Ectomycorrhizal Diversity Research Articles

Ectomycorrhizal diversity associated with Cedrus deodara and Pinus wallichiana in the Kashmir Himalaya, India.

The present study was undertaken to document the ectomycorrhizal diversity associated with the Cedrus deodara and Pinus wallichiana in the Kashmir Himalaya, India. The extensive field surveys carried out in the Kashmir Himalaya at five study sites resulted in the collection and identification of 76 potential ectomycorrhizal fungal species associated with the Cedrus deodara and Pinus wallichiana. Maximum 32 number of species were found associated with Pinus wallichiana, 19 with Cedrus deodara and 25 species were found growing in association with both the conifers. The present study reveals that Cedrus deodara and Pinus wallichiana in the Kashmir Himalaya, India harbour diverse ectomycorrhizal fungal species.

Profiling functions of ectomycorrhizal diversity and root structuring in seedlings of Norway spruce (Picea abies) with fast‐ and slow‐growing phenotypes

We studied the role of taxonomical and functional ectomycorrhizal (ECM) fungal diversity in root formation and nutrient uptake by Norway spruce (Picea abies) seedlings with fast- and slow-growing phenotypes. Seedlings were grown with an increasing ECM fungal diversity gradient from one to four species and sampled before aboveground growth differences between the two phenotypes were apparent. ECM fungal colonization patterns were determined and functional diversity was assayed via measurements of potential enzyme activities of eight exoenzymes probably involved in nutrient mobilization. Phenotypes did not vary in their receptiveness to different ECM fungal species. However, seedlings of slow-growing phenotypes had higher fine-root density and thus more condensed root systems than fast-growing seedlings, but the potential enzyme activities of ectomycorrhizas did not differ qualitatively or quantitatively. ECM species richness increased host nutrient acquisition potential by diversifying the exoenzyme palette. Needle nitrogen content correlated positively with high chitinase activity of ectomycorrhizas. Rather than fast- and slow-growing phenotypes exhibiting differing receptiveness to ECM fungi, our results suggest that distinctions in fine-root structuring and in the belowground growth strategy already apparent at early stages of seedling development may explain later growth differences between fast- and slow-growing families.

Microbial community structure of soils under four productivity classes of aspen forests in northern British Columbia

Trembling aspen (Populus tremuloides) is widely distributed in North American forests. Increased stand productivity with resource availability has been reported, but the relationship between soil microbial community structure and stand productivity remains unclear. To examine soil microbial composition of 4 aspen stand productivity classes, we assessed soil properties, microbial biomass and respiration, and bacterial and ectomycorrhizal diversity. Most variables showed no significant differences between productivity classes. However, mean values for basal respiration (0.05 to 27.99 μg CO2-C·g−1 soil·h−1), bacterial biomass, and metabolic quotient (0.08 to 5.22 CO2-C·mg−1 Cmic·h−1) were lowest in low productivity (Class 1) sites. Bacteria to fungi ratios were significantly lower (P = 0.05) in Class 1 compared to other classes. Microbial biomass ranged from 1.39 to 8.11 mg Cmic·g−1 soil. Thirty-seven distinct aspen ectomycorrhizas (ECM) were characterized, 21 were considered rare (from ≤3 trees). ECM richness did not differ significantly between classes, although relative abundance for some types did. Canonical correspondence analysis showed productivity class explained most microbial community variation, e.g., ECM fungi (80% explained) and soil bacteria (46%). Despite some differences, we could not identify statistically significant bacterial or ECM assemblages linked to stand productivity. Results may reflect a strong association between microbial processes and the dominant host, aspen. Aspen associated with widely distributed fungi common to all classes, possibly facilitating its survival and growth, including on sites exhibiting low pH and low soil fertility.

Individual tree genotypes do not explain ectomycorrhizal biodiversity in soil cores of a pure stand of beech (Fagus sylvatica L.)

Niche differentiation is a common explanation for high ectomycorrhizal diversity. In monocultures and on small spatial scales, the number of variable factors that may provide niches decreases. Still, even in the restricted volume of a soil core, typically more than one ectomycorrhizal species is found. We tested the hypothesis that roots of different individual beech genotypes provide niches on a small spatial scale in a pure beech (Fagus sylvatica L.) stand in the North-eastern Lowlands of Germany. Fourteen ectomycorrhizal species, as determined by ITS sequencing and phylograms were patchily distributed along an 81 m long transect with ten transect points. All root segments in the three species richest soil cores and the surrounding beeches were genotyped by microsatellite PCR. In each of the three soil cores, roots of two host genotypes were present that corresponded to the two closest mature trees. We found that the different root genotypes did not carry different sets of ectomycorrhizal species even at the high species resolution provided through our study. Therefore, the hypothesis of tree genotypes contributing to ectomycorrhizal biodiversity at the analyzed beech stand has to be rejected. Exploration types and stochastic processes are discussed as alternative explanations for the species richness and distributions in the analyzed soil cores. To the best of our knowledge, this is the first report that links ectomycorrhizal biodiversity in a soil core to the individual genotype of an angiosperm host.

Ectomycorrhizal diversity at five different tree species in forests of the Taunus Mountains in Central Germany

Ectomycorrhizal fungi were investigated on five different forest tree species growing in pure stands on the south slope of the Taunus Mountains, which are situated at the northern end of the Rhine rift valley in Central Germany. Mycorrhizal fungi accompanying the genus Xerocomus were identified and their frequencies counted. Using ITS markers, 22 different fungal species were identified down to species level and 6 down to genus level. On European beech (Fagus sylvatica) 16 fungal species and 4 genera were identified and on Sessile oak (Quercus petraea) 16 ectomycorrhizal species and 2 genera were determined. On both deciduous trees we observed exclusively: Cortinarius subsertipes, Genea hispidula, Lactarius quietus, Tylopilus felleus and a Melanogaster genus. On Norway spruce (Picea abies) we identified 13 different mycorrhizal species and 3 different genera, on Silver fir (Abies alba) 12 species and 3 genera, and in association with European larch (Larix decidua) 11 species and 3 genera. On these conifers Cortinarius anomalus, Lactarius necator and a Piloderma genus occurred exclusively. Comparisons with published data of ectomycorrhizal diversity on the same five tree species, growing in different areas of Germany and Europe, led to the conclusion that there is relative site specificity for ectomycorrhizal communities. Upper soil compartments of the stands investigated in the Taunus Mountainssuffer from soil acidification (pH-H20 ~3.7 to ~4.8). However, a clear correlation between upper soil pH-values and fungal diversity was not observed. On the other hand, nitrate concentrations in upper soil compartments (~26 to ~91 kgNO3-/ha) were higher in older stands as compared to younger ones. Higher nitrate concentrations in upper soils correlated with lower numbers of mycorrhizal individuals.

Ectomycorrhizal diversity enhances growth and nitrogen fixation of Acacia mangium seedlings

Increasing interest has been given so far to the role of mycorrhizal symbiosis on plant diversity and ecosystem productivity. However much remains unknown about the effect of ectomycorrhizal fungal diversity on plant growth and rhizobial symbiosis. The purpose of this study is to investigate the influence of ectomycorrhizal diversity on root nodulation and plant nutrient uptake during plant growth. A gradient of ectomycorrhizal diversity was created (ranged from one to six fungal isolates) on Australian Acacia (Acacia mangium) seedlings grown on a phosphate-deficient soil in controlled conditions. The results clearly show (i) an enhancement of A. mangium growth due to ectomycorrhizal fungal inoculation, (ii) as well as significant effects of increasing ectomycorhizal diversity and soil ectomycorrhizal mycelium density on whole plant biomass and plant nutrient uptake. They also reveal an effect of ectomycorrhizal diversity effect on the functioning of the nitrogen-fixing symbiosis. These results emphasize the need to manage soil ectomycorrhizal potential (abundance and diversity of ectomycorrhizal mycelium) in forest management practices in order to optimize N2 fixation and seedling growth, leading thus to dramatic improvements in outplanting performances with fast-growing tree legumes on various reafforestation sites, more particularly in tropical and Mediterranean areas.

Effect of chronic ammonium nitrate addition on the ectomycorrhizal community in a black spruce stand1This article is one of a selection of papers from the 7th International Conference on Disturbance Dynamics in Boreal Forests.

Observed modifications of ectomycorrhizal (ECM) communities have been connected to the increased N depositions of the 20th century. Because of their narrow niche width, small disturbances of soil conditions can produce greater effects on the fungal species than on their host trees. This study investigated the ECM community in a black spruce ( Picea mariana (Mill.) BSP) stand subjected to long-term additions of 9 and 30 kg N·ha–1·year–1 of ammonium nitrate, representing 3 and 10 times the atmospheric N deposition at the site, respectively. Root tip vitality and ECM presence were detected on samples collected from the organic horizon and ECM were classified into morphotypes according to their morphological and anatomical characters. In the control, 80.6% of the root tips were vital, 76.5% of them showing ECM colonization. Higher root tip vitality and mycorrhization were observed in the treated plots. Forty-one morphotypes were identified, most of them detected at the higher N inputs. Results diverging from the expectations of a reduction in ECM presence and diversity could be related to a higher growth rate of the trees following fertilization. The repeated application of small N doses could have been a better imitation of natural inputs from atmospheric deposition and could have provided more reliable responses of ECM to treatment.

Below-ground ectomycorrhizal communities: the effect of small scale spatial and short term temporal variation

Ectomycorrhizal (ECM) associations are an important form of symbiosis for the majority of tree species. In forest ecosystems where nutrients are often limited, ECM associations are vital for seedling establishment and tree survival. ECM communities are often very species rich and frequently follow the log normal distribution—with a few species being abundant and many species being rare. Much of the current knowledge of ECM communities has been revealed through a combination of above-ground sporocarp and below-ground root tip analyses. However, above-ground surveys of ECM communities reveal largely different findings regarding ECM diversity and community structure to below-ground surveys. Therefore below-ground surveys are vital to our understanding of ECM biology, ecology and community dynamics. In this article I review the recent findings regarding how ECM communities vary both spatially and temporally in forests. Spatial variation occurs at the centimetre scale both horizontally and vertically in forests, and can be explained by the separation of the ECM community into distinct niches. Temporal variation occurs over relatively short time scales, with ECM communities showing large changes even on a monthly basis. I then apply the niche concept to ECM fungi, and review a recent theory, ECM functional morphology, and examine how this may be used to explain a significant amount of spatial and temporal variation in forest ECM communities. The functional morphology theory is particularly useful in explaining patterns of ECM community variation across the distinct successional stages of the forest cycle. However, the effect of other abiotic and biological variables on ECM communities should not be ignored. Finally, as ECM communities are non-randomly distributed and vary widely in species richness over time, I lay out a sampling strategy to provide representative samples of the actual ECM community in the study area. Using (i) an extensive sampling methodology, (ii) separation of samples at distances greater than levels of spatial autocorrelation, and (iii) samples collected throughout the year, over a number of years, an ample picture of the ECM community in temperate forests can be collected.

Correspondence of ectomycorrhizal diversity and colonisation of willows (Salix spp.) grown in short rotation coppice on arable sites and adjacent natural stands

Willows (Salix spp.) are mycorrhizal tree species sometimes cultivated as short rotation coppice (SRC) on arable sites for energy purposes; they are also among the earliest plants colonising primary successional sites in natural stands. The objective of this study was to analyse the degree of colonisation and diversity of ectomycorrhizal (EM) communities on willows grown as SRC in arable soils and their adjacent natural or naturalized stands. Arable sites usually lack ectomycorrhizal host plants before the establishment of SRC, and adjacent natural or naturalized willow stands were hypothesized to be a leading source of ectomycorrhizal inoculum for the SRC. Three test sites including SRC stands (Salix viminalis, Salix dasyclados, and Salix schwerinii) and adjacent natural or naturalized (Salix caprea, Salix fragilis, and Salix × mollissima) stands in central Sweden were investigated on EM colonisation and morphotypes, and the fungal partners of 36 of the total 49 EM fungi morphotypes were identified using molecular tools. The frequency of mycorrhizas in the natural/naturalized stands was higher (two sites) or lower (one site) than in the corresponding cultivated stands. Correspondence analysis revealed that some EM taxa (e.g. Agaricales) were mostly associated with cultivated willows, while others (e.g. Thelephorales) were mostly found in natural/naturalized stands. In conclusion, we found strong effects of sites and willow genotype on EM fungi formation, but poor correspondence between the EM fungi abundance and diversity in SRC and their adjacent natural/naturalized stands. The underlying mechanism might be selective promotion of some EM fungi species by more effective spore dispersal.

Ectomychorrizal DB: a symbiotic association database.

Ectomycorrhizal (ECM) fungal species, a "Symbiotic" relationship between tress and fungi in forest has a great ecological and economic importance. Here is an attempt to describe database named "EctomycorrhizalDB", addressing ECM diversity of Central Himalaya (Kumaun region), with special emphasis on their characterization, physical properties and morphological features along with specifications. This database would help the scientific community to draw a better understanding of the environmental factors that affects species diversity. The database is available for free at http://www.kubic.nic.in/ectomychorhiza.

Similar taxonomic richness but different communities of ectomycorrhizas in native forests and non-native plantation forests

This investigation sought to examine if there was a difference between the ectomycorrhizal (ECM) communities in plots of native oak and introduced Scots pine and Sitka spruce forest. The ECM communities in four plots of each forest type were described, from five soil cores collected in each plot, by morphotyping, internal transcribed spacer (ITS)-restriction fragment length polymorphism matching of mycorrhizas and sporocarps and ITS sequencing. Fifty-one distinct taxa were distinguished; 25 were identified to species level, 11 to genus and 15 remained unidentified. Seventy-one ECM species were recorded as sporocarps from the forest plots; most (43 species) were found in the Sitka spruce plots. The below-ground ECM communities of the different forest types did not differ significantly with respect to species richness of taxa on roots, but differed in species composition. Multivariate analysis produced a clear separation of the communities of the different forest types using below-ground data, but the above-ground sporocarp data did not separate the forest types. Moreover, results of a Mantel test found no relationship between the above- and below-ground similarity matrices. The oak plots had the most distinctive ECM community, with Laccaria amethystina and Elaphomyces granulatus being frequent. The Sitka spruce plots showed the lowest intra-forest type similarity and were often dominated by "nursery type" ectomycorrhizas. There was only 10% similarity between the above- and below-ground ECM species in these plots, different colonisation methods of ectomycorrhizal taxa and insufficient below-ground sampling being possible reasons for this disparity. Our results indicate that plantations of non-native Sitka spruce can support similar levels of ECM diversity as native forests.

Ectomycorrhizal fungal diversity, tree diversity and root nutrient relations in a mixed Central European forest

Knowledge is limited about whether root nutrient concentrations are affected by mixtures of tree species and interspecific root competition. The goal of this field study was to investigate root nutrient element concentrations in relation to root and ectomycorrhizal (EM) diversity in six different mixtures of beech (Fagus sylvatica), ash (Fraxinus excelsior) and lime (Tilia sp.) in an old-growth, undisturbed forest ecosystem. Root biomass and nutrient concentrations per tree taxon as well as the abundance and identity of all EM fungi were determined in soil cores of a volume of 1 L (r=40 mm, depth=200 mm). Stand-level nutrient concentrations in overall root biomass and H' (Shannon-Wiener diversity) were obtained by pooling the data per stand. At stand level, Shannon H' for roots and aboveground tree species abundance were correlated. H' for roots and EM fungi were not correlated because of the contribution of ash roots that form only arbuscular mycorrhizal but no EM associations. Nutrient element concentrations in roots showed taxon-related differences and increased in the following order: beech ≤ lime < ash with the exception of calcium (Ca), which was lower in ash. Stand-level concentrations of Ca, magnesium, potassium and sulfur in roots increased with increasing tree diversity because of two effects: increasing contribution of ash roots to the mixture and increasing Ca accumulation in beech roots with increasing root diversity. On a small scale, increasing root diversity, but not EM diversity, was correlated with decreasing P concentrations in beech roots pointing to interspecific tree competition. Nitrogen (N) concentrations of beech roots were unaltered in relation to root and EM diversity. Opposing behavior was observed for lime and ash: the N concentrations in lime roots increased, whereas those in ash roots decreased with increasing EM diversity in a given soil volume. This suggests that EM diversity facilitates N acquisition of lime roots at the expense of non-EM ash.

Biodiversity of Ectomycorrhizal fungi of Pahalgam forests (Jammu &amp; Kashmir)

The present paper describes the rich ectomycorrhizal diversity existing in forests of Pahalgam in district Anantnag of Kashmir valley. Eight hitherto unreported ectomycorrhizal fungi from Jammu and Kashmir State, collected and identified during the survey conducted in March - October 2006 are described.

Morphological and molecular analyses of ectomycorrhizal diversity in Pinus densiflora seedlings

Using ectomycorrhizal root tip morphotyping (anatomical and morphological identification) and molecular analysis (internal transcribed spacer region amplification and sequencing), we assessed diversity and composition of the ectomycorrhizal fungal community colonizing P. densiflora seedlings (from 1 to 5 years ) in a naturally regenerating area of a mature forest, in Dongning County of Hei Longjiang Province, China. A total of 22 ectomycorrhizal taxa were determined on the roots of 100 seedlings. The most frequent species was Cenococcum geophilum, which colonized 31.2% of the root tips and occurred in 93.8% of the all samples. It was followed by Clavulina cinerea, Thelephora sp.2, and Russula albidula. They colonized in 22.7%, 17.5%, 13.4% of the root tips and occurred in 63.4%, 42.6%, 29.3% of the samples respectively. These results suggested that ectomycorrhizal diversity increased in P. densiflora seedlings with increasing age.

Potential link between plant and fungal distributions in a dipterocarp rainforest: community and phylogenetic structure of tropical ectomycorrhizal fungi across a plant and soil ecotone

*Relatively little is known about diversity or structure of tropical ectomycorrhizal communities or their roles in tropical ecosystem dynamics. In this study, we present one of the largest molecular studies to date of an ectomycorrhizal community in lowland dipterocarp rainforest. *We sampled roots from two 0.4 ha sites located across an ecotone within a 52 ha forest dynamics plot. Our plots contained > 500 tree species and > 40 species of ectomycorrhizal host plants. Fungi were identified by sequencing ribosomal RNA genes. *The community was dominated by the Russulales (30 species), Boletales (17), Agaricales (18), Thelephorales (13) and Cantharellales (12). Total species richness appeared comparable to molecular studies of temperate forests. Community structure changed across the ecotone, although it was not possible to separate the role of environmental factors vs host plant preferences. Phylogenetic analyses were consistent with a model of community assembly where habitat associations are influenced by evolutionary conservatism of functional traits within ectomycorrhizal lineages. *Because changes in the ectomycorrhizal fungal community parallel those of the tree community at this site, this study demonstrates the potential link between the distribution of tropical tree diversity and the distribution of tropical ectomycorrhizal diversity in relation to local-scale edaphic variation.

Ectomycorrhizal fungal communities of pedunculate and sessile oak seedlings from bare-root forest nurseries

In this study, we present the detailed molecular investigation of the ectomycorrhizal (ECM) community of Quercus petraea and Quercus robur seedlings grown in bare-root forest nurseries. In all tested oak samples, mycorrhizal colonization was nearly 100%. Morphological observation and molecular investigations (sequencing of fungal ITS rDNA) revealed a total of 23 mycorrhizal taxa. The most frequent and abundant fungal taxa were Hebeloma sacchariolens, Tuber sp., and Peziza sp.; from the detected fungal taxa, 20 were noted for Q. petraea and 23 for Q. robur. Depending on the nursery, the species richness of identified ECM fungal taxa for both oak species ranged from six to 11 taxa. The mean species richness for all nurseries was 5.36 and 5.82 taxa per Q. petraea and Q. robur sample, respectively. According to the analysis of similarity, ECM fungal communities were similar for Q. petraea and Q. robur (R = 0.019; p = 0.151). On the other hand, detected fungal communities were significantly different between nurseries (R = 0.927; p < 0.0001). Using the Spearman rank correlation, it was determined that the ectomycorrhizal diversity (in terms of richness, the Shannon diversity, evenness, and Simpson dominance indices) is significantly related to the soil parameters of each nursery. We conclude that individual nursery may be considered as separate ecological niches that strongly discriminate diversity of ECM fungi.

Ectomycorrhizal lifestyle in fungi: global diversity, distribution, and evolution of phylogenetic lineages

The ectomycorrhizal (EcM) symbiosis involves a large number of plant and fungal taxa worldwide. During studies on EcM diversity, numerous misidentifications, and contradictory reports on EcM status have been published. This review aims to: (1) critically assess the current knowledge of the fungi involved in the EcM by integrating data from axenic synthesis trials, anatomical, molecular, and isotope studies; (2) group these taxa into monophyletic lineages based on molecular sequence data and published phylogenies; (3) investigate the trophic status of sister taxa to EcM lineages; (4) highlight other potentially EcM taxa that lack both information on EcM status and DNA sequence data; (5) recover the main distribution patterns of the EcM fungal lineages in the world. Based on critically examining original reports, EcM lifestyle is proven in 162 fungal genera that are supplemented by two genera based on isotopic evidence and 52 genera based on phylogenetic data. Additionally, 33 genera are highlighted as potentially EcM based on habitat, although their EcM records and DNA sequence data are lacking. Molecular phylogenetic and identification studies suggest that EcM symbiosis has arisen independently and persisted at least 66 times in fungi, in the Basidiomycota, Ascomycota, and Zygomycota. The orders Pezizales, Agaricales, Helotiales, Boletales, and Cantharellales include the largest number of EcM fungal lineages. Regular updates of the EcM lineages and genera therein can be found at the UNITE homepage http://unite.ut.ee/EcM_lineages . The vast majority of EcM fungi evolved from humus and wood saprotrophic ancestors without any obvious reversals. Herbarium records from 11 major biogeographic regions revealed three main patterns in distribution of EcM lineages: (1) Austral; (2) Panglobal; (3) Holarctic (with or without some reports from the Austral or tropical realms). The holarctic regions host the largest number of EcM lineages; none are restricted to a tropical distribution with Dipterocarpaceae and Caesalpiniaceae hosts. We caution that EcM-dominated habitats and hosts in South America, Southeast Asia, Africa, and Australia remain undersampled relative to the north temperate regions. In conclusion, EcM fungi are phylogenetically highly diverse, and molecular surveys particularly in tropical and south temperate habitats are likely to supplement to the present figures. Due to great risk of contamination, future reports on EcM status of previously unstudied taxa should integrate molecular identification tools with axenic synthesis experiments, detailed morphological descriptions, and/or stable isotope investigations. We believe that the introduced lineage concept facilitates design of biogeographical studies and improves our understanding about phylogenetic structure of EcM fungal communities.

Beech carbon productivity as driver of ectomycorrhizal abundance and diversity

We tested the hypothesis that carbon productivity of beech (Fagus sylvatica) controls ectomycorrhizal colonization, diversity and community structures. Carbon productivity was limited by long-term shading or by girdling. The trees were grown in compost soil to avoid nutrient deficiencies. Despite severe limitation in photosynthesis and biomass production by shading, the concentrations of carbohydrates in roots were unaffected by the light level. Shade-acclimated plants were only 10% and sun-acclimated plants were 74% colonized by ectomycorrhiza. EM diversity was higher on roots with high than at roots with low mycorrhizal colonization. Evenness was unaffected by any treatment. Low mycorrhizal colonization had no negative effects on plant mineral nutrition. In girdled plants mycorrhizal colonization and diversity were retained although (14)C-leaf feeding showed almost complete disruption of carbon transport from leaves to roots. Carbohydrate storage pools in roots decreased upon girdling. Our results show that plant carbon productivity was the reason for and not the result of high ectomycorrhizal diversity. We suggest that ectomycorrhiza can be supplied by two carbon routes: recent photosynthate and stored carbohydrates. Storage pools may be important for ectomycorrhizal survival when photoassimilates were unavailable, probably feeding preferentially less carbon demanding EM species as shifts in community composition were found.

Ectomycorrhizal fungal communities of oak savanna are distinct from forest communities

Oak savanna is one of the most endangered ecosystems of North America, with less than 0.02% of its original area remaining. Here we test whether oak savanna supports a unique community of ectomycorrhizal fungi, a higher diversity of ectomycorrhizal fungi or a greater proportional abundance of ascomycete fungi compared with adjacent areas where the absence of fire has resulted in oak savanna conversion to oak forest. The overall fungal community was highly diverse and dominated by Cenococcum geophilum and other ascomycetes, Cortinarius, Russula, Lactarius and Thelephoraceae. Oak savanna mycorrhizal communities were distinct from oak forest communities both aboveground (sporocarp surveys) and belowground (RFLP identification of ectomycorrhizal root tips); however total diversity was not higher in oak savanna than oak forests and there was no evidence of a greater abundance of ascomycetes. Despite not having a higher local diversity than oak forests, the presence of a unique fungal community indicates that oak savanna plays an important role in maintaining regional ectomycorrhizal diversity.

Influence of host species on ectomycorrhizal communities associated with two co-occurring oaks (Quercus spp.) in a tropical cloud forest

Interactions between host tree species and ectomycorrhizal fungi are important in structuring ectomycorrhizal communities, but there are only a few studies on host influence of congeneric trees. We investigated ectomycorrhizal community assemblages on roots of deciduous Quercus crassifolia and evergreen Quercus laurina in a tropical montane cloud forest, one of the most endangered tropical forest ecosystems. Ectomycorrhizal fungi were identified by sequencing internal transcribed spacer and partial 28S rRNA gene. We sampled 80 soil cores and documented high ectomycorrhizal diversity with a total of 154 taxa. Canonical correspondence analysis indicated that oak host was significant in explaining some of the variation in ectomycorrhizal communities, despite the fact that the two Quercus species belong to the same red oak lineage (section Lobatae). A Tuber species, found in 23% of the soil cores, was the most frequent taxon. Similar to oak-dominated ectomycorrhizal communities in temperate forests, Thelephoraceae, Russulaceae and Sebacinales were diverse and dominant.