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Figure 4 from: Joshi A, Lanjekar VB, Dhakephalkar PK, Callaghan TM, Griffith GW, Dagar SS (2018) Liebetanzomyces polymorphus gen. et sp. nov., a new anaerobic fungus (Neocallimastigomycota) isolated from the rumen of a goat. MycoKeys 40: 89-110. https://doi.org/10.3897/mycokeys.40.28337
Figure 4 Phase contrast (A, C, E, G), fluorescence (B, D, F, H) and confocal (I) microscopic images of Liebetanzomycespolymorphus showing elongate (A–B) and triangular (C–D) sporangium filled with zoospores. Nuclei were seen in sporangium but not in sporangiophore (B) or rhizoidal system (F, H, I). No constrictions were observed in rhizoids. Scanning electron microscopy images of elongate (J) and globose (K) sporangium showing monocentric thallus. Scale bar: 20 µM (A–I); 10 µM (J–K).
Figure 2 from: Joshi A, Lanjekar VB, Dhakephalkar PK, Callaghan TM, Griffith GW, Dagar SS (2018) Liebetanzomyces polymorphus gen. et sp. nov., a new anaerobic fungus (Neocallimastigomycota) isolated from the rumen of a goat. MycoKeys 40: 89-110. https://doi.org/10.3897/mycokeys.40.28337
Figure 2 Microscopic features of Liebetanzomycespolymorphus showing pleomorphism in sporangial and rhizoidal structures, when grown on different carbon sources like rice straw (A), wheat straw (B), cellulose (C), xylan (D), starch (E), cellobiose (F), lactose (G), maltose (H), sucrose (I), glucose (J), xylose (K) and fructose (L). The exogenous sporangia appearing on a sporangiophore (A–B) and endogenous sporangia of different shapes (C–L) are shown. Scale bar: 20 µM.
Figure 3 from: Joshi A, Lanjekar VB, Dhakephalkar PK, Callaghan TM, Griffith GW, Dagar SS (2018) Liebetanzomyces polymorphus gen. et sp. nov., a new anaerobic fungus (Neocallimastigomycota) isolated from the rumen of a goat. MycoKeys 40: 89-110. https://doi.org/10.3897/mycokeys.40.28337
Figure 3 Microscopic images of Liebetanzomycespolymorphus. On rice straw (A–F) sporangia of varying sizes and shapes, like elongate (A), ellipsoid (B), ovoid (C), clavate (E) and globose (F). The zoospore cyst (A–C arrowed) is also visible, highlighting bipolar germination. Sporangiophore of varying length and shape, from short to long (A), sometimes eggcup shaped (C) and constricted (E arrowed) is shown. The sporangia with a papilla (D arrowed) and septum (B, C, D, E starred) are also indicated. Sporangia and thalli of irregular morphology on xylose (G–I) and cellobiose (J–L), including some pseudo-intercalary sporangia (J–L) can be observed. Scale bar: 20 µM.
Figure 1 from: Joshi A, Lanjekar VB, Dhakephalkar PK, Callaghan TM, Griffith GW, Dagar SS (2018) Liebetanzomyces polymorphus gen. et sp. nov., a new anaerobic fungus (Neocallimastigomycota) isolated from the rumen of a goat. MycoKeys 40: 89-110. https://doi.org/10.3897/mycokeys.40.28337
Figure 1 Macroscopic and microscopic features of Liebetanzomycespolymorphus. Colony morphology on agar roll tubes (A–C), showing the development of a colony attached (A) to a straw particle (arrowed), dense growth in the centre surrounded by numerous sporangia and zoospores (B–C) causing expansion of colony size. Growth in liquid medium showing a biofilm-like growth (D). Zoospores are spherical and Uniflagellate (E–F) or biflagellate (G). Germinating zoospore (H) showing a zoospore cyst (arrowed), presence and absence of sporangiophore indicating the endogenous and exogenous type of sporangial development (I) and different shapes of sporangia (I, J). Early stages of thallus development showing a single (K), bifurcated (L) and multifurcated (M) rhizoidal system. Scale bar: 1 mm (A–C); 10 µM (E–M).
Figure 3 from: Zhou Y-M, Zhi J-R, Ye M, Zhang Z-Y, Yue W-B, Zou X (2018) Lecanicillium cauligalbarum sp. nov. (Cordycipitaceae, Hypocreales), a novel fungus isolated from a stemborer in the Yao Ren National Forest Mountain Park, Guizhou. MycoKeys 43: 59-74. https://doi.org/10.3897/mycokeys.43.30203
Figure 3 Lecanicilliumcauligalbarum. a Synnemata emerged from the corpse of a stemborer (Lepidoptera) b Culture plate, showing the front (upper) and the back (lower) of the colony, cultured on PDA medium c–e Phialides solitary or in 2–3 whorls f–g Conidia. Scale bars: 10 mm (b, c, e), 5 μm (d, f, g).
Figure 2 from: Zhou Y-M, Zhi J-R, Ye M, Zhang Z-Y, Yue W-B, Zou X (2018) Lecanicillium cauligalbarum sp. nov. (Cordycipitaceae, Hypocreales), a novel fungus isolated from a stemborer in the Yao Ren National Forest Mountain Park, Guizhou. MycoKeys 43: 59-74. https://doi.org/10.3897/mycokeys.43.30203
Figure 2 Phylogenetic relationships of the form genus Lecanicillium, Akanthomyces, Samsoniella, Blackwellomyces, Hevansia and related genera in the Cordycipitaceae. Statistical support values (≥ 0.5/50%) are shown at the nodes for BI posterior probabilities/ML boostrap support.
Figure 1 from: Zhou Y-M, Zhi J-R, Ye M, Zhang Z-Y, Yue W-B, Zou X (2018) Lecanicillium cauligalbarum sp. nov. (Cordycipitaceae, Hypocreales), a novel fungus isolated from a stemborer in the Yao Ren National Forest Mountain Park, Guizhou. MycoKeys 43: 59-74. https://doi.org/10.3897/mycokeys.43.30203
Figure 1 Phylogenetic analysis of the isolated strains GZUIFRZHJ01 and GZUIFRZHJ02 and related species derived from a combined dataset of partial ITS+SSU+LSU+TEF+RPB1+RPB2 sequences. Statistical support values (≥ 0.5/50%) are shown at the nodes for BI posterior probabilities/ML boostrap support.
Supplementary material 1 from: Trovão J, Tiago I, Soares F, Paiva DS, Mesquita N, Coelho C, Catarino L, Gil F, Portugal A (2019) Description of Aeminiaceae fam. nov., Aeminium gen. nov. and Aeminium ludgeri sp. nov. (Capnodiales), isolated from a biodeteriorated art-piece in the Old Cathedral of Coimbra, Portugal. MycoKeys 45: 57-73. https://doi.org/10.3897/mycokeys.45.31799
: Data type: species data
Figure 2 from: Trovão J, Tiago I, Soares F, Paiva DS, Mesquita N, Coelho C, Catarino L, Gil F, Portugal A (2019) Description of Aeminiaceae fam. nov., Aeminium gen. nov. and Aeminium ludgeri sp. nov. (Capnodiales), isolated from a biodeteriorated art-piece in the Old Cathedral of Coimbra, Portugal. MycoKeys 45: 57-73. https://doi.org/10.3897/mycokeys.45.31799
Figure 2 Aeminiumludgeria Colony appearance on PDA b Colony appearance on MEA+10% NaCl (w/v) c Colony appearance on DG-18 d Colony appearance on PDA after maturation e Colony appearance on MEA+10% NaCl (w/v) after maturation f Colony appearance on DG-18 after maturation g Initial simple, branched, septate hyphae becoming toruloid-like (scale 20 μm) h Differentiated, toruloid-like hyphae and mature chains of arthroconidia (scale 50 μm) i Intercalary and terminal conidial chains (scale 20 μm); j typical aspect of arthroconidia (scale 20 μm)
Supplementary material 5 from: Trovão J, Tiago I, Soares F, Paiva DS, Mesquita N, Coelho C, Catarino L, Gil F, Portugal A (2019) Description of Aeminiaceae fam. nov., Aeminium gen. nov. and Aeminium ludgeri sp. nov. (Capnodiales), isolated from a biodeteriorated art-piece in the Old Cathedral of Coimbra, Portugal. MycoKeys 45: 57-73. https://doi.org/10.3897/mycokeys.45.31799
: Data type: species data
Figure 1 from: Trovão J, Tiago I, Soares F, Paiva DS, Mesquita N, Coelho C, Catarino L, Gil F, Portugal A (2019) Description of Aeminiaceae fam. nov., Aeminium gen. nov. and Aeminium ludgeri sp. nov. (Capnodiales), isolated from a biodeteriorated art-piece in the Old Cathedral of Coimbra, Portugal. MycoKeys 45: 57-73. https://doi.org/10.3897/mycokeys.45.31799
Figure 1 Bayesian 50% majority rule consensus tree based on an LSU/rpb2/ITS concatenated alignment, containing representative sequences from the order Capnodiales. The new strains are shown in bold. Bayesian posterior probabilities (BP) ≥ 0.95 are presented at the nodes. The tree was rooted to Parastagonosporanodorum CBS 110109. The scale bar specifies 0.2 expected changes per site.
Supplementary material 4 from: Trovão J, Tiago I, Soares F, Paiva DS, Mesquita N, Coelho C, Catarino L, Gil F, Portugal A (2019) Description of Aeminiaceae fam. nov., Aeminium gen. nov. and Aeminium ludgeri sp. nov. (Capnodiales), isolated from a biodeteriorated art-piece in the Old Cathedral of Coimbra, Portugal. MycoKeys 45: 57-73. https://doi.org/10.3897/mycokeys.45.31799
: Data type: statistical data
Supplementary material 3 from: Trovão J, Tiago I, Soares F, Paiva DS, Mesquita N, Coelho C, Catarino L, Gil F, Portugal A (2019) Description of Aeminiaceae fam. nov., Aeminium gen. nov. and Aeminium ludgeri sp. nov. (Capnodiales), isolated from a biodeteriorated art-piece in the Old Cathedral of Coimbra, Portugal. MycoKeys 45: 57-73. https://doi.org/10.3897/mycokeys.45.31799
: Data type: statistical data
Supplementary material 2 from: Trovão J, Tiago I, Soares F, Paiva DS, Mesquita N, Coelho C, Catarino L, Gil F, Portugal A (2019) Description of Aeminiaceae fam. nov., Aeminium gen. nov. and Aeminium ludgeri sp. nov. (Capnodiales), isolated from a biodeteriorated art-piece in the Old Cathedral of Coimbra, Portugal. MycoKeys 45: 57-73. https://doi.org/10.3897/mycokeys.45.31799
: Data type: phylogenetic data
Figure 4 from: Khuna S, Suwannarach N, Kumla J, Meerak J, Nuangmek W, Kiatsiriroat T, Lumyong S (2019) Apophysomyces thailandensis (Mucorales, Mucoromycota), a new species isolated from soil in northern Thailand and its solubilization of non-soluble minerals. MycoKeys 45: 75-92. https://doi.org/10.3897/mycokeys.45.30813
Figure 4 Apophysomycesthailandensis SDBR-CMUS26 (holotype). A colony on potato dextrose agar B Colony on malt extract agar C Colony on Czapek agar D Branched, aseptate hyphae E Funnel-shaped apophysis F Slightly trapezoidal sporangiospores. Scale bars: 10 mm (A–C), 10 µm (D–E), 20 µm (F).
Figure 3 from: Khuna S, Suwannarach N, Kumla J, Meerak J, Nuangmek W, Kiatsiriroat T, Lumyong S (2019) Apophysomyces thailandensis (Mucorales, Mucoromycota), a new species isolated from soil in northern Thailand and its solubilization of non-soluble minerals. MycoKeys 45: 75-92. https://doi.org/10.3897/mycokeys.45.30813
Figure 3 Solubilization index of the ability to solve non-soluble mineral by Apophysomycesthailandensis. Data are means of three replicates. Error bar at each point indicates ± SD. Different letters above each graph indicate that the means are significantly different by Tukey's test (P < 0.05)
Figure 2 from: Khuna S, Suwannarach N, Kumla J, Meerak J, Nuangmek W, Kiatsiriroat T, Lumyong S (2019) Apophysomyces thailandensis (Mucorales, Mucoromycota), a new species isolated from soil in northern Thailand and its solubilization of non-soluble minerals. MycoKeys 45: 75-92. https://doi.org/10.3897/mycokeys.45.30813
Figure 2 Solubilization of non-soluble minerals in agar media by Apophysomycesthailandensis SDBR-CMUS26 (holotype). A Ca3(PO4)2B CuCO3•Cu(OH)2C CuO D ZnCO3E FePO4F MnO G Feldspar H Kaolin. Scale bars: 10 mm. Fungal colonies in E and F were cut for the solubilization area (halo zone) observation.
Figure 1 from: Khuna S, Suwannarach N, Kumla J, Meerak J, Nuangmek W, Kiatsiriroat T, Lumyong S (2019) Apophysomyces thailandensis (Mucorales, Mucoromycota), a new species isolated from soil in northern Thailand and its solubilization of non-soluble minerals. MycoKeys 45: 75-92. https://doi.org/10.3897/mycokeys.45.30813
Figure 1 Phylogenetic tree derived from maximum likelihood analysis of a combined ITS, LSU, and H3 genes of 28 sequences. Saksenaeavasiformis and S.erythrospora were used as outgroup. Numbers above branches are the bootstrap statistics percentages (left) and Bayesian posterior probabilities (right). Branches with bootstrap values ≥ 50% are shown at each branch and the bar represents 0.1 substitutions per nucleotide position. The fungal isolates from this study are in bold. Superscript T = type species.
FIGURE 32 in Revision of the Old World species of the genus Tephritis (Diptera, Tephritidae) with a pair of isolated apical spots
FIGURE 32. Tephritis theryi—habitus, paratype♀. Scale bar = 1 mm.
FIGURES 18a–b in Revision of the Old World species of the genus Tephritis (Diptera, Tephritidae) with a pair of isolated apical spots
FIGURES 18a–b. Tephritis heiseri: a—habitus ♀; b—abdomen, dorsal.
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Allen Brain Atlas
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OpenNeuro
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