Our Work

This deliverable contributes to INSPIRE’s project ambition to advance the foundations of Inclusive Gender Equality in the European R&I ecosystem by providing a synthesis of the cross-cutting…

This deliverable contributes to INSPIRE’s project ambition to advance the foundations of Inclusive Gender Equality in the European R&I ecosystem by providing a synthesis of the cross-cutting themes found in the empirical work carried out across Work Package 3 (WP3). Two key points are addressed directly for policy makers and change agents in the European Research Area (ERA) working on Inclusive Gender Equality: how to advance the conceptual, methodological, and practical foundations of Inclusive Gender Equality Plans (IGEPs) and Inclusive Gendered Innovation (IGI) as instruments capable of producing structural change, while addressing intersectional inequalities and making innovations with demonstrated benefits for scientific quality and societal relevance. INSPIRE data show that whether equality policies produce real change or remain symbolic depends not only on what happens within organisations but also on how research funding and innovation are governed at the organisational, national, and EU levels. Each level sets different conditions for how research agendas are formulated and evaluated, how resources are allocated, and whose knowledge and needs research is designed to serve. Addressing this complexity requires governance tools that can operate across all three levels simultaneously, in a structurally uneven, politically contested, and epistemically fragmented ecosystem. This synergies analysis forms the foundation for developing guiding principles to advance IGE from an intersectional perspective. Because national policy frameworks, historical trajectories, and institutional cultures vary significantly across the ERA, these principles must enable meaningful contextualisation without sacrificing coherence. The deliverable is structured in three parts: first, the introduction situates the project's ambition and analytical approach. Second, we present three cross-cutting themes that emerged from the project's empirical research and respond to the questions of where, who and how: context, actors, and governance structures. Third, we present a set of guiding principles for change agents and policymakers working in the R&I ecosystem in the ERA, derived from the convergence of evidence across these themes. The principles are organised addressing different moments of the policy process: the diagnostic moment, the design moment and the infrastructure necessary to sustain the changes over time. The principles also address the issue of different contexts in the ERA, the need to have intersectionality as political practice, the participatory processes necessary to tailor policies, the need to have common standards of governance infrastructures and integrate IGI into R&I funding and practice, investment and conditions for evidence infrastructure and system learning and, finally, the relevance of recognising, resourcing and protecting equality work and expertise in the organisational, national and ERA levels.

Aureobasidium catharanthi Senwanna, Kodchasee, J. Kumla & N. Suwannar. sp. nov.Fig. 9Etymology.Refers to the host genus Catharanthus, from which this species was isolated.Type.THAILAND • Phay…

Aureobasidium catharanthi Senwanna, Kodchasee, J. Kumla & N. Suwannar. sp. nov.Fig. 9Etymology.Refers to the host genus Catharanthus, from which this species was isolated.Type.THAILAND • Phayao Province, Mueang District, isolated from vinca flower (Catharanthus roseus; Apocynaceae, Gentianales), Aug 2024, P. Kodchasee, C. Senwanna, J. Kumla and N. Suwannarach, holotype = CMUB 40140 (preserved in metabolically inactive state), living culture (ex-type) = SDBR-CMU 842 = GMBCC 2503.Cultural characteristics.After 14 days of incubation at 25 ° C in the dark, colonies on PDA reaching 36–44 mm diam., surface flat, spreading, round with radiating margin, velvety, olive brown (4 E 6), with grayish yellow (4 B 6) at the margin; on MEA reaching 55–60 mm diam., surface flat, spreading with lobate margin, velvety, shiny, grayish yellow (4 B 6), with olive brown (4 E 5) mixed with grayish yellow (4 B 6) at the margin; on OA 60–68 mm diam., surface flat, spreading with filiform, entire margin, velvety, slimy, light gray (3 D 1), with dark gray (3 F 1) at the margin.Description.Anamorph in vitro dematiaceous hyphomycetes. Vegetative hyphae (3.9 –) 5.0–10.0 (– 16.0) μm, hyaline to brown, branched, septate, smooth, thin-walled, becoming light brown to brown with age, constricted at the septa, thick-walled. Conidiogenous cells (6.8 –) 9.3–13.0 (– 20.1) × 4.0–6.0 μm (x ̄ = 10.2 × 5.3 μm, n = 25), undifferentiated, intercalary, terminal, producing conidia percurrently from short lateral denticles, or differentiated on hyphae, occasionally elongated, solitary, light brown to brown. Conidia obovoid to ellipsoidal, or subglobose, hyaline, aseptate, occasionally with an indistinct truncated base and a hilum, smooth-walled, guttulate, (5.4 –) 6.8–11.5 (– 14.2) × (3.3 –) 4–5.3 (– 6.4) μm (x ̄ = 8.9 × 4.7 μm, n = 150), budding occasionally observed. Chlamydospores (8.0 –) 9.5–14.8 (– 18.1) μm wide (x ̄ = 12.2 μm, n = 30), frequent produced in aerial hyphae, mostly intercalary, solitary or in branched chains, globose to subglobose, light to dark brown, smooth-, thick-walled, septate, 1–2 cells, constricted near the septa. Endoconidia absent.Fermentation of glucose is negative. D - glucose, galactose, sorbose, N - acetyl glucosamine (weak), ribose, xylose, L - arabinose, D - arabinose, L - rhamnose, sucrose, maltose, α - α - trehalose, methyl- α - D - glucoside (weak), cellobiose, salicin (weak), melibiose, lactose (weak), raffinose, melizitose, glycerol (weak), erythritol (weak), ribitol (weak), glucitol, mannitol, galactitol, myo - inositol, D - glucono- 1, 5 - lactone (weak), D - gluconate, D - glucuronate, D - galacturonic acid (weak), DL - lactate (weak), succinate (weak), citrate (weak), ethanol, and xylitol are assimilated, but inulin, soluble starch, and methanol are not assimilated. Ammonium sulfate, ethylamine hydrochloride, L - lysine, cadaverine, and creatine are assimilated as sole nitrogen sources. Potassium nitrate and sodium nitrite are not assimilated. After 3 weeks, light brown sediment formed in D - glucose, D - galactose, L - sorbose, salicin, D - galacturonic acid, succinate, and citrate, while dark brown sediment formed in N - acetyl glucosamine, ribitol, D - glucono- 1, 5 - lactone, D - gluconate, D - glucuronate, and xylitol. Black sediment formed in methyl- α - D - glucoside, glycerol, and erythritol, while white sediment observed in ethanol.Cardinal temperatures for growth.Minimum 10 ° C, optimum in the range of 25 ° C to 30 ° C. No growth at 4 ° C and 37 ° C.Additional strains examined.THAILAND • Phayao Province, Mueang District, isolated from vinca flower (Catharanthus roseus; Apocynaceae, Gentianales), Aug 2024, P. Kodchasee, C. Senwanna, J. Kumla and N. Suwannarach, living culture = SDBR-CMU 812.Habitat and distribution.Flowers of Catharanthus roseus. Known only from northern Thailand.Notes.Phylogenetic analyses showed that A. catharanthi formed a distinct monophyletic lineage and was sister to A. bougainvilleae, with 77 % MLBS and 0.96 BIPP support (Fig. 2). The differences in sequence data, morphological characteristics, and physiological traits between A. catharanthi and A. bougainvilleae are described above. Therefore, A. catharanthi is introduced here as a new species.

Aureobasidium castaneae C. M. Tian & N. Jiang, Journal of Fungi 7 (1, no. 64): 11 (2021)Fig. 8Cultural characteristics.After 14 days of incubation at 25 ° C in the dark, colonies on PDA reachi…

Aureobasidium castaneae C. M. Tian & N. Jiang, Journal of Fungi 7 (1, no. 64): 11 (2021)Fig. 8Cultural characteristics.After 14 days of incubation at 25 ° C in the dark, colonies on PDA reaching 34–45 mm diam., surface flat, spreading, round with radiating, irregular margin, velvety, slimy, pale yellow (2 A 3), becoming olive brown (4 E 5) at the margin; on MEA reaching 28–35 mm diam., surface flat, spreading, round with radiating, irregular margin, velvety, slimy, dark brown (6 F 8) at center, becoming olive brown (4 E 5) to smoke brown (4 E 2) and white at the margin; on OA 32–45 mm diam., surface flat, spreading with irregular margin, velvety, slimy, pale yellow (2 A 3), becoming brownish gray (4 E 2), yellowish brown (5 E 8) at the margin.Description.Anamorph in vitro dematiaceous hyphomycetes. Vegetative hyphae 2.0–5.0 (– 6.6) μm wide, mostly hyaline, branched, septate, smooth, thin-walled, becoming light brown to brown, guttulate, thick-walled. Conidiogenous cells (4.8 –) 6.0–14.0 (– 16.0) × 2.5–6.0 (– 6.7) μm (x ̄ = 9.7 × 4.6 μm, n = 25), undifferentiated from hyphae, intercalary, rarely terminal, producing conidia percurrently from indistinct lateral denticles, giving rise to conidia that aggregate in a mucoid mass, or differentiated from hyphae, occasionally elongated, solitary, erect to lightly curved, hyaline becoming lightly melanized with age. Conidia (4.3 –) 5.0–9.0 (– 11.0) × (2.5 –) 3.0–4.5 (– 5.6) μm (x ̄ = 7 × 3.7 μm, n = 150), obovoid to ellipsoid, globose to subglobose, hyaline, becoming light brown to brown with age, aseptate, occasionally with an indistinct truncated base and a hilum, guttulate, smooth-walled, budding occasionally observed. Endoconidia (2.9 –) 3.4–5.6 × 1.6–2.5 μm (x ̄ = 4.0 × 1.9 μm, n = 25), obovoid to ellipsoid, hyaline, occasionally seen in intercalary hyphal cells.Cardinal temperatures for growth.Minimum 10 ° C, optimum in the range of 25 ° C to 30 ° C. No growth at 4 ° C and 37 ° C.Strains examined.THAILAND • Chiang Mai, Mueang District, Suthep, isolated from American cassia flower (Senna spectabilis; Fabaceae, Fabales), Aug 2024, P. Kodchasee, C. Senwanna, J. Kumla and N. Suwannarach, living culture = SDBR-CMU 835.Habitat and distribution.Leaf spots of Castanea henryi in China (Jiang et al. 2021); flowers of Senna spectabilis in Thailand (this study).Notes.Phylogenetic analysis showed that strain SDBR-CMU 835 clustered with A. castaneae CFCC 54591 (ex-type) in the same clade, with strong statistical support (100 % MLBS and 0.97 BIPP) (Fig. 2). The LSU and ITS sequences of strain SDBR-CMU 835 showed 100 % similarity to those of A. castaneae CFCC 54591. The morphology of strain SDBR-CMU 835 is consistent with the description provided by Jiang et al. (2021). Therefore, this strain was identified as A. castaneae. In addition, an updated description of the melanized structures of the species is provided. Prior to this study, A. castaneae was reported on Castanea henryi in China (Jiang et al. 2021). This study represents the first report of A. castaneae in Thailand.

Aureobasidium bougainvilleae Senwanna, Kodchasee, J. Kumla & N. Suwannar. sp. nov.Fig. 7Etymology.Refers to the host genus Bougainvillea, from which this species was isolated.Type.THAILAND • …

Aureobasidium bougainvilleae Senwanna, Kodchasee, J. Kumla & N. Suwannar. sp. nov.Fig. 7Etymology.Refers to the host genus Bougainvillea, from which this species was isolated.Type.THAILAND • Phayao Province, Mueang District, isolated from bougainvillea (Bougainvillea hybrid; Nyctaginaceae, Caryophyllales), Aug 2024, P. Kodchasee, C. Senwanna, J. Kumla and N. Suwannarach, holotype = CMUB 40141 (preserved in metabolically inactive state), living culture (ex-type) = SDBR-CMU 858 = GMBCC 2509.Cultural characteristics.After 14 days of incubation at 25 ° C in the dark, colonies on PDA reaching 56–60 mm diam., surface flat, spreading, round with radiating, irregular margin, velvety, grayish brown (6 E 3), with grayish yellow (4 B 6) at the margin; on MEA reaching 35–44 mm diam., surface flat, spreading, round with radiating, lobate margin, velvety, brownish gray (4 E 2), grayish brown (6 E 3), and black at the margin; on OA 62–67 mm diam., surface flat, spreading with filiform, entire margin, velvety, slimy, pale orange (6 A 3), with yellowish brown (5 E 8), light brown (6 D 4) at the margin.Description.Anamorph in vitro dematiaceous hyphomycetes. Vegetative hyphae 3.0–11.0 (– 19.0) μm, hyaline to brown, branched, septate, smooth, thin-walled, becoming light to dark brown with age, constricted at the septa, thick-walled. Conidiogenous cells 5.0–15.0 (– 17.0) × 3.5–8.8 μm (x ̄ = 12.2 × 5.1 μm, n = 25), undifferentiated, intercalary, terminal, producing conidia percurrently from indistinct, short lateral denticles, giving rise to conidia that aggregate in a mucoid mass, or differentiated on hyphae, occasionally elongated, solitary, becoming brown with age. Conidia (3.8 –) 6.0–11.5 (– 13.5) × (2.5 –) 3.5–7.0 (– 9.4) μm (x ̄ = 8.7 × 4.7 μm, n = 180), obovoid to ellipsoidal, elongated, or globose to subglobose, hyaline becoming light to dark brown with age, aseptate, occasionally with an indistinct truncated base and a hilum, smooth-walled, guttulate, budding occasionally observed. Chlamydospores (8.2 –) 10.1–16.0 (– 20.0) μm wide (x ̄ = 13.3 μm, n = 30), produced in aerial hyphae, mostly intercalary, solitary or in branched chains, globose to subglobose, pigmented, light to dark brown, smooth-, thick-walled, septate, 1–2 cells, constricted near the septa. Endoconidia absent.Fermentation of glucose is negative. D - glucose, galactose, sorbose, N - acetyl glucosamine, ribose, xylose, L - arabinose, D - arabinose, L - rhamnose, sucrose (weak), maltose, α - α - trehalose, methyl- α - D - glucoside, cellobiose, salicin, melibiose, lactose, raffinose, melizitose, glycerol, erythritol, ribitol, glucitol, mannitol, galactitol, myo - inositol, D - glucono- 1, 5 - lactone, D - gluconate, D - glucuronate, D - galacturonic acid (weak), DL - lactate (weak), succinate, citrate (weak), ethanol, and xylitol are assimilated, but inulin, soluble starch, and methanol are not assimilated. Ammonium sulfate, ethylamine hydrochloride, L - lysine, cadaverine, and creatine are assimilated as sole nitrogen sources. Potassium nitrate and sodium nitrite are not assimilated. After 3 weeks, light brown sediment formed in D - glucose, raffinose, and D - galacturonic acid, while dark brown sediment formed in N - acetylglucosamine, D - xylose, L - rhamnose, maltose, α - α - trehalose, methyl- α - D - glucoside, cellobiose, salicin, melibiose, lactose, myo - inositol, D - glucono- 1, 5 - lactone, citrate, and xylitol. Black sediment formed in D - galactose, L - sorbose, D - arabinose, glycerol, erythritol, D - mannitol, and D - gluconate.Cardinal temperatures for growth.Minimum 10 ° C, optimum in the range of 25 ° C to 30 ° C. No growth at 4 ° C and 37 ° C.Additional strains examined.THAILAND • Phayao Province, Mueang District, isolated from bougainvillea (Bougainvillea hybrid; Nyctaginaceae, Caryophyllales), Aug 2024, P. Kodchasee, C. Senwanna, J. Kumla and N. Suwannarach, living culture = SDBR-CMU 859.Habitat and distribution.Flowers of Bougainvillea hybrid. Known only from northern Thailand.Notes.Phylogenetic analyses showed that A. bougainvilleae strains SDBR-CMU 858 (ex-type) and SDBR-CMU 859 formed a distinct monophyletic lineage that was sister to A. catharanthi, with 77 % MLBS and 0.96 BIPP support (Fig. 2). The rpb 2, tef 1, and tub sequences of A. bougainvilleae differed from those of A. catharanthi by 4.96 % (47 / 948 bp, including gaps), 9.29 % (25 / 269 bp, including gaps), and 2.93 % (12 / 409 bp, including gaps), respectively. Morphologically, colonies of A. bougainvilleae on PDA, MEA, and OA were grayish brown with a grayish-yellow margin, brownish gray with a grayish-brown to black margin, and pale orange with a light brown margin, respectively. In contrast, colonies of A. catharanthi were olive brown with grayish-yellow margins on PDA, grayish yellow mixed with olive brown and with grayish-yellow margins on MEA, and light gray with dark gray margins on OA. Although the conidial size ranges of A. bougainvilleae and A. catharanthi overlapped, the conidia of A. bougainvilleae became brown at maturity, whereas those of A. catharanthi remained hyaline. Aureobasidium bougainvilleae can be distinguished from A. catharanthi by its ability to assimilate D - xylose, D - arabinose, L - rhamnose, maltose, α, α - trehalose, cellobiose, melibiose, lactose, raffinose, ribitol, D - mannitol, myo - inositol, D - glucuronate, succinate, and ethanol, with sediment formation observed during growth on these carbon sources (Table 1). Thus, A. bougainvilleae is described here as a new species based on phylogenetic analysis and morphological characteristics.

This thesis provides information about the na’t chapters within «Layli and Majnun,» the third epic of Navoi’s «Khamsa,» and analyzes their artistic features through…

This thesis provides information about the na’t chapters within «Layli and Majnun,» the third epic of Navoi’s «Khamsa,» and analyzes their artistic features through poetic devices. It also demonstrates that the organic connection between the divine love expressed in the na’ts and the metaphorical love is reflected in the plot.

Aureobasidium anthicola Senwanna, Kodchasee, J. Kumla & N. Suwannar. sp. nov.Fig. 6Etymology.Refers to “ inhabiting flowers, ” the substrate from which this species was first isolated.…

Aureobasidium anthicola Senwanna, Kodchasee, J. Kumla & N. Suwannar. sp. nov.Fig. 6Etymology.Refers to “ inhabiting flowers, ” the substrate from which this species was first isolated.Type.THAILAND • Phayao Province, Mueang District, isolated from bridal bouquet flower (Plumeria pudica; Apocynaceae, Gentianales), Aug 2024, P. Kodchasee, C. Senwanna, J. Kumla and N. Suwannarach, holotype = CMUB 40138 (preserved in metabolically inactive state), living culture (ex-type) = SDBR-CMU 851 = GMBCC 2507.Cultural characteristics.After 14 days of incubation at 25 ° C in the dark, colonies on PDA reaching 35–43 mm diam., surface flat, spreading, round with radiating margin, velvety, concentric, light gray (3 D 1) at center, pale orange (6 A 3), olive brown (4 E 5); on MEA reaching 30–37 mm diam., surface flat, spreading, round with radiating margin, velvety, brownish gray (4 E 2) to black, with olive brown at the margin; on OA 36–40 mm diam., surface flat, spreading with filiform, with entire margin, wrinkled, light gray (3 D 1) at center, pale orange (6 A 3) mixed with olive brown (4 E 5).Description.Anamorph in vitro dematiaceous hyphomycetes. Vegetative hyphae (1.9 –) 2.9–7.7 (– 9) μm wide, hyaline to dark brown, branched, septate, smooth, thin-walled, becoming light brown to brown or golden brown with age, constricted at the septa. Conidiogenous cells (7.0 –) 9.1–14.0 (– 16.0) × 4.0–6.0 (– 8.9) μm (x ̄ = 11.4 × 6.2 μm, n = 25), undifferentiated, intercalary, terminal, producing conidia percurrently from indistinct, short lateral denticles, giving rise to conidia that aggregate in a mucoid mass, or differentiated on hyphae, hyaline to dark brown in age, occasionally elongated, solitary. Conidia (4.2 –) 6.3–10.5 (– 13.0) × (2.5 –) 3.4–6.0 (– 8.0) μm (x ̄ = 8.3 × 4.2 μm, n = 200), obovoid to ellipsoidal, hyaline to light brown, aseptate, guttulate, smooth-walled, becoming light brown to brown with ages. Chlamydospores (5.7 –) 7.2–10.4 (– 12.3) μm wide (x ̄ = 8.7 μm, n = 45), produced in aerial hyphae, mostly intercalary, solitary or in branched chains, subglobose to ellipsoidal, pigmented, light to dark brown, smooth-, thick-walled, septate, constricted near the septa. Endoconidia (2.7 –) 3.6–6.0 (– 6.6) × 2.2–3.1 (– 3.7) μm (x ̄ = 4.8 × 2.8 μm, n = 40), ellipsoidal, hyaline, occasionally seen in intercalary hyphal cells.Fermentation of glucose is negative. D - glucose, galactose, sorbose, N - acetyl glucosamine, ribose, xylose, L - arabinose, D - arabinose, L - rhamnose, sucrose, maltose, α - α - trehalose, methyl- α - D - glucoside, cellobiose, salicin, melibiose, lactose, raffinose, melizitose, glycerol, erythritol, ribitol, glucitol, mannitol, galactitol, myo - inositol, D - glucono- 1, 5 - lactone, D - gluconate, D - glucuronate, D - galacturonic acid, DL - lactate, succinate, citrate, ethanol, and xylitol are assimilated, but inulin, soluble starch, and methanol are not assimilated. Ammonium sulfate, ethylamine hydrochloride, L - lysine, cadaverine, and creatine are assimilated as sole nitrogen sources. Potassium nitrate and sodium nitrite are not assimilated. After 3 weeks, light brown pigmentation was observed in salicin, D - glucono- 1, 5 - lactone, and D- glucuronate, while dark brown sediment formed in D - galactose, D - arabinose, sucrose, methyl- α - D - glucoside, raffinose, and D - gluconate.Cardinal temperatures for growth.Minimum 10 ° C, optimum in the range of 25 ° C to 30 ° C. No growth at 4 ° C and 37 ° C.Additional strains examined.THAILAND • Chiang Mai Province, Mueang District, Suthep, isolated from Fukien tea flower (Ehretia microphylla; Boraginaceae, Boraginales), Jul 2024, P. Kodchasee, C. Senwanna, J. Kumla and N. Suwannarach, living culture = SDBR-CMU 821.Habitat and distribution.Flowers of Ehretia microphylla and Plumeria pudica. Known only from northern Thailand.Notes.Based on the multilocus phylogenetic analyses, A. anthicola SDBR-CMU 821 and SDBR-CMU 851 (ex-type) formed a well-supported monophyletic lineage (100 % MLBS and 0.99 BIPP) that was sister to A. florigenum (Fig. 2). The rpb 2 and tef 1 sequences of A. anthicola differed from those of A. florigenum by 1.74 % (17 / 977 bp, including gaps) and 1.88 % (5 / 266 bp, including gaps), respectively. Additionally, the PHI test confirmed the genetic distinctiveness of A. anthicola and A. florigenum (Fig. 4). Morphologically, colonies of A. anthicola on OA differed from those of A. florigenum by having a pale orange mixed with olive-brown color, whereas A. florigenum produced yellowish-white colonies mixed with light gray and with a brownish-gray margin. Aureobasidium anthicola produced endoconidia, whereas A. florigenum did not. Based on physiological characteristics, A. anthicola differed from A. florigenum by producing light brown pigment when grown in salicin, D - glucono- 1, 5 - lactone, and D - glucuronate, which was not produced by A. florigenum. In addition, differences in sediment formation were observed during carbon assimilation (Table 1). Therefore, A. anthicola is introduced as a new species in the A. thailandense group.

Aureobasidium albui Jumbam & Aime, Persoonia 54: 171 (2025)Fig. 5Cultural characteristics.After 14 days of incubation at 25 ° C in the dark, colonies on PDA reaching 32–40 mm diam., surf…

Aureobasidium albui Jumbam & Aime, Persoonia 54: 171 (2025)Fig. 5Cultural characteristics.After 14 days of incubation at 25 ° C in the dark, colonies on PDA reaching 32–40 mm diam., surface flat, spreading, round with radiating, irregular margin, velvety, slimy, fluffy, yellowish white (2 A 2), paler at the margin; on MEA reaching 40–50 mm diam., spreading, round with radiating, irregular margin, velvety, slimy, grayish brown (7 F 3) at center, becoming yellowish brown (5 E 4) to smoke brown (4 E 2) and white at the margin; on OA 35–47 mm diam., surface flat, spreading with entire margin, velvety, fluffy, whitish gray, light gray at the margin.Description.Anamorph in vitro dematiaceous hyphomycetes. Vegetative hyphae (2.6 –) 3.5–7.5 (– 9.6) μm wide, mostly hyaline, branched, septate, smooth, thin-walled; become light brown to brown with age, constricted at the septa, thick-walled. Conidiogenous cells (4.4 –) 6.0–11.0 (– 16.2) × 2.5–5.4 (– 6.7) μm (x ̄ = 8.6 × 4.3 μm, n = 25), mostly undifferentiated, intercalary, rarely terminal, producing conidia percurrently from indistinct, short lateral denticles, or differentiated on hyaline hyphae, occasionally elongated, solitary, becoming light brown to dark brown with age. Conidia (4.3 –) 5.9–9.8 (– 13.6) × (2.3 –) 3.2–5.6 (– 7.0) μm (x ̄ = 8.0 × 4.4 μm, n = 180), fusoid, obovoid to ellipsoidal or occasionally elongate, hyaline to light brown, aseptate, guttulate, smooth-walled, becoming brown with age, budding occasionally observed. Chlamydospores (5 –) 6.5–9.5 (– 11.2) μm wide (x ̄ = 8.1 μm, n = 35), produced in aerial hyphae, mostly intercalary, solitary or in branched chains, subglobose to ellipsoidal, pigmented, light to dark brown, smooth-, thick-walled, septate, 1–2 cells, constricted near the septa. Endoconidia (3.7 –) 4.2–5.8 × 2.3–3.5 μm (x ̄ = 4.9 × 2.9 μm, n = 20), obovoid to ellipsoidal, hyaline, occasionally seen in intercalary hyphal cells.Cardinal temperatures for growth.Minimum 4 ° C, optimum in the range of 25 ° C to 30 ° C. No growth at 37 ° C.Strain examined.THAILAND • Chiang Mai Province, Mueang District, Suthep, isolated from white cheesewood flower (Alstonia scholaris; Apocynaceae, Gentianales), Sep 2024, P. Kodchasee, C. Senwanna, J. Kumla and N. Suwannarach, living culture = SDBR-CMU 866.Habitat and distribution.Phylloplane of Cyrtomium falcatum and unidentified leaf in the USA (Jumbam et al. 2025); flowers of Alstonia scholaris in Thailand (this study).Notes.In the phylogenetic tree, strain SDBR-CMU 866 formed a well-supported clade with A. albui NRRL 61482 (ex-type), with 100 % MLBS and 1.0 BIPP support (Fig. 2). Morphologically, strain SDBR-CMU 866 is generally consistent with the type description of A. albui by Jumbam et al. (2025); however, detailed observations of some structures (e. g., conidiophores and conidiogenous cells) were not provided. Therefore, strain SDBR-CMU 866 was identified as A. albui, and an updated morphological description of the species is provided herein. Prior to this study, A. albui had been reported only from the leaf phylloplane in the USA (Jumbam et al. 2025). This study represents the first report of A. albui in Thailand.

By applying unsupervised machine learning techniques, this cross-sectional study provides a novel approach to enhance the clinical interpretation of body composition in newly diagnosed patients with g…

By applying unsupervised machine learning techniques, this cross-sectional study provides a novel approach to enhance the clinical interpretation of body composition in newly diagnosed patients with gastrointestinal cancers, a population at high risk of malnutrition. To investigate the clinical relevance of this approach, we evaluated the association between the identified body composition profiles, nutritional risk, and health-related quality of life. Our findings indicate that male patients with a low muscle profile had a threefold higher risk of malnutrition. Nevertheless, malnutrition risk emerged as the only determinant of poorer quality of life, underscoring the importance of monitoring nutritional status throughout the cancer continuum. In this context, integrating body composition profiles into the assessment of gastrointestinal cancer patients may improve nutritional risk stratification and support the implementation of early, tailored, multimodal interventions. Further studies are warranted to evaluate longitudinal changes in body composition profiles and their association with clinically relevant outcomes.

Updated the Figure 1 scripts for compatibility with MetaPathNet v0.99.5. Changes: updated MetaPathNet function names; updated the README and software requirements; corrected the C00346 compound annot…

Updated the Figure 1 scripts for compatibility with MetaPathNet v0.99.5. Changes: updated MetaPathNet function names; updated the README and software requirements; corrected the C00346 compound annotation; refined the Panel D permutation-distribution plotting code.

AMDGPU v2.7.1 Diff since v2.7.0 Merged pull requests: Switch to CompilerCaching.jl. (#961) (@maleadt) Group all Julia Github Actions PRs into a single one (#985) (@luraess) Allow Enzyme test to fail …

AMDGPU v2.7.1 Diff since v2.7.0 Merged pull requests: Switch to CompilerCaching.jl. (#961) (@maleadt) Group all Julia Github Actions PRs into a single one (#985) (@luraess) Allow Enzyme test to fail (#993) (@luraess) Increase evals from 1 to 4 in the benchmark suite (#999) (@luraess) Support ROCm 7.14+ versioned core-* library layout (#1000) (@luraess) Make versioninfo() robust to version-probe crashes (#1001) (@luraess) don't pick up device libs in current dir during precompilation (#1003) (@simeonschaub) don't return reshaped array from mapreducedim! (#1004) (@simeonschaub) use AMDGPU_LLVM_Backend_jll instead of in-tree backend (#1005) (@simeonschaub) Reduce per-kernel allocations from 12 down to 1 (#1009) (@pxl-th) support DocumenterVitepress 0.3 (#1010) (@luraess) Closed issues: Trying install AMDGPU on ubuntu 26.04 with no success. (#920) Discovery will fail on ROCm 7.14 — libraries move to /opt/rocm/core-<ver>/lib (#986)