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Figure 3 from: Ezekiel CN, Kraak B, Sandoval-Denis M, Sulyok M, Oyedele OA, Ayeni KI, Makinde OM, Akinyemi OM, Krska R, Crous PW, Houbraken J (2020) Diversity and toxigenicity of fungi and description of Fusarium madaense sp. nov. from cereals, legumes and soils in north-central Nigeria. MycoKeys 67: 95-124. https://doi.org/10.3897/mycokeys.67.52716
Figure 3 The first of 1000 equally parsimonious trees obtained from Maximum-Parsimony (MP) analysis of RPB2 sequences of 76 isolates of Fusarium and Neocosmospora spp. Numbers on the nodes are MP bootstrap values (BS) and Maximum-Likelihood BS values above 70%. Branch lengths are proportional to distance. Ex-type and ex-epitype strains are indicated with T and ET, respectively. The names of 17 species complexes of Fusarium are shown in grey. Nigerian isolates obtained in this study are shown in red together with their geographical origin and source of isolation. The internal square shows MP statistics as follows: TL = tree length, CI = consistency index, RI = retention index and HI = homoplasy index.
Supplementary material 1 from: Ezekiel CN, Kraak B, Sandoval-Denis M, Sulyok M, Oyedele OA, Ayeni KI, Makinde OM, Akinyemi OM, Krska R, Crous PW, Houbraken J (2020) Diversity and toxigenicity of fungi and description of Fusarium madaense sp. nov. from cereals, legumes and soils in north-central Nigeria. MycoKeys 67: 95-124. https://doi.org/10.3897/mycokeys.67.52716
Tables S1, S2
Figure 2 from: Ezekiel CN, Kraak B, Sandoval-Denis M, Sulyok M, Oyedele OA, Ayeni KI, Makinde OM, Akinyemi OM, Krska R, Crous PW, Houbraken J (2020) Diversity and toxigenicity of fungi and description of Fusarium madaense sp. nov. from cereals, legumes and soils in north-central Nigeria. MycoKeys 67: 95-124. https://doi.org/10.3897/mycokeys.67.52716
Figure 2 Distribution of fungal species in food and soil in two states A Nasarawa state B Niger state C combined/both states) in north-central Nigeria.
Figure 4 from: Ezekiel CN, Kraak B, Sandoval-Denis M, Sulyok M, Oyedele OA, Ayeni KI, Makinde OM, Akinyemi OM, Krska R, Crous PW, Houbraken J (2020) Diversity and toxigenicity of fungi and description of Fusarium madaense sp. nov. from cereals, legumes and soils in north-central Nigeria. MycoKeys 67: 95-124. https://doi.org/10.3897/mycokeys.67.52716
Figure 4 The first of 24 equally parsimonious trees obtained from Maximum-Parsimony (MP) analysis of BenA, CaM, RPB1, RPB2 and TEF-1a sequences of 42 isolates of Fusarium spp. Numbers on the nodes are MP bootstrap values (BS) and Maximum-Likelihood BS values above 70%. Branch lengths are proportional to distance. Ex-type strains are indicated with T. Strains corresponding to new species described here are shown in bold. The internal square shows MP statistics as follows: TL = tree length, CI = consistency index, RI = retention index and HI = homoplasy index.
Figure 5 from: Ezekiel CN, Kraak B, Sandoval-Denis M, Sulyok M, Oyedele OA, Ayeni KI, Makinde OM, Akinyemi OM, Krska R, Crous PW, Houbraken J (2020) Diversity and toxigenicity of fungi and description of Fusarium madaense sp. nov. from cereals, legumes and soils in north-central Nigeria. MycoKeys 67: 95-124. https://doi.org/10.3897/mycokeys.67.52716
Figure 5 Fusarium madaense sp. nov. (ex-type culture CBS 146669). A–C aspect of colonies on PDA, OA and SNA, respectively, after 14 d at 24°C in the dark D colony reverse on OA (up) and PDA (down) after 14 d at 24 °C in the dark E–G, J aerial conidiophores and phialides H, I sporodochia formed on the surface of carnation leaves K, L sporodochial conidiophores M, N chlamydospores O, P microconidia Q sporodochial conidia. Scale bars: 100 μm (H, I); 20 μm (J); 10 μm (all others).
Figure 1 from: Ezekiel CN, Kraak B, Sandoval-Denis M, Sulyok M, Oyedele OA, Ayeni KI, Makinde OM, Akinyemi OM, Krska R, Crous PW, Houbraken J (2020) Diversity and toxigenicity of fungi and description of Fusarium madaense sp. nov. from cereals, legumes and soils in north-central Nigeria. MycoKeys 67: 95-124. https://doi.org/10.3897/mycokeys.67.52716
Figure 1 Overall incidence of fungal genera recovered from food and soil in two states in north-central Nigeria.
Supplementary material 3 from: Meidl P, Furneaux B, Tchan KI, Kluting K, Ryberg M, Guissou M-L, Soro B, Traoré A, Konomou G, Yorou NS, Rosling A (2021) Soil fungal communities of ectomycorrhizal dominated woodlands across West Africa. MycoKeys 81: 45-68. https://doi.org/10.3897/mycokeys.81.66249
Datafile 3
Supplementary material 1 from: Meidl P, Furneaux B, Tchan KI, Kluting K, Ryberg M, Guissou M-L, Soro B, Traoré A, Konomou G, Yorou NS, Rosling A (2021) Soil fungal communities of ectomycorrhizal dominated woodlands across West Africa. MycoKeys 81: 45-68. https://doi.org/10.3897/mycokeys.81.66249
Datafile 1
Supplementary material 2 from: Meidl P, Furneaux B, Tchan KI, Kluting K, Ryberg M, Guissou M-L, Soro B, Traoré A, Konomou G, Yorou NS, Rosling A (2021) Soil fungal communities of ectomycorrhizal dominated woodlands across West Africa. MycoKeys 81: 45-68. https://doi.org/10.3897/mycokeys.81.66249
Datafile 2
Supplementary material 5 from: Meidl P, Furneaux B, Tchan KI, Kluting K, Ryberg M, Guissou M-L, Soro B, Traoré A, Konomou G, Yorou NS, Rosling A (2021) Soil fungal communities of ectomycorrhizal dominated woodlands across West Africa. MycoKeys 81: 45-68. https://doi.org/10.3897/mycokeys.81.66249
Table S1 and Figs S1–S4
Supplementary material 4 from: Meidl P, Furneaux B, Tchan KI, Kluting K, Ryberg M, Guissou M-L, Soro B, Traoré A, Konomou G, Yorou NS, Rosling A (2021) Soil fungal communities of ectomycorrhizal dominated woodlands across West Africa. MycoKeys 81: 45-68. https://doi.org/10.3897/mycokeys.81.66249
Datafile 4
Figure 6 from: Meidl P, Furneaux B, Tchan KI, Kluting K, Ryberg M, Guissou M-L, Soro B, Traoré A, Konomou G, Yorou NS, Rosling A (2021) Soil fungal communities of ectomycorrhizal dominated woodlands across West Africa. MycoKeys 81: 45-68. https://doi.org/10.3897/mycokeys.81.66249
Figure 6 Taxonomic composition to family level of ECM fungi in gallery forest and woodlands. Abundance measured as fraction of reads (A) and richness measured as fraction of species hypotheses (SH) (B).
Figure 3 from: Meidl P, Furneaux B, Tchan KI, Kluting K, Ryberg M, Guissou M-L, Soro B, Traoré A, Konomou G, Yorou NS, Rosling A (2021) Soil fungal communities of ectomycorrhizal dominated woodlands across West Africa. MycoKeys 81: 45-68. https://doi.org/10.3897/mycokeys.81.66249
Figure 3 Species accumulation curves for each plot. Curves are based on SHs, by sequencing depth (A) and number of trees sampled (B), presented separately for three gallery forest sites (left panels) and six woodland sites (right panels). Points represent the observed species richness at the actual sequencing depth and trees sampled in A, B respectively. Thin lines represent the accumulation curve calculated by rarefaction (darker) and extrapolation (lighter); shaded regions represent the associated 95% confidence intervals. Dotted lines represent the asymptotic estimate for each site.
Figure 4 from: Meidl P, Furneaux B, Tchan KI, Kluting K, Ryberg M, Guissou M-L, Soro B, Traoré A, Konomou G, Yorou NS, Rosling A (2021) Soil fungal communities of ectomycorrhizal dominated woodlands across West Africa. MycoKeys 81: 45-68. https://doi.org/10.3897/mycokeys.81.66249
Figure 4 NMDS ordination of fungal communities based on Bray-Curtis dissimilarity of species hypothesis-based community composition, grouped into woodland (W) and gallery forests (GF) samples, for All fungi, axis 1–2 (A) and axis 2–3 (B), and for ECM fungi, axis 1–2 (C) and axis 3–4 (D). Stress value = 0.1902 for all fungi and 0.1723 for ECM fungi. Ellipses represent 95% confidence intervals around the mean of each vegetation type.
Figure 5 from: Meidl P, Furneaux B, Tchan KI, Kluting K, Ryberg M, Guissou M-L, Soro B, Traoré A, Konomou G, Yorou NS, Rosling A (2021) Soil fungal communities of ectomycorrhizal dominated woodlands across West Africa. MycoKeys 81: 45-68. https://doi.org/10.3897/mycokeys.81.66249
Figure 5 Fungal guild assignment of the soil fungal community in gallery forest and woodlands. Abundance measured as fraction of reads (A) and richness measured as fraction of species hypotheses (SH) (B) Guilds representing less than 2% of both abundance and richness are grouped together in "other".
Figure 2 from: Meidl P, Furneaux B, Tchan KI, Kluting K, Ryberg M, Guissou M-L, Soro B, Traoré A, Konomou G, Yorou NS, Rosling A (2021) Soil fungal communities of ectomycorrhizal dominated woodlands across West Africa. MycoKeys 81: 45-68. https://doi.org/10.3897/mycokeys.81.66249
Figure 2 NMDS ordination of tree communities based on Bray-Curtis dissimilarities between sites, based on total basal areas of each ECM trees species separately and all non-ECM trees combined. The nine sites were classified into two distinct woodland types, woodlands in red and gallery forests in blue. Site abbreviations: Bissandougou Forest Reserve (BISS-W), Moussaya Forest Reserve (MOUS-W), Kota Waterfall (KOTA-G and KOTA-W), Kouadianikro Forest Reserve (KDNK-W), Kou Forest Reserve (KOUF-G), Niangoloko Forest Reserve (NIAN-W) and Farako Forest Reserve (FA01-W and FA15-W). ECM tree species abbreviations: Afzelia africana (Aa), Ac: Anthonotha crassifolia (Ac), Bg: Berlinia grandiflora (Bg), Id: Isoberlinia doka (Id), I. tomentosa (It), Monotes kerstingii (Mk), Uapacaguineensis (Ug) and Uapaca togoensis (Ut).
Figure 1 from: Meidl P, Furneaux B, Tchan KI, Kluting K, Ryberg M, Guissou M-L, Soro B, Traoré A, Konomou G, Yorou NS, Rosling A (2021) Soil fungal communities of ectomycorrhizal dominated woodlands across West Africa. MycoKeys 81: 45-68. https://doi.org/10.3897/mycokeys.81.66249
Figure 1 Sampling sites of the West African Centre for Tropical Mycology's 2018 National Geographic Explorer Grant expedition. Shapes and colors separate the different woodland types with blue circles for gallery forests and red triangles for woodlands. With site names (abbreviations): Bissandougou (BISS-W), Moussaya (MOUS-W), Kota (KOTA-G and KOTA-W), Kouadianikro (KDNK-W), Kou (KOUF-G), Niangoloko (NIAN-W) and Farako (FA01-W and FA15-W). The dotted line represents the route taken on the sampling trip, beginning on the coast of Benin and concluding in Ivory Coast. Ecoregions are from White (1983), digitized in Olson et al. (2001).
HOUJIKI MATAMDA SHRIMATBHAGWAT KI MARU OIBA
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Figure 9 from: Evangelista DA, Chan K, Kaplan KI, Wilson MM, Ware JL (2015) The Blattodea s.s. (Insecta, Dictyoptera) of the Guiana Shield. ZooKeys 475: 37-87. https://doi.org/10.3897/zookeys.475.7877
Figure 9 - Xestoblatta berenbaumae sp. n. A Dorsal view of abdomen showing the simple tergal gland (DECBA2023) B, C Hooked left phallomere D Ventral medial phallomere (L2vm) E Right phallomere. R2e – external sclerite, R2i – internal sclerite, R2c – cleft sclerite F Posterior view of abdomen showing paraprocts and subgenital plate. RS-right stylus, LS-left stylus with small translucent ball at tip, LP-left paraproct reduced and specialized with polydentate spine, RP-unspecialized right paraproct. Illustration is a composite of multiple individuals G Dorsal view of sub-genital plate (DECBA1967) H Head of adult male I Hindwing (DECBA0801). Photos and illustrations contributed by Kayla Kaplan and Dominic A. Evangelista.
Figure 4 from: Evangelista DA, Chan K, Kaplan KI, Wilson MM, Ware JL (2015) The Blattodea s.s. (Insecta, Dictyoptera) of the Guiana Shield. ZooKeys 475: 37-87. https://doi.org/10.3897/zookeys.475.7877
Figure 4 - Epilampra sodali. A Adult male dorsal view (DECBA0401) B Juvenile dorsal view (DECBA2163). Add scale bar.
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