A total of 130 samples exhibiting leaf and stem lesions were collected from various host plants in the orders Poales and Asparagales across different locations in Iran (Isfahan, Mazandaran, and West Azarbaijan Provinces) between 2010 and 2022, and the important collection information was recorded (Rathnayaka et al., 2024). Subsequently, they were brought to the laboratory for further analysis. Small sections, approximately 0.5 × 0.5 cm², were cut from the interface between healthy and diseased tissue. These sections were disinfected by submerging them in a diluted bleach solution (2% sodium hypochlorite) for 2 min, followed by three thorough rinses in sterile distilled water, and then blotted dry on sterile filter paper. The disinfected sections were then transferred to Potato Dextrose Agar (PDA, 39 g/L, Merck, Germany) plates supplemented with streptomycin sulfate and penicillin G (150 ppm each). The plates were incubated at 23 ± 2°C under cool white fluorescent light with a 12-h photoperiod for 5 days. Fungi growing out from the margins of plant sections were transferred into new PDA plates and purified via single-spore or hyphal tip methods. Furthermore, infected plant samples were incubated in moist chambers at 25°C until formation of conidial mass was observed. The incubated samples were inspected under a stereomicroscope, and single spores were then transferred to PDA at 23°C–25°C using a fine sterile needle. All identified isolates were deposited as pure cultures in the fungal culture collections at the Iranian Research Institute of Plant Protection (IRAN) and Urmia University (FCCUU).

Mycelial disks (5 mm in diameter) were excised from the actively growing margins of 7-day-old cultures and placed on fresh PDA, Corn Meal Agar (CMA, 17 g/L, Quelab, Montreal, Canada), and Malt Extract Agar (MEA, 50 g/L, Quelab, Montreal, Canada) media plates. The plates were incubated in the dark at 25°C for 7 days. Subsequently, the characteristics of the colonies, including color, pattern, and diameter, were observed and recorded. The color of the colonies was recorded using Rayner’s (1970) color charts. The micro-morphological characteristics were observed using 10- to 14-day-old cultures on tap water agar plates with autoclaved wheat straw (TWA–wheat straw) or leaves of the host plant. The cultures were subjected to near-ultraviolet light on a 12-h diurnal cycle at 23°C–25°C, as described by Sivanesan (1987) and Hernández-Restrepo et al. (2018). Fungal structures, such as hyphae, conidiophores, conidiogenous cells, conidia, ascocarps, asci, and ascospores, were measured (20–50 measurements per structure) and photographed using an Olympus AX70 microscope with differential interference contrast (DIC) illumination from slide mounts prepared with either clear lactic acid or lactophenol cotton blue staining solutions. Images were edited with Adobe Photoshop 2020 v. 2.10.8 software (Adobe Inc., San Jose, California). Taxonomic novelties were registered in MycoBank (www.MycoBank.org; Crous et al., 2004).

Total genomic DNA was extracted from the mycelial mass of each isolate harvested from 10-day-old PDA Petri dishes using the method described by Ahmadpour et al. (2021). The internal transcribed spacer (ITS−rDNA) region, parts of glyceraldehyde-3-phosphate dehydrogenase (GAPDH), and the translation elongation factor-1 alpha (TEF1) genes were amplified using the primer pairs ITS1/ITS4 (White et al., 1990), gpd1/gpd2 (Berbee et al., 1999), and TEF1-983F/TEF1-2218R (Rehner and Buckley, 2005), respectively. Polymerase chain reaction (PCR) was performed in the SimpliAmp™ Thermal Cycler (Applied Biosystems™, Thermo Fisher Scientific Corp., USA) with a final volume of 30 μl. The PCR mixture comprised of 0.4 μM of each primer, 10 μl of a ready master mix (Taq DNA Polymerase 2× Master Mix Red, 2 mM MgCl₂, Ampliqon Company, Denmark), and approximately 10 ng of DNA. The PCR amplification conditions were as follows: an initial denaturation at 95°C for 5 min, followed by 35 cycles of denaturation at 95°C for 45 s, annealing at 62°C–57°C (annealing temperature decreased by 0.5°C per cycle in the first 12 cycles) for 45 s, extension at 72°C for 45 s, and a final extension step at 72°C for 7 min. Amplicons were visualized on a 1% agarose gel stained with FluoroVue^TM Nucleic Acid Gel Stain (SMOBIO Technology Inc., China), and the sizes of amplicons were determined using a FluoroBand^TM 100 bp+3K Fluorescent DNA Ladder (SMOBIO Technology Inc., China). The amplified products were cleaned and sequenced by Macrogen Corp. (Seoul, South Korea) using the same primer sets that were used for PCR amplification. The sequences derived from this study were submitted to GenBank ( Table 1 ).

The initial identification of the isolates involved utilizing newly generated sequences of ITS−rDNA, GAPDH, and TEF1 with the NCBI Basic Local Alignment Search Tool (BLAST) (www.ncbi.nlm.nih.gov/blast/). Subsequently, pairwise sequence comparisons were performed between novel species and their closely related taxa using the same BLAST tool. DNA sequences from the type or representative species were obtained from GenBank ( Table 1 ) and used in the analyses. A multi-locus phylogenetic analysis was conducted on a combined dataset comprising the three genes/regions (ITS−rDNA + GAPDH + TEF1). Multiple sequence alignment was done using the online alignment tool MAFFT version 7 (https://mafft.cbrc.jp/alignment/server/) (Katoh et al., 2019). The best-fit substitution models were determined with the Akaike Information Criterion (AIC) in MrModeltest 2.3 (Nylander, 2004). The maximum likelihood (ML) and maximum parsimony (MP) analyses were conducted via the CIPRES Science Gateway portal (accessible at https://www.phylo.org/) (Miller et al., 2012) using RAxML-HPC BlackBox v. 8.2.12 (utilizing the GTR + GAMMA model and 1,000 bootstrapping iterations) (Stamatakis, 2014) and PAUP on ACCESS v. 4.a168 (using the heuristic search option and branch swapping with the tree–bisection–reconnection (TBR) algorithm with 1,000 bootstrapping replicates) (Swofford, 2002) tools, respectively. Descriptive tree statistics [tree length (TL), consistency index (CI), retention index (RI), and homoplasy index (HI)] were calculated for trees generated in the parsimony analysis. Bayesian phylogenetic inference (BI) and Bayesian posterior probabilities (BPP) were conducted in MrBayes v. 3.2.7 (Ronquist et al., 2012) with the Markov chain Monte Carlo (MCMC) method (four chains, 1,000,000 generations, 1,000 sampling frequency, and 25% burn-in phase). In all phylogenetic analyses, Curvularia affinis (CBS 154.34) and Curvularia lunata (CBS 730.96) were used as the outgroup taxa (Manamgoda et al., 2014; Tan et al., 2016; Bhunjun et al., 2020; Ferdinandez et al., 2022). The generated phylogenetic trees were viewed using FigTree v. 1.4.4 (Rambaut, 2019) and further edited using graphic design software, Adobe Illustrator^® CC 2020.

Genealogical Concordance Phylogenetic Species Recognition (GCPSR) was used to test for significant recombinant events (Quaedvlieg et al., 2014). Three-locus concatenated datasets (ITS−rDNA + GAPDH + TEF1) with closely related species were used for the analyses. The data were analyzed using SplitsTree 5 software employing the pairwise homoplasy index (PHI or Φw) test (Bruen et al., 2006; Huson and Bryant, 2006). PHI test results indicating a value less than 0.05 (Φw < 0.05) suggest the presence of significant recombination within the dataset. To visualize the relationships between novel taxa and their closely related counterparts, split graphs were constructed using concatenated datasets. The LogDet transformation and split decomposition options were used for this purpose.

A total of 85 isolates were obtained from various hosts (Poales and Asparagales plants). All isolates were examined based on their morphology. Representative isolates were then selected from various plant hosts for phylogenetic analyses. PCR amplifications produced DNA fragments of approximately 540 bp for ITS−rDNA, 545 bp for GAPDH, and 850 bp for TEF1. A total of 104 ITS−rDNA, 102 GAPDH, and 95 TEF1 sequences were subjected to multiple sequence alignment (nucleotides + gaps) resulting in 505-, 494-, and 898-character datasets, respectively. A combination of three gene sequences from 104 strains yielded a dataset with 1,897 characters, of which, 1,472 characters were constant, 112 characters were variable and parsimony uninformative, and 313 were parsimony informative. The most parsimonious tree yielded the following metrics: TL = 937, CI = 0.574, RI = 0.842, HI = 0.426. The nucleotide substitution model GTR + I + G was identified by MrModeltest 2.3 for all ITS−rDNA, GAPDH, and TEF1 datasets. The ML, MP, and BI phylogenetic analyses produced trees with similar topology and showed no significant conflicts. The combined dataset analysis of RAxML generated the best-scoring tree ( Figure 1 ) with a final ML optimization likelihood value of −8,235.239283. Estimated base frequencies were as follows: A = 0.229913, C = 0.302740, G = 0.236579, T = 0.230767; substitution rates AC = 1.001686, AG = 2.714677, AT = 1.255930, CG = 0.832074, CT = 6.025850, GT = 1.000000; gamma distribution shape parameter α = 0.731765. Based on morphological characteristics and multi-locus phylogeny (ITS−rDNA, GAPDH, and TEF1), nine Bipolaris species were identified: Bipolaris avrinica sp. nov., B. azarbaijanica sp. nov., B. banihashemii sp. nov., B. hedjaroudei sp. nov., B. hemerocallidis sp. nov., B. iranica sp. nov., B. persica sp. nov., Bipolaris crotonis, and B. salkadehensis. B. crotonis is a new record for Iran’s funga. Also, the phylogenetic relationship of B. salkadehensis with related species was re-defined using sequences from three genomic regions, and several new hosts were identified for this species worldwide. All identified taxa clustered with high statistical support values in the phylogenetic tree ( Figure 1 ). Each species was thoroughly illustrated, described, and discussed in terms of morphology, habitat, distribution, and phylogenetic relationships with other Bipolaris species.

Bipolaris avrinica A. Ahmadpour, Z. Heidarian, Y. Ghosta, Z. Alavi & F. Alavi, sp. nov. ( Figure 2 ).

MycoBank No: MB 854730

Etymology: The name refers to Avrin Mountain, located in Khoy County, West Azarbaijan Province, where the holotype was collected.

Diagnosis: Differs from Bipolaris adikaramae and B. yamadae by the abundant production of secondary conidiophores and conidia in culture media.

Type: IRAN, West Azarbaijan Province, Khoy County, on infected leaves of Setaria sp. (Poaceae, Poales), 10 September 2020, A. Ahmadpour, (IRAN 18493F, holotype, dried culture; ex-type culture IRAN 4806C).

Description: Lesions on infected leaves of Setaria sp., 1- to 10-mm long, gray color at the center with dark brown margins. Sexual morph: Undetermined. Asexual morph: On TWA Hyphae 2- to 5-μm wide, pale brown to brown, smooth, septate, branched. Conidiophores (125–)185–500(–600) × 4–6 µm ( x ¯ ± SD = 342.5 ± 157.5 × 5 ± 1 μm, n = 50), mononematous, semi- to macronematous, arising singly or rarely in groups, unbranched, straight to flexuous, septate, geniculate, pale brown to brown, paler toward the apex, rarely swollen at the base. Secondary conidiophores are frequently formed in culture media and conidia attached to primary conidiophores. Conidiogenous cells (6–)8–21(–16) × 4–7 μm ( x ¯ ± SD = 14.5 ± 6.5 × 5.5 ± 1.5 μm, n = 50), mono- to polytretic, sympodial proliferation, integrated, terminal or intercalary, subcylindrical to slightly swollen, pale brown to brown, smooth-walled, with thickened and darkened scars. Conidia (45–)50–87(–100) × 10–13 µm ( x ¯ ± SD = 68.5 ± 18.5 × 12 ± 1 μm, n = 50), pale brown to brown, smooth walled, straight to curved, fusoid to cylindrical, occasionally ellipsoidal, tapering toward rounded ends, (6–)7–10(–11)-distoseptate, germinated mono- or bipolar; hila 1.5- to 2.5-μm wide, inconspicuous, flat, thickened, and darkened. Stroma, chlamydospores, and microconidiation were not observed.

Culture characteristics: Colonies on PDA reaching 50 mm in diameter after 7 days at 25°C in the dark, circular, margin irregular, cottony appearance, gray with white to gray aerial mycelia; reverse gray olivaceous. Colonies on MEA reaching 38-mm diameter, circular, margin irregular, cottony appearance, white with white aerial mycelia; reverse brown to pale brown from the center to the margin. Colonies on CMA reaching 52 mm in diameter, circular, margin entire, hairy appearance with concentric rings, gray with sparse white to gray aerial mycelia; reverse olivaceous brown at the center and a hyaline margin.

Additional material examined: IRAN, West Azarbaijan Province, Khoy County, on infected leaves of Setaria sp. (Poaceae, Poales), 10 September 2020, A. Ahmadpour, isolate FCCUU 1012.

Host and distribution: Setaria sp. in Iran (this study).

Notes: Based on the phylogenetic analyses, B. avrinica is closely related to B. adikaramae and B. yamadae (MLBS/MPBS/BIPP = 100/98/1.0) ( Figure 1 ). A comparison of nucleotide differences in ITS−rDNA, GAPDH, and TEF1 indicates that B. avrinica (IRAN 4806C) differs from B. adikaramae (USJCC–0008) by 1/511 bp [0.19%, with one gap (0%)] in ITS−rDNA, 3/550 bp (0.54%) in GAPDH, and 3/763 bp (0.39%) in TEF1 and from B. yamadae (CBS 202.29) by 1/511 bp [0.54%, with one gap (0%)] in ITS−rDNA, 4/480 bp (0.83%) in GAPDH, and 4/763 bp (0.52%) in TEF1. The PHI analysis confirms that B. avrinica shows no significant genetic recombination with closely related species (Φw = > 0.05, Figure 3 ). Bipolaris avrinica can be differentiated by its abundant production of secondary conidiophores and conidia in cultures, a feature absent in B. adikaramae and B. yamadae. Additionally, B. avrinica has smaller conidia [(45–)50–87(–100) × 10–13 μm] compared to B. yamadae [(60–)65–100(–120) × (12–)14–18 μm] (Manamgoda et al., 2014; Ferdinandez et al., 2022). The production of secondary conidiophores and secondary conidia has been observed in B. cookei and B. microstegii grown on culture media (Manamgoda et al., 2014). However, B. avrinica is phylogenetically distinct from these species ( Figure 1 ). Bipolaris yamadae has been reported from several hosts, including Oryza sp., Euphorbia sp., Panicum spp. (P. capillare, P. implicatum, P. maximum, and P. miliaceum), Saccharum officinarum, and Setaria plicata (Manamgoda et al., 2014; Marin-Felix et al., 2017a; Farr et al., 2024). Bipolaris adikaramae has been isolated from yellow lesions on the leaf of Panicum maximum in Sri Lanka (Ferdinandez et al., 2022). Based on morphological and molecular evidence, we propose B. avrinica as a new species.

Bipolaris azarbaijanica A. Ahmadpour, Z. Heidarian, Y. Ghosta, Z. Alavi & F. Alavi, sp. nov. ( Figure 4 ).

MycoBank No: MB 854731

Etymology: The name refers to the West Azarbaijan Province, where the holotype was collected.

Diagnosis: Differs from Bipolaris chusqueae by the shape (fusoid to cylindrical) and size (longer and wider) of conidia.

Type: IRAN, West Azarbaijan Province, Salmas County, on leaves of Setaria sp. (Poaceae, Poales), 10 September 2015, A. Ahmadpour/Z. Heidarian, (IRAN 18208F, holotype, dried culture; ex-type culture IRAN 4776C).

Description: Leaf spots on Setaria sp., 1- to 10-mm long, gray at the center with a red-brown margin. Sexual morph: Undetermined. Asexual morph: On TWA: Hyphae 3- to 5-μm wide, pale brown to brown, smooth, septate, branched. Conidiophores (112–)140–300(–450) × 5–7 µm ( x ¯ ± SD = 220 ± 80 × 6 ± 1 μm, n = 50), mononematous, semi- to macronematous, arising singly or in groups, unbranched, straight to flexuous, septate, geniculate, pale brown to brown, paler toward the apex, swollen at the base. Conidiogenous cells (8–)10–22(–25) × 5–8 μm ( x ¯ ± SD = 16 ± 6 × 6.5 ± 1.5 μm, n = 50), mono- to polytretic, sympodial proliferation, integrated, terminal or intercalary, subcylindrical to slightly swollen, pale brown to brown, smooth walled to slightly verruculose, with thickened and darkened scars. Conidia (44–)50–80(–84) × 11–15 µm ( x ¯ ± SD = 65 ± 15 × 13 ± 2 μm, n = 50), pale brown to brown, smooth walled, straight to slightly curved, broadly fusoid to cylindrical, occasionally ellipsoidal to clavate, tapering toward the rounded ends, apical and basal cells paler than the median cells, (4–)5–9(–10)-distoseptate, germination mono- or bipolar; hila 2- to 3-μm wide, flat to slightly protuberant, thickened, and darkened. Stroma, chlamydospores, and microconidiation were not observed.

Culture characteristics: Colonies on PDA reaching 73 mm in diameter after 7 days at 25°C in the dark, circular, margin entire, gray at the center with white to gray aerial mycelia, white at the margin; reverse olivaceous gray at the center, margin pale brown. Colonies on MEA reaching 68 mm in diameter, circular, margin entire, cottony appearance, gray at the center, white at the margin with white aerial mycelia; reverse brown to pale brown. Colonies on CMA reaching 65 mm in diameter, circular, margin entire, hairy appearance, olivaceous gray with sparse white to gray aerial mycelia; reverse olivaceous gray at the center and a hyaline margin.

Additional material examined: Iran, West Azarbaijan Province, Salmas County, on leaves of Setaria sp. (Poaceae, Poales), 10 September 2015, A. Ahmadpour/Z. Heidarian, isolate FCCUU 1010.

Host and distribution: Setaria sp. in Iran (this study).

Notes: Bipolaris azarbaijanica is phylogenetically closely related to B. chusqueae (MLBS/MPBS/BIPP = 100/96/1.0) ( Figure 1 ). The pairwise DNA sequence comparison revealed that B. azarbaijanica is distinct from B. chusqueae. A comparison of nucleotide differences in ITS−rDNA and GAPDH indicates that B. azarbaijanica (IRAN 4776C) differs from B. chusqueae (SGO 166370) by 3/525 bp (0.57%) in ITS−rDNA and 6/531 bp (1.12%) in GAPDH. The PHI analysis confirms that B. azarbaijanica has no significant genetic recombination with closely related species (Φw = > 0.05, Figure 5 ). Morphologically, B. azarbaijanica can be differentiated by the shape of the conidia (broadly fusoid to cylindrical vs. subcylindrical to narrowly clavate in B. chusqueae), and longer and wider conidia [(44–)50–80(–84) × 11–15 µm vs. (17–)26–50(–68) × 10–12(–15) μm in B. chusqueae] (Lebeuf et al., 2023). Bipolaris chusqueae has been reported from Chusquea cumingii (Bambusoideae, Poales) in Chile (Lebeuf et al., 2023).

Bipolaris banihashemii A. Ahmadpour, Z. Heidarian, Y. Ghosta, Z. Alavi & F. Alavi, sp. nov. ( Figure 6 ).

MycoBank No: MB 854732

Etymology: Named in honor of Dr. Zia Banihashemi, emeritus Professor of Shiraz University, Iran, who significantly contributed to the knowledge of mycology and plant pathology in Iran.

Diagnosis: Differs from Bipolaris variabilis and B. zeae by the size of conidiophores and the shape and size of the conidia.

Type: IRAN, West Azarbaijan Province, Khoy County, on infected leaves of Setaria sp. (Poaceae, Poales), 20 September 2010, A. Ahmadpour, (IRAN 18244F, holotype, dried culture; ex-type IRAN 3389C).

Description: Leaf spots on Setaria sp., 1- to 5-mm long, gray at the center with red-brown margins. Sexual morph: Undetermined. Asexual morph: On TWA Hyphae 3- to 5-μm wide, pale brown to brown, smooth, septate, branched. Conidiophores (150–)260–400(–450) × 5–7 µm ( x ¯ ± SD = 330 ± 70 × 5 ± 1 μm, n = 50), mononematous, semi- to macronematous, arising singly or in groups, unbranched, straight to flexuous, septate, geniculate, pale brown to brown, paler toward the apex, swollen at the base. Conidiogenous cells (7–)9–23(–28) × 5–8 μm ( x ¯ ± SD = 16 ± 7 × 6.5 ± 1.5 μm, n = 50), mono- to polytretic, sympodial proliferation, integrated, terminal or intercalary, subcylindrical to slightly swollen, pale brown to brown, smooth walled to slightly verruculose, with thickened and darkened scars. Conidia (28–)38–62(–68) × 9–13 µm ( x ¯ ± SD = 50 ± 18.5 × 11 ± 2 μm, n = 50), golden brown, smooth walled, straight, cylindrical to fusoid, occasionally ellipsoidal, tapering toward rounded ends, end cells often cut off by a thick dark septum, (4–)5–8(–9)-distoseptate, germination mono- or bipolar; hila 2- to 3-μm wide, truncate, slightly protruding, thickened, and darkened. Stroma, chlamydospores, and microconidiation were not observed.

Culture characteristics: Colonies on PDA reaching 67 mm in diameter after 7 days at 25°C in the dark, circular, margin entire, olivaceous green at the center, white at the margin with white to gray aerial mycelia; reverse gray olivaceous to olivaceous black with a hyaline margin. Colonies on MEA reaching 35 mm in diameter, circular, margin irregular, cottony appearance, white with white aerial mycelia; reverse brown to pale brown from the center to the margin. Colonies on CMA reaching 62 mm in diameter, circular, margin entire, hairy appearance, olivaceous gray with sparse white to gray aerial mycelia; reverse olivaceous gray at the center and a hyaline margin.

Additional materials examined: IRAN, West Azarbaijan Province, Khoy County, on infected leaves of Setaria sp. (Poaceae, Poales), 20 September 2010, A. Ahmadpour, isolate IRAN 3388C; ibid. on infected leaves of Setaria sp. (Poaceae, Poales), 20 September 2010, A. Ahmadpour, isolate IRAN 3387C.

Host and distribution: Setaria sp. in Iran (this study).

Notes: Based on multi-locus phylogenetic analyses, B. banihashemii clustered closely with B. variabilis and B. zeae (MLBS/MPBS/BIPP = 100/86/0.99) ( Figure 1 ). A comparison of nucleotide differences in ITS−rDNA, GAPDH, and TEF1 indicates that B. banihashemii (IRAN 3389C) differs from B. variabilis (CBS 127716) by 1/548 bp [0.18%, with one gap (0%)] in ITS−rDNA, 4/577 bp (0.69%) in GAPDH, and 1/642 bp (0.15%) in TEF1 and from B. zeae (BRIP 11512) by 3/577 bp (0.52%) in GAPDH and 2/712 bp (0.28%) in TEF1. The PHI analysis confirms that B. banihashemii has no significant genetic recombination with closely related species (Φw = > 0.05, Figure 7 ). Bipolaris variabilis can be differentiated by having longer conidiophores (up to 1,600 μm vs. up to 450 μm in B. banihashemii), shape of conidia (verruculose walled, straight or slightly curved, globose to obclavate conidia vs. smooth walled, straight, cylindrical to fusoid conidia in B. banihashemii), and wider conidia (10–19.5 vs. 9–13 μm in B. banihashemii) (Marin-Felix et al., 2017a). Bipolaris zeae differs from B. banihashemii in producing shorter conidiophores (up to 370 vs. 450 μm in B. banihashemii) and longer and wider conidia [(30–)40–80(–120) × 12–18(–21) μm vs. (28–)38–62(–68) × 9–13 µm in B. banihashemii] (Sivanesan, 1987; Manamgoda et al., 2014).

Bipolaris hedjaroudei A. Ahmadpour, Z. Heidarian, Y. Ghosta, Z. Alavi & F. Alavi, sp. nov. ( Figure 8 ).

MycoBank No: MB 854733

Etymology: Named in honor of Dr. Ghorbanali Hedjaroud, emeritus Professor of Tehran University, who significantly contributed to the knowledge of mycology in Iran.

Diagnosis: Differs from Bipolaris microstegii, B. victoriae, B. zeicola, and B. woodii by having longer conidiophores, smaller conidia, and production of sexual morph (homothallic species) in culture media.

Type: IRAN, West Azarbaijan Province, Khoy County, on infected leaves of Setaria sp. (Poaceae, Poales), 10 September 2020, A. Ahmadpour, (IRAN 18492F, holotype, dried culture; ex-type IRAN 4805C).

Description: On infected leaves of Setaria sp., leaf lesions 1- to 10-mm long, gray at the center and red-brown at the margins. Sexual morph: On sterile leaves of Setaria sp. in TWA medium Ascomata pseudothecial, (300–)400–550(–600) × (290–)300–500(–550) μm ( x ¯ ± SD = 475 ± 75 × 400 ± 100 μm, n = 20), solitary, scattered, superficial or slightly embedded, globose to subglobose or oval, dark brown to black, unilocular with a short ostiolate neck, with long brown setae and conidiophores bearing conidia developing on the upper part of the ascoma. Ostiolar neck 10–20× 8–12 μm ( x ¯ ± SD = 15 ± 5 × 10 ± 2 μm, n = 20), conical, central, filled with masses of hyaline cells frequently covering the apex of the neck. Peridium (ascomata wall) 30- to 35-μm wide, composed of layers of pigmented thick-walled cells. Pseudoparaphyses 2- to 3-μm wide, hyaline, septate, filamentous, simple to branched. Asci (136–)150–200(–212) × (15–)17–20 (–22) μm ( x ¯ ± SD = 150 ± 50 × 18.5 ± 1.5 μm, n = 20), with eight ascospores coiled in a tight helix, bitunicate, cylindrical to clavate, occasionally obclavate–fusoid, straight or curved, with short pedicel. Ascospores 170–250 × 5–7 μm ( x ¯ ± SD = 210± 40 × 6 ± 1 μm, n = 50), hyaline, filiform to flagelliform, tapering toward the rounded ends, tightly coiled inside the ascus, 7–13 septate, with a thin mucilaginous sheath visible in water mounts. Asexual morph: On TWA Hyphae 2- to 5-μm wide, pale brown to brown, smooth, septate, branched. Conidiophores (125–)175–250(–325) × 5–7 µm ( x ¯ ± SD = 212.5 ± 37.5 × 6 ± 1 μm, n = 50), mononematous, semi- to macronematous, arising mostly singly or rarely in groups, unbranched, straight to flexuous, septate, geniculate, pale brown to brown, paler toward the apex, swollen at the base. Conidiogenous cells (6–)8–22(–25) × 5–8 μm ( x ¯ ± SD = 15 ± 7 × 6.5 ± 1.5 μm, n = 50), mono- to polytretic, sympodial proliferation, integrated, terminal or intercalary, subcylindrical to slightly swollen, pale brown to brown, smooth walled to slightly verruculose, with thickened and darkened scars. Conidia (25–)32–60(–62) × 15–17 µm ( x ¯ ± SD = 46 ± 14 × 16 ± 1 μm, n = 50), brown to dark brown, smooth walled, straight to slightly curved, broadly fusiform, occasionally ellipsoidal to obclavate, tapering toward the rounded ends, apical and basal cells paler than the median cells, end cells often cut off by a thick dark septum, (4–)5–8(–9)-distoseptate, germinated mono- or bipolar; hila 2- to 3-μm wide, conspicuous, brown, slightly protuberant, thickened, and darkened. Stroma, chlamydospores, and microconidiation were not observed.

Culture characteristics: Colonies on PDA reaching 65 mm in diameter after 7 days at 25°C in the dark, circular, margin entire, velvety, gray at the center and white at the margin, with gray to white aerial mycelia; reverse brown to pale brown from the center to the margin. Colonies on MEA reaching 61 mm in diameter, circular, margin entire, cottony appearance, white with white aerial mycelia; reverse brown to pale brown from the center to the margin. Colonies on CMA reaching 61 mm in diameter, circular, margin entire, hairy appearance, gray with sparse white to gray aerial mycelia; reverse olivaceous brown at the center and a hyaline margin.

Additional material examined: Iran, West Azarbaijan Province, Khoy County, on infected leaves of Setaria sp. (Poaceae, Poales), 10 September 2020, A. Ahmadpour, isolate FCCUU 1013.

Host and distribution: Setaria sp. in Iran (this study).

Notes: Bipolaris hedjaroudei is phylogenetically closely related to B. victoriae, B. microstegii, B. zeicola, and B. woodii ( Figure 1 ). Pairwise sequence similarity analyses of three genomic regions in B. hedjaroudei distinguished it from closely related taxa. A comparison of nucleotide differences in ITS−rDNA, GAPDH, and TEF1 indicates that B. hedjaroudei (IRAN 4805C) differs from B. microstegii (CBS 132550) by 2/507 bp (0.39%) in ITS−rDNA, 5/539 bp (0.92%) in GAPDH, and 8/763 bp [1.04%, with two gaps (0%)] in TEF1; from B. victoriae (CBS 327.64) by 1/480 bp (0.20%) in GAPDH and 6/763 bp [0.78%, with two gaps (0%)] in TEF1; from B. woodii (BRIP 12239) by 2/512 bp (0.39%) in ITS−rDNA, 9/550 bp [1.63%, with one gap (0%)] in GAPDH, and 8/761 bp [1.05%, with two gaps (0%)] in TEF1; and from B. zeicola (FIP 532) by 2/437 bp [0.45%, with one gap (0%)] in ITS−rDNA, 1/480 bp (0.20%) in GAPDH, and 6/763 bp [0.78%, with two gaps (0%)] in TEF1. The PHI analysis confirms that B. hedjaroudei has no significant genetic recombination with closely related species (Φw = > 0.05, Figure 7 ). Bipolaris hedjaroudei can be differentiated by having longer conidiophores (up to 325 μm vs. up to 250 μm in B. victoriae, up to 270 μm in B. zeicola, up to 250 μm in B. woodii) and smaller conidia [(25–)32–60(–62) × 15–17 µm vs. (25–)55–90(–110) × (10–)12–16(–19) μm in B. victoriae, (45–)65–90(–105) × (10–)15–19(–22) μm in B. zeicola, (60–)69–76(–86) × (10–)12.5–13.5(–15) μm in B. woodii] (Manamgoda et al., 2014; Tan et al., 2016). Bipolaris microstegii differs from B. hedjaroudei in producing secondary conidiophores and conidia, longer conidiophores (up to 750 μm vs. up to 325 μm in B. hedjaroudei), and accentuated septa (Manamgoda et al., 2014). Bipolaris victoriae and B. zeicola have been reported on various poaceous hosts and caused destructive diseases in oat and maize, respectively (Manamgoda et al., 2014; Farr et al., 2024). Bipolaris hedjaroudei is a homothallic species that forms sexual morph abundantly on TWA medium containing host leaves after 21–30 days. In contrast, B. victoriae and B. zeicola are heterothallic species, and the sexual morph of B. microstegii and B. woodii has not been recorded yet (Manamgoda et al., 2014; Tan et al., 2016).

Bipolaris hemerocallidis A. Ahmadpour, Z. Heidarian, Y. Ghosta, Z. Alavi & F. Alavi, sp. nov. ( Figure 9 ).

MycoBank No: MB 854734

Etymology: Named after the host genus, Hemerocallis, from which the holotype was collected.

Diagnosis: Differs from Bipolaris axonopicola by having longer conidiophores.

Type: IRAN, Isfahan Province, Isfahan County, Flower Garden, on leaves of Hemerocallis fulva (Asphodelaceae, Asparagales), 7 October 2013, A. Ahmadpour/Z. Heidarian, (IRAN 18206F, holotype, dried culture; ex–type IRAN 4774C).

Description: Associated with leaves of Hemerocallis fulva. Sexual morph: Undetermined. Asexual morph: On TWA Hyphae 2- to 5-μm wide, pale brown to brown, smooth, septate, branched. Conidiophores (180–)230–550(–600) × 5–7 µm ( x ¯ ± SD = 390 ± 160 × 6 ± 1 μm, n = 50), mononematous, semi- to macronematous, arising singly or in groups, unbranched, straight to flexuous, septate, geniculate, pale brown to brown, paler toward the apex, swollen at the base. Conidiogenous cells (5–)7–21(–25) × 5–8 μm ( x ¯ ± SD = 14± 7 × 6.5 ± 1.5 μm, n = 50), mono- to polytretic, sympodial proliferation, integrated, terminal or intercalary, subcylindrical to slightly swollen, pale brown to brown, smooth walled to slightly verruculose, with thickened and darkened scars. Conidia (38–)40–52(–60) × 9–11 µm ( x ¯ ± SD = 46 ± 6 × 10 ± 1 μm, n = 50), pale brown to brown, smooth walled, straight to slightly curved, broadly fusoid to cylindrical, occasionally ellipsoidal to clavate, tapering toward the rounded ends, apical and basal cells paler than the median cells, (4–)5–9(–10)-distoseptate, germinated mono- or bipolar; hila 2- to 3-μm wide, truncate, slightly protruding, thickened, and darkened. Stroma, chlamydospores, and microconidiation were not observed.

Culture characteristics: Colonies on PDA reaching 65 mm in diameter after 7 days at 25°C in the dark, circular, margin entire, olivaceous green at the center with white to gray aerial mycelia, white at the margin; reverse olivaceous gray to olivaceous black. Colonies on MEA reaching 55 mm in diameter, circular, margin entire, cottony appearance, olivaceous gray to gray, with white to gray aerial mycelia; reverse brown to pale brown from the center to the margin. Colonies on CMA reaching 60 mm in diameter, circular, margin entire, hairy appearance, olivaceous gray with sparse white to gray aerial mycelia; reverse olivaceous brown at the center with a hyaline margin. Sterile ascomata were produced on TWA medium containing leaves of the host plant. However, these structures remained sterile (without asci and ascospores) after 3–6 months of incubation.

Additional material examined: IRAN, Isfahan Province, Isfahan County, Flower Garden, on leaves of Hemerocallis fulva (Asphodelaceae, Asparagales), 7 October 2013, A. Ahmadpour/Z. Heidarian, isolate FCCUU 1011.

Host and distribution: Associated with leaves of Hemerocallis fulva in Iran (this study).

Notes: Bipolaris hemerocallidis is phylogenetically close to B. axonopicola (MLBS/MPBS/BIPP = 100/100/1.0) ( Figure 1 ). The pairwise DNA sequence comparison revealed that B. hemerocallidis is distinct from B. axonopicola. A comparison of nucleotide differences in ITS−rDNA, GAPDH, and TEF1 indicates that B. hemerocallidis (IRAN 4774C) differs from B. axonopicola (BRIP 11740) by 6/532 bp [1.12%, with four gaps (0%)] in ITS−rDNA, 17/546 bp (3.11%) in GAPDH and 4/788 bp (0.50%) in TEF1. The PHI analysis confirms that B. hemerocallidis has no significant genetic recombination with closely related species (Φw = > 0.05, Figure 5 ). Bipolaris hemerocallidis can be differentiated by having longer conidiophores (up to 600 μm vs. up to 250 μm in B. axonopicola) (Tan et al., 2016). Bipolaris axonopicola is only known on Axonopus fissifolius (Poaceae) in Australia (Tan et al., 2016). In this study, B. hemerocallidis was isolated from the leaves of Hemerocallis fulva (Asphodelaceae, Asparagales) in the greenhouse.

Bipolaris iranica A. Ahmadpour, Z. Heidarian, Y. Ghosta, Z. Alavi & F. Alavi, sp. nov. ( Figure 10 ).

MycoBank No: MB 854735

Etymology: Named after the country “Iran” where the holotype was collected.

Diagnosis: Differs from Bipolaris heveae, B. microlaenae, and B. simmondsii by having much longer conidiophores and accentuated transverse septa.

Type: IRAN, West Azarbaijan Province, Khoy County, on infected leaves of Cynodon dactylon (Poaceae, Poales), 20 September 2010, A. Ahmadpour, (IRAN 18207F, holotype, dried culture; ex–type IRAN 4775C).

Description: Leaf lesions on Arundo donax, Cynodon dactylon, Echinochloa colona, Hordeum vulgare, Sorghum halepense, and Triticum aestivum, 1- to 10-mm long. Sexual morph: Undetermined. Asexual morph: On TWA Hyphae 2- to 5-μm wide, pale brown to brown, smooth, septate, branched. Conidiophores (125–)187–480(–550) × 7–8 µm ( x ¯ ± SD = 337.5 ± 146.5 × 7.5 ± 0.5 μm, n = 50), mononematous, macronematous, arising singly or in groups, simple, straight to flexuous, septate, geniculate, with cell walls thicker than vegetative hyphae, pale brown to brown, paler toward the apex, basal cell swollen and darker than the other cells, up to 10 μm in diameter Conidiogenous cells (8–)10–24(–28) × 6–8 μm ( x ¯ ± SD = 17 ± 7 × 7 ± 1 μm, n = 50), mono- to polytretic, proliferating sympodially, integrated, terminal or intercalary, subcylindrical to slightly swollen, pale brown to dark brown, smooth walled to slightly verruculose, with thickened and darkened scars. Conidia (70–)85–100(–110)× 15–20 µm ( x ¯ ± SD = 92.5 ± 7.5 × 17.5 ± 2.5 μm, n = 50), brown to dark brown, smooth walled, straight to curved, mostly navicular to fusoid, rarely cylindrical to clavate, taper toward rounded ends, apical and basal cells paler than the median cells, septa accentuated at maturity, (6–)8–11(–13)-distoseptate, germinated mono- or bipolar; hila 2- to 3-μm wide, flat to slightly protuberant, thickened, and darkened. Stroma, chlamydospores, and microconidiation were not observed.

Culture characteristics: Colonies on PDA reaching 58 mm in diameter after 7 days at 25°C in the dark, circular, margin entire, olivaceous gray at the center with white to gray aerial mycelia, white at the margin; reverse olivaceous gray to olivaceous black with a hyaline margin. Colonies on MEA reaching 42 mm in diameter, circular, margin entire, cottony appearance, white with white aerial mycelia; reverse brown to pale brown from the center to the margin. Colonies on CMA reaching 66 mm in diameter, circular, margin entire, olivaceous gray with sparse gray aerial mycelia; reverse olivaceous gray at the center and a hyaline margin.

Additional materials examined: IRAN, West Azarbaijan Province, Miyandoab County, on infected leaves of Sorghum halepense (Poaceae, Poales), 11 July 2013, A. Ahmadpour/Z. Heidarian, isolate FCCUU 1005; ibid. on infected leaves of Echinochloa colona (Poaceae, Poales), 23 September 2014, A. Ahmadpour/Z. Heidarian, isolate FCCUU 1007; West Azarbaijan Province, Urmia County, on infected leaves of Arundo donax (Poaceae, Poales), 20 September 2014, A. Ahmadpour/Z. Heidarian, isolate FCCUU 1006; West Azarbaijan Province, Bukan County, on infected leaves of Hordeum vulgare (Poaceae, Poales), 20 October 2014, A. Ahmadpour/Z. Heidarian, isolate FCCUU 1008; West Azarbaijan Province, Khoy County, on infected leaves of Triticum aestivum (Poaceae, Poales), 22 May 2021, A. Ahmadpour, isolate FCCUU 1009.

Hosts and distribution: Arundo donax, Cynodon dactylon, Echinochloa colona, Hordeum vulgare, Sorghum halepense, and Triticum aestivum in Iran (this study).

Notes: Based on the results of phylogenetic analyses ( Figure 1 ), B. iranica isolates clustered well in a separate lineage with 100% ML, 100% MP bootstrap, and 1.0 BI posterior probability values, representing a new taxon. The pairwise DNA sequence comparison revealed that B. iranica is distinct from related taxa, B. heveae, B. microlaenae, and B. simmondsii. A comparison of nucleotide differences in ITS−rDNA, GAPDH, and TEF1 indicates that B. iranica (IRAN 4775C) differs from B. heveae (CBS 241.92) by 5/539 bp [0.92%, with four gaps (0%)] in ITS−rDNA, 11/490 bp (2.24%) in GAPDH and 6/770 bp (0.77%) in TEF1; from B. microlaenae (BRIP 15613) by 2/534 bp (0.37%) in ITS−rDNA, 11/543 bp (2.02%) in GAPDH, and 12/788 bp (1.52%) in TEF1; and from B. simmondsii (BRIP 12030) by 3/536 bp [0.55%, with one gap (0%)] in ITS−rDNA, 13/536 bp (2.42%) in GAPDH, and 7/788 bp (0.88%) in TEF1. The PHI analysis confirms that B. iranica has no significant genetic recombination with closely related species (Φw = > 0.05, Figure 11 ). Bipolaris iranica is morphologically similar to B. heveae, B. microlaenae, and B. simmondsii; however, it can be distinguished by its much longer conidiophores (up to 550 μm vs. up to 335 μm in B. heveae, and up to 240 μm in B. simmondsii), and its accentuated septa, which are absent in B. heveae, B. microlaenae, and B. simmondsii (Manamgoda et al., 2014; Tan et al., 2016). Bipolaris heveae is known to cause diseases on rubber trees (Hevea brasiliensis) across various tropical countries, including Cambodia, the Dominican Republic, Ghana, Guatemala, Haiti, Honduras, Indonesia, Mexico, Nigeria, the Philippines, Sri Lanka, and the United States. Unlike B. iranica, this pathogen does not infect grass species and is restricted to its specific host plant (Manamgoda et al., 2014; Farr et al., 2024). Furthermore, B. microlaenae and B. simmondsii have only been documented in Australia, where they cause leaf spots on Zoysia macrantha (Tan et al., 2016).

Bipolaris persica A. Ahmadpour, Z. Heidarian, Y. Ghosta, Z. Alavi & F. Alavi, sp. nov. ( Figure 12 )

MycoBank No: MB 854736

Etymology: The name refers to the old name of Iran, Persia, from where the holotype was collected.

Diagnosis: Differs from Bipolaris heveae, B. microlaenae, and B. simmondsii by having longer conidiophores and accentuated transverse septa.

Type: IRAN, West Azarbaijan Province, Mahabad County, on infected leaves of Cynodon dactylon (Poaceae, Poales), 20 June 2015, A. Ahmadpour, (IRAN 18209F, holotype, dried culture; ex-type IRAN 4777C).

Description: Leaf spots on Cynodon dactylon, 1- to 10-mm long, with dark brown spots. Sexual morph: Undetermined. Asexual morph: On TWA Hyphae 2- to 5-μm wide, pale brown to brown, smooth, septate, branched. Conidiophores (210–)250–330(–350) × 6–7 µm ( x ¯ ± SD = 290 ± 40 × 6.5 ± 0.5 μm, n = 50), mononematous, macronematous, arising singly or in groups, simple, straight to flexuous, septate, geniculate, with cells wall thicker than those of vegetative hyphae, pale brown to brown, paler toward the apex, basal cell swollen and darker than the other cells, up to 10 μm in diameter. Conidiogenous cells (7–)10–25(–30) × 6–8 μm ( x ¯ ± SD = 17.5 ± 7.5 × 7 ± 1 μm, n = 50), mono- to polytretic, proliferating sympodially, integrated, terminal or intercalary, subcylindrical to slightly swollen, pale brown to brown, smooth walled to slightly verruculose, with thickened and darkened scars. Conidia (62–)80–95(–100)× 13–20 µm ( x ¯ ± SD = 87.5 ± 7.5 × 16.5 ± 3.5 μm, n = 50), brown to dark brown, smooth walled, curved, mostly navicular to fusoid, tapering toward the rounded ends, apical and basal cells paler than the median cells, septa accentuated at maturity, (6–)7–10(–11)-distoseptate, germinated mono- or bipolar; hila 2- to 3-μm wide, flat, thickened, and darkened. Stroma, chlamydospores, and microconidiation were not observed.

Culture characteristics: Colonies on PDA reaching 68 mm in diameter after 7 days at 25°C in the dark, circular, margin entire, olivaceous gray with white to gray aerial mycelia, sporulation abundant; reverse olivaceous gray at the center with hyaline margin. Colonies on MEA reaching 58 mm in diameter, circular, margin entire, cottony appearance, gray at the center, white at the margin with white to gray aerial mycelia; reverse olivaceous gray with hyaline margin. Colonies on CMA reaching 53 mm in diameter, circular, margin entire, olivaceous green with white to gray aerial mycelia; reverse olivaceous gray to olivaceous black and a hyaline margin.

Additional material examined: IRAN, West Azarbaijan Province, Mahabad County, on infected leaves of Cynodon dactylon (Poaceae, Poales), 20 June 2015, A. Ahmadpour, isolate FCCUU 1004.

Host and distribution: Cynodon dactylon in Iran (this study).

Notes: Bipolaris persica is phylogenetically closely related to B. heveae, B. iranica, B. microlaenae, and B. simmondsii ( Figures 1 , 11 ). Pairwise DNA sequence comparison revealed that B. persica is distinct from its closely related taxa. A comparison of nucleotide differences in ITS−rDNA, GAPDH, and TEF1 indicates that B. persica (IRAN 4777C) differs from B. heveae (CBS 241.92) by 1/500 bp [0.20%, with one gap (0%)] in ITS−rDNA, 13/481 bp (2.70%) in GAPDH, and 7/731 bp (0.95%) in TEF1; from B. iranica (IRAN 4775C) by 4/500 bp [0.80%, with three gaps (0%)] in ITS−rDNA, 15/504 bp (2.97%) in GAPDH, and 8/744 bp (1.07%) in TEF1; from B. microlaenae (BRIP 15613) by 4/500 bp [0.80%, with three gaps (0%)] in ITS−rDNA, 17/516 bp (3.29%) in GAPDH, and 8/744 bp (1.07%) in TEF1; and from B. simmondsii (BRIP 12030) by 4/500 bp [0.80%, with three gaps (0%)] in ITS−rDNA, 9/545 bp (1.65%) in GAPDH, and 3/744 bp (0.40%) in TEF1. The PHI analysis further confirms that B. iranica has no significant genetic recombination with closely related species (Φw = > 0.05, Figure 11 ). Morphologically, Bipolaris persica can be differentiated from closely related taxa by its longer conidiophores (up to 350 μm vs. up to 240 μm in B. simmondsii), and by its accentuated septa, which are absent in B. heveae, B. microlaenae, and B. simmondsii (Manamgoda et al., 2014; Tan et al., 2016). However, B. persica shares overlapping morphological characteristics and the same host with B. iranica, complicating their differentiation. Unlike B. persica, B. iranica has a broader host range, including Arundo donax, Cynodon dactylon, Echinochloa colona, Hordeum vulgare, Sorghum halepense, and Triticum aestivum (this study). Consequently, using molecular tools is essential for accurately distinguishing Bipolaris species and identifying any cryptic species.

Bipolaris crotonis Sivan., Trans. Br. mycol. Soc. 84(3): 404 (1985) ( Figure 13 ).

Description: Leaf spots on Eleusine indica, gray at the center and dark brown margins. Sexual morph: Undetermined. Asexual morph: On TWA Hyphae 3- to 6-μm wide, pale brown to brown, smooth, septate, branched. Conidiophores (60–)100–300(–325) × 5–7 µm ( x ¯ ± SD = 200± 100 × 6 μm, n = 50), mononematous, semi- to macronematous, arising singly or mostly in groups, unbranched, straight to flexuous, septate, geniculate, pale brown to brown, paler toward the apex, swollen at the base. Conidiogenous cells (9–)11–26(–30) × 5–8 μm ( x ¯ ± SD = 18.5 ± 7.5 × 6.5 ± 1.5 μm, n = 50), mono- to polytretic, proliferating sympodially, integrated, terminal or intercalary, subcylindrical to slightly swollen, hyaline to pale brown, smooth walled to slightly verruculose, with thickened and darkened scars. Conidia (62–)75–100(–120) × 17–25 µm ( x ¯ ± SD = 87.5 ± 12.5 × 21 ± 4 μm, n = 50), straight, brown to dark golden brown, smooth walled, broadly ellipsoidal, fusoid to obclavate, tapering toward the rounded ends, apical and basal cells paler than the median cells, (5–)7–9(–11)-distoseptate, germinated mono- or bipolar; hila 2- to 3-μm wide, truncate, slightly protruding, thickened, and darkened. Stroma, chlamydospores, and microconidiation were not observed.

Culture characteristics: Colonies on PDA reaching 45 mm in diameter after 7 days at 25°C in the dark, circular, margin entire, velvety, gray at the center and white at the margin, with sparse gray aerial mycelia; reverse brown to pale brown from the center to the margin. Colonies on MEA reaching 40 mm in diameter, circular, margin entire, cottony appearance, gray at the center, white at the margin, with floccose aerial mycelia; reverse brown to pale brown from the center to the margin. Colonies on CMA reaching 50 mm in diameter, hairy appearance, olivaceous gray, with sparse gray aerial mycelia; reverse olivaceous gray at the center and a hyaline margin.

Material examined: IRAN, Mazandaran Province, Nour County, from leaf spots of Eleusine indica (Poaceae, Poales), 10 September 2022, Hashemlou E., living culture IRAN 4807C.

Hosts: Croton sp., Eleusine indica (Sivanesan, 1987; Manamgoda et al., 2014; Farr et al., 2024).

Distribution: Australia, Iran (this study), Papua New Guinea, Samoa, and Vanuatu (Sivanesan, 1987; Manamgoda et al., 2014; Farr et al., 2024).

Notes: Bipolaris crotonis is morphologically similar and phylogenetically related to B. sorokiniana ( Figure 1 ) and can be differentiated by having longer conidia [(51–)60–110(–138) × (14–)20–25(–32) µm vs. (31–)40–72(–100) × 15–25(–27) μm in B. sorokiniana] (Sivanesan, 1987; Manamgoda et al., 2014). This species is heterothallic, and sexual morph can be developed by crossing compatible isolates in Sach^’s agar medium (Manamgoda et al., 2014). Tan et al. (2014) reported that B. eleusines is phylogenetically similar to B. crotonis and synonymized it under B. crotonis based on nomenclatural priority. Bipolaris crotonis was first reported on decaying leaves of Croton sp. (Euphorbiaceae) (Sivanesan, 1985; Manamgoda et al., 2014) and was later identified on Eleusine indica (Poaceae) (Tan et al., 2014; Bhunjun et al., 2020). This species has also been reported as the causal agent of black point disease in wheat on the North China Plain (Xu et al., 2018) and as an endophytic fungus associated with Dillenia indica, an ethnomedicinal plant (Prasher and Kumar, 2021). To the best of our knowledge, this is the first report of B. crotonis in Iran.

Bipolaris salkadehensis Ahmadpour & Heidarian, Mycotaxon 120: 302 (2012) ( Figure 14 ).

Description: Culm spots on Scirpus acutus, 1- to 20-mm long, with dark brown spots. Sexual morph: Undetermined. Asexual morph: on TWA Hyphae 3- to 5-μm wide, pale brown to brown, smooth, septate, branched. Conidiophores (225–)260–400(–590) × 6–7 µm ( x ¯ ± SD = 330 ± 70 × 6.5 ± 0.5 μm, n = 50), mononematous, semi- to macronematous, arising singly or in groups, unbranched, straight to flexuous, septate, geniculate, pale brown to brown, paler toward the apex, swollen at the base. Conidiogenous cells (8–)10–24(–30) × 5–8 μm ( x ¯ ± SD = 16 ± 6 × 6.5 ± 1.5 μm, n = 50), smooth walled, mono- to polytretic, proliferating sympodially, integrated, terminal or intercalary, subcylindrical to slightly swollen, subhyaline or pale brown to brown. Conidia (32–)52–70(–93) × 11–15 µm ( x ¯ ± SD = 61 ± 9 × 13 ± 2 μm, n = 50), brown to dark brown, smooth walled to slightly verruculose, straight to slightly curved, subcylindrical to fusoid, occasionally obclavate to clavate, tapering toward the rounded apex, median cells brown to dark brown, apical and basal cells paler than the median cells being subhyaline to pale brown, end cells often cut off by a thick dark septum, (3–)5–8(–10)-distoseptate, germinated mono- or bipolar; hila 2- to 4-μm wide, flat to slightly protuberant, thickened, and darkened. Stroma, chlamydospores, and microconidiation were not observed.

Culture characteristics: Colonies on PDA reaching 60 mm in diameter after 7 days at 25°C in the dark, circular, margin entire, olivaceous gray to olivaceous brown with white to gray aerial mycelia; reverse gray olivaceous to olivaceous black at the center, white at the margin. Colonies grow more slowly on MEA, reaching 40 mm in diameter, circular, with irregular margin, gray at the center, white at the margin, with floccose aerial mycelia; reverse brown. Colonies on CMA reaching 51 mm in diameter, hairy appearance, olivaceous gray, with sparse gray aerial mycelia; reverse olivaceous gray.

Materials examined: IRAN, West Azarbaijan Province, Khoy County, on infected culms of Scirpus acutus (Cyperaceae, Poales), 10 September 2020, A. Ahmadpour, living culture IRAN 3382C; ibid. on infected leaves of Sparganium erectum (Typhaceae, Poales), 20 September 2010, A. Ahmadpour, living culture BI 1 = IRAN 3385C; ibid. on infected leaves of Cladium mariscus (Cyperaceae, Poales), 20 September 2010, A. Ahmadpour, living culture BI 4 = IRAN 3386C; ibid. on infected leaves of Setaria sp. (Poaceae, Poales), 25 September 2013, A. Ahmadpour, living culture FCCUU 1002; West Azarbaijan Province, Miyandoab County, on infected leaves of Sorghum halepense (Poaceae, Poales), 10 July 2013, A. Ahmadpour/Z. Heidarian, living culture IRAN 3383C; ibid. on infected leaves of Arundo donax (Poaceae, Poales), 10 July 2013, A. Ahmadpour/Z. Heidarian, living culture FCCUU 1001; ibid. on infected leaves of Hordeum vulgare (Poaceae, Poales), 10 May 2014, A. Ahmadpour/Z. Heidarian, living culture FCCUU 1003.

Hosts: Arundo donax, Cladium mariscus, Hordeum vulgare, Scirpus acutus, Setaria sp., Sorghum halepense, and Sparganium erectum (Ahmadpour et al., 2012a; Farr et al., 2024; this study).

Distribution: Iran (Ahmadpour et al., 2012a; this study).

Notes: Bipolaris salkadehensis was originally reported from infected leaves of Sparganium erectum (Sparganiaceae) and Cladium mariscus (Cyperaceae) with brown oval to elliptical lesions based on morphological characteristics and molecular data obtained from ITS−rDNA sequences (Ahmadpour et al., 2012a). In this study, two additional genes, GAPDH and TEF1, were sequenced for the ex-type isolate (Bi 1 = IRAN 3385C) as well as for other isolates from various plant hosts ( Table 1 ) and used in phylogenetic analyses. Bipolaris salkadehensis isolates clustered well in a separate lineage with 100% ML, 100% MP bootstrap, and 1.0 BI posterior probability values ( Figure 1 ). This species is morphologically similar to B. cynodontis and B. setariae (Sivanesan, 1987; Ahmadpour et al., 2012a). However, the conidia of B. cynodontis are smaller in size (30–75 × 10–16 μm), have three to nine (commonly seven to eight) distoseptate, and without cut-off in end cells (Sivanesan, 1987; Ahmadpour et al., 2012a). The conidia of B. setariae are fusoid to navicular, pale to mid golden brown, 5–10 distoseptate, 45–100 (mostly 50–70) × 10–15 μm, without cut-off in end cells, and lighter than those of B. salkadehensis (Sivanesan, 1987; Ahmadpour et al., 2012a). Zibani et al. (2025) have reported that B. salkadehensis exhibits low virulence as a pathogen of corn in Algeria. To the best of our knowledge, Arundo donax, Hordeum vulgare, Scirpus acutus, Setaria sp., and Sorghum halepense are newly identified hosts for this species.