0174 | −1.7 |
All fungi | NGS | P | every 3 yr (winter) | 3 | TF | Georgia, USA | 4 | 668 | 4 | 680.5 | 0.0185 | 1.9 | |
All fungi | NGS | P | every 3 yr (summer) | 7 | TF | Georgia, USA | 4 | 668 | 4 | 659.75 | −0.0124 | −1.2 | |
All fungi | NGS | P | every 6 yr (summer) | 10 | TF | Georgia, USA | 4 | 668 | 4 | 687.5 | 0.0288 | 2.9 | |
Olsson and Jonsson 2010 | WIF | sporocarp survey | P | 1 | BF | Sweden | 150 | 2.0 | 150 | 1.2 | −0.5008 | −39.4 | |
Rincón et al. 2014 | ECM | morphotyping + molecular ID | W | 14 | TF | Spain | 3 | 11.9 | 3 | 10.0 | −0.1796 | −16.4 | |
ECM | morphotyping + molecular ID | W | 3 | TF | Spain | 3 | 11.9 | 3 | 9.0 | −0.2832 | −24.7 | ||
Robinson et al. 2008 | All fungi | sporocarp survey | W | 1 | TF | Australia | 4 | 39.41 | 4 | 27.94 | −0.3440 | −29.1 | |
Román and Miguel 2005 | ECM | hyphal morphotype | P | 1 | TF | Spain | 5 | 6 | 5 | 5.2 | −0.1431 | −13.3 | |
Smith et al. 2004 | ECM | morphotyping + molecular ID | P | 1 | TF | Oregon, USA | 4 | 10.3 | 4 | 10 | −0.0247 | −2.4 | |
ECM | morphotyping + molecular ID | P | 1 | TF | Oregon, USA | 4 | 9.5 | 4 | 1.8 | −1.6917 | −81.6 | ||
Sun et al. 2015 | All fungi | NGS | W | 2 | BF | Finland | 10 | 121.5 | 10 | 181.3 | 0.4002 | 49.2 | |
All fungi | NGS | W | 42 | BF | Finland | 10 | 121.5 | 10 | 143.9 | 0.1692 | 18.4 | ||
All fungi | NGS | W | 60 | BF | Finland | 10 | 121.5 | 10 | 129 | 0.0599 | 6.2 | ||
All fungi | NGS | W | 60 | BF | Finland | 10 | 121.5 | 10 | 130.8 | 0.0738 | 7.7 | ||
Trappe et al. 2009 | ECM | sporocarp survey | P | 3 | TF | Oregon, USA | 8 | 69 | 8 | 55 | −0.2268 | −20.3 | |
ECM | sporocarp survey | P | 3 | TF | Oregon, USA | 4 | 69 | 4 | 81 | 0.1603 | 17.4 | ||
ECM | sporocarp survey | P | 3 | TF | Oregon, USA | 4 | 69 | 4 | 81 | 0.1603 | 17.4 | ||
Trusty 2009 | ECM | morphotyping + molecular ID | W | 5 | TF | Montana, USA | 3 | 2.17 | 3 | 1.58 | −0.3173 | −27.2 | |
Tuininga and Dighton 2004 | ECM | hyphal morphotype | P | every 4 yr | 0.3 | TF | New Jersey, USA | 3 | 9.4 | 3 | 9.1 | −0.0389 | −3.8 |
ECM | hyphal morphotype | P | every 8 yr | 0.3 | TF | New Jersey, USA | 3 | 10.6 | 3 | 8.6 | −0.2164 | −19.5 | |
Xiang et al. 2015 | AM | NGS | W | 1 | BF | China | 6 | 74.34 | 6 | 8.68 | −0.5919 | −44.7 | |
AM | NGS | W | 1 | BF | China | 6 | 74.34 | 6 | 12.84 | −0.7641 | −53.4 | ||
AM | NGS | W | 11 | BF | China | 6 | 74.34 | 6 | 15.09 | −0.1392 | −13.0 | ||
AM | NGS | W | 11 | BF | China | 6 | 74.34 | 6 | 15.85 | −0.4945 | −39.0 |