identifier	taxonID	type	CVterm	format	language	title	description	additionalInformationURL	UsageTerms	rights	Owner	contributor	creator	bibliographicCitation
DB578615C5705B27BA46D29A15810478.text	DB578615C5705B27BA46D29A15810478.taxon	http://purl.org/dc/dcmitype/Text	http://rs.tdwg.org/ontology/voc/SPMInfoItems#GeneralDescription	text/html	en	Delicatispora Blaszk., Niezgoda & B. T. Goto 2025	<html xmlns:mods="http://www.loc.gov/mods/v3">
    <body>
        <div>
            <p> Delicatispora Błaszk., Niezgoda &amp; B. T. Goto gen. nov.</p>
            <p>Fig. 1, Suppl. material 1</p>
            <p>Etymology.</p>
            <p>Latin, Delicati and spora, referring to the delicate spores produced by the type species of the genus.</p>
            <p>Type genus.</p>
            <p> Delicatispora indica (Błaszk., Wubet &amp; Harikumar) , Błaszk., Niezgoda &amp; B. T. Goto,  comb. nov.</p>
            <p>Basionym.</p>
            <p> Glomus indicum Błaszk., Wubet &amp; Harikumar.</p>
            <p>Synonym.</p>
            <p> Dominikia indica (Błaszk., Wubet &amp; Harikumar) Błaszk., Chwat &amp; Kovács.</p>
            <p>Diagnosis.</p>
            <p> Differs from other genera of  Glomerales in nucleotide composition of sequences of the 45 S nuc rDNA region (see “ Discussion ” for details). </p>
            <p>Genus description.</p>
            <p>As that in Błaszkowski et al. (2010 b).</p>
        </div>
    </body>
</html>
	https://treatment.plazi.org/id/DB578615C5705B27BA46D29A15810478	Public Domain	No known copyright restrictions apply. See Agosti, D., Egloff, W., 2009. Taxonomic information exchange and copyright: the Plazi approach. BMC Research Notes 2009, 2:53 for further explanation.		Pensoft via Plazi	Błaszkowski, Janusz;Zubek, Szymon;Milczarski, Paweł;Malinowski, Ryszard;Niezgoda, Piotr;Goto, Bruno Tomio	Błaszkowski, Janusz, Zubek, Szymon, Milczarski, Paweł, Malinowski, Ryszard, Niezgoda, Piotr, Goto, Bruno Tomio (2025): New taxa and a combination in Glomerales (Glomeromycota, Glomeromycetes). MycoKeys 112: 253-276, DOI: 10.3897/mycokeys.112.136158
60062287D34E5DBF8C6FD9F6B3F88A50.text	60062287D34E5DBF8C6FD9F6B3F88A50.taxon	http://purl.org/dc/dcmitype/Text	http://rs.tdwg.org/ontology/voc/SPMInfoItems#GeneralDescription	text/html	en	Delicatispora indica (Błaszkowski & Zubek & Milczarski & Malinowski & Niezgoda & Goto 2025) Blaszk., Niezgoda & B. T. Goto 2025	<html xmlns:mods="http://www.loc.gov/mods/v3">
    <body>
        <div>
            <p> Delicatispora indica (Błaszk., Wubet &amp; Harikumar) Błaszk., Niezgoda &amp; B. T. Goto comb. nov.</p>
            <p>Fig. 1, Suppl. material 1</p>
            <p>Etymology.</p>
            <p>Latin, referring to India where this species was originally found.</p>
            <p>Specimens examined.</p>
            <p> Poland. Spores from single-species cultures established from spores extracted from trap pot cultures inoculated with rhizosphere soil and root fragments of  Euphorbia heterophylla L. from coastal sands of Alappuzha in Kerala State of South India (90 ° 55 ' N, 76.0 ° 46 ' E) and  Lactuca sativa L. cultivated in Asmara, Eritrea, North East Africa (15 ° 28 ' N, 38 ° 55 ' E), 10 Apr 2009, J. Błaszkowski (holotype: slide with spores no. LPPDSE 3113; isotypes: slides with spores nos. LPPDSE 3108–3112 and 3114–3133), and two slides at OSC. </p>
            <p>Diagnosis.</p>
            <p> As that of  Delicatispora (see above). </p>
            <p>Description.</p>
            <p>As that in Błaszkowski et al. (2010 b).</p>
            <p>Ecology and distribution.</p>
            <p> Originally found in two trap pot cultures inoculated with rhizosphere soils and root fragments of  E. heterophylla from coastal sands of Alappuzha in Kerala State of South India and  L. sativa cultivated in Asmara, Eritrea, Northeast Africa. The geographic positions of the sampled sites, physicochemical properties of their soils, and features of mycorrhizal structures formed in single-species cultures of this fungus, are given in Błaszkowski et al. (2010 b). Based on ≥ 98 % SSU rDNA sequence identity to uncultured AMF sequences available in public databases, suggested to have also been present in various states of the USA, Estonia, and Australia (Błaszkowski et al. 2010 b). In the USA, also found associated with roots of  Panicum virgatum L. in Wisconsin, as resulted from phylogenetic analyses of our 45 S alignment with the MT 765488, MT 765651, and MT 765457 environmental sequences with&gt; 96 % identity to 45 S sequences of  D. indica (data not shown). </p>
        </div>
    </body>
</html>
	https://treatment.plazi.org/id/60062287D34E5DBF8C6FD9F6B3F88A50	Public Domain	No known copyright restrictions apply. See Agosti, D., Egloff, W., 2009. Taxonomic information exchange and copyright: the Plazi approach. BMC Research Notes 2009, 2:53 for further explanation.		Pensoft via Plazi	Błaszkowski, Janusz;Zubek, Szymon;Milczarski, Paweł;Malinowski, Ryszard;Niezgoda, Piotr;Goto, Bruno Tomio	Błaszkowski, Janusz, Zubek, Szymon, Milczarski, Paweł, Malinowski, Ryszard, Niezgoda, Piotr, Goto, Bruno Tomio (2025): New taxa and a combination in Glomerales (Glomeromycota, Glomeromycetes). MycoKeys 112: 253-276, DOI: 10.3897/mycokeys.112.136158
DE6C09F5C5D658FCB1906F6B7F7D5A93.text	DE6C09F5C5D658FCB1906F6B7F7D5A93.taxon	http://purl.org/dc/dcmitype/Text	http://rs.tdwg.org/ontology/voc/SPMInfoItems#GeneralDescription	text/html	en	Dominikia paraminuta Blaszk., Niezgoda & B. T. Goto 2025	<html xmlns:mods="http://www.loc.gov/mods/v3">
    <body>
        <div>
            <p> Dominikia paraminuta Błaszk., Niezgoda &amp; B. T. Goto sp. nov.</p>
            <p>Fig. 2 A – H</p>
            <p>Specimens examined.</p>
            <p> Poland. Pomeranian Province, spores from single-species cultures established from spores extracted from trap pot cultures inoculated with rhizosphere soil and root fragments of  Ammophila arenaria from the Hel Peninsula maritime dunes (54 ° 45 ' 31 " N, 18 ° 30 ' 38 " E and 54 ° 41 ' 58 " N, 18 ° 40 ' 36 " E), 14 Aug 2012, J. Błaszkowski (holotype: slide with spores Z + ZT Myc 0067480; isotypes: slides with spores nos. 3979–3987, LPPDSE). </p>
            <p>Etymology.</p>
            <p>Latin, paraminuta, referring to D. minuta, the phylogenetic sister of this new species.</p>
            <p>Diagnosis.</p>
            <p> Differs from  D. minuta , the phylogenetic sister, in (i) morphometric features of spores and their spore wall, (ii) the spore wall structure, (iii) phenotypic properties of spore wall layer 1, and (iv) nucleotide composition of sequences of the 45 S nuc rDNA region (see “ Discussion ” for details). </p>
            <p>Description.</p>
            <p>Forming loose to compact hypogeous clusters with five to ca. 25 randomly distributed spores and sterile hyphae (Fig. 2 A – D). Spores glomoid, arising blastically at tips of subtending hyphae (Fig. 2 A, B, F, G) branched from a parent hypha continuous with a mycorrhizal extraradical hypha. Spores hyaline; globose to subglobose; (23 –) 31 (– 39) µm diam; rarely ovoid to oblong, 14–33 × 26–71 µm; with one subtending hypha (Fig. 2 A – G). Spore wall composed of three hyaline layers (layers 1–3; Fig. 2 D – G). Layer 1, forming the spore surface, uniform (without visible sublayers), semi-permanent, (0.8 –) 1.3 (– 2.0) µm thick when smooth, often with local thickenings, (1.2 –) 2.1 (– 3.8) µm thick, randomly distributed on the spore surface, rarely strongly or completely sloughed off in aged spores (Fig. 2 D – G). Layer 2 laminate, permanent, smooth, (1.0 –) 1.4 (– 2.0) µm thick, consisting of very thin, &lt;0.5 µm, sublayers tightly adherent to and not separating from each other even in vigorously crushed spores (Fig. 2 D – G). Layer 3 uniform, permanent, smooth, ca. 0.6–0.8 µm thick, usually tightly adherent to the inner surface of layer 2 and, therefore, difficult to detect. Layers 1–3 do not stain in Melzer’s reagent (Fig. 2 E – G). Subtending hypha hyaline; straight or recurved, usually cylindrical to funnel-shaped, rarely slightly constricted at the spore base, (3.8 –) 5.7 (– 9.5) µm wide at the spore base (Fig. 2 A, B, F, G). Wall of subtending hypha hyaline; (1.6 –) 2.2 (– 2.9) µm thick at the spore base; composed of three layers continuous with spore wall layers 1–3 (Fig. 2 F, G). Pore (1.0 –) 1.9 (– 5.8) µm diam, usually open (Fig. 2 F), very rarely occluded by a curved septum connecting the inner surfaces of subtending hyphal wall layer 3; septum 0.4–0.6 µm thick, located ca. 2.0 µm below the spore base (Fig. 2 G). Sterile hyphae hyaline, (2.8 –) 4.4 (– 5.2) µm wide (Fig. 2 B, C). Germination unknown.</p>
            <p>Ecology and distribution.</p>
            <p> In the field,  D. paraminuta probably lived in arbuscular mycorrhizal symbiosis with roots of  A. arenaria that colonized maritime sand dunes near Chałupy and Jastarnia on the Hel Peninsula, northern Poland. However, no molecular analyses were performed to confirm this assumption. In single-species cultures with  P. lanceolata as host plant,  D. paraminuta formed mycorrhiza with arbuscules, vesicles, and intra- and extraradical hyphae (Fig. 2 H). These structures stained clearly [pale violet (16 A 3) to deep violet (16 E 8)] in 0.1 % Trypan blue. Phylogenetic analyses with the 45 S alignment used in this study and environmental sequences with&gt; 96 % identity to 45 S sequences of  D. paraminuta , revealed by BLASTn, indicated that  D. paraminuta was previously recognized in grasslands and unspecified sites in China (data not shown). </p>
        </div>
    </body>
</html>
	https://treatment.plazi.org/id/DE6C09F5C5D658FCB1906F6B7F7D5A93	Public Domain	No known copyright restrictions apply. See Agosti, D., Egloff, W., 2009. Taxonomic information exchange and copyright: the Plazi approach. BMC Research Notes 2009, 2:53 for further explanation.		Pensoft via Plazi	Błaszkowski, Janusz;Zubek, Szymon;Milczarski, Paweł;Malinowski, Ryszard;Niezgoda, Piotr;Goto, Bruno Tomio	Błaszkowski, Janusz, Zubek, Szymon, Milczarski, Paweł, Malinowski, Ryszard, Niezgoda, Piotr, Goto, Bruno Tomio (2025): New taxa and a combination in Glomerales (Glomeromycota, Glomeromycetes). MycoKeys 112: 253-276, DOI: 10.3897/mycokeys.112.136158
65C2AB47776550409DA8BCE5E0056791.text	65C2AB47776550409DA8BCE5E0056791.taxon	http://purl.org/dc/dcmitype/Text	http://rs.tdwg.org/ontology/voc/SPMInfoItems#GeneralDescription	text/html	en	Macrodominikia compressa (Sieverd., Oehl, Palenz., Sánchez-Castro & G. A. Silva) Blaszk., Niezgoda & B. T. Goto	<html xmlns:mods="http://www.loc.gov/mods/v3">
    <body>
        <div>
            <p> Macrodominikia compressa (Sieverd., Oehl, Palenz., Sánchez-Castro &amp; G. A. Silva) emend. Błaszk., Niezgoda &amp; B. T. Goto</p>
            <p>Figs 3 A – H, 4 A, B</p>
            <p>Specimens examined.</p>
            <p> Poland. Pomeranian Province, spores from a trap pot culture inoculated with rhizosphere soil and root fragments of  Ammophila arenaria from the Hel Peninsula maritime dunes (54 ° 36 ' 42 " N, 18 ° 48 ' 29 " E), 5 Aug 2021, P. Niezgoda (slides with spores nos. 3988–3990, LPPDSE). Switzerland. Two slides with holotype sporocarps and spores deposited under the accession number Z + ZT Myc 52538. Brazil. Thirty-three isotypic spores deposited under the URM 85721 accession number. </p>
            <p>Diagnosis.</p>
            <p> Differs from other genera of  Dominikiaceae in (i) having subtending hyphae with a strong bend and locally very narrow lumen due to large thickening present on the inner surfaces of the subtending hyphal walls and (ii) nucleotide composition of sequences of the 45 S nuc rDNA region (see “ Discussion ” for details). </p>
            <p>Description.</p>
            <p>Forming loose to compact hypogeous clusters with 3–33 randomly distributed spores (Fig. 3 A), and spores singly in the soil. Spores glomoid, arising blastically at tips of subtending hyphae (Figs 3 B, D – H, 4 B) either branched from a parent hypha continuous with a mycorrhizal extraradical hypha (spores in clusters), or directly continuous with a mycorrhizal extraradical hypha (single spores). Spores pale yellow (4 A 3) to brownish yellow (5 C 8); globose to subglobose; (19 –) 62 (– 100) µm diam; rarely ovoid to oblong 22–81 × 66–134, to irregular; with one subtending hypha (Figs 3 A – H, 4 A, B). Spore wall composed of four layers (layers 1–4; Figs 3 B – H, 4 A, B). Layer 1, forming the spore surface, evanescent, flexible, hyaline, (0.6 –) 0.9 (– 1.4) µm thick, usually slightly swelling in PVLG and then easier to detect (Fig. 3 B – H), occasionally strongly or completely sloughed off in aged spores (Fig. 4 A, B). Layer 2 uniform (without visible sublayers), permanent, flexible to semi-flexible, smooth, hyaline, (0.8 –) 1.2 (– 1.5) µm thick, tightly adherent to layer 3 (Figs 3 B – H, 4 A, B). Layer 3 laminate, semi-rigid, smooth, pale yellow (4 A 3) to brownish yellow (5 C 8), (2.8 –) 3.8 (– 6.3) µm thick, consisting of very thin, &lt;0.5 µm thick, sublayers tightly adherent to and not separating from each other even in vigorously crushed spores (Figs 3 B – H, 4 A, B). Layer 4 uniform, flexible to semi-flexible, smooth, concolorous with or slightly lighter than layer 3, (0.8 –) 1.0 (– 1.3) µm thick, usually only slightly separating from the lower surface of layer 3 even in vigorously crushed spores (Figs 3 B – H, 4 A, B). Layers 1–4 do not stain in Melzer’s reagent (Fig. 3 B – H). Subtending hypha concolorous with or slightly lighter than the spores; straight or recurved, usually cylindrical to funnel-shaped, rarely slightly constricted at the spore base, (9.6 –) 14.2 (– 20.4) µm wide at the spore base (Figs 3 A, B, D – H, 4 B). Walls of subtending hypha concolorous with or slightly lighter than the spores; usually with thickenings of unequal size, (5.8 –) 7.2 (– 11.0) µm vs. (4.0 –) 5.1 (– 6.0) µm thick, present on the inner, opposite surfaces of the walls, making the subtending hyphal lumen more or less curved and narrow when seen in a plan view (Fig. 3 A, D, E, H); less often, both walls have the same or similar thickness, (4.0 –) 6.3 (– 8.1) µm (Fig. 3 G); subtending hyphal walls composed of four layers continuous with spore wall layers 1–4 (Fig. 3 B, D, E – H). Pore (1.0 –) 2.4 (– 7.0) µm diam, open (Fig. 3 D, E) or occluded by a curved septum continuous with spore wall layer 4; septum 0.6–1.0 µm thick, located at or up to 8.2 µm below the spore base (Fig. 3 G, H); subtending hyphal lumen rarely occluded by an additional septum located up to 22 µm below the spore base. Sterile hyphae hyaline, (1.8 –) 4.2 (– 5.6) µm wide. Germination unknown.</p>
            <p>Ecology and distribution.</p>
            <p> Results from our studies conclude that in the field  M. compressa probably lived in arbuscular mycorrhizal symbiosis with roots of  A. arenaria that colonized maritime dunes near Hel on the Hel Peninsula in northern Poland. However, no molecular analyses were performed to confirm this assumption. In a trap pot culture,  M. compressa produced abundant spore communities. Oehl et al. (2014) found this species, as  G. compressum , in ten locations in Switzerland, southwestern Germany, and northeastern France. It occurred in grasslands and crop rotation systems located at altitudes between 230–1505 m asl., with soils with a wide range of pH (5.7–8.0), organic carbon (9.8–45.8 g kg - 1), and different levels of plant available phosphate. There is no sequence in GenBank with&gt; 96 % identity to the 45 S sequence  M. compressa , which would suggest the presence of this species in other regions of the world. </p>
        </div>
    </body>
</html>
	https://treatment.plazi.org/id/65C2AB47776550409DA8BCE5E0056791	Public Domain	No known copyright restrictions apply. See Agosti, D., Egloff, W., 2009. Taxonomic information exchange and copyright: the Plazi approach. BMC Research Notes 2009, 2:53 for further explanation.		Pensoft via Plazi	Błaszkowski, Janusz;Zubek, Szymon;Milczarski, Paweł;Malinowski, Ryszard;Niezgoda, Piotr;Goto, Bruno Tomio	Błaszkowski, Janusz, Zubek, Szymon, Milczarski, Paweł, Malinowski, Ryszard, Niezgoda, Piotr, Goto, Bruno Tomio (2025): New taxa and a combination in Glomerales (Glomeromycota, Glomeromycetes). MycoKeys 112: 253-276, DOI: 10.3897/mycokeys.112.136158
93569CDEC68350689D8C34906ADFADF8.text	93569CDEC68350689D8C34906ADFADF8.taxon	http://purl.org/dc/dcmitype/Text	http://rs.tdwg.org/ontology/voc/SPMInfoItems#GeneralDescription	text/html	en	Microkamienskia perpusilla (Blaszk. & Kovacs) Corazon-Guivin, G. A. Silva & Oehl	<html xmlns:mods="http://www.loc.gov/mods/v3">
    <body>
        <div>
            <p> Microkamienskia perpusilla (Błaszk. &amp; Kovács) Corazon-Guivin, G. A. Silva &amp; Oehl</p>
            <p>Fig. 4 C, D</p>
            <p>Basionym.</p>
            <p> Glomus perpusillum Błaszk. &amp; Kovács.</p>
            <p>Synonym.</p>
            <p> Kamienskia perpusilla (Błaszk. &amp; Kovács) Błaszk., Chwat &amp; Kovács.</p>
            <p>Specimens examined.</p>
            <p> Poland. Pomeranian Province, spores from single-species cultures established from spores extracted from a trap pot culture inoculated with rhizosphere soil and root fragments of  Ammophila arenaria from the Hel Peninsula maritime dunes (54 ° 47 ' 35 " N, 18 ° 24 ' 69 " E), 7 Aug 2021, P. Niezgoda (slides with spores nos. 3991–3996, LPPDSE). </p>
            <p>Diagnosis.</p>
            <p> Differs from  Mk. peruviana , the phylogenetic sister (Fig. 1), in (i) morphometric features of the spore wall, the spore subtending hypha, and the pore connecting the subtending hyphal lumen with the spore interior, (ii) phenotypic properties of spore wall layer 1 and subtending hyphal wall layer 1, and (iii) nucleotide composition of sequences of the 45 S nuc rDNA region (Błaszkowski et al. 2009 a; Corazon-Guivin et al. 2019 b; see “ Discussion ” for details). </p>
            <p>Notes.</p>
            <p> The morphological features of Isolate 524 (Fig. 4 C, D), here recognized to be conspecific with  Mk. perpusilla , were nearly identical to those originally defined for  G. perpusillum (Błaszkowski et al. 2009 a) . The only discrepancy was the lack of plasticity and contractibility of spore wall layer 2 in Isolate 524, which were considered unique features of  G. perpusillum . </p>
        </div>
    </body>
</html>
	https://treatment.plazi.org/id/93569CDEC68350689D8C34906ADFADF8	Public Domain	No known copyright restrictions apply. See Agosti, D., Egloff, W., 2009. Taxonomic information exchange and copyright: the Plazi approach. BMC Research Notes 2009, 2:53 for further explanation.		Pensoft via Plazi	Błaszkowski, Janusz;Zubek, Szymon;Milczarski, Paweł;Malinowski, Ryszard;Niezgoda, Piotr;Goto, Bruno Tomio	Błaszkowski, Janusz, Zubek, Szymon, Milczarski, Paweł, Malinowski, Ryszard, Niezgoda, Piotr, Goto, Bruno Tomio (2025): New taxa and a combination in Glomerales (Glomeromycota, Glomeromycetes). MycoKeys 112: 253-276, DOI: 10.3897/mycokeys.112.136158
