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FIGURE 2 in Nomenclature of Caroxylon imbricatum s.lat. (Amaranthaceae / Chenopodiaceae), with a new combination at variety rank

FIGURE 2. Isolectotype of Chenopodium baryosmon (≡ Salsola baryosma), eventually the only actual specimen of the species seen by Schultes (by courtesy of the Bayerische Staatssammlungen München, M).

FIGURE 1. A in New lichen species from Thailand, new combinations and new additions to the Thai lichen biota

FIGURE 1. A. Acanthothecis consocians (J.S. & K.K., KK37067; scale 0.5 mm); B. Caloplaca bassiae (J.K. & K.K, KJK 41911; scale 0.4 mm); C. Chapsa pulchra (K.K. et al., KK 39153; scale 0.5 mm); D. Constrictolumina leucostoma (K.K. et al., KK 40863; scale 0.5 mm); E. Allographa stictilabiata, section through ascoma showing the striate exciple (scale 100 μm); F. Allographa stictilabiata (K.K. & Poengsungnoen, KK 38768; scale 1 mm); G. Graphis aphaneomicrospora (K.K. et al., KK 38387; scale 0.8 mm); H. Graphis balaghatensis (J.S. & K.K., KJK 41380; scale 0.5 mm).

FIGURE 3. A in New lichen species from Thailand, new combinations and new additions to the Thai lichen biota

FIGURE 3. A. Pseudotopeliopsis longispora (J.K. & K.K, KJK 41893; scale 0.5 mm); B. Ramonia minima, ascomata (holotype; scale 0.2 mm); C. Ramonia minima, section through ascoma (scale 25 μm; inlay, ascospores (scale 5 μm); D. Sclerophyton seriale (J.K. & K.K, KJK 42013; scale 1 mm); E. Traponora macrospora (K.K. et al., KK 36844; scale 0.2 mm); F. Trinathotrema stictideum (Vongshewarat s.n. RAMK; scale 0.3 mm).

FIGURE 2. A in New lichen species from Thailand, new combinations and new additions to the Thai lichen biota

FIGURE 2. A. Graphis indica (J.K. & K.K, KJK 41769; scale 1 mm); B. Leucodecton occultum (J.K. & K.K, KJK 41952; scale 0.25 mm); C. Phaeographopsis palaeotropica, ascomata with a distinct black mazaedium (J.K. & K.K, KJK 41398; scale 0.5 mm); D. Phaeographopsis palaeotropica, ascomata lacking a mazaedium (J.K. & K.K, KJK 41395; scale 0.4 mm); E. Platygramme australis (J.K. & K.K, KJK 41279; scale 0.5 mm); F. Platygramme commutabilis (Sutjaritturakan 4225, KJK 42227; scale 1 mm); G. Platygramme discurrens (Sutjaritturakan 4895, KJK 42217; scale 0.3 mm); H. Platygramme subcolubrosa (J.S. & K.K., KK 41534; scale 0.5 mm).

FIGURE 7 in Combined multi-gene backbone tree for the genus Coniochaeta with two new species from Uzbekistan

FIGURE 7. Coniochaeta coluteae (from isotype culture MFLUCC 17-2299) a. Culture on MEA from above after 4 weeks. b. Culture on MEA from below after 4 weeks. c, d. Hyphal strands on the culture. e–j. Conidiogenous cells on hyphal cells (arrow heads: conidiogenesis). k. Conidia. Scale bars: c,d=200 μm, e–k=5 μm.

FIGURE 6 in Combined multi-gene backbone tree for the genus Coniochaeta with two new species from Uzbekistan

FIGURE 6. Coniochaeta coluteae (holotype TASM 6104) a, b. Ascomata on the substrate. c, d. Vertical section of ascoma. e, f. Ostiole. g. Section of peridium (in water). h. Section of peridium (in 5% KOH). i. Paraphyses. j. Ascus apex in Congo Red. k. Ascospores. l–n. Asci (arrowheads show germ slits in n). Scale bars: a=500 μm, b=200 μm, c=100 μm, d=50 μm, e, f=20 μm, g–i, l–n=10 μm, j, k=5 μm.

FIGURE 3 in Combined multi-gene backbone tree for the genus Coniochaeta with two new species from Uzbekistan

FIGURE 3. Results of the PHI test of closely related species (a C. acaciae, b C. coluteae) using both LogDet transformation and splits decomposition. New species described in this study are indicated in red, type strains are in boldface.

FIGURE 5 in Combined multi-gene backbone tree for the genus Coniochaeta with two new species from Uzbekistan

FIGURE 5. Coniochaeta acaciae (from isotype culture MFLUCC 17-2298) a. Culture on MEA from above after 4 weeks. b. Culture on MEA from below after 4 weeks. c. Hyphal strands on the culture. d–i. Conidiogenous cells on hyphal cells. j. Conidia. Scale bars: c=200 μm, d–j=5 μm.

FIGURE 4 in Combined multi-gene backbone tree for the genus Coniochaeta with two new species from Uzbekistan

FIGURE 4. Coniochaeta acaciae (holotype TASM 6103) a, b. Ascomata on the substrate. c, d. Vertical section of ascoma. e. Section of peridium (in water). f. Section of peridium (in 5% KOH). g. Ostiole. h. Setae. i. Ascus apex in Congo Red. j–l. Ascospores (arrow heads show germ slits in l). m–o. Asci. Scale bars: a=500 μm, b=200 μm, c,d=100 μm, e–h=20 μm, i=10 μm, j–o=5 μm.

FIGURE 1 in Combined multi-gene backbone tree for the genus Coniochaeta with two new species from Uzbekistan

FIGURE 1. Maximum likelihood tree revealed by RAxML from an analysis of the LSU rDNA matrix of Coniochaeta, showing the phylogenetic position of C. acaciae and C. coluteae. MP, ML bootstrap supports (≥50%) and Bayesian posterior probabilities (≥0.9PP) support are given above or below the branches respectively. The tree was rooted with Chaetosphaeria garethjonesii (MFLUCC 15-1012) and C. jonesii (MFLUCC 15-1015). New species proposed in this study are indicated in red, and type strains are in boldface.

FIGURE 2. Steiropteris alstonii. A in Steiropteris alstonii (Thelypteridaceae), a new species from Colombia, and some new combinations in the family

FIGURE 2. Steiropteris alstonii. A. Detail of the abaxial side of segments showing venation, false veins and sori. B. Detail of the setose indusium.

FIGURE 2 in Iris tibetica, a new combination in I. ser. Lacteae (Iridaceae) from China: evidence from morphological and chloroplast DNA analyses

FIGURE 2. Median-joining network based on combined sequences of four cpDNA regions, depicting the relationships among haplotypes of 136 individuals from 59 localities across the geographic range of Iris ser. Lacteae. Each white circle represents a haplotype and the size of the circle is proportional to the number of individuals with that haplotype. Haplotype codes correspond to those in Table 1. Black dots indicate missing haplotypes (extinct or not sampled). Haplotypes of A, B, and C haplogroups are encircled with thin lines.

FIGURE 4 in Iris tibetica, a new combination in I. ser. Lacteae (Iridaceae) from China: evidence from morphological and chloroplast DNA analyses

FIGURE 4. Phylogenetic analysis of Iris ser. Lacteae based on psbA–trnH/rps4–trnS/trnS–trnG/trnL–trnF sequences. Neighbour-joining tree is shown with bootstrap values in 1000 replicates for NJ/MP/ML analyses (shown only when> 50%) above the branches and Bayesian posterior probabilities more than PP = 0.90 below the branches. Clades I and II within I. ser. Lacteae are indicated. Haplotypes and locality codes are given in Table 1.

FIGURE 1 in Iris tibetica, a new combination in I. ser. Lacteae (Iridaceae) from China: evidence from morphological and chloroplast DNA analyses

FIGURE 1. Map showing the locations of Iris ser. Lacteae samples analyzed in the present study (created with http://www. spatialepidemiology.net). The locality codes are given in Table 1.

FIGURE 3 in Iris tibetica, a new combination in I. ser. Lacteae (Iridaceae) from China: evidence from morphological and chloroplast DNA analyses

FIGURE 3. Genetic clustering of Iris ser. Lacteae haplotypes from 136 individuals inferred with the program BAPS. Each vertical column corresponds to one haplotype, and black vertical lines separate haplotypes from the different localities. Locality codes are given in Table 1. Different colours represent the different genetic cluster (blue-cluster 1, red-cluster 2, green-cluster 3). (a) Mixture clustering results revealing three clusters with a posterior marginal probability of 0.80; (b) Bar plot from the admixture results. The vertical bars are split into several colours when there is evidence for the admixture (P <0.05). Localities are ordered according to latitude, from south to north.

opennotspecifiedMay 2024View details →

TABLE 1 in Myxotrichum persicum sp. nov., and two new combinations in the genus Myxotrichum

TABLE 1. Isolates used in the phylogenetic analysis.<table><tbody><tr><th>Taxon</th><th>Strain</th><th>Origin</th><th>GenBank accession number</th><th>References</th></tr></tbody><tbody><tr><th></th><td></td><td></td><td>ITS</td><td>LSU</td><td>MCM7</td><td>RPB1</td><td></td></tr><tr><th>Amorphotheca resinae</th><td>ATCC 22711= DAOM 170427</td><td>Jet fuel, Canada</td><td>EU030278</td><td>EU030280</td><td>–</td><td>–</td><td>Seifert et al. (2007)</td></tr><tr><th>Amorphotheca resinae</th><td>ATCC 11841= CBS Creosote-treated 184.54 wooden pole, USA</td><td>AY251067</td><td>EU040231</td><td>–</td><td>–</td><td>Crous et al. (2007), Braun et al. (2003)</td></tr><tr><th></th><td></td><td></td><td>ITS LSU MCM7 RPB1</td><td></td></tr><tr><th>Amorphotheca resinae</th><td>NBRC 31773= ATCC 11274= CBS 187.54</td><td>Cosmetic face cream, ‘Nivea’, The Netherlands</td><td>LC646545</td><td>LC646546</td><td>LC646547</td><td>LC646548</td><td>Hirose et al. (2022)</td></tr><tr><th>Amorphotheca resinae (IT)</th><td>ATCC 200942= CBS 406.68</td><td>Soil, Australia</td><td>AF393726</td><td>AY352592</td><td>–</td><td>–</td><td>Park et al. (unpublished), Managbanag et al. (unpublished)</td></tr><tr><th>Byssoascus striatosporus (T)</th><td>CBS:642.66= UAMH 3572</td><td>Soil, Canada</td><td>AF062817</td><td>AB040688</td><td>LC639221</td><td>LC639257</td><td>Hambleton et al. (1998), Sugiyama & Mikawa (2001), Hirose et al. (2022)</td></tr><tr><th>Hyphodiscus hyaloscyphoides (T)</th><td>NBRC 104869</td><td>Decaying wood of Betula sp., Japan</td><td>LC639297</td><td>LC639333</td><td>LC639237</td><td>LC431668</td><td>Hirose et al. (2022)</td></tr><tr><th>Myxotrichum albicans (T)</th><td>CGMCC 16488</td><td>Pinus koraiensis leaf litter, China</td><td>MH378419</td><td>MH971222</td><td>–</td><td>–</td><td>Liang et al. (2019)</td></tr><tr><th>Myxotrichum arcticum (T)</th><td>UAMH 7565</td><td>Forest soil, USA</td><td>AF062810</td><td>–</td><td>–</td><td>–</td><td>Hambleton et al. (1998)</td></tr><tr><th>Myxotrichum cancellatum (T)</th><td>ATCC 15316= CBS:426.62= UAMH 1911</td><td>Frozen blueberry pastry, USA</td><td>MH858197</td><td>LC639315</td><td>LC639219</td><td>LC639255</td><td>Vu et al. (2019), Hirose et al. (2022)</td></tr><tr><th>Myxotrichum carminoparum (T)</th><td>CBS 224.31= UAMH 1597</td><td>Wood pulp, Norway</td><td>AF062812</td><td>LC639307</td><td>LC639211</td><td>LC639247</td><td>Hambleton et al. (1998), Hirose et al. (2022)</td></tr><tr><th>Myxotrichum chartarum</th><td>NBRC 31717= UAMH 1997</td><td>Soil, Japan</td><td>AF062813</td><td>LC639331</td><td>LC639235</td><td>LC639271</td><td>Hambleton et al. (1998), Hirose et al. (2022)</td></tr><tr><th>Myxotrichum circinatum (T)</th><td>ATCC 34526= IFM 41295=CBS 129.77= UAMH 1890</td><td>Soil, USA</td><td>MN627784</td><td>MN627782</td><td>LC639234</td><td>LC639270</td><td>RangelGrimaldo et al. (2020)</td></tr><tr><th>Myxotrichum deflexum</th><td>CBS:544.72</td><td>Soil, Kuwait</td><td>MH860562</td><td>MH872267</td><td>–</td><td>–</td><td>Vu et al. (2019)</td></tr><tr><th>Myxotrichum deflexum (NT)</th><td>CBS 228.61</td><td>Soil, Canada</td><td>AF062814</td><td>LC639308</td><td>LC639212</td><td>LC639248</td><td>Hambleton et al. (1998), Hirose et al. (2022)</td></tr><tr><th>Myxotrichum flavoroseum (T)</th><td>ATCC 34529= IFM 41293= CBS 130.77= UAMH 1051</td><td>Soil, USA</td><td>NR_158362</td><td>AB359419</td><td>LC639233</td><td>LC639269</td><td>RangelGrimaldo et al. (2020)</td></tr><tr><th>Myxotrichum persicum</th><td>IRAN 3775C</td><td>Seed endophyte of Aegilops triuncialis, Iran</td><td>OR053729</td><td>OR053730</td><td>–</td><td>–</td><td>This study</td></tr><tr><th>Myxotrichum setosum</th><td>UAMH 3835</td><td>Soil, Canada</td><td>AF062815</td><td>–</td><td>–</td><td>–</td><td>Hambleton et al. (1998)</td></tr><tr><th>Myxotrichum stipitatum (NT)</th><td>NBRC 31721= UAMH 1510</td><td>Sand dune, England</td><td>AF062816</td><td>LC639332</td><td>LC639236</td><td>LC639272</td><td>Hambleton et al. (1998), Hirose et al. (2022)</td></tr><tr><th>Oidiodendron boninense (T)</th><td>NBRC 115413= DH 1175</td><td>Root of Vaccinium boninense, Japan</td><td>LC639290</td><td>LC639326</td><td>LC639230</td><td>LC639266</td><td>Hirose et al. (2022)</td></tr><tr><th>Oidiodendron cereale</th><td>UAMH 1522</td><td>Peat soil, Canada</td><td>AF062788</td><td>–</td><td>–</td><td>–</td><td>Hambleton et al. (1998)</td></tr><tr><th></th><td></td><td></td><td>ITS LSU MCM7 RPB1</td><td></td></tr><tr><th>Oidiodendron cereale</th><td>CCF 3193</td><td>Digestive tract of Acarus siro from seeds of Papaver somniferum, Czech Republic</td><td>LC639291</td><td>LC639327</td><td>LC639231</td><td>LC639267</td><td>Hirose et al. (2022)</td></tr><tr><th>Oidiodendron chlamydosporicum (T)</th><td>ATCC 18448= CBS 403.69= UAMH 6520</td><td>Soil, Canada</td><td>AF062789</td><td>NG_ 064071</td><td>LC639218</td><td>LC639254</td><td>Hambleton et al. (1998), Vu et al. (2019)</td></tr><tr><th>Oidiodendron citrinum</th><td>CBS:129229</td><td>USA</td><td>MH865252</td><td>MH876692</td><td>–</td><td>–</td><td>Vu et al. (2019)</td></tr><tr><th>Oidiodendron citrinum (T)</th><td>UAMH 1525</td><td>Soil, Canada</td><td>AF062790</td><td>–</td><td>–</td><td>–</td><td>Hambleton et al. (1998)</td></tr><tr><th>Oidiodendron clavatum (T)</th><td>21-64-D</td><td>Cicindela transbaicalica, Korea</td><td>LC683775</td><td>LC683776</td><td>–</td><td>–</td><td>Lee et al. (2022)</td></tr><tr><th>Oidiodendron echinulatum</th><td>UAMH 8467</td><td>Soil, Canada</td><td>AF062791</td><td>–</td><td>–</td><td>–</td><td>Hambleton et al. (1998)</td></tr><tr><th>Oidiodendron echinulatum</th><td>ATCC 16287= CBS:113.65</td><td>Soil, Germany</td><td>LC639276</td><td>LC639304</td><td>LC639208</td><td>LC639244</td><td>Hirose et al. (2022)</td></tr><tr><th>Oidiodendron eucalypti</th><td>DH 0313= NBRC 115396</td><td>Root of Rhododendron tomentosum, Japan</td><td>LC639283</td><td>LC639319</td><td>LC639223</td><td>LC639259</td><td>Hirose et al. (2022)</td></tr><tr><th>Oidiodendron eucalypti (T)</th><td>CBS 144423= CPC 32659</td><td>Eucalyptus maidenii, Australia</td><td>NR_160624</td><td>NG_ 064544</td><td>–</td><td>–</td><td>Crous et al. (2018)</td></tr><tr><th>Oidiodendron flavum</th><td>CBS 524.69= UAMH 1524</td><td>Soil, Canada</td><td>AF062792</td><td>LC639316</td><td>LC639220</td><td>LC639256</td><td>Hambleton et al. (1998), Hirose et al. (2022)</td></tr><tr><th>Oidiodendron fuscum (T)</th><td>CBS 238.31= UAMH 8511</td><td>Wood pulp, Norway</td><td>AF062807</td><td>LC639309</td><td>LC639213</td><td>LC639249</td><td>Hambleton et al. (1998), Hirose et al. (2022)</td></tr><tr><th>Oidiodendron griseum</th><td>CBS 249.33= UAMH 1403</td><td>Wood pulp, Sweden</td><td>AF062793</td><td>LC639310</td><td>LC639214</td><td>LC639250</td><td>Hambleton et al. (1998), Hirose et al. (2022)</td></tr><tr><th>Oidiodendron maius (T)</th><td>UAMH 1540</td><td>Soil, Canada</td><td>AF062798</td><td>LC639313</td><td>LC639217</td><td>LC639253</td><td>Hambleton et al. (1998), Hirose et al. (2022)</td></tr><tr><th>Oidiodendron mellicola</th><td>DH 1211= NBRC 115401</td><td>Honey from persimmon, Japan</td><td>LC639300</td><td>LC639336</td><td>LC639240</td><td>LC639274</td><td>Hirose et al. (2022)</td></tr><tr><th>Oidiodendron mellicola (T)</th><td>CBS:143839= FMR 15683</td><td>Decanted and filtered blossom honey, Spain</td><td>LT906544</td><td>–</td><td>–</td><td>–</td><td>RodríguezAndrade et al. (2019)</td></tr><tr><th>Oidiodendron muniellense (T)</th><td>CBS 113932= IMI 391998</td><td>Rotten basidiocarp, Spain</td><td>AJ634700</td><td>LC639302</td><td>LC639206</td><td>LC639242</td><td>Calduch et al. (2004), Hirose et al. (2022)</td></tr><tr><th>Oidiodendron myxotrichoides (T)</th><td>IMI 388795</td><td>Litter, Spain</td><td>AJ635314</td><td>–</td><td>–</td><td>–</td><td>Calduch et al. (2002)</td></tr><tr><th>Oidiodendron nigrum (IT)</th><td>CBS:321.31</td><td>Wood pulp, Norway</td><td>MH855228</td><td>MH866680</td><td>–</td><td>–</td><td>Vu et al. (2019)</td></tr><tr><th>Oidiodendron periconioides</th><td>CBS:126939</td><td>Unknown, USA</td><td>MH864342</td><td>MH875787</td><td>–</td><td>–</td><td>Vu et al. (2019)</td></tr><tr><th>Oidiodendron periconioides (T)</th><td>ATCC 18449=CBS 391.69</td><td>Soil, Canada</td><td>AF062802</td><td>LC639311</td><td>LC639215</td><td>LC639251</td><td>Hambleton et al. (1998), Hirose et al. (2022)</td></tr><tr><th></th><td></td><td></td><td>ITS LSU MCM7 RPB1</td><td></td></tr><tr><th>Oidiodendron pilicola</th><td>DH 0252= NBRC 115402</td><td>Pinus pumila leaf litter, Japan</td><td>LC639282</td><td>LC639318</td><td>LC639222</td><td>LC639258</td><td>Hirose et al. (2022)</td></tr><tr><th>Oidiodendron pilicola</th><td>CBS 141.72= UAMH 7526</td><td>Soil, Sweden</td><td>AF062787</td><td>–</td><td>–</td><td>–</td><td>Hambleton et al. (1998)</td></tr><tr><th>Oidiodendron ramosum (T)</th><td>CBS 113931= IMI 391997</td><td>Rotten basidiocarp, Spain</td><td>AJ634701</td><td>LC639301</td><td>LC639205</td><td>LC639241</td><td>Calduch et al. (2004), Hirose et al. (2022)</td></tr><tr><th>Oidiodendron reticulatum (T)</th><td>CBS 113933= IMI 391999</td><td>Soil, Spain</td><td>AJ634699</td><td>LC639303</td><td>LC639207</td><td>LC639243</td><td>Calduch et al. (2004), Hirose et al. (2022)</td></tr><tr><th>Oidiodendron rhodogenum</th><td>CBS 237.31= UAMH 1405</td><td>Sludge in pulp strainers, Norway</td><td>AF062803</td><td>–</td><td>–</td><td>–</td><td>Hambleton et al. (1998)</td></tr><tr><th>Oidiodendron rhodogenum</th><td>CBS 401.69</td><td>Forest soil, Canada</td><td>LC639280</td><td>LC639312</td><td>LC639216</td><td>LC639252</td><td>Hirose et al. (2022)</td></tr><tr><th>Oidiodendron scytaloides (T)</th><td>UAMH 6521</td><td>Forest soil, Sweden</td><td>AF062804</td><td>–</td><td>–</td><td>–</td><td>Hambleton et al. (1998)</td></tr><tr><th>Oidiodendron setiferum (T)</th><td>CBS 114896= UAMH 5715</td><td>House dust, Japan</td><td>AF062805</td><td>LC639305</td><td>LC639209</td><td>LC639245</td><td>Hambleton et al. (1998), Hirose et al. (2022)</td></tr><tr><th>Oidiodendron tenuissimum</th><td>UAMH 8513= CBS 315.95</td><td>Leaf litter, Spain</td><td>AF062806</td><td>–</td><td>–</td><td>–</td><td>Hambleton et al. (1998)</td></tr><tr><th>Oidiodendron tenuissimum</th><td>NBRC 115410= DH 0894</td><td>Roots of Rhododendron sp., Japan</td><td>LC639287</td><td>LC639323</td><td>LC639227</td><td>LC639263</td><td>Hirose et al. (2022)</td></tr><tr><th>Oidiodendron tokumasui (T)</th><td>DH 1137= NBRC:115411</td><td>Root of Vaccinium boninense, Japan</td><td>LC639289</td><td>LC639325</td><td>LC639229</td><td>LC639265</td><td>Hirose et al. (2022)</td></tr><tr><th>Oidiodendron truncatum (T)</th><td>CBS 222.65= UAMH 1399</td><td>Soil, Canada</td><td>AF062809</td><td>LC639306</td><td>LC639210</td><td>LC639246</td><td>Hambleton et al. (1998), Hirose et al. (2022)</td></tr><tr><th>Skoua asexualis (T)</th><td>CBS 144072= FMR 16572</td><td>Decanted, filtered honey, Spain</td><td>LT964668</td><td>LT964669</td><td>–</td><td>–</td><td>Rodríguez-Andrade et al. (2019)</td></tr><tr><th>Skoua fertilis</th><td>FMR 16571</td><td>Honey, Spain</td><td>LR585992</td><td>LT965027</td><td>–</td><td>–</td><td>Rodríguez-Andrade et al. (2019)</td></tr><tr><th>Skoua fertilis</th><td>NBRC 115406= DH 1205</td><td>Honey from apple, Japan</td><td>LC639299</td><td>LC639335</td><td>LC639239</td><td>LC639273</td><td>Hirose et al. (2022)</td></tr><tr><th>Skoua fertilis (NT)</th><td>5159(C)</td><td>Overwintering bee bread of Apis mellifera, Denmark</td><td>-</td><td>KR139934</td><td>–</td><td>–</td><td>Wynns (2015)</td></tr><tr><th>Venturiocistella japonica</th><td>NBRC 106633</td><td>Apothecium produced on leaf of Cercidiphyllum japonica, Japan</td><td>LC639298</td><td>LC639334</td><td>LC639238</td><td>LC431669</td><td>Hirose et al. (2022)</td></tr></tbody></table>...continued on the next page...continued on the next page...continued on the next pageSequences with underlined numbers are generated in this study, others are from GenBank. (T), ex-type; (IT), ex-isotype; (NT), exneotype strains. CBS, Westerdijk Fungal Biodiversity Institute, Utrecht, The Netherlands; IRAN, Iranian Fungal Culture Collection, Iranian Research Institute of Plant Protection, Tehran, Iran; ATCC, American Type Culture Collection, Manassas, VA, USA; CGMCC, China General Microbiological Culture Collection Center, Institute of Microbiology, Chinese Academy of Sciences, Beijing, China; DAOM, Plant Research Institute, Department of Agriculture (Mycology), Ottawa, Canada; DH, Dai Hirose, Nihon University, Japan; FMR, Facultad de Medicina, Reus, Tarragona, Spain; IFM, Medical Mycology Research Center, Chiba University, Chiba, Japan through the National Bioresource Project, Japan; UAMH, University of Alberta Microfungus Collection and Herbarium, Devonian Botanic Garden, Edmonton, Alberta, Canada.

opennotspecifiedJan 2020View details →

FIGURE 2 in A new species and a new combination of Amomum Roxb. (Zingiberaceae) from Sikkim Himalaya, India

FIGURE 2. Amomum raoii: A. inflorescence; B. infructescence. Amomum raoii var. oblongum: C inflorescence; D. infructescence.

opennotspecifiedJan 2020View details →

FIGURE 1. Amomum raoii. A. a in A new species and a new combination of Amomum Roxb. (Zingiberaceae) from Sikkim Himalaya, India

FIGURE 1. Amomum raoii. A. a part of leafy shoot; B. ligule; C. inflorescence; D. outer bract; E. bracteole; F. flower; G. calyx; H. corolla lobes; I. stamen; J. labellum; K. ovary with epigynous glands and style; L. stigma; M. c.s. of ovary; N. fruit; O. seed. Drawn by V.P. Thomas.

opennotspecifiedMar 2020View details →

FIGURE 1. Parkinsonia glauca. A—Flowering branch. B—Fruiting branch. C in Parkinsonia glauca (Caesalpinioideae, Leguminosae), a new combination and status

FIGURE 1. Parkinsonia glauca. A—Flowering branch. B—Fruiting branch. C—Spine and stipule. D—Bipinnate leaf with one pair of pinnae. E—Bracts. F—Flower. G—Petals. H—Stamens. I—Ovary and ovules. J—Fruit. K—Seed. (A, E, F, G, H and I drawn from: T.M. Pedersen 13958 MBM; B, C and D: W. Fischer 20 NY.) Drawn by Klei Rodrigo Sousa.