Leotia cf. lubrica forms arbutoid mycorrhiza with Comarostaphylis arbutoides (Ericaceae)

Arbutoid mycorrhizal plants are commonly found as understory vegetation in forests worldwide where ectomycorrhiza-forming trees occur. Comarostaphylis arbutoides (Ericaceae) is a tropical woody plant and common in tropical Central America. This plant forms arbutoid mycorrhiza, whereas only associations with Leccinum monticola as well as Sebacina sp. are described so far. We collected arbutoid mycorrhizas of C. arbutoides from the Cerro de la Muerte (Cordillera de Talamanca), Costa Rica, where this plant species grows together with Quercus costaricensis. We provide here the first evidence of mycorrhizal status for the Ascomycete Leotia cf. lubrica (Helotiales) that was so far under discussion as saprophyte or mycorrhizal. This fungus formed arbutoid mycorrhiza with C. arbutoides. The morphotype was described morphologically and anatomically. Leotia cf. lubrica was identified using molecular methods, such as sequencing the internal-transcribed spacer (ITS) and the large subunit (LSU) ribosomal DNA regions, as well as phylogenetic analyses. Specific plant primers were used to confirm C. arbutoides as the host plant of the leotioid mycorrhiza.


Introduction
The tropical woody plant Comarostaphylis arbutoides Lindl. (Ericaceae) is common in tropical Central America (c. 2,500-3,430 m height above sea level (a.s.l.)), where it can form extensive thickets. Based on fruit and flower morphology, anatomy, and phytochemistry, this plant is a member of the subfamily Arbutoideae (Hileman et al. 2001;Fig. 1a). The Arbutoideae also include the circumboreal Arctostaphylos uva-ursi and species of Arbutus that are all known to form arbutoid mycorrhiza (Molina and Trappe 1982a;Münzenberger et al. 1992;Osmundson et al. 2007). The mycorrhizal fungus induces the branching of the lateral roots to form mostly, with some exceptions (Molina and Trappe 1982a), a pinnate-cruciate branching pattern that is typical for this mycorrhizal type (Massicotte et al. 1993). The arbutoid mycorrhiza is characterized by a hyphal mantle, a paraepidermal Hartig net and intracellular hyphae penetrating the living epidermal cells of the host (Münzenberger et al. 1992;Selosse et al. 2007). Suberization of the outer cortical layer leads to the formation of an exodermis and prevents penetration of the fungus into deeper root cell layers (Münzenberger et al. 1992;Massicotte et al. 1993).
C. arbutoides is a refuge plant for ectomycorrhizal fungi as it shares these fungi with ectomycorrhizal tropical trees such as Quercus costaricensis (Halling and Mueller 2003;Kühdorf et al. 2014). After forest clearcutting of the economically important forest trees, arbutoid mycorrhizal plants host the ectomycorrhizal fungi that contribute to forest recovery later on (Dahlberg 1990;Visser 1995;Molina et al. 1997;Horton et al. 1999;Hagerman et al. 2001). Ectomycorrhizal fungi of Arbutoideae show identical morphology (apart from, e.g., host-depending branching pattern and habit dimensions) and hyphal mantle anatomy as the ectomycorrhiza (ECM) of other hosts such as Pinus, Picea, Pseudotsuga, and Quercus (Zak 1976a, b;Molina and Trappe 1982b;Mühlmann and Göbl 2006;Kühdorf et al. 2014). The ericaceous hosts Arbutus menziesii and A. uva-ursi lack mycorrhizal specificity, which means numerous ectomycorrhizal fungi are able to colonize these ericads (Molina and Trappe 1982a;Acsai and Largent 1983a, b;Massicotte et al. 1994;Richard et al. 2005;Kennedy et al. 2012). Osmundson et al. (2007) were the first to describe the arbutoid mycorrhiza of C. arbutoides and Leccinum monticola anatomically and molecularly. To date, only one more morphotype has been described in literature (Kühdorf et al. 2014). However, Halling and Mueller (2004) mention that species of other mycorrhizal genera such as Tricholoma, Cortinarius, Russula, and Laccaria are likely associates of C. arbutoides.
The ecology of the helotialean fungi is diverse. Members of the Helotiales have been described as plant pathogens, ECM and ericoid mycorrhiza formers, terrestrial and aquatic saprobes, and wood rot fungi (Wang et al. 2006a). The genus Leotia (Helotiales) is globally distributed (Wang et al. 2006a, b), whereas the ecological role of the Ascomycete is not clear. Species of Leotia and Microglossum are found usually on humus-rich soil, sometimes on decaying wood, but rarely on leaf litter (Arora 1986). Leotia was already recorded as mycorrhiza-forming fungus by Molina et al. (1992). This status was later speculated to be saprotrophic by Rinaldi et al. (2008) based on insufficient evidence. Both Zeller et al. (2007) and Seitzman et al. (2011) later found the 13 C signature of the species L. lubrica comparable with those of ectomycorrhizal fungi and therefore, conclude that this fungus should be mycorrhizal. Furthermore, L. lubrica was reported to form ECM with diverse plant species such as Quercus rotundifolia, Polygonum sp., and Nothofagus menziesii (Branco and Ree 2010;Gao and Yang 2010;Orlovich et al. 2013). However, these records have been proven by DNA sequencing only and were not further described.
The genus Leotia contains three species of inoperculate discomycetes with stipitate-capitate ascomata. They are constructed, at least in part, of tissues built-up of hyphae imbedded in a gelatinous matrix (Zhong and Pfister 2004). They are distinguished by the color of their fresh ascomata: species with a yellow stipe and yellow hymenia are assigned to Leotia lubrica, those with an entirely green ascomata to Leotia atrovirens. Species of Leotia viscosa have a yellow stalk and green hymenia (Durand 1908;Mains 1956;Grund and Harrison 1967).
Here, we describe arbutoid mycorrhizal systems morphologically and anatomically according to Agerer (1991), formed by L. cf. lubrica and C. arbutoides from the Cerro de la Muerte (Cordillera de Talamanca), Costa Rica. L. cf. lubrica was identified using molecular methods such as internal-transcribed spacer (ITS) and large subunit (LSU) sequencing as well as phylogenetic analysis. Plant primers were used to sequence the ITS region of C. arbutoides from the same arbutoid mycorrhiza as used for fungal analysis.

Site description and sampling
Sampling was conducted at two forest sites around the Mountain Cerro de la Muerte (  Fine root systems of C. arbutoides were collected during the rainy seasons in October 2010 and 2011. For this, a soil corer (diameter, 3 cm; length, 40 cm) was used at distances of 50 and 100 cm from the trunk. Within these 2 years, a total of 60 soil cores were taken and analyzed. At the University of Costa Rica, turgid and apparently healthy morphotypes were sorted out using a stereomicroscope. Systems with the same morphological features (e.g., color, hydrophobicity presence, emanating elements, and rhizomorphs) were assigned to one morphotype. For further analyses, the morphotypes were preserved in 2 % glutaraldehyde with 0.1 M sodium cacodylate buffer (Münzenberger et al. 2009) for light microscopy or dried on silica gel for DNA extraction, respectively. Identification of each morphotype is based on their respective sequence type. The genus Leotia was proven genetically in six soil cores.

DNA extraction, PCR, and sequencing
One unramified root tip per morphotype was used for DNA extraction using the DNeasy Plant Mini Kit (Qiagen, Hilden, Germany) following the manufacturer's recommendations. For phylogenetic analysis at family and species level, the ribosomal nuclear LSU and the ITS region from the ribosomal DNA (rDNA) were amplified. For this purpose, the primer combinations LR0R/LR5 (Moncalvo et al. 2000) and ITS1F/ ITS4 (Gardes and Bruns 1993;White et al. 1990) were used. To identify the plant from mycorrhizal roots without coamplifying fungal DNA, the angiosperm-specific ITS primer pair ITS-5A/ITS-241r was amplified (Osmundson et al. 2007). Direct sequencing of PCR products was performed using the PCR primers as sequencing primers. Sequencing service was facilitated by GATC Biotech AG (Konstanz, Germany).

Identification and phylogenetic analysis
All fungal sequences obtained for ITS and LSU rDNA were analyzed and edited using Chromas Lite v2.01 software (http://technelysium.com.au). Sequence comparisons were performed in the NCBI database (http://www.ncbi.nlm.nih. gov/) using Megablast, and the database UNITE (Kõljalg et al. 2005; http://unite.ut.ee/) using BLASTn. To calculate the phylogenetic tree of the ITS region, the 100 most similar sequences for each reference sequence in NCBI database were downloaded and complemented with an additional search in the nucleotide database and sequences of other publications as well. Alignment was performed with the program MAFFT v7 (Katoh et al. 2002) using the FFT-NS-2 alignment algorithm. To estimate phylogenetic relationships, we used maximum likelihood and Bayesian approaches. Maximum likelihood analyses was performed using RAxML (v7. 3.2; Stamatakis 2006; Stamatakis et al. 2008) in a parallelized version supplied by Bioportal (http://bioportal.uio.no/) with eight parallel processors and trees inferred from 10,000 rapid bootstrap analyses as starting trees in a heuristic search for the tree with the highest likelihood. GTRCAT was used in the heuristic search and the final evaluation of the best tree found was based on the GTR + Gamma model. The Bayesian analyses were performed using MrBayes v3.2.1 (Ronquist et al. 2012) on an iMac (2.9 GHz Quad-Core Intel Core i5). The GTR+Gamma model was in effect, and four chains in two parallel runs were performed for 2,000,000 generations. The first 50,000 trees were discarded before calculating the posterior probabilities.

Microscopy
The morphological and anatomical description of the mycorrhizas was carried out according to Agerer (1987Agerer ( -2012Agerer ( , 1991, and using the online key of DEEMY Rambold 2004-2014). The iodine reaction specially adapted to Ascomycetes was done after Baral (1987Baral ( , 2009. Anatomical studies are based on 15 mycorrhizal systems. Drawings were performed by using an interference contrast microscope (BX50F-3, Olympus Corporation, Tokyo, Japan) connected with a drawing tube. All drawings were made at a thousandfold magnification.
For semi-thin sections, the mycorrhizas were fixed with 2 % glutaraldehyde in 0.1 M sodium cacodylate buffer (pH 7.2) at room temperature until further processing. Thereafter, six washes in 0.1 M sodium cacodylate buffer were performed. Samples were postfixed in 1 % osmium tetroxide in the same buffer for 1 h under light exclusion at room temperature. After six washes in double-distilled water, samples were dehydrated by immersion for 15 min each in 25, 50, 70, and 95 % acetone and three times for 1 h in 100 % acetone (Münzenberger et al. 2009). The mycorrhizal tips were embedded in Spurr's plastic (Spurr 1969) and sectioned with a diamond knife on an Ultracut Reichert Ultramicrotome (W. Reichert-LABTEC, Wolfratshausen, Germany). The sections (0.5 μm thick) were stained with crystal violet and investigated by use of a light microscope (Zeiss Axioskop 50, Oberkochen, Germany).

Fruit bodies of L. lubrica
During 2 years of sampling, fruit bodies of L. lubrica were found only once and were coincidentally documented. For that reason, no further genetic investigations were carried out to clearly identify the fungus. As the three species of the genus Leotia are easy to distinguish morphologically, the ascomata ( Fig. 1b) were preliminary identified as L. lubrica, based on the yellow color of both the stipe and the hymenium.

Results
Morpho-anatomical description of the mycorrhiza Leotia cf. lubrica-C. arbutoides Morphological characters (Fig. 1c) Mycorrhizal systems arbutoid, with 0-1 (4) orders of ramification, solitary or in small numbers, up to 2.8 mm long, main axis at 0.3 mm diameter; mantle surface hydrophilic and smooth to moderately hairy, of contact exploration type or short-distance exploration type. Unramified ends straight to slightly bent, cylindric, not inflated, 0.1-0.7 (1.4) μm long, 0.2-0.3 (0.1) μm diameter, mantle consistently transparent and yellowish to light orange, older parts dark orange to ochre. Surface of unramified ends smooth to occasionally hairy, cortical cells (correspond to epidermal cells) visible. Cystidia not distinct under stereomicroscope magnification. Rhizomorphs not found. Sclerotia not observed.
Anatomical characters of the mantle in plan views (Figs. 2 and 3a-d) Mantle plectenchymatous throughout, all hyphae clampless and smooth; laticifers are lacking. Outer mantle layers (Figs. 2a and 3a) hyphae arranged net-like; hyphae frequently branched, often with merged hyphal tips, matrix lacking (mantle type E; Agerer 1991); hyphae septate, even and straight, not constricted at septa; hyphae with closed anastomoses, anastomosal bridge long, mostly thinner than hyphae; hyphae with numerous oily droplets, droplets light yellow to light orange; cytoplasm colorless; hyphae 10-90 μm long, 0.7-3.1 μm diameter; cell walls 0.2-0.4 μm thick; septa as thick as cell walls and often difficult to discern due to frequent droplets. Middle mantle layers (Figs. 2d, e and 3b) contain a nongelatinous matrix, hyphae irregularly interwoven, repeatedly branched and septate, colorless, no discernible pattern; frequently merged hyphal tips, hyphae at distal end simple; hyphae 15-50 (90) μm long, 0.9-2.4 μm diameter; cell walls 0.2 μm thick; septa as thick as cell walls; anastomoses frequently and very variable in shape; anastomoses open or closed by a simple septum; anastomosal bridge long, short, or almost lacking; bridge thinner or thicker than hyphae or as thick as hyphae; cell walls of anastomoses as thick as remaining wall; anastomoses close to hyphal tips not found. Inner mantle layers (Figs. 2f, h and 3c) ring-like arrangement of hyphal bundles; hyphae even or irregularly inflated, at distal end simple or slightly inflated; hyphae rarely septate, colorless; hyphae (7) 20-130 μm long, 1.5-3.9 μm diameter; cell walls 0.2-0.3 μm thick, septa as thick as cell walls; anastomoses frequently, anastomoses open, with short bridge or bridge almost lacking, bridge thinner or thicker than hyphae, or as thick as hyphae; cell walls of anastomoses as thick as remaining walls; anastomoses close to hyphal tips also present. Very tip (Figs. 2g, h and 3d) inner mantle layers similar to remaining part but without hyphal bundles; hyphae often irregularly inflated, many hyphae with hyphal tips; outer and middle mantle layers organized as older parts of the mantle.
Anatomical characters of emanating elements (Fig. 2b, c) Rhizomorphs lacking. Emanating hyphae rare to frequently, not specifically distributed; hyphae even, not striking, sometimes one-side branched, sometimes with open anastomoses; hyphal tips sometimes merged with hyphae; some hyphae in bundles; hyphae at distal end simple; hyphae straight and even, up to 500 μm long, maybe longer since often observed without hyphal tip, 2.3-4.2 μm diameter; cell walls 0.5-1.2 μm thick, not constricted at septa, septa 0.2-0.3 (0.6) μm thick, septa often difficult to discern due to frequent droplets; cell wall light yellow to light orange, cytoplasm light dirty blue, oily droplets same color as cell wall; lacking are clamps, elbow-like protrusions, and intrahyphal hyphae. Cystidia not found.
Color reactions with different reagents (mantle preparations and emanating hyphae) Acetic acid: no reaction; congo red: no reaction; cotton blue: hyphae of outer mantle layer with blue cytoplasm and blue (sometimes reddish) oily droplets, emanating hyphae with violet (sometimes reddish) cell walls, blue cytoplasm, and red to red brown oily droplets; ethanol 70 %: no reaction; Fe(II)SO 4 : no reaction; guaiac: no reaction; KOH 10 %: no reaction; lactic acid: no reaction; Lugol's solution: no reaction; Melzer's reagent: no reaction; NH 4 OH: no reaction; sulpho-vanillin: no reaction; H 2 SO 4 concentration: no reaction; toluidine blue: hyphae of outer mantle layer with patchy pale blue to blue cytoplasm and red oily droplets, emanating hyphae with violet cell walls, patchy pale blue to blue cytoplasm, and red oily droplets.

Phylogenetic analyses
A total of 399 root tips were analyzed genetically, of which ten were identified as Leotia cf. lubrica. All leotioid sequences were deposited in NCBI GenBank under the accession numbers KF836622-KF836631 (LSU) and KF836612-KF836621 (ITS), respectively. In all samples, C. arbutoides (KF419121) was proven as host tree.
The sequenced LSU rDNA region of the ten arbutoid mycorrhizas of C. arbutoides resulted in sequences with a length of 890-913 bp (KF836622-KF836631), in which the overlapping area was different in five positions within these samples. Sequence comparison with BLASTn in NCBI database resulted in matches mainly belonging to the order Helotiales, where the Leotiaceae L. lubrica (AY789359) showed the highest similarity values (Table 1). In UNITE, best values were reached with the Helotiaceae Unguiculariopsis thallophila (UDB016232), which also belongs to the Helotiales. In the sequenced 563-616 bp long ITS region (KF836612-KF836621) of the arbutoid mycorrhizas of C. arbutoides, 30 positions were different in the overlapping area. Sequences obtained from NCBI and UNITE comparison with ITS sequences belong to members of the genus Leotia (Table 1), whereby UNITE provides lower similarity values.
The Bayesian and RAxML phylogenies, generated by ITS sequences are concordant. Both trees show the same grouping structure, supported by high posterior probabilities (PP) in the Bayesian analysis and by typically lower bootstraps (BS) in the RAxML analysis (Fig. 4). The phylogenetic analysis in Fig. 4 reveals that the three species of the genus Leotia are paraphyletic and split in several groups. Members of the species L. atrovirens can be found in two groups (III and IV), whereby both are highly supported (PP 1/BS 100, each). Samples of L. lubrica are also divided and can be found exclusively in group II (PP 1/BS 99) on the one hand, and as a large complex together with L. viscosa samples in group I (PP 1/BS 78) on the other. In this L. lubrica/viscosa complex, Fig. 2 Arbutoid mycorrhiza of Leotia cf. lubrica-Comarostaphylis arbutoides. a-f Plan view of different mantle layers, emanating hyphae and anastomoses; bars, 10 μm: a outer mantle layer with ramified hyphae, irregularly arranged; hyphae with numerous oily droplets; anastomoses with closed long bridge (arrowheads); b bundle of emanating hyphae, hyphae with oily droplets; c simple and branched emanating hyphae; d middle mantle layer with repeatedly branched hyphae, densely arranged; anastomoses with short or long bridge, bridge closed or open (single arrowheads); merged hyphal tips, some with remnants of a partly solved septum (double arrowheads); e different anastomoses of the middle mantle layer; f inner mantle layer with ring-like arrangement of hyphal bundles, some hyphae irregularly inflated; anastomoses (arrowheads); g inner mantle layer close to the very tip with many irregularly inflated hyphae, many hyphae with hyphal tips; different anastomoses (arrowheads); h anastomoses of both the inner mantle layer and the inner mantle layer close to very tip, anastomosis close to the hyphal tip again several subgroups (a-f) are formed, containing exclusively L. lubrica (b, d, e, f; PP 1/BS 90-100) and L. viscosa (c; PP 1/BS 98) species, respectively, as well as a mixture of L. lubrica and L. viscosa samples (a).
All investigated leotioid arbutoid mycorrhizas of C. arbutoides can be found in group I, whereby eight group together (PP 1/BS 98) and nest within samples of L. lubrica (subgroup e; PP 1/BS 90). Therefore, these samples were identified as L. cf. lubrica species. The other two mycorrhizas do not group to a specific Leotia species. KKM 317 (KF836615) can be found among various L. lubrica and L. viscosa samples within subgroup a, which is not well supported, whereas the sample KKM 147 (KF836613) does not cluster in one of the above mentioned subgroups.

Discussion
The classification of Ascomycota was traditionally based on the morphology of their fruit bodies, whereas, molecular studies showed that such morphologically defined groups can be phylogenetically misleading (Wang et al. 2006a, b). Currently, the five orders Cyttariales, Erysiphales, Helotiales, Rhytismatales, and Thelebolales are placed in the ascomycetous class Leotiomycetes (Hibbett et al. 2007). The genus Leotia Pers. belongs to the Leotiaceae (Helotiales) whose final composition of genera is not fully resolved. Currently, Lumbsch and Huhndorf (2009) place the genera Geocoryne, Gelatinipulvinella, Leotia, Microglossum, Neobulgaria, and Pezoloma into this family. Sufficient molecular information of currently included genera is rarely or not at all available in NCBI database. Therefore, further reinterpretations within the Leotiaceae family are expected. Nevertheless, the obtained LSU rDNA sequences of the ten arbutoid mycorrhizas of C. arbutoides (KF836622-KF836631) identify them as members of the genus Leotia (Table 1).
Thus far, a detailed phylogenetic investigation within the genus Leotia has been carried out only by Zhong and Pfister (2004). They combined morphological information with phylogenetic analyses and found four groups within the genus Fig. 3 a-  Group I comprises all L. viscosa and some L. lubrica samples, which are characterized by a yellow stipe in fresh and dry condition, respectively. Another group (II) exclusively formed by L. lubrica samples, however, showed a green stipe when dry. The species L. atrovirens is divided into two groups (III and IV) and differ from each other by the presence or absence of gel in their stipes. Genetically, eight of ten arbutoid mycorrhizas of C. arbutoides collected in Costa Rica were identified as L. cf. lubrica. The other two leotioid mycorrhizas samples KKM 147 (KF836613) and KKM 317 (KF836615) still remain unidentified, whereby the first one represents a further genotype within the L. lubrica/viscosa complex, because it does not cluster in a specific subgroup within group I. However, those two leotioid mycorrhizas are also assumed to be L. lubrica species, since they were found as mycorrhizal partner of C. arbutoides. This suggests a high genetic variability of L. lubrica species assigned to group I.
The stipes of the L. lubrica fruit bodies found at site I, were not further investigated regarding a possible color change in dried condition or genetically. As pointed out by Zhong and Pfister (2004), it is difficult to distinguish between L. lubrica species of group I and II, as both have a yellow stipe in fresh conditions. Thus, it is not possible to clearly assign the found fruit bodies to one of both groups. However, thus far mycorrhizal associations are only known from group I L. lubrica samples, not from L. lubrica species belonging to group II. Among C. arbutoides, the species Q. rotundifolia, Polygonum sp., and N. menziesii are reported as host plants of leotioid ECMs (Branco and Ree 2010;Gao and Yang 2010;Orlovich et al. 2013). Orlovich et al. (2013) additionally indicate that Leotia perhaps interact in some way with other ectomycorrhizal fungi, since the fungus was found with either Russula, Clavulina, or Laccaria at the same root tip. Tedersoo et al. (2009) identified L. lubrica from ectomycorrhizal roots formed by Basidiomycota and the Rhamnaceae Pomaderris apetala (FN298733) and suggest a secondary colonization of ECMs by this fungal species (Tedersoo et al. 2010). However, such secondary mycorrhizal association for the described leotioid arbutoid mycorrhizas of C. arbutoides is not assumed. Color of leotioid mycorrhiza is similar to the fruit bodies of L. lubrica and all investigated samples show the same morpho-and anatomotype. Additionally, semi-thin sections reveal a mantle, Hartig net, as well as intracellular hyphae, typical for mycorrhizas of the Arbutoideae (Fig. 3e, f). However, only samples of L. cf. lubrica clustering in subgroup e were investigated, so no conclusion can be made if there are morphological or anatomical differences regarding the leotioid mycorrhizas KKM 147 (KF836613) and KKM 317 (KF836615).
The L. cf. lubrica arbutoid mycorrhiza is morphologically characterized by a hydrophilic, consistently transparent and  yellowish colored mantle. According to Rambold (2004-2014), these features are in common with the ECM of the Basidiomycete Entoloma nitidum (Montecchio et al. 2006). Given their smooth to moderately hairy surface, the leotioid arbutoid mycorrhiza is assigned to the contact exploration type or short distance exploration type (Agerer 2001). By contrast, the mantle of the E. nitidum ECM features abundant rhizomorphs and is therefore assigned to the medium distance exploration type (Montecchio et al. 2006). Anatomically, all mantle layers lack a matrix and offer hyphae with clamps, which make it also different from the leotioid mycorrhiza. Anatomically, the L. cf. lubrica arbutoid mycorrhiza is characterized by a continuous plectenchymatous mantle, wherein the middle mantle layer is embedded in a nongelatinous matrix. Anastomoses can be found in all layers, showing various types. Emanating hyphae also show anastomoses, which confirm them as such structures and not as cystidia (Agerer 1999). The yellowish droplets are another characteristic feature, only found in emanating hyphae and in hyphae of the outer mantle layer. The ECM of the hypogeous Ascomycete Gautieria inapire (Palfner and Horak 2001) also show a plectenchymatous mantle in all layers with clampless hyphae and oily droplets, which do not stain in sulpho-vanillin Rambold 2004-2014). However, it differs from L. cf. lubrica arbutoid mycorrhiza in having cystidia, emanating hyphae, and rhizomorphs. A matrix is also present, but shows, by subgroups (a-f) after Zhong and Pfister (2004) contrast, a gelatinous condition and can be found only in the inner mantle layer.
Color reactions of the leotioid arbutoid mycorrhiza are observed with cotton blue and toluidine blue, which are restricted to the hyphae of the outer mantle layer, emanating hyphae, and the droplets within. Both chemicals cause a metachromatic reaction due to the color change of droplets to red. Additionally, cell walls of the emanating hyphae turn violet in cotton blue and are thus cyanophil. In contrast, other applied chemicals cause no reaction, for instance, dissolution of the droplets.
Evidence of amyloidity or dextrinoidity in fungal structures is an important characteristic feature in taxonomy (Baral 1987;Rambold 2004-2014). These blue (amyloid) or red to red-brown (dextrinoid) iodinebased reactions are induced by Melzer's reagent as well as Lugol's solution. According to Baral (1987) there exists a special case of amyloidity, called hemiamyloidity. Here, Lugol's solution provokes a red reaction, whereas Melzer's reagent yields no reaction at all due to chloral hydrate contained within. However, a pretreatment with KOH causes a blue reaction in both, Lugol's and Melzer's. This hemiamyloid color reaction is so far only known in Ascomycetes, including many Helotiales (Baral 2009). Among mycologists, Melzer's reagent is prefered over Lugol's solution. This makes it more difficult to observe clearly a hemiamyloid reaction as Melzer's reagent solely used may falsely indicate inamyloidity (Baral 2009). For that reason, a possible hemiamyloid reaction of Ascomycete mycorrhizas could be overlooked. Regardless which treatment was applied, the arbutoid mycorrhiza of L. cf. lubrica reacts inamyloid. Zhong and Pfister (2004) confirm this reaction also for the cap of the ascoma for all three species of the genus Leotia.
The present study is the first morpho-anatomical proof that the species L. cf. lubrica is actually mycorrhizal. Besides C. arbutoides (Ericaceae) as mycorrhizal partner, an association likewise with Q. costaricensis has not been found as it was shown for the Basidiomycete Sebacina sp. (Kühdorf et al. 2014). However, an ectomycorrhizal association with Q. costaricensis is likewise assumed, since Branco and Ree (2010) reported a leotioid ECM with Q. rotundifolia. Nevertheless, it is interesting that mycorrhizas of L. lubrica were overlooked so far, although the fungus occurs worldwide. One possibility could be a low competitive ability, e.g., due to slow colonization of root tips (Kennedy 2010). In addition, a dual lifestyle (mycorrhizal as well as saprotrophic) may be also possible, as is known for the ectomycorrhizal Basidiomycete Laccaria bicolor (Vincent et al. 2012). However, these assumptions need further investigation. Further sampling could reveal if group II L. lubrica species also have the potential to be mycorrhizal or if this ability is limited to members of group I.