Table 4.
Clade/Taxon1 | Conidiomata | Conidiogenous layer | Conidia | Origin2 | Reference |
---|---|---|---|---|---|
Diaporthe amygdali clade | |||||
Diaporthe amygdali | |||||
Diaporthe amygdali (Delacr.) Udayanga, Crous & K.D. Hyde ≡Fusicoccum amygdali Delacr. CBS 126679ET |
Pycnidia subglobose to ampulliform, dark brown to black, exuding white to cream conidial droplets, 240–390 μm diam × 140–160 μm high (on host), 160–220 μm diam × 120–300 μm high (in culture) |
Conidiophores subcylindrical, hyaline, seldom branched, 7.4–36.3 × 1.5–3.2 μm (x̄= 14.5 × 2.3 μm, n = 380) Conidiogenous cells cylindrical, tapering towards apex, hyaline, periclinal thickening and collarette present, 5–20 × 1.5–3.2 μm, (x̄ = 9.8 × 2.3 μm, n = 380) |
Alpha conidia ovoid-ellipsoid, mostly with one end obtuse and the other acute, hyaline, aseptate, eguttulate to biguttulate, (4.18–)6.27–6.32(–9.64) × (1.63–)2.36–2.38(–3.31) μm, (x̄= 6.3 × 2.37 μm, n = 2100) Beta andgamma conidia not observed |
Host: on branches of Prunus amygdalus with symptoms of cankers or dieback Country: Portugal Ecological group: pathogen |
Diogo et al . (2010) |
Diaporthe chongqingensis Y.S. Guo & G.P. Wang. CGMCC 3.19603T |
Pycnidia globose, grey to black, exuding yellowish translucent conidial droplets from ostiole, 285–744 μm diam |
Conidiophores cylindrical, straight to sinuous, hyaline, septate, branched, 11–24.1 × 1.6–2.9 μm (x̄= 16 × 2.1 μm, n = 30) Conidiogenous cells cylindrical, straight or slightly curved, hyaline, rough, periclinal thickening present |
Alpha conidia fusiform, acutely rounded at one end, hyaline, aseptate, multiguttulate, 5.5–7.5 × 2–3 μm (x̄= 6.4 × 2.3 μm, n = 50; L/W = 2.8). Beta and gamma conidia not observed |
Host: on branches of Pyrus pyrifolia with symptoms of shoot canker Country: China (Chongqing) Ecological group: pathogen |
Guo et al . (2020) |
Diaporthe fusicola Y.H. Gao & L. Cai. HMAS 244837H |
Pycnidia subglobose to globose, with hairy necks, exuding yellowish translucent conidial droplets, aggregated in more or less cohesive clusters with variable number of pycnidia of variable morphology and dimensions, 175–500 μm diam |
Conidiophores ampulliform, hyaline, 1-septate, unbranched, densely aggregated, 6.5–12.5 × 2–6 μm Conidiogenous cells cylindrical, straight, terminal, tapering towards apex, hyaline, phialidic, 14–26 × 1.5–2.5 μm |
Alpha conidia fusoid, tapering towards ends, hyaline, aseptate, mostly biguttulate, 5.4–7.9 × 1.6–2.7 μm (x̄= 6.7 × 2 μm, n = 60) Beta and gamma conidia not observed |
Host: on diseased leaves of Lithocarpus glaber Country: China (Zhejiang) Ecological group: potential pathogen |
Gao et al . (2015) |
Diaporthe garethjonesii Dissanayake, Tangthirasunun & K.D. Hyde MFLU 13-0261H |
Pycnidia globose, unilocular, black, ostiolate, 85–125 μm diam× 80–100 μm high (x̄= 115 × 85 μm, n = 10) |
Conidiophores cylindrical, straight to sinuous, hyaline, smooth, 5–12 × 1–1.5 μm Conidiogenous cells cylindrical, terminal and lateral, slightly tapering towards apex, phialidic, 0.5–1 μm diam |
Alpha conidia fusoid to ellipsoid, straight, tapering towards ends, obtuse apex, hyaline, aseptate, guttulate, 5–6 × 2–3 μm Beta conidia curved or hamate, straight, hyaline, aseptate, smooth, less common than alpha conidia, 40–50 × 3–4 μm Gamma conidia not observed |
Host: on unknown dead leaves Country: Thailand Ecological group: saprophyte |
Hyde et al . (2016) |
Diaporthe kadsurae C.M. Tian & Q. Yang CFCC 52586T |
Pycnidia nearly flat, discoid, uniloculate and undivided, ectostromatic disc brown to dark, with one ostiole, 475–525 μm diam | Conidiophores cylindrical, straight or slightly curved, hyaline, unbranched, densely aggregated, tapering towards apex, 7–11 × 1.8–2.9 μm |
Alpha conidia oval or fusoid, tapering towards apex, hyaline, aseptate, biguttulate, 5.5–7.5 × 2.1–2.9 μm (x̄= 6.5 × 2.5 μm, n = 60) Beta and gamma conidia not observed |
Host: on symptomatic branches of Kadsura longipedunculata Country: China (Jiangxi) Ecological group: potential pathogen |
Yang et al . (2018) |
Diaporthe mediterranea M. León, Rodríguez-Reina & Armengol CBS 146754T |
Pycnidia globose or irregular, dark brown to black, exuding whitish translucent to creamy conidial droplets from ostiole (x̄ = 527 μm diam, n = 30) |
Conidiophores reduced to conidiogenous cells Conidiogenous cells cylindrical, straight, hyaline, smooth, densely aggregated (x̄ = 15.5 × 2.2 μm, n = 30) |
Alpha conidia fusiform, acute ends, hyaline, aseptate, multiguttulate (x̄= 6.6 × 2.4 μm, n = 30) Beta andgamma conidia not observed |
Host: on twig canker of Prunus amygdalus Country: Spain Ecological group: pathogen |
León et al . (2020) |
Diaporthe nannuoshanensis S.T. Huang, J.W. Xia, X.G. Zhang & Zhuang Li* SAUCC 194.91T |
Pycnidia globose to subglobose, black, brown to dark brown, coated with white and greyish hyphae, exuding cream conidial droplets from central ostiole, 275–530 μm diam × 205–435 μm high |
Conidiophores cylindrical, straight to sinuous, hyaline, smooth, eguttulate to biguttulate, densely aggregated, branched, 7.5–14 × 1.5–2.5 μm (x̄= 10.5 × 2.1 μm, n = 20) Conidiogenous cells cylindrical, ampulliform, straight or sinuous, terminal and lateral, tapering towards apex, phialidic, neck up to 4.0 μm long, 1–1.5 μm wide |
Beta conidia filiform, straight, bent or hamate, acutely rounded apex, truncate base, slightly narrowing towards apex, hyaline, aseptate, smooth, 20.5–24 × 1.5–2 μm (x̄= 22.3 × 1.7 μm, n = 50) Alpha andgamma conidia not observed |
Host: on leaf spots of Camellia sinensis Country: China (Yunnan) Ecological group: potential pathogen |
Huang et al . (2021a) |
Diaporthe ovoidea Y.H. Gao & L. Cai HMAS 244835H |
Pycnidia globose, exuding cream conidial droplets from ostiole, 140–250 μm diam |
Conidiophores reduced to conidiogenous cells Conidiogenous cells cylindrical, straight or slightly curved, tapering towards apex, single to multi-septate, rough, guttulate, phialidic, (12.3–)14.2–23.6(–26.5) × 1.6–2.3 μm (x̄= 18.7 × 1.9 μm, n = 30) |
Alpha conidia ovoid to fusoid, mostly with one end obtuse and the other acute, hyaline, aseptate, eguttulate to biguttulate, 5.3–8.3 × 1.7–3 μm (x̄= 6.7 × 2.3 μm, n = 60) Beta conidia filiform, curved, with rounded ends, hyaline, aseptate, eguttulate, 16.1–25 × (1–)1.2–1.5(–1.8) μm (x̄= 20.7 × 1.4 μm, n = 30) Gamma conidia not observed |
Host: on leaf spots of Lithocarpus glaber Country: China (Zhejiang) Ecological group: potential pathogen |
Gao et al . (2015) |
“Diaporthe sinensis ” Jayaward.,Manawas., X.H. Li, J.Y. Yan & K.D. Hyde JZBH 3340167H |
Pycnidia globose, dark brown to black, 360–900 μm (x̄= 500 μm, n = 20) diam |
Conidiophores reduced to conidiogenous cells Conidiogenous cells simple, terminal, hyaline, smooth |
Alpha conidia oval, obtuse ends, hyaline, aseptate, 4–7 × 2–3 μm (x̄= 5 × 3 μm, n = 40) Beta and gamma conidia not observed |
Host: on dead leaves of Camellia sinensis Country: China (Fujian) Ecological group: saprophyte or potential pathogen |
Manawasinghe et al . (2021) |
Phomopsis ternstroemiae Y.H. Gao, W. Sun & L. Cai HMAS 244234T |
Pycnidia globose, white to dark brown, exuding yellowish translucent conidial droplets from ostiole, 180–390 μm diam | Conidiophores cylindrical, hyaline, branched, single to multi-septate, rough, 13.9–18.2 × 1.8–2.4 μm |
Alpha conidia fusiform to ellipsoidal, tapering towards ends or obtuse at one end, hyaline, aseptate, biguttulate, very often with several additional smaller guttules, 6.2–10.7 × 2.0–3.4 μm (x̄= 7.51 × 2.61 μm, n = 60) Beta andgamma conidia not observed |
Host: leaf spots of Ternstroemia gymnanthera Country: China (Zhejiang) Ecological group: potential pathogen |
Gao et al . (2014) |
Diaporthe brasiliensis clade | |||||
Diaporthe brasiliensis | |||||
Diaporthe brasiliensis R.R. Gomes, Glienke & Crous CBS 133183T |
Pycnidia globose to conical, brown to black, ostiolate, with globose conidial masses, white to pale-luteous, 70–160 μm diam × 60–140 μm high, with necks of 60–130 μm high. |
Conidiophores cylindrical, filiform, straight to curved, hyaline, 1–3-septate, (17–)20–27(–30) × 2(–4) μm Conidiogenous cells cylindrical, filiform, straight to curved, with flared collarette and slight periclinal thickening, (7–)8–12(–14) × 2(–3) μm |
Alpha conidia ellipsoid to irregular, bluntly rounded apex, obtuse to subtruncate base, hyaline, aseptate, bi- to multiguttulate, 6–7(–8) × 2–3 μm Beta andgamma conidia not observed |
Host: on a leaf of Aspidosperma tomentosum Country: Brazil (Rio de Janeiro) Ecological group: endophyte |
Gomes et al . (2013) |
Diaporthe caatingaensis | |||||
Diaporthe caatingaensis J.D.P. Bezerra, L.M. Paiva, G.A. Silva, C.M. Souza-Motta & Crous CBS 141542T |
Pycnidia globose to subglobose-conical, dark brown to black, with hyaline to pale conidial masses at neck apex, up to 465 μm diam, with long black necks up to 510 μm tall |
Conidiophores cylindrical, straight to sinuous, hyaline, 3–5-septate, smooth, densely aggregated, sometimes branched, 30–37.5 × 2(–2.5) μm Conidiogenous cells cylindrical, terminal, with distinct collarette at apex and slight periclinal thickening, phialidic, 16–23.5 × 1–2(–2.5) μm |
Alpha conidia fusoid to ellipsoid, tapering towards ends, subobtuse to obtuse apex, subtruncate to truncate base, hyaline, aseptate, smooth, guttulate, (6.5–)8.5–9.5(–10.5) × (1.5–)2(–2.5) μm Beta andgamma conidia not observed |
Host: on Tacinga inamoena Country: Brazil (Pernambuco) Ecological group: endophyte |
Crous et al . (2006a) |
Diaporthe pygmaeae sp. nov. | |||||
Diaporthe pygmaeae D.S. Pereira & A.J.L. Phillips CDP 1370T |
Pycnidia globose to subglobose, black, exuding white to pale conidial droplets, up to 210 μm diam |
Conidiophores mostly reduced to conidiogeneous cells, doliiform to subcylindrical, hyaline to subhyaline, aseptate to 1–3-septate, smooth, densely aggregated, unbranched Conidiogenous cells terminal, cylindrical, tapering towards apex, straight or slightly curved, hyaline, aseptate, rarely 1-septate, smooth, unbranched, rarely 1-branched, occasionally with minute, inconspicuous collarette, with periclinal thickenings,8.0–19.0(–31.6) × 1.9–3.9(–4.8) μm |
Alpha conidia fusoid to ellipsoid, acute ends, hyaline, aseptate, smooth, eguttulate, often with granular contents (7.8–)8.0–10.0(–10.7) × 2.4–3.5(–4.0) μm (x̄= 9.0 × 2.9 μm, n = 150) Beta andgamma conidia not observed |
Host: on foliar lesions of Phoenix roebelenii Country: Portugal Ecological group: potential pathogen |
Present study |
Diaporthe eucommiae clade | |||||
Diaporthe eucommiae | |||||
Diaporthe araliae-chinensis S.Y. Wang, Yong Wang bis & Y. Li* GUCC 412.7T |
Pycnidia globose or subglobose, deep green to black, up to 1 mm diam |
Conidiophores reduced to conidiogeneous cells Conidiogenous cells cylindrical, subulate, mostly straight, slightly tapering towards apex, hyaline, simple, smooth, densely aggregated, with inconspicuous periclinal thickening, 12–20 × 1.5–2.5 μm (x̄= 16.5 × 2 μm, n = 20) |
Alpha conidia fusoid to ellipsoidal, asymmetrical, mostly straight, tapering towards ends, hyaline, aseptate, smooth, 5.5–9.5 × 2–3 μm (x̄= 7.5 × 2.4 μm, n = 30) Beta andgamma conidia not observed |
Host: on leaves of Aralia chinensis Country: China (Guizhou) Ecological group: UN |
Hyde et al . (2023) |
Diaporthe australiana R.G. Shivas, Akinsanmi & Y.P. Tan* BRIP 66145T |
Pycnidia globose or irregular, dark brown to black, exuding whitish to pale yellow conidial droplets from central ostioles, up to 1 mm diam |
Conidiophores with an irregularly polygonal basal cell, hyaline, smooth, densely aggregated, 15 × 25 μm Paraphyses intermingled among conidiophores, tapering towards apex (1–2 μm wide), hyaline, 1–3-septate, smooth, up to 70 μm long Conidiogenous cells cylindrical, straight or flexuous, hyaline, phialidic, 10–20 × 1–2.5 μm |
Alpha conidia fusiform, acute ends, hyaline, aseptate, guttulate, 5–8.5 × 1.5–2 μm Beta andgamma conidia not observed |
Host: on husk rot of Macadamia sp. Country: Australia (New South Wales) Ecological group: pathogen |
Wrona et al . (2020) |
Diaporthe eucalyptorum Crous & R.G. Shivas* CBS 132525T |
Pycnidia subglobose, black, exuding white to cream conidial droplets from central ostioles, up to 350 μm |
Conidiophores r educed to conidiogeneous cells or straight to sinuous, hyaline, up to 4-septate, unbranched or branched below, smooth, densely aggregated, 15–60 × 3–4 μm Paraphyses c ylindrical, flexuous, hyaline, 1–3-septate, unbranched or branched below, smooth, up to 70 μm long, 2–3 μm wide at base Conidiogenous cells cylindrical, slightly tapering towards apex (1–1.5 μm diam), terminal and lateral, phialidic, with visible periclinal thickening and flared collarette (up to 2 μm long), surrounded by a prominent flaring mucoid sheath, 10–30 × 2–3 μm |
Alpha conidia fusoid, tapering towards ends, straight, subobtuse apex, subtruncate base, hyaline, aseptate, smooth, guttulate, (5.5–)6.5–7(–8) × (2–)2.5(–3) μm Beta and gamma conidia not observed |
Host: on leaf spots of Eucalyptus sp. Country: Australia (Queensland) Ecological group: potential pathogen |
Crous et al . (2012) |
Diaporthe eucommiae (F.X. Chao & P.K. Chi) Y.H. Gao & L. Cai* ≡ Phomopsis eucommiae F.X. Chao & P.K. Chi SCHM 0020H |
Pycnidia triangular to oblate, dark brown, ostiolate, uniloculate, 60–110 μm diam |
Conidiophores hyaline, branched Conidiogenous cells hyaline, phialidic |
Alpha conidia fusiform to ellipsoid, hyaline, aseptate, mono- to biguttulate, 3.9–4.7 × 1–1.7 μm Beta conidia filiform, straight to curved, hyaline, aseptate,6.6–14.9 × 0.33–0.66 μm Gamma conidia not observed |
Host: on leaf spots of Eucommia ulmoides Country: China (Guangdong) Ecological group: potential pathogen |
Cao & Chi (1990); Gao et al . (2017) |
Diaporthe fujianensis Jayaward., Manawas., X.H. Li, J.Y. Yan & K.D. Hyde* JZB 320149T |
Pycnidia globose, black | Conidiogenous cells terminal, hyaline, smooth |
Alpha conidia oval or ellipsoidal, obtuse ends, hyaline, aseptate, 4–6 × 2–3 μm (x̄= 5 × 2.5 μm, n = 30) Beta andgamma conidia not observed |
Host: on dead shoots of Camellia sinensis Country: China (Fujian) Ecological group: saprophyte or potential pathogen |
Manawasinghe et al . (2021) |
Diaporthe fusiformis Jayaward., Manawas., X.H. Li, J.Y. Yan & K.D. Hyde* JZB 320154T |
Pycnidia globose, black |
Conidiophores reduced to conidiogenous cells Conidiogenous cells hyaline, smooth, clustered |
Alpha conidia fusiform, angular ends, hyaline, aseptate, eguttulate, 8–5 × 2–3 μm (x̄= 7 × 2 μm, n = 40) Beta conidia filiform, hamate, tapering towards ends, hyaline, aseptate, 23–32 × 1.2–1.6 μm (x̄= 27 × 1.5 μm, n = 40) Gamma conidia not observed |
Host: on dead leaves of Camellia sinensis Country: China (Fujian) Ecological group: saprophyte or potential pathogen |
Manawasinghe et al . (2021) |
Diaporthe globoostiolata Monkai & S. Lumyong* MFLUCC 23-0025T |
Pycnidia subconical to subglobose, dark brown to black, with black ostiolar necks, uniloculate, 90–120 × 110–180 μm |
Conidiophores reduced to conidiogeneous cells Conidiogenous cells subcylindrical to ampulliform, slightly tapering towards apex, hyaline, terminal, monophialidic, with periclinal thickening and a prominent collarette, 3.5–11.4 × 1.4–3.7 μm (x̄= 6.5 × 2.2 μm, n = 30) |
Alpha conidia fusiform to ellipsoid, obtuse ends, hyaline, aseptate, smooth, mono- to biguttulate, 6–9.6 × 1.8–2.8 μm (x̄= 7.6 × 2.2 μm, n = 30) Beta conidia filiform, tapering towards apex, straight to slightly curved, truncate base, hyaline, smooth, eguttulate, 13.2–22 × 1–1.8 μm (x̄= 16.8 × 1.4 μm, n = 30) Gamma conidia not observed |
Host: on dead leaves of a member of Fagaceae Country: Thailand Ecological group: saprophyte |
Monkai et al . (2023) |
Diaporthe hongkongensis R.R. Gomes, Glienke & Crous* (CBS 115448T) |
Pycnidia g lobose, with central ostiole, exuding a creamy conidial cirrhus, up to 200 μm diam |
Conidiophores r educed to conidiogeneous cells Paraphyses hyaline, up to 4-septate, frequently branched below, smooth, with a clavate terminal cell, up to 80 μm long and apex of 2–8 μ diam Conidiogenous cells ampulliform to subcylindrical, with prominent apical tapper, hyaline, smooth, with periclinal thickening and minute collarette (1 μm long), phialidic, 5–12 × 2–4 μm |
Alpha conidia fusiform, tapering towards ends, mostly straight, acutely rounded apex, truncate base, hyaline, aseptate, smooth, granular to guttulate, (5–)6–7(–8) × (2–)2.5(–3) μm Beta conidia spindle-shaped, mostly curved in upper part, acutely rounded apex, truncate base, widest in mid region, hyaline, smooth, 18–22 × 1.5–2 μm Gamma conidia ellipsoid-fusoid, subobtuse apex, truncate base, hyaline, aseptate, smooth, 10–13 × 2 μm |
Host: on fruit of Dichroa febrifuga Country: Hong Kong Ecological group: UN |
Gomes et al . (2013) |
Diaporthe lithocarpi (Y.H. Gao, W. Sun & L. Cai) Y.H. Gao & L. Cai ≡ Phomopsis lithocarpi Y.H. Gao, W. Sun & L. Cai CGMCC 3.15175T |
Pycnidia globose to subglobose, dark brown to black, exuding cream conidial droplets from ostioles, 120–270 μm diam | Conidiophores cylindrical, frequently curved, tapering towards apex, hyaline, septate, rough, 12–15.4 × 1.9–2.6 μm |
Alpha conidia fusiform, tapering towards ends, hyaline, aseptate, biguttulate, 5.7–8.1 × 2.1–3.2 μm (x̄= 7 × 2.6 μm, n = 30) Beta conidia filiform, curved or hamate, obtuse ends, hyaline, aseptate, eguttulate, 17.6–28.1 × 0.92–1.81 μm (x̄= 23.6 × 1.4 μm, n = 30) Gamma conidia not observed |
Host: on leaf spots of Lithocarpus glaber Country: China (Zhejiang) Ecological group: potential pathogen |
Gao et al . (2014); Tan & Shivas (2023) |
Diaporthe lagerstroemiae (C.Q. Chang, M.M. Xiang & P.K. Chi) Y.H. Gao & L. Cai* ≡ Phomopsis lagerstroemiae C.Q. Chang, M.M. Xiang & P.K. Chi SCHM 3608H |
Pycnidia mostly triangular or ampullate, rarely compressed-triangular, eustromatic, unilocular, olivaceous brown to dark brown, wall becoming darker and thicker towards ostiole, 110–150 × 65–125 μm |
Conidiophores filiform, hyaline, septate, simple or branched, 11–35 × 1.4–2.1 μm Conidiogenous cells hyaline, phialidic, enteroblastic |
Alpha conidia fusiform, acute ends, hyaline, aseptate, biguttulate, 6–8.1 × 1.5–1.9 μm Beta conidia filiform, curved or hamate, rarely abnormal, clavate, straight or somewhat curved, hyaline, aseptate, 12–15 × 0.9–1.2 μm Gamma conidia not observed |
Host: on branches of Lagerstroemia indica Country: China (Hunan) Ecological group: UN |
Chang et al . (2005a); Gao et al . (2017) |
Diaporthe rhodomyrti C.M. Tian & Qin Yang* CFCC 53101T |
Pycnidia globose or rostrate, black, often exuding translucent conidial droplets from ostioles, 500–850 μm diam |
Conidiophores reduced to conidiogenous cells Conidiogenous cells cylindrical, straight, tapering towards apex, hyaline, septate, unbranched, (14.5–)15.5–23(–25.5) × 1.5–2 μm (n = 30; L/W = 8.5–13) |
Alpha conidia ellipsoidal, hyaline, aseptate, biguttulate, 6–7(–8.5) × 2–2.5(–3) μm (n = 30; L/W = 2.8–3.3) Beta conidia filiform, straight to sinuous, hyaline, aseptate, eguttulate, (15–)16.5–21.5(–23) × 1–1.5 μm (n = 30; L/W = 15.5–16.5) Gamma conidia not observed |
Host: On leaves of Rhodomyrtus tomentosa Country: China (Jiangxi) Ecological group: potential pathogen |
Cao et al . (2022) |
Diaporthe theobromatis H. Dong, J.W. Xia & X.G. Zhang* SAUCC 102221T |
Pycnidia globose, dark brown to black, covered with short hyphae, exuding whitish translucent to yellowish conidial droplets from ostioles |
Conidiophores cylindrical, hyaline, septate, branched, 14–21 × 1–2 μm Conidiogenous cells cylindrical, straight, tapering towards apex, hyaline, terminal, phialidic, 4.5–12 × 1–2 μm |
Alpha conidia ellipsoid or falcate, acute ends, hyaline, aseptate, mono- to biguttulate, 5–12 × 1.5–2.5 μm Beta conidia filiform, hamate or curved, hyaline, smooth, 15–25 × 1–2 μm Gamma conidia not observed |
Host: on leaf spot of Theobroma cacao Country: China (Yunnan) Ecological group: potential pathogen |
Dong et al . (2020) |
Diaporthe aseana | |||||
Diaporthe aseana Dissan., Tangthir. & K.D. Hyde MFLUCC 12-0299aT |
Pycnidia globose, black, unilocular, ostiolate, 140–200 × 220–300 μm (x̄= 185 × 260 μm, n = 10) |
Conidiophores cylindrical, straight to sinuous, hyaline, smooth, densely aggregated, 8–15 × 2–3 μm Conidiogenous cells cylindrical, slightly tapering towards apex, terminal and lateral, phialidic, 6–10 × 2–3 μm |
Alpha conidia fusoid to ellipsoidal, subobtuse apex, tapering towards ends, straight, hyaline, aseptate, smooth, guttulate, 6–9 × 2–3 μm Beta and gamma conidia not observed |
Host: on an unknown dead leaf Country: Thailand Ecological group: saprophyte |
Hyde et al . (2016) |
Diaporthe tectonigena Doilom, Dissan. & K.D. Hyde* MFLUCC 12-0767T |
Pycnidia subglobose or variable, black, with an elongated black neck, multilocular, exuding hyaline to yellowish, reddish brown to umber, white to cream conidial droplets from central ostioles, (170–)270–310(–360) × (165–)280–295(–320) μm (x̄= 265 × 268 μm, n = 25) |
Conidiophores cylindrical, straight or slightly curved, rounded to obtuse apex, wider at base, hyaline, septate, branched or unbranched, smooth, in dense clusters, 9–32 × 1.8–3.7 μm Conidiogenous cells cylindrical, slightly tapering towards apex, terminal, phialidic, 2–5 × 1.3–3.9 μm |
Alpha conidia oblong to ellipsoid, bluntly rounded apex, obtuse to subtruncate base, hyaline, aseptate, smooth, multiguttulate, (5–)7.3–7.8(–8.3) × 2.5–3.5 μm (x̄= 7.2 × 2.9 μm, n = 30) Beta conidia filiform, curved or hamate, subtruncate base, hyaline, aseptate, (16–)29–30(–34) × 1.4–2 μm (x̄= 28 × 1.7 μm, n = 30) Gamma conidia ellipsoid-fusoid, acutely rounded apex, subtruncate base, hyaline, aseptate, smooth, multiguttulate, (9–)10–12(–14) × 1.7–3.2 μm (x̄= 11 × 2.3 μm, n = 30) |
Host: on a twig dieback of Tectona grandis Country: Thailand Ecological group: potential pathogen |
Doilom et al . (2016) |
Diaporthe xishuangbanica | |||||
Diaporthe xishuangbanica Y.H. Gao & L. Cai CGMCC 3.18283T |
Pycnidia globose, 180–310 μm diam | Conidiophores cylindrical, straight, sometimes sinuous or lateral, branched, phialidic, 13–34.5 × 1.5–3 μm (x̄= 20.9 × 2.1 μm, n = 40) |
Alpha conidia fusiform, hyaline, aseptate, multiguttulate, 7–9.5 × 2.5–3.5 μm (x̄= 8.3 × 2.8 μm, n = 30) Beta and gamma conidia not observed |
Host: on diseased leaves of Camellia sinensis Country: China (Yunnan) Ecological group: potential pathogen |
Gao et al . (2017) |
Diaporthe foeniculina clade | |||||
Diaporthe cytosporella | |||||
“Diaporthe chamaeropis ” (Cooke) R.R. Gomes, Glienke & Crous CBS 454.81 |
Pycnidia globose, black, exuding creamy conidial droplets from central ostioles, up to 400–600 μm diam |
Conidiophores cylindrical, straight to sinuous, hyaline, 1–5-septate, smooth, densely aggregated, branched, 10–50 × 2–2.5 μm Conidiogenous cells cylindrical, terminal and lateral, slightly tapering towards apex (1–1.5 μm diam), with visible periclinal thickening, phialidic, 10–20 × 1.5–2 μm |
Alpha conidia fusoid to ellipsoid, tapering towards ends, straight, subobtuse apex, subtruncate base, hyaline, aseptate, smooth, guttulate, (5–)6–8(–9) × 2(–2.5) μm Beta conidia spindle-shaped, curved, acutely rounded apex, truncate base, tapering from lower third towards apex, hyaline, aseptate, smooth, (20–)22–27(–30) × 1.5(–2) μm Gamma conidia not observed |
Host: on a dead part of leaf ofChamaerops humilis Country: Greece Ecological group: saprophyte |
Gomes et al . (2013) |
Diaporthe cytosporella (Penz. & Sacc.) Udayanga & Castl. ≡ Phoma cytosporella Penz. & Sacc. CBS 137020ET |
Pycnidia globose, with an elongated black neck, often exuding a yellowish conidial cirrus from ostiole, up to 450 μm diam, 65–100 μm high |
Conidiophores cylindrical, ampulliform, wider at base, hyaline, smooth, branched or unbranched, occurring in dense clusters, 7–18 × 1–2 μm Conidiogenous cells cylindrical, terminal, slightly tapering towards apex (0.5–1 μm), phialidic |
Alpha conidia ovate to ellipsoidal, subtruncate base, hyaline, aseptate, smooth, bi- to multiguttulate, (6.9–)8–9(–12.6) × (2.3–)2.6–3.2 μm (x̄= 8.8 × 3 μm, n = 30) Beta andgamma conidia not observed |
Host: on Citrus limon Country: Spain Ecological group: UN |
Udayanga et al . (2014b) |
Diaporthe pimpinellae Abeywickrama, Camporesi, Dissan. & K.D. Hyde* MFLU 19-0563H |
Pycnidia as black dots (on host), 150–250 μm diam × 150–200 μm high |
Conidiophores cylindrical, straight to sinuous, terminal, hyaline, aseptate, densely aggregated, slightly tapering towards apex Conidiogenous cells cylindrical, terminal and lateral, phialidic, 2–4 × 4–8 μm |
Alpha conidia fusiform or oval, hyaline, aseptate, single to biguttulate, 6–8 × 2–3 μm Beta andgamma conidia not observed |
Host: on aerial stems of Pimpinella peregrina Country: Thailand Ecological group: saprophyte |
Yuan et al . (2020) |
“Diaporthe cinerascens ” | |||||
“Diaporthe cinerascens ” Sacc. CBS 719.96 |
Pycnidia globose, black, exuding creamy-luteous conidial droplets from central ostioles, up to 300 μm diam |
Conidiophores cylindrical, straight to sinuous, hyaline, 1–3-septate, smooth, densely aggregated, branched, 17–30 × 2–3 μm Conidiogenous cells cylindrical, terminal and lateral, slightly tapering towards apex (1.5–2 μm diam), collarette mostly absent and slightly flared when present, with visible periclinal thickening, phialidic, 8–18 × 2–3 μm |
Alpha conidia fusoid to ellipsoid, tapering towards ends, subobtuse apex, subtruncate base, hyaline, aseptate, smooth, guttulate, 7–8(–9) × (2.5–)3 μm Gamma conidia ellipsoid to fusoid, acutely rounded apex, subtruncate base, hyaline, aseptate, smooth, 8–12 × 3 μm Beta conidia not observed |
Host: on branch of Ficus carica Country: Bulgaria Ecological group: UN |
Gomes et al . (2013) |
Diaporthe diospyricola | |||||
Diaporthe diospyricola Crous CBS 136552T |
Pycnidia globose, black, exuding creamy conidial droplets from central ostioles, up to 400 μm diam |
Conidiophores c ylindrical, straight to sinuous, hyaline, 2–4-septate, smooth, densely aggregated, branched, 20–50 × 2.5–4 μm Conidiogenous cells cylindrical, terminal and lateral, slightly tapering towards apex (1–1.5 μm diam), with visible periclinal thickening, phialidic, 7–15 × 1.5–2.5 μm |
Alpha conidia fusoid to ellipsoid, tapering towards ends, straight, subobtuse apex, subtruncate base, hyaline, aseptate, smooth, guttulate, (5.5–)6–7(–7.5) × (2–)2.5(–3) μm Beta conidia spindle-shaped, curved, acutely rounded apex, truncate base, tapering from lower third towards apex, hyaline, aseptate, smooth, (18–)25–27(–30) × 1.5(–2) μm Gamma conidia not observed |
Host: on leaves of Diospyros whyteana Country: South Africa Ecological group: UN |
Crous et al . (2013) |
Diaporthe foeniculina | |||||
Diaporthe foeniculina (Sacc.) Udayanga & Castl. ≡ Phoma foeniculina Sacc. CBS 111553ET |
Pycnidia globose to subglobose, with an elongated, black neck, often exuding a yellowish drop- like conidial cirrus from ostiole, 400–700 μm diam × (300–)500–800(–930) μm high |
Conidiophores cylindrical, straight to sinuous, hyaline, smooth, unbranched, 9–15(–18) × 1–2 μm Conidiogenous cells cylindrical, terminal, slightly tapering towards apex (0.5–1 μm diam) |
Alpha conidia ellipsoidal or fusiform, rarely with subtruncate base, hyaline, aseptate, smooth, eguttulate, bi- or multiguttulate, (7.5–)8.5–9(–9.2) × (2–)2.3–2.5(–2.7) μm (x̄= 8.8 × 2.4 μm, n = 30) Beta conidia hamate or slightly curved, acute apex, subtruncate base, hyaline, aseptate, eguttulate, (20–)22–28(–29) × (1.1–)1.4–1.6(–2) μm (x̄= 25.1 × 1.5 μm, n = 30) Gamma conidia not observed |
Host: on dead stems of Foeniculum vulgare Country: Portugal Ecological group: saprophyte |
Udayanga et al . (2014b) |
Diaporthe baccae L. Lombard, G. Polizzi & Crous CBS 136972T |
Pycnidia globose to conical, brown to black, eustromatic, multilocular, occasionally with ostiolate necks, surface covered with hyphae, exuding cream to pale conidial droplets from central ostioles, up to 650 μm diam |
Conidiophores cylindrical, straight to sinuous, hyaline, 1–3-septate, smooth, densely aggregated, branched, 20–57 × 2–3 μm Conidiogenous cells cylindrical, terminal and lateral, slightly tapering towards apex, with visible periclinal thickening, phialidic, 9–23 × 1–2 μm |
Alpha conidia fusoid to ellipsoid, tapering towards ends, straight, subobtuse apex, subtruncate base, hyaline, aseptate, smooth, guttulate, (6–)7–9 × 2–3 μm (x̄= 8 × 2 μm) Beta conidia spindle-shaped, acutely rounded apex, truncate base, tapering from lower third towards apex, hyaline, aseptate, smooth, (17–)20–24(–26) × 1–2 μm (x̄= 22 × 2 μm) Gamma conidia not observed |
Host: on Vaccinium corymbosum Country: Italy Ecological group: UN |
Lombard et al . (2014) |
Diaporthe neotheicola A.J.L. Phillips & J.M. Santos CBS 123208T |
Pycnidia of variable morphology and dimensions, globose to subglobose, cone-shaped, naked or covered with dense layer of hyphae, exuding translucent yellow conidial droplets, 420–730 μm diam × 280–1130 μm high |
Conidiophores cylindrical, hyaline, smooth, unbranched, single- to multi-septate, intermingled with long, septate and highly branched paraphyses, 6.7–23.5 × 1.6–3.1 μm Conidiogenous cells cylindrical to filiform, tapering towards apex, with periclinal thickening, phialidic, of two types, terminal (10.6–19.1 × 1.4–2.4 μm) and lateral (branched-like aspect of conidiophore) (2.6–9.8 × 1–1.6 μm) |
Alpha conidia fusoid, obtuse ends, hyaline, aseptate, mostly biguttulate, with basal conidiogenous scar, (6.6–)7.6–8(–9.5) × (1.9–)2.2–2.3(–2.6) μm (x̄= 7.8 × 2.2 μm, n = 50) Beta conidia filiform, curved, with rounded ends, hyaline, aseptate, eguttulate, (21.5–)25.7–26.7(–30.3) × (0.8–)1(–1.1) μm (x̄= 26.2 × 1 μm, n = 50) Gamma conidia not observed |
Host: on Foeniculum vulgare Country: Portugal Ecological group: UN |
Santos & Phillips (2009) |
Diaporthe ravennica Thambug., Camporesi & K.D. Hyde MFLU 16–0665H |
Stromata multiloculate, with subglobose or irregular locules of 140–275 μm diam × 65–175 μm high (x̄= 190 × 108 μm, n = 5), ostiolate or inostiolate, up to 500 μm diam |
Conidiophores cylindrical, straight to sinuous, hyaline, smooth, unbranched, 12–23 × 1.2–1.8 μm (x̄= 16.4 × 1.5 μm, n = 40) Conidiogenous cells cylindrical, terminal, slightly tapering towards apex, phialidic |
Alpha conidia ellipsoidal or fusiform, hyaline, aseptate, smooth, eguttulate, bi- or multiguttulate, (6.4–)7.2–10.5 × 1.7–2.8 μm (x̄= 8.6 × 2.3 μm, n = 40) Beta conidia filiform, slightly curved, acute apex, subtruncate base, hyaline, aseptate, eguttulate, 21–32(–38) × (1–)1.2–1.7 μm (x̄= 26.4 × 1.3 μm, n = 30) Gamma conidia not observed |
Host: on dead branches of Tamarix sp. Country: Italy Ecological group: saprophyte |
Thambugala et al . (2016) |
Diaporthe rhoicola Crous CBS 129528T |
Pycnidia flattened, multilocular, up to 600 μm diam |
Conidiophores subcylindrical, hyaline, 1–3-septate, smooth, unbranched or branched (below or above), 20–40 × 2–3 μm Conidiogenous cells subcylindrical, terminal, tapering towards a truncate apex (1–1.5 μm), with a flaring collarette (up to 5 μm wide and long), smooth, 15–25 × 2–3 μm Paraphyses intermingled among conidiophores, subcylindrical, hyaline, smooth, branched or unbranched, up to 80 μm long, 2–3 μm wide |
Alpha conidia subcylindrical to fusoid-ellipsoidal, obtuse apex, widest in middle, tapering to a truncate base (1 μm diam), hyaline, aseptate, smooth, guttulate, (7–)8–9(–10) × 3(–3.5) μm Beta and gamma conidia not observed | Host: on leaf spots of Rhus pendulina Country: South Africa Ecological group: potential pathogen |
Crous et al . (2011a) |
Diaporthe nigra Brahmanage & K.D. Hyde* JZBH 320170H |
Pycnidia globose or irregular, multiloculate, black |
Conidiophores reduced to conidiogeneous cells or rarely short, compressed cylindrical, straight to sinuous, hyaline, smooth, branched, densely aggregated, 8–25 × 1–3 μm (x̄= 20 × 1.5 μm) Conidiogenous cells subcylindrical to ampulliform, phialidic, with flared collarette and visible periclinal thickening, 190–295 × 120–175 μm (x̄= 270 × 160 μm) |
Alpha conidia ovate to ellipsoidal, obtuse to subtruncate base, straight, hyaline, aseptate, smooth, biguttulate, 17–28 × 7–7.5 μm (x̄= 25 × 7.2 μm) Beta andgamma conidia not observed |
Host: on dead aerial stem of Ballota nigra Country: Italy Ecological group: saprophyte |
Hyde et al . (2020a) |
Diaporthe rumicicola Manawasinghe, Camporesi & K.D. Hyde* MFLU 18-0739H |
Pycnidia ampulliform, ostiolate, with elongate black neck, 98–280 μm (x̄= 208 μm, n = 10) diam (on host) |
Conidiophores reduced to conidiogeneous cells on host, with paraphyses observed on culture Conidiogenous cells integrated, clustered, hyaline, smooth, enteroblastic with percurrent annelations |
Alpha conidia hyaline, smooth, mono- or bi- guttulate, 3–5 × 2–3 μm (x̄= 3.5 × 2.5 μm, n = 30) Beta and gamma conidia not observed |
Host: on dead aerial stem of Rumex sp. Country: Italy Ecological group: saprophyte |
Hyde et al . (2019) |
Diaporthe zaobaisu Y.S. Guo & G.P. Wang* CGMCC 3.19598T |
Pycnidia globose or irregular, dark brown to black, 235–445 μm diam |
Conidiophores cylindrical, straight, hyaline, 1-septate, densely aggregated, 6–13 × 2.5–4 μm Conidiogenous cells ampulliform, tapering towards apex, hyaline, terminal, phialidic, 8.5–12 × 2.5–3 μm |
Alpha conidia fusiform, hyaline, aseptate, biguttulate, 5.5–8.5 × 2–3 μm (x̄= 6.4 × 2.3 μm, n = 50; L/W = 2.8) Beta conidia filiform, curved, tapering towards ends, hyaline, aseptate, 21.5–28 × 1–1.4 μm (x̄= 24.5 × 1.1 μm, n = 41; L/W = 22.3) Gamma conidia not observed |
Host: on branches with shoot cankers symptoms of Pyrus bretschneideri Country: China (Yunnan) Ecological group: pathogen |
Guo et al . (2020) |
Diaporthe forlicesenica | |||||
Diaporthe forlicesenica Bundhun, Camporesi & K.D. Hyde ≡ Diaporthe dorycnii Dissan., Camporesi & K.D. Hyde MFLUCC 17-1015T |
Pycnidia globose, brown to black, up to 420 μm diam × 380 μm high |
Conidiophores cylindrical, slightly tapering towards apex, straight to sinuous, hyaline, terminal, densely aggregated, 21–35 × 1.5–2.5 μm Conidiogenous cells subcylindrical, filiform, straight, tapering towards apex, 13–19 × 2–3 μm |
Alpha conidia fusiform or oval, obtuse ends, hyaline, biguttulate, 9–13.5 × 3–4 μm (x̄= 11 × 4 μm) Beta andgamma conidia not observed |
Host: on dead aerial stem of Dorycnium hirsutum Country: Italy Ecological group: saprophyte |
Bundhun et al . (2021); Dissanayake et al . (2017) |
Diaporthe glabrae clade | |||||
Diaporthe glabrae | |||||
Diaporthe alangii C.M. Tian & Qin Yang* CFCC 52556T |
Pycnidia discoid (ectostromatic disc), uniloculate and undivided, black, with one ostiole, 135–330 μm diam | Conidiophores cylindrical, straight, hyaline, unbranched, phialidic, 6–12 × 1.4–2 μm |
Alpha conidia ellipsoidal, mostly with one end obtuse and the other acute, hyaline, aseptate, occasionally submedian constriction, biguttulate, 6.5–8 × 2 μm (x̄= 7 × 2 μm, n = 30) Beta andgamma conidia not observed |
Host: on symptomatic branches of Alangium kurzii Country: China (Zhejiang) Ecological group: potential pathogen |
Yang et al . (2018) |
Diaporthe conferta H. Dong, J.W. Xia & X.G. Zhang* SAUCC 194.9T |
Pycnidia subglobose or irregular, black, covered with short hyphae, exuding yellowish translucent conidial droplets from ostioles |
Conidiophores cylindrical, straight to slightly curved, tapering towards apex, wider at base, hyaline, septate, branched or unbranched, smooth, in dense clusters, 5–25 × 2–3 μm Conidiogenous cells cylindrical, straight, tapering towards apex, terminal, phialidic, 5–15 × 2–3 μm |
Alpha conidia ellipsoidal or oval, bluntly rounded apex, obtuse base, hyaline, aseptate, smooth, biguttulate, 5–7 × 2–3 μm Beta andgamma conidia not observed |
Host: on leaf spots of Elaeagnus conferta Country: China (Yunnan) Ecological group: potential pathogen |
Dong et al . (2021) |
Diaporthe glabrae (C.Q. Chang, Z.D. Jiang & P.K. Chi) Y.H. Gao & L. Cai ≡ Phomopsis glabrae C.Q. Chang, Z.D. Jiang & P.K. Chi SCHM 3622H |
Pycnidia globose or triangular, eustromatic, unilocular, olivaceous to brown, 75–140 × 53–95 μm |
Conidiophores hyaline, septate, simple or branched, 7.5–20 × 1.6–2.5 μm Conidiogenous cells hyaline, phialidic, enteroblastic |
Alpha conidia oblong-ellipsoidal, obtuse ends, hyaline, aseptate, biguttulate, 5–7.4 × 1.6–2.1 μm Beta conidia filiform, mostly hamate, hyaline, aseptate, 13.5–22.5 × 0.6–1 μm Gamma conidia not observed |
Host: on branches of Bougainvillea glabra Country: China (Fujian) Ecological group: UN |
Chang et al . (2005b); Gao et al . (2017) |
Diaporthe hubeiensis Dissanayake, X.H. Li & K.D. Hyde* JZB 320123T |
Pycnidia subglobose, ostiolate, with up to 100 μm black cylindrical necks, up to 510 μm diam | Conidiophores reduced to conidiogeneous cells |
Alpha conidia ellipsoidal to cylindrical, blunt ends, hyaline, aseptate, smooth, biguttulate, 5.6–7.1 × 1–3.1 μm (x̄= 6.1 × 1.8 μm, n = 40) Beta conidia filiform, tapering towards ends, 17–27 × 1–1.5 μm (x̄= 24 × 1.5 μm, n = 40) Gamma conidia not observed |
Host: on diseased trunk of Vitis vinifera Country: China (Hubei) Ecological group: pathogen |
Manawasinghe et al . (2019) |
Diaporthe morindae M. Luo, W. Guo, M. P. Zhao, Manawas., K. D. Hyde & C. P. You* ZHKUCC 22-0072T |
Pycnidia oblate, subglobose, flask or irregularly shaped, uni or multilocular, 50–380 × 30–160 μm (x̄= 170 × 90 μm) | Conidiogenous cells hyaline, phialidic |
Alpha conidia ellipsoidal or torque circular, blunt ends, hyaline, aseptate, mono- or biguttulate, 6–7 × 2–4 μm (x̄= 6 × 3 μm) Beta andgamma conidia not observed |
Host: on healthy stems and roots of Morinda officinalis Country: China (Guangdong) Ecological group: endophyte |
Luo et al . (2022) |
Diaporthe tectonae Doilom, A.J. Dissanayake & K.D. Hyde* MFLUCC 12-0777T |
Pycnidia subglobose or irregular, black, with an elongated black neck, exuding hyaline to yellowish, white to cream conidial droplets from central ostioles, (460–)725–820(–1385) × (500–)900–1035(–2075) μm (x̄ = 773 × 918 μm, n = 25) |
Conidiophores cylindrical, straight or slightly curved, tapering towards apex, wider at base, hyaline, septate, branched or unbranched, smooth, in dense clusters, 11–18 × 1–2 μm Conidiogenous cells cylindrical, slightly tapering towards apex (0.5–1 μm), terminal, phialidic, 1.5–5.2 × 0.9–1.7 μm |
Alpha conidia oblong to ellipsoidal, bluntly rounded apex, obtuse to subtruncate base, hyaline, aseptate, smooth, mono- to mostly biguttulate, (4–)5.5–6(–6.8) × 2–2.9 μm (x̄= 5.5 × 2.6 μm, n = 30) Beta conidia rare, cylindrical, flexuous, hamate, rounded apex, subtruncate base, hyaline, aseptate, smooth, 10–13.5 × 1.3–1.7 μm (x̄= 12 × 1.5 μm, n = 10) Gamma conidia ellipsoid-fusoid, acutely rounded apex, subtruncate base, hyaline, aseptate, smooth, (7–)8–9(–10.6) × 1.3–2.1 μm (x̄= 8.5 × 1.8 μm, n = 30) |
Host: on dieback lesions of twigs of Tectona grandis Country: Thailand Ecological group: potential pathogen |
Doilom et al . (2016) |
Diaporthe xishuangbannaensis Hongsanan & K.D. Hyde* ≡ Diaporthe chinensis H. Dong, J.W. Xia & X.G. Zhang SAUCC 194.30T |
Pycnidia subglobose or irregular, black, covered with short hyphae, exuding whitish translucent to yellowish conidial droplets from ostioles |
Conidiophores cylindrical, straight to slightly curved, tapering towards apex, wider at base, hyaline, septate, branched or unbranched, smooth, in dense clusters, 4–20 × 1–3 μm Conidiogenous cells cylindrical, straight, tapering towards apex, terminal, phialidic, 5–7 × 2–3.5 μm |
Alpha conidia ellipsoidal or oval, bluntly rounded apex, obtuse base, hyaline, aseptate, smooth, biguttulate, 5–7 × 2–3.5 μm Beta conidia rare, filiform, hamate or curved, hyaline, smooth, 17–25 × 1–1.5 μm Gamma conidia rare, obovate to clavate, hyaline, 2–4-guttulate 7–10 × 1.5–2 μm |
Host: on leaf spots of Litchi chinensis Country: China (Yunnan) Ecological group: potential pathogen |
Dong et al . (2021); Hongsanan et al . (2023) |
Diaporthe celtidis | |||||
Diaporthe celtidis Tennakoon, C.H. Kuo & K.D. Hyde MFLUCC 20-0180T |
Pycnidia globose to subglobose, dark brown to black, thin-walled, ostiolate, exuding light brown to pale yellow conidial droplets from ostioles, up to 500 μm diam |
Conidiophores sometimes reduced to conidiogenous cells, hyaline, 1-septate Conidiogenous cells subcylindrical, tapering towards apex, determinate, unbranched, smooth, phialidic, enteroblastic, 6–10 × 1.2–2.6 μm (x̄= 7.5 × 1.7 μm, n = 20) |
Alpha conidia oval to cylindrical, straight to slightly curved, rounded apex, hyaline, aseptate, smooth, biguttulate, 5–6 × 2–3 μm (x̄= 5.3 × 2.5 μm, n = 40) Beta andgamma conidia not observed |
Host: on dead leaves of Celtis formosana Country: Taiwan Ecological group: saprophyte |
Tennakoon et al . (2021) |
Diaporthe tulliensis | |||||
Diaporthe tulliensis R.G. Shivas, Vawdrey & Y.P. Tan BRIP 62248aT |
Pycnidia subglobose, ostiolate, beaks absent or up to 1 mm long, exuding cream to pale yellow conidial droplets from ostioles, up to 500 μm diam |
Conidiophores reduced to conidiogeneous cells Conidiogenous cells cylindrical, tapering towards apex, hyaline, 15–20 × 1.5–2.5 μm |
Alpha conidia oval to cylindrical, rounded apex, obconically truncate base, hyaline, aseptate, (4.5–)5–7 × 2–2.5(–3) μm Beta conidia scarce, flexuous, hamate, hyaline, aseptate, 25–30 × 1(–1.5) μm Gamma conidia not observed |
Host: on rotted stem end of fruit of Theobroma cacao Country: Australia (Queensland) Ecological group: UN |
Crous et al . (2015) |
Diaporthe inconspicua clade | |||||
Diaporthe inconspicua | |||||
Diaporthe inconspicua R.R. Gomes, Glienke & Crous* URM 7775 |
Pycnidia globose, dark brown to black, ostiolate, exuding yellowish conidial droplets from ostioles, 424–954 × 371–742 μm |
Conidiophores cylindrical, straight to sinuous, hyaline, 0–2-septate, sometimes branched, in dense clusters, 11–21.5 × 2–2.5 μm Conidiogenous cells cylindrical, terminal, phialidic, (2–)5.5–8.5(–14.5) × (1.5–)2–2.5 μm |
Alpha conidia ellipsoidal to fusoid, acute ends, hyaline, aseptate, smooth, eguttulate, 5.5–6.5 × 1.5–2 μm Beta conidia filiform, straight to curved, tapering towards apex, truncate base, hyaline, aseptate, eguttulate, (17.5–)20–26(–28) × 1–1.5 μm Gamma conidia not observed |
Host: on Poincianella pyramidalis Country: Brazil Ecological group: endophyte |
Gomes et al . (2013); Bezerra et al . (2018) |
Diaporthe lutescens S.T. Huang, J.W. Xia, X.G. Zhang & Z. Li* SAUCC 194.36T |
Pycnidia subglobose, black, exuding white creamy conidial droplets from central ostioles |
Conidiophores subcylindrical, straight or slightly curved, obtuse apex, wider at base, hyaline, septate, unbranched, smooth, 10.2–17 × 1.8–3 μm Conidiogenous cells cylindrical, straight to sinuous, tapering towards apex, terminal, phialidic, 5.7–9.1 × 1.4–2.6 μm |
Beta conidia filiform, straight or slightly curved, subtruncate base, enlarged towards apex, hyaline, aseptate, 20.8–28.8 × 1.2–2 μm (x̄= 25.3 × 1.4 μm, n = 20) Alpha andgamma conidia not observed |
Host: on leaf spots of Chrysalidocarpus lutescens Country: China (Yunnan) Ecological group: potential pathogen |
Sun et al . (2021) |
Diaporthe pseudoinconspicua T.G.L. Oliveira, J.D.P. Bezerra, A.R. Machado, Souza-Motta & O.M.C. Magalh.* URM 7874T |
Pycnidia globose to subglobose, dark brown to black, exuding yellowish conidial droplets from ostioles, 200–320 × 160–190 μm |
Alpha conidiophores straight to sinuous, hyaline, branched, aggregated, 14.5–21.5(–23.5) × 2.5–3 μm Beta conidiophores straight to sinuous, hyaline, septate, branched, smooth, aggregated, 10.5–16(–18) × 2–2.5(–3) μm Conidiogenous cells straight to sinuous, bifurcate, hyaline, phialidic, (9–)10.5–13.5 × 2–2.5(–3) μm |
Alpha conidia fusoid, one end rounded and the other acute, hyaline, aseptate, bi- to multiguttulate, 5–7.5(–8.5) × 2–2.5(–3.5) μm Beta conidia filiform, straight to curved, one end obtuse and the other truncate, hyaline, aseptate, 18–21(–25.5) × 1–1.5(–2) μm Gamma conidia not observed |
Host: on branches of Poincianella pyramidalis Country: Brazil Ecological group: endophyte |
Crous et al . (2018) |
“Diaporthe pterocarpi ” (S. Hughes) Udayanga, Xing Z. Liu & K.D. Hyde MFLUCC 10-0572ET |
Pycnidia globose, 100–120 μm diam, later conical, with a slightly elongated black neck, exuding dirty white, spiral conidial cirri from ostioles, up to 100 μm diam, 65–100 μm high |
Conidiophores ampulliform, straight to sinuous, hyaline, unbranched, smooth, 10–15 × 1–2 μm Conidiogenous cells cylindrical, slightly tapering towards apex (0.5–1 μm), terminal, phialidic |
Alpha conidia fusiform, subtruncate base, hyaline, aseptate, biguttulate, rarely 3-guttulate, smooth, (5–)6–7(–9) × (2–)2.5(–3) μm Beta andgamma conidia not observed |
Host: on leaf spot of Pterocarpus indicus Country: Thailand Ecological group: potential pathogen |
Udayanga et al . (2012b) |
Diaporthe samaneae Monkai & S. Lumyong* SDBR-CMU470T |
Pycnidia subglobose to ovoid, elongate, dark brown to brown, ostiolate, multiloculate, 300–480 × 290–740 μm |
Conidiophores subcylindrical, straight to sinuous, hyaline to pale brown, septate, branched, smooth, tightly aggregated, 7.5–31.7 × 1.5–2.7 μm (x̄= 19 × 2 μm, n = 30) Conidiogenous cells subcylindrical to ampulliform, tapering towards apex, hyaline, terminal, with periclinal thickening and a prominent collarette, 5.2–14.3 × 1.5–2.7 μm (x̄= 9.7 × 2 μm, n = 30) |
Alpha conidia ellipsoid to elongate fusiform, obtuse apex, subtruncate base, hyaline, aseptate, smooth, eguttulate, forming basipetal chains of two or more conidia on phialidic neck, 7–11 × 1.8–2.8 μm (x̄= 8.4 × 2.4 μm, n = 30) Beta andgamma conidia not observed |
Host: on dead wood of Samanea saman Country: Thailand Ecological group: saprophyte |
Monkai et al . (2023) |
Diaporthe inconspicua R.R. Gomes, Glienke & Crous* URM 7775 |
Pycnidia globose, dark brown to black, ostiolate, exuding yellowish conidial droplets from ostioles, 424–954 × 371–742 μm |
Conidiophores cylindrical, straight to sinuous, hyaline, 0–2-septate, sometimes branched, in dense clusters, 11–21.5 × 2–2.5 μm Conidiogenous cells cylindrical, terminal, phialidic, (2–)5.5–8.5(–14.5) × (1.5–)2–2.5 μm |
Alpha conidia ellipsoidal to fusoid, acute ends, hyaline, aseptate, smooth, eguttulate, 5.5–6.5 × 1.5–2 μm Beta conidia filiform, straight to curved, tapering towards apex, truncate base, hyaline, aseptate, eguttulate, (17.5–)20–26(–28) × 1–1.5 μm Gamma conidia not observed |
Host: on Poincianella pyramidalis Country: Brazil Ecological group: endophyte |
Gomes et al . (2013); Bezerra et al . (2018) |
Diaporthe isoberliniae | |||||
Diaporthe isoberliniae Crous CBS 137981T |
Pycnidia g lobose, black, exuding creamy conidial droplets from central ostioles, up to 300 μm diam |
Conidiophores c ylindrical, straight to sinuous, hyaline, 2–3-septate, branched, smooth, densely aggregated, 15–40 × 3–4 μm Conidiogenous cells cylindrical, slightly tapering towards apex (1 μm diam), terminal and lateral, with periclinal thickening and flared collarette (up to 4 μm long), phialidic, 10–14 × 2.5–3 μm |
Alpha conidia fusoid-ellipsoid, tapering towards ends, subobtuse apex, subtruncate base, hyaline, aseptate, smooth, guttulate, (6.5–)8–9(–10) × (2.5–)3(–3.5) μm Beta and gamma conidia not observed |
Host: on Isoberlinia angolensis Country: Zambia Ecological group: UN |
Crous et al . (2014b) |
Diaporthe isoberliniae Crous STMA 18245, STMA 18291 |
Pycnidia g lobose or irregular, dark brown to black, exuding white to cream or yellow conidial droplets from ostioles, 200–460 μm diam | Conidiophores cylindrical to subcylindrical, subhyaline base to pale olivaceous, hyaline apex, 1–3-septate, smooth, densely aggregated, 13–42 × 1.5–4 μm Conidiogenous cells cylindrical to subcylindrical, tapering towards apex, terminal or lateral, hyaline, phialidic, (5.5–)6.5–14 × 1.5–3 μm |
Alpha conidia ellipsoid to obovoid, or fusoid-ellipsoid, rounded or subobtuse apex, acutate or subtruncate base, hyaline, aseptate, bi- to multiguttulate, 5.5–9(–10) × 2–3(–3.5) μm Beta conidia less frequent, filiform, curved, tapering towards apex, hyaline, aseptate, eguttulate, 11.5–27.5 × 1–2 μm Gamma conidia less frequent, broadly fusiform, straight to slightly curved, rarely sinuose, acutate or filiform apex, filiform base, hyaline, aseptate, multiguttulate, 10–18.5(–21) × 1.5–2.5 μm |
Host: on Pittosporum manii Country: Cameroon Ecological group: endophyte |
Lambert et al . (2023) |
Diaporthe pungensis S.T. Huang, J.W. Xia, X.G. Zhang & Z. Li* SAUCC 194.112T |
Pycnidia globose or subglobose, dark brown to black, thin-walled, exuding white creamy conidial droplets from ostioles |
Conidiophores cylindrical, straight to sinuous, hyaline, aseptate, unbranched, smooth, 11–14.5 × 1.5–2.3 μm Conidiogenous cells cylindrical, terminal, phialidic, 8–9.5 × 1–2.5 μm |
Alpha conidia ellipsoidal to fusoid, subobtuse apex, subtruncate base, hyaline, aseptate, smooth, 2–3-guttulate, 6–8.5 × 2–3.3 μm (x̄= 6.6 × 2.5 μm, n = 20) Beta conidia filiform, slightly curved, tapering towards apex, truncate base, hyaline, aseptate, eguttulate, 24–28.9 × 1–2 μm (x̄= 26.9 × 1.4 μm, n = 20) Gamma conidia not observed |
Host: on leaf spots of Elaeagnus pungens Country: China (Yunnan) Ecological group: potential pathogen |
Sun et al . (2021) |
Diaporthe leucospermi clade | |||||
Diaporthe acaciarum | |||||
Diaporthe acaciarum Crous & M.J. Wingf. CBS 138862T |
Pycnidia globose, black, exuding creamy conidial droplets from central ostioles, up to 300 μm diam |
Conidiophores cylindrical, straight to sinuous, hyaline, 2–3-septate, branched, smooth, densely aggregated, 20–30 × 2.5–4 μm Conidiogenous cells cylindrical, with a slight apical taper (1–1.5 μm diam), terminal and intercalary, with periclinal thickening and collarette (up to 2 μm long), phialidic, 15–25 × 2–3 μm |
Alpha conidia fusoid-ellipsoid, tapering towards ends, straight, subobtuse apex, subtruncate base, hyaline, aseptate, smooth, biguttulate, (6–)6.5–7(–7.5) × (2–)2.5(–3) μm Beta conidia spindle-shaped, acutely rounded apex, truncate base, tapering from lower third towards base, hyaline, aseptate, smooth, (20–)25–35(–40) × 1.5(–2) μm Gamma conidia not observed |
Host: on thorns of Acacia tortilis Country: Tanzania Ecological group: UN |
Crous et al . (2014a) |
Diaporthe beilharziae | |||||
Diaporthe beilharziae R.G. Shivas, Jacq. Edwards & Y.P. Tan BRIP 54792IT |
Pycnidia subglobose, beaks absent or less than 300 μm, exuding pale yellow to salmon conidial droplets from ostioles, up to 250 μm diam |
Conidiophores reduced to conidiogenous cells or ampulliform to cylindrical, hyaline to pale yellowish brown, 1-septate, 5–15 × 1.5–3.5 μm Conidiogenous cells cylindrical, flexuous, tapering towards apex, hyaline, 5–20 × 1.5–3 μm |
Alpha conidia oval to cylindrical, rounded apex, obconically truncate base, hyaline, aseptate, mostly biguttulate, (5.5–)6.5–9(–10) × 2–2.5(–3) μm Beta conidia scarce, flexuous, hyaline, 15–25 × 1–1.5 μm Gamma conidia not observed |
Host: on leaf spot of Indigofera australis Country: Australia (New South Wales) Ecological group: potential pathogen |
Tan et al . (2013) |
Diaporthe leucospermi | |||||
Diaporthe leucospermi Crous & Summerell CBS 111980T |
Pycnidia dark brown, exuding a creamy conidial cirrus from central ostiole, up to 300 μm diam |
Conidiophores reduced to conidiogeneous cells or subcylindrical, hyaline, pale brown at base, 1–3-septate, smooth, 15–30 × 2–3 μm Conidiogenous cells subcylindrical, with an apical taper, terminal or lateral, with periclinal thickening and flaring collarette (1 μm long), phialidic, 10–15 × 2–3 μm |
Alpha conidia ellipsoid, tapering to acutely rounded apex and obtuse to truncate base, hyaline, aseptate, smooth, biguttulate, flattened hilum (1 μm diam), (6–)7(–8) × (2.5–)3 μm
Beta conidia spindle-shaped, prominently hooked in apical part, acute apex, truncate base, hyaline, aseptate, smooth, (20–)25–30(–35) × (1–)1.5 μm Gamma conidia not observed |
Host: on leaves of Leucospermum sp. Country: Australia (New South Wales) Ecological group: UN |
Crous et al . (2011b) |
Diaporthe pyracanthae L. Santos & A. Alves CBS 142384T |
Pycnidia dark brown, exuding a creamy to white conidial cirrus from central ostiole |
Conidiophores reduced to conidiogeneous cells or subcylindrical, hyaline, smooth Conidiogenous cells subcylindrical, with an apical taper, hyaline, smooth, phialidic |
Alpha conidia fusiform to ellipsoid, rounded apex, obtuse to truncate base, hyaline, aseptate, smooth, frequently biguttulate, 6.7–6.8 × 2.2–2.4 μm (interpreted from means, n = 100) Beta conidia filiform, frequently hooked in apical part, acute apex, truncate base, hyaline, aseptate, smooth, 26.8–30 × 1.3 μm (interpreted from means, n = 100) Gamma conidia infrequent, fusoid, acutely rounded apex, subtruncate base hyaline, aseptate, smooth |
Host: on branch canker of Pyracantha coccinea Country: Portugal Ecological group: pathogen |
Santos et al . (2017b) |
Diaporthe rossmaniae S. Hilário, I. Amaral, L. Santos & A. Alves MUM 19.30T |
Pycnidia brown to black, exuding a creamy white to yellow conidial cirrus |
Conidiophores reduced to conidiogeneous cells Conidiogenous cells subcylindrical, hyaline to gold, smooth, x̄= 7.4 × 1.9 μm (n = 30) |
Alpha conidia ellipsoid, rounded apex, obtuse to truncate base, hyaline, aseptate, smooth, mono to biguttulate, x̄= 6.8 × 2.5 μm (n = 100) Beta conidia filiform, frequently hooked in apical part, acute apex, truncate base, hyaline, aseptate, smooth, x̄= 25.7 × 1.2 μm (n = 100) Gamma conidia not observed |
Host: on twig lesions of Vaccinium corymbosum Country: Portugal Ecological group: pathogen |
Hilário et al . (2020) |
Diaporthe micheliae | |||||
Diaporthe chimonanthi (C.Q. Chang, M.M. Xiang & P.K. Chi) Y.H. Gao & L. Cai* ≡ Phomopsis chimonanthi C.Q. Chang, M.M. Xiang & P.K. Chi SCHM 3614H |
Pycnidia triangular or tuberous, eustromatic, unilocular, 150–238 × 130–230 μm |
Conidiophores slim, hyaline, septate, branched, 13–25 × 1.6–2.5 μm Conidiogenous cells hyaline, phialidic, enteroblastic |
Alpha conidia fusiform, somewhat obtuse base, hyaline, aseptate, biguttulate, 6.6–8.8 × 1.8–2.2 μm Beta conidia mostly filiform, curved or hamate, rarely abnormal, clavate, straight or somewhat curved, hyaline, aseptate, 15–18 × 1–1.5 μm Gamma conidia not observed |
Host: on branches of Chimonanthus praecox Country: China (Hunan) Ecological group: UN |
Chang et al . (2005a); Gao et al . (2017) |
Diaporthe micheliae Y.H. Gao & L. Cai ≡Phomopsis micheliae C.Q. Chang, Z.D. Jiang & P.K. Chi SCHM 3603H |
Pycnidia tuberous or irregular, eustromatic, unilocular, wall becoming darker and thicker towards ostiole, 85–188 × 55–118 μm |
Conidiophores hyaline, septate, simple, rarely branched, 8.5–19.5 × 1.6–2.6 μm Conidiogenous cells hyaline, phialidic, enteroblastic |
Alpha conidia fusiform, acute ends, hyaline, aseptate, biguttulate, 6.5–8.2 × 1.6–2 μm Beta conidia filiform, straight or hamate, hyaline, aseptate, 9–23 × 0.5–0.8 μm Gamma conidia not observed |
Host: on branches of Michelia alba Country: China (Fujian) Ecological group: UN |
Chang et al . (2005b); Gao et al . (2017) |
Diaporthe middletonii R.G. Shivas, L. Morin, S.M. Thomps. & Y.P. Tan* BRIP 54884eT |
Pycnidia subglobose, multilocular, necks absent or up to 200 μm, exuding cream conidial droplets from a few ostioles, up to 300 μm diam |
Conidiophores reduced to conidiogenous cells or cylindrical, hyaline to pale yellowish brown, 1-septate, 10–25 × 1.5–3.5 μm Conidiogenous cells cylindrical, hyaline, 5–20 × 1.5–2.5 μm |
Alpha conidia fusiform to cylindrical, rounded apex, obconically truncate base, hyaline, aseptate, mostly biguttulate, (5–)6–7.5(–8) × 2–2.5(–3) μm Beta conidia scarce, mostly J-shaped, flexuous, hyaline, aseptate, 20–35 × 1–1.5 μm Gamma conidia not observed |
Host: on stem of Rapistrum rugosum Country: Australia (Queensland) Ecological group: UN |
Thompson et al . (2015) |
Diaporthe myracrodruonis | |||||
Diaporthe myracrodruonis A.P.S.L. Pádua, T.G.L. Oliveira, Souza-Motta, X.L. Fan & J.D.P. Bezerra URM 7972T |
Pycnidia globose to subglobose, dark brown to black, thin-walled, exuding whitish to light cream conidial droplets from ostioles, (424)636–954(–975) × (286–)318–795(–901) μm |
Conidiophores straight to sinuous, moderately curved, tapering towards apex, thick at base, hyaline, occasionally branched, smooth, phialidic, (5–)6–9(–11) × 1.5–2(–2.5) μm Conidiogenous cells cylindrical, terminal, phialidic, (2–)5.5–8.5(–14.5) × (1.5–)2–2.5 μm |
Alpha conidia fusoid or elongated ellipsoid, attenuating towards ends, hyaline, aseptate, smooth 2.5–3.5(–4) × 1–1.5 μm Beta conidia sickle-shaped, curved, curved and slightly tapered apex, truncate base, hyaline, aseptate, smooth, 18–20(–24) × 0.7–1 μm Gamma conidia not observed |
Host: on leaves of Myracrodruon urundeuva Country: Brazil Ecological group: endophyte |
da Silva et al . (2019) |
Diaporthe sackstonii | |||||
Diaporthe caryae C.M. Tian & Qin Yang* CFCC 52563T |
Pycnidia n early flat, discoid, uniloculate and undivided, ectostromatic disc brown to dark, with one ostiole, 310–325 μm diam | Conidiophores cylindrical, sometimes inflated, hyaline, unbranched, phialidic, 7–11 × 1.4–2.2 μm |
Alpha conidia ellipsoidal or fusiform, obtuse ends, hyaline, aseptate, eguttulate, 7–8.5 × 2.1–2.5 μm (x̄= 8 × 2.3 μm, n = 30) Beta conidia filiform, straight or hamate, tapering towards apex, subtruncate base, hyaline, aseptate, eguttulate, 15.5–34 × 1.1–1.4 μm (x̄= 27.5 × 1.2 μm, n = 30) Gamma conidia not observed |
Host: on symptomatic twigs of Carya illinoensis Country: China (Beijing) Ecological group: potential pathogen |
Yang et al . (2018) |
Diaporthe juglandigena S.Y. Wang, Yong Wang bis* GUCC 422.16T |
Pycnidia irregular globose to subglobose, exuding black conidial masses surrounded by white mycelium and drops of water, up to 2 mm diam |
Conidiophores reduced to conidiogenous cells Conidiogenous cells subulate, cylindrical, straight to sinuous, tapering towards apex, hyaline, simple, rarely branched above, smooth, slightly thicker, densely aggregated, 19–34 × 1–2.5 μm (x̄= 27 × 1.7 μm, n = 20) |
Alpha conidia fusoid to ellipsoidal, asymmetrical, tapering towards ends, mostly straight, hyaline, aseptate or 1-septate, smooth, frequently guttulate, 5–8 × 2–3 μm (x̄= 6.4 × 2.3 μm, n = 30) Beta conidia infrequent, filiform, mostly curved, acute apex, hyaline, aseptate, eguttulate, smooth, 23–36 × 1–2 μm (x̄= 31 × 1.3 μm, n = 10) Gamma conidia not observed |
Host: on peel of Juglans regia Country: China (Guizhou) Ecological group: potential pathogen |
Wang et al . (2022) |
Diaporthe machili S.T. Huang, J.W. Xia, W.X. Sun & X.G. Zhang* SAUCC 194.111T |
Pycnidia globose to subglobose, black, exuding cream conidial droplets from central ostioles | Conidiophores mostly ampulliform, cylindrical, straight or slightly curved, swelling at base, tapering towards apex, hyaline, septate, unbranched, guttulate, densely aggregated, 7–11.4 × 1.8–2.8 μm |
Beta conidia J-shaped, filiform, mostly curved, swelling in middle, tapering towards ends, hyaline, aseptate, 29–39 × 1.3–1.5 μm (x̄= 32.5 × 1.4 μm, n = 20) Alpha and gamma conidia not observed |
Host: on diseased leaves of Machilus pingii Country: China (Yunnan) Ecological group: potential pathogen |
Huang et al . (2021b) |
Diaporthe orixae Q.T. Lu & Z. Zhang* KUNCC 21–10714T |
Pycnidia globose to conical, brown to dark brown, ostiolate, with short necks (36–88 × 49–73 μm), smooth or covered by sparce hyaline hyphae, 98–509 × 55–360 μm diam |
Conidiophores reduced to conidiogeneous cells or subcylindrical to cylindrical, hyaline, rarely septate Conidiogenous cells subcylindrical to cylindrical, rarely tapering towards apex, hyaline, with collarette and prominent periclinal thickening, 2–4.2 × 1–2.5 μm |
Alpha conidia oblong to ellipsoid, bluntly rounded apex, obtuse base, hyaline, aseptate, multiguttulate, 3.5–5.5 × 1.5–3 μm Beta andgamma conidia not observed |
Host: on stems of Orixa japonica Country: China (Guizhou) Ecological group: endophyte |
Lu et al . (2022) |
Diaporthe sackstonii R.G. Shivas, S.M. Thomps. & Y.P. Tan BRIP 54669bT |
Pycnidia multilocular, with necks up to 0.5 mm, exuding cream conidial droplets from ostioles, up to 1 mm diam |
Conidiophores reduced to conidiogenous cells or filiform, hyaline to pale yellowish brown, septate, 15–40 × 1.5–3 μm Conidiogenous cells cylindrical to lageniform, tapering toward apex, hyaline, 10–15 × 1.5–3 μm |
Alpha conidia fusiform, rounded apex, obconically truncate base, hyaline, aseptate, 6–7(–8) × 2–2.5 μm Beta and gamma conidia not observed |
Host: on petiole of Helianthus annuus Country: Australia (Queensland) Ecological group: UN |
Thompson et al . (2015) |
Diaporthe serafiniae | |||||
Diaporthe serafiniae R.G. Shivas, S.M. Thomps. & Y.P. Tan BRIP 55665bT |
Pycnidia multilocular, with necks up to 1.5 mm, exuding cream conidial droplets from most ostioles, up to 2 mm diam |
Conidiophores fusiform, hyaline to pale yellowish brown, 1-septate, 15–25 × 1.5–3.5 μm Conidiogenous cells cylindrical, flexuous, tapering towards apex, hyaline, 5–20 × 1.5–2.5 μm |
Alpha conidia fusiform, rounded apex, narrowed towards base, hyaline, aseptate, biguttulate, 5.5–7 (–8) × 1.5–2.5(–3) μm Beta andgamma conidia not observed |
Host: on seed of an ornamental variety of Helianthus annuus Country: Australia (Queensland) Ecological group: UN |
Thompson et al . (2015) |
Diaporthe longicolla clade | |||||
Diaporthe longicolla | |||||
Diaporthe longicolla (Hobbs) J.M. Santos, Vrandečić & A.J.L. Phillips ≡ Phomopsis longicolla Hobbs ATCC 60325T |
Pycnidia globose, black, stromatic, uni- or multilocular, with prominent necks more than 200 μm long opening by an apical ostiole, locules uniostiolate or multiostiolate, up to 500 μm diam |
Conidiophores hyaline, septate, simple or usually branched, 3.5–24 × 1–4 μm Conidiogenous cells filiform, hyaline, phialidic |
Alpha conidia ellipsoid to fusiform, hyaline, aseptate, guttulate, 5–9.5 × 1.5–3.5 μm Beta conidia rare, filiform, hamate, hyaline Gamma conidia not observed |
Host: seeds, pods, and stems of Glycine max Country: USA (Ohio) Ecological group: pathogen |
Hobbs (1985); Santos et al . (2011) |
Diaporthe megabiguttulata M. Luo, W. Guo, Manawas., M.P. Zhao, K.D. Hyde & C.P. You* ZHKUCC 22-0067T |
Pycnidia oblate or hemispherical, uni- or multilocular, 50–440 × 40–270 μm (x̄= 180 × 120 μm) | Conidiogenous cells hyaline, phialidic |
Alpha conidia ellipsoid or lanceolate, one end obtuse and the other acute, hyaline, aseptate, biguttulate, 5–10 × 2–3 μm (x̄= 6 × 2 μm) Beta conidia hamate or curved, hyaline, truncate base, 20–30 × 1–2 μm (x̄= 30 × 1 μm) Gamma conidia not observed |
Host: on stem of Morinda officinalis Country: China (Guangdong) Ecological group: endophyte |
Luo et al . (2022) |
Diaporthe unshiuensis F. Huang, K.D. Hyde & Hong Y. Li* CGMCC 3.17566T |
Pycnidia globose, subglobose or irregular, dark brown | Conidiophores cylindrical, slightly tapering towards apex, hyaline, smooth, 14.3–24.2 × 1.4–2.6 μm (x̄= 19.5 × 2 μm) |
Alpha conidia ellipsoidal or clavate, truncate base, hyaline, aseptate, smooth, biguttulate, 5.2–7.5 × 2–3.9 μm (x̄= 6.5 × 2.8 μm; L/W = 2.4) Beta and gamma conidia not observed |
Host: on melanose fruit of Citrus unshiu Country: China (Zhejiang) Ecological group: potential pathogen |
Huang et al . (2015) |
Diaporthe morindendophytica | |||||
Diaporthe morindendophytica M. Luo, W. Guo, Manawas., M.P. Zhao, K.D. Hyde & C.P. You ZHKUCC 22-0069T |
Pycnidia oblate, subglobose or irregular, uni- or multilocular, exuding black conidial droplets from ostioles, 40–200 × 30–130 μm (x̄= 120 × 70 μm) | Conidiogenous cells hyaline, phialidic |
Alpha conidia ellipsoid, torque circular or lanceolate, blunts ends, or one end slightly pointed, hyaline, aseptate, biguttulate, 5–10 × 2–3 μm (x̄= 6 × 3 μm) Beta conidia linear, curved, hyaline, 20–30 × 1–2 μm (x̄= 20 × 2 μm) Gamma conidia not observed |
Host: on stem of Morinda officinalis Country: China (Guangdong) Ecological group: endophyte |
Luo et al . (2022) |
Diaporthe tectonendophytica | |||||
Diaporthe tectonendophytica Doilom, Dissan. & K.D. Hyde MFLUCC 13-0471T |
Pycnidia subglobose or irregular, black, with an elongated black neck, exuding hyaline to yellowish, reddish brown to umber, white to cream conidial droplets from central ostioles, (250–)550–675(–1048) × (300–)770–1000(–1490) μm (x̄= 542 × 660 μm, n = 25) |
Conidiophores cylindrical, straight or slightly curved, rounded to obtuse at apex, wider at base, hyaline, septate, branched or unbranched, smooth, in dense clusters, 15–36 × 1.5–2.5 μm Conidiogenous cells cylindrical, slightly tapering towards apex (0.5–1 μm), terminal, phialidic, 4–8 × 1.5–2 μm |
Alpha conidia ellipsoid, bluntly rounded apex, obtuse to subtruncate base, hyaline, aseptate, smooth, mono- to mostly biguttulate, (3.8–)4.8–5.4(–6) × 1.7–2.7 μm (x̄= 5 × 2.2 μm, n = 30) Beta conidia filiform, curved or hamate, subtruncate base, hyaline, aseptate, (14–)24.5–25.5(–29.3) × 1–1.6 μm (x̄= 23 × 1.3 μm, n = 30) Gamma conidia not observed |
Host: on branches of Tectona grandis Country: Thailand Ecological group: endophyte |
Doilom et al . (2016) |
Diaporthe ueckeri | |||||
Diaporthe durionigena L.D. Thao, L.T. Hien, N.V. Liem, H.M. Thanh & T.N. Khanh* VTCC 930005T |
Pycnidia globose to subglobose, black, with up to six well-defined necks per conidioma, 200–400 μm diam |
Conidiophores reduced to conidiogeneous cells Conidiogenous cells cylindrical, hyaline, 10–18 × 2.5–3.5 μm |
Alpha conidia rare or absent, ellipsoidal, hyaline, aseptate, smooth, biguttulate, (5.6–)6.1–7.5(–7.9) × (1.8–)2.1–2.7(–3) μm Beta conidia hamate, hyaline, aseptate, (17.8–)20.3–26.1(–31.2) × 1.1–1.5(–1.7) μm Gamma conidia not observed |
Host: on branches of Durio zibethinus Country: Vietnam Ecological group: UN |
Crous et al . (2020, 2021a) |
Diaporthe miriciae R.G. Shivas, S.M. Thomps. & Y.P. Tan BRIP 54736jT |
Pycnidia multilocular, with necks up to 1 mm, exuding pale yellow conidial droplets from some ostioles |
Conidiophores reduced to conidiogeneous cells or cylindrical to obclavate, hyaline to subhyaline, 1–2-septate, 10–20 × 1.5–3 μm Conidiogenous cells cylindrical to obclavate, tapering towards apex, hyaline, 5–12 × 1.5–3 μm |
Alpha conidia fusiform to oval, rounded apex, narrowed base, hyaline, aseptate, 6–7.5(–9) × 2–2.5(–3) μm Beta conidia hamate, flexuous, hyaline, aseptate, 20–35 × 1–1.5 μm Gamma conidia not observed |
Host: on stubble of Helianthus annuus Country: Australia (New South Wales) Ecological group: UN |
Thompson et al . (2015) |
Diaporthe passifloricola Crous & M.J. Wingf.* CBS 141329T |
Pycnidia globose, black, with short black necks, exuding creamy conidial droplets from central ostioles, up to 250 μm diam |
Conidiophores cylindrical, straight to sinuous, hyaline, 2–3-septate, branched, smooth, densely aggregated, 20–50 × 3–4 μm Conidiogenous cells cylindrical, tapering towards apex (1–1.5 μm), terminal and lateral, phialidic, with periclinal thickening, 7–20 × 1.5–2.5 μm |
Alpha conidia fusoid-ellipsoid, tapering towards end, subobtuse apex, subtruncate base, hyaline, aseptate, smooth, guttulate, (5–)6–7(–9) × 2.5(–3) μm Beta conidia spindle-shaped, tapering from lower third towards apex, curved, acutely rounded apex, truncate base, hyaline, aseptate, (20–)22–25(–27) × 1.5(–2) μm Gamma conidia not observed |
Host: on leaf spots of Passiflora foetida Country: Malaysia Ecological group: potential pathogen |
Crous et al . (2016b) |
Diaporthe rosae Samarak. & K.D. Hyde* MFLUCC 17-2658 |
Pycnidia globose to pyriform, reddish brown, coriaceous, with elongate necks, 95–160 μm (x̄ = 123.9 μm, n = 22) long, 35–75 μm (x̄= 54.9 μm, n = 10) high, 80–140 μm (x̄= 110.9 μm, n = 10) diam at base |
Conidiophores reduced to conidiogenous cells or straight, hyaline, septate, branched, smooth, 10–19 × 1.9–3.3 μm (x̄= 15 × 2.6 μm, n = 20) Alpha conidiogenous cells ampulliform, slightly tapering towards apex, phialidic, with periclinal thickening, 13 × 1–2.5 μm (x̄= 9.9 × 2 μm, n = 25) Beta conidiogenous cells ampulliform, slightly tapering towards apex, phialidic, with periclinal thickening and flared collarette, 7.7–15 × 1.2–2.3 μm (x̄= 12.5 × 1.9 μm, n = 10) |
Alpha conidia ovate to ellipsoidal, subtruncate base, hyaline, aseptate, smooth, often biguttulate, 5.5–7.5 × 2–3 μm (x̄= 6.5 × 2.5 μm, n = 30; L/W = 2.6) Beta conidia scarce, fusiform to hooked, subtruncate base, hyaline, aseptate, smooth, 12.5–18 × 1–2 μm (x̄= 14.6 × 1.4 μm, n = 10; L/W = 10.4) Gamma conidia not observed |
Host: on dead pedicel of Rosa sp. Country: Thailand Ecological group: saprophyte |
Wanasinghe et al . (2018) |
Diaporthe thunbergiicola Udayanga & K.D. Hyde* MFLUCC 12-0033T |
Pycnidia subglobose to ovate, with an elongated black neck 100–200 μm long, often exuding a yellowish conidial cirrus from ostiole, 100–200 μm diam |
Conidiophores ampulliform, cylindrical to subcylindrical, with larger basal cell, hyaline, unbranched or branched at the basal cell, smooth, 6–14 × 1–2 μm (x̄= 11 × 1.5 μm, n = 30) Conidiogenous cells cylindrical, slightly tapering towards apex (0.5–1 μm), terminal, phialidic |
Alpha conidia ovate to ellipsoidal, subtruncate base, hyaline, aseptate, smooth, biguttulate, 5.7–7.5 × 2–3 μm (x̄= 6.6 × 2.8 μm, n = 30) Beta and gamma conidia not observed |
Host: on diseased leaves of Thunbergia laurifolia Country: Thailand Ecological group: potential pathogen |
Liu et al . (2015) |
Diaporthe ueckeri Udayanga & Castl. CBS 139283T |
Pycnidia g lobose, with an elongated black neck 200–300 μm long, often exuding a yellowish conidial cirrus from ostiole, 150–200 μm diam |
Conidiophores ampulliform, long, slender, hyaline, unbranched, smooth, (9–)12–28(–30) × 1.5–2.5 μm Conidiogenous cells cylindrical, slightly tapering towards apex (0.5–1 μm), terminal, phialidic |
Alpha conidia ellipsoidal, subtruncate base, hyaline, aseptate, smooth, often biguttulate, (6–)6.4–8.3(–8.6) × (2–)2.3–3 μm (x̄= 7.2 × 2.6 μm, n = 30) Beta andgamma conidia not observed |
Host: on crown of Cucumis melo Country: USA (Oklahoma) Ecological group: potential pathogen |
Udayanga et al . (2015) |
Diaporthe vochysiae S.A. Noriler, R.R. Gomes & C. Glienke LGMF 1583T |
Pycnidia globose to conical, brown to black, with necks 90 μm long, outer surface smooth, ostiolate, with globose, predominantly yellow and yellow to reddish brown conidial mass, 328 × 367 μm |
Conidiophores subcylindrical to cylindrical, tapering towards apex, hyaline, 1–3-septate, rarely branched above the septa, 21–29 × 2.1–3.3 μm Conidiogenous cells subcylindrical, tapering towards apex, hyaline, with slight periclinal thickening and flared collarette, (13.5–)12.2–14.8(–15) × 3(–5) μm |
Alpha conidia oblong to ellipsoid, bluntly rounded apex, obtuse base, hyaline, aseptate, biguttulate, (2.8–)3–4(–4.2) × (1.5–)2 μm Beta andgamma conidia not observed |
Host: on leaf of Vochysia divergens Country: Brazil (Mato Grosso do Sul) Ecological group: endophyte |
Noriler et al . (2019) |
Diaporthe rudis clade | |||||
Diaporthe asheicola | |||||
Diaporthe asheicola L. Lombard & Crous MFLU 15-2966 |
Pycnidia globose, flask-like to conical, brown to black, eustromatic, unilocular, with ostiolate necks, outer surface smooth, exuding a globose white, pale-yellow to yellow conidial mass or cirrus, up to 530 μm diam and 290–420 μm high |
Alpha conidiophores cylindrical, filiform, aseptate, rarely branched, 8–35 × 2–3 μm (x̄= 27 × 2 μm, n = 20) (alpha ), 10–27 × 1–2 μm (x̄= 16 × 1.5 μm, n = 20) (beta ) Conidiogenous cells subcylindrical, tapering towards apex, with periclinal thickening and collarette, phialidic, 3–15 × 1–2 μm (x̄= 10 × 1.5 μm,n = 20) (alpha ), 7–14 × 1–2 μm (x̄= 11 × 1.5 μm, n = 20) (beta ) |
Alpha conidia fusoid to ellipsoidal, acutely rounded apex, obtuse to subtruncate base, multiguttulate, rarely biguttulate, 6–9 × 2–3 μm (x̄ = 8 × 2 μm, n = 20) Beta conidia straight, curved or hamate, 20–25 × 1–2 μm (x̄= 23 × 1 μm, n = 20) Gamma conidia not observed |
Host: on a stem of Fraxinus pennsylvanica Country: Russia Ecological group: saprophyte |
Lombard et al . (2014); Chethana et al . (2021b) |
Diaporthe australafricana | |||||
Diaporthe australafricana Crous & van Niekerk CBS 111886T |
N/A # | N/A # |
Alpha conidia fusoid, obtuse ends, biguttulate to eguttulate, 5–5.5(–6) × 1.5–2 μm Beta and gamma conidia not observed |
Host: on Vitis vinifera Country: South Africa Ecological group: UN |
van Niekerk et al . (2005) |
Diaporthe crousii | |||||
Diaporthe crousii S. Hilário, L. Santos & A. Alves MUM 19.29T |
Pycnidia ellipsoid, brown to black, exuding yellow conidial mass from o stiole |
Conidiophores reduced to conidiogeneous cells Conidiogenous cells cylindrical, straight, hyaline, aggregated, x̄= 21.9 × 1.5 μm (n = 30) |
Alpha conidia ellipsoid, rounded apex, obtuse to truncate base, hyaline, aseptate, smooth, biguttulate, x̄= 5.7 × 2.3 μm (n = 100) Gamma conidia infrequent, hyaline, aseptate, smooth, x̄= 10.6 × 1.5 μm (n = 8) Beta conidia not observed |
Host: on dieback lesions of Vaccinium corymbosum Country: Portugal Ecological group: pathogen |
Hilário et al . (2020) |
Diaporthe cynaroidis | |||||
Diaporthe cynaroidis Marinc., M.J. Wingf. & Crous MFLU 14-0847 |
Pycnidia globose to pyriform, black, coriaceous, with an elongated neck, often exuding a yellowish white conidial cirrus from ostiole, 265–300 μm diam at base × 125–140 μm high (x̄= 280 × 135 μm, n = 10) |
Conidiophores ampulliform, straight to sinuous, hyaline, smooth, unbranched, 4–6 × 4.5–8 μm (x̄= 4.6 × 6.6 μm, n = 20) Conidiogenous cells cylindrical, slightly tapering towards apex, terminal, phialidic, 8–14 × 1.5–3 μm (x̄= 11.2 × 2.2 μm, n = 20) |
Alpha conidia ovate to ellipsoidal, subtruncate base, hyaline, aseptate, smooth, often biguttulate, 5.8–7.5 × 2.5–3.5 μm (x̄= 6.4 × 2.8 μm, n = 10) Beta andgamma conidia not observed |
Host: on a dead aerial stem of Eupatorium cannabinum Country: Italy Ecological group: saprophyte |
Marincowitz et al . (2008); Hyde et al . (2020a) |
Diaporthe salicicola R.G. Shivas, Jacq. Edwards & Y.P. Tan* VPRI 32789T |
Pycnidia with ostiolar beaks mostly up to 400 μm long |
Conidiophores cylindrical, straight, hyaline, 1–3-septate, unbranched, 10–25 × 2–3 μm Conidiogenous cells cylindrical, tapering towards apex, terminal, hyaline, phialidic, 10–20 × 2–3 μm |
Alpha conidia cylindrical to oval, rounded apex, slightly attenuated base, hyaline, aseptate, (4–)5–7(–8) × 1.5–2.5 μm Beta and gamma conidia not observed |
Host: on leaf spot of Salix purpurea Country: Australia (Tasmania) Ecological group: potential pathogen |
Tan et al . (2013) |
Diaporthe patagonica | |||||
Diaporthe patagonica M. Zapata, M.A. Palma, M.J. Anninat & E. Piontelli CBS 145291T |
Pycnidia globose, flask-shaped, eustromatic, convoluted to unilocular, brown to black, with black cylindrical ostiolate necks up to 1 mm, outer surface smooth, exuding light yellow to cream conidial mass, up to 550 μm diam |
Conidiophores reduced to conidiogenous cells or cylindrical, straight, hyaline, smooth, densely aggregated Conidiogenous cells cylindrical, slightly tapering towards apex, terminal and lateral, phialidic, with inconspicuous periclinal thickening, 10.5–22 × 1–2.5 μm |
Alpha conidia fusoid to ellipsoid, tapering towards ends, straight, hyaline, aseptate, smooth, mostly biguttulate, (5.5–)6–7.5(–10) × (2–)2.5(–3) μm (x̄= 7 × 2.4 μm) Beta conidia spindle shaped, some straight, mostly curved towards one end, subacute apex, lightly truncate base, hyaline, aseptate, smooth, (12–)16–22(–28.5) × 1–1.5 μm (x̄= 18.8 × 1.3 μm) Gamma conidia scarcely observed |
Host: on branches of Aristotelia chilensis with dieback symptoms Country: Chile Ecological group: potential pathogen |
Zapata et al . (2020) |
Diaporthe rudis | |||||
Diaporthe rudis (Fr.) Nitschke ≡ Sphaeria rudis Fr. CBS 109292ET |
Pycnidia globose, 200–250 μm diam, and 400–500 μm diam at maturity |
Conidiophores cylindrical, ampulliform, straight to sinuous, hyaline, smooth, branched, 20–45 × 2–2.4 μm Paraphyses abundant among conidiophores, 20–40 × 1–2 μm Conidiogenous cells cylindrical, terminal, slightly tapering towards apex (0.5–1 μm), phialidic |
Alpha conidia ovate to ellipsoidal, subtruncate base, hyaline, aseptate, smooth, biguttulate, (6.3–)7–8(–8.7) × 2–2.5 μm (x̄= 7.5 × 2.2 μm, n = 30) Beta conidia fusiform or hooked, subtruncate base, hyaline, aseptate, smooth, 27–31(–35.2) × (3–)3.4–3.8(–4.2) μm (x̄= 29.5 × 3.6 μm, n = 30) Gamma conidia fusiform, subtruncate base, hyaline, aseptate, smooth, mostly biguttulate, (10–)14–15 × 1–2 μm (x̄= 14.4 × 1.7 μm, n = 30) |
Host: on stem of Laburnum anagyroides Country: Austria Ecological group: UN |
Udayanga et al . (2014b) |
Diaporthe viticola Nitschke CBS 113201ET |
Pycnidia black, exuding white or pale-yellow conidial mass |
Conidiophores tapering towards apex, septate, branched, branches arising from immediately below the septa, 17–34 × 1.5–2.5 μm (in culture), 18–24 × 2–3 μm (on host, some unbranched) Conidiogenous cells hyaline, aperture apical, channel minute, with funnel-shaped collarette up to 6 μm long, integrated, enteroblastic, phialidic, 10–14 × 1.5–2.5 μm (in culture), 10–14 × 2 μm (on host) |
Alpha conidia oblong to elliptical, hyaline, aseptate, smooth, biguttulate, 5–7 × 2.5 μm (in culture), 7–9 × 2–3 μm (on host) Beta conidia straight or curved or hamate, hyaline, smooth, 16–28 × 1 μm Gamma conidia not observed |
Host: on Vitis vinifera Country: Portugal Ecological group: UN |
Phillips (1999); van Niekerk et al . (2005); Udayanga et al . (2014b) |
1 Taxa synonymised in the present study are noted with a superscript asterisk (*); status of the strains or specimens on which the morphological data is based is noted by superscript ET (ex-epitype), H (holotype) and T (ex-type).
2 UN = unknown, i.e. information not mentioned by the respective authors; the ecological group “potential pathogen” stands for species recovered from symptomatic tissues, but for which pathogenicity tests were not conducted to prove their pathogenicity.
#N/A = not available, i.e. feature not mentioned by the respective authors in the taxonomic description of the species.
Note: several species of the Diaporthe clades treated (including some synonymised in the present study) were excluded from this synopsis due to lack of morphological data regarding their asexual morphs. Some details about their collections are given below.
Diaporthe amygdali clade: D. sterilis Lombard, Polizzi & Crous was introduced by Lombard et al. (2014) as a pathogen on Vaccinium corymbosum in Italy, based on the diagnosis of sequence data, since no sporulation was observed for five different isolates (including the ex-type strain CBS 136969) on different media or on sterilised organic material placed on the media; D. sterilis was synonymised under D. amygdali by Hilário et al. (2021a).
Diaporthe eucommiae clade: D. tuyouyouiae Y.P. Tan, Bishop-Hurley & R.G. Shivas was introduced by Tan & Shivas (2023) from a leaf spot on Decalobanthus peltatus in Queensland (Australia), based on the diagnosis of sequence data obtained apparently from the type specimen (BRIP 75017a), and no taxonomic description was provided. D. xylocarpi M.S. Calabon & E.B.G. Jones (as D. salinicola Dayar.) was introduced by Dayarathne et al. (2020) as a saprophyte on decaying submerged wood of Xylocarpus sp. in Thailand, based on morpho-molecular analyses [the species name was validly published by Calabon et al. (2023)]; however, only the sexual morph was observed on the host tissue, and no sporulation was observed in culture; both species are synonymised here under D. eucommiae.
Diaporthe foeniculina clade: D. parva Y.S. Guo & G.P. Wang was introduced by Guo et al. (2020) as a pathogen on branches with shoot cankers symptoms of Pyrus bretschneideri, based on the diagnosis of sequence data, since the isolates formed globose or irregular, dark brown to black conidiomata-like structure that remained sterile on different media or on sterilised organic material under different conditions.
Diaporthe glabrae clade: D. etinsideae Y.P. Tan, Grice & R.G. Shivas was introduced by Tan & Shivas (2022) on Annona muricata in Queensland (Australia), based on the diagnosis of sequence data obtained apparently from the type specimen (BRIP 64096a), and no taxonomic description was provided; D. etinsideae is synonymised here under D. tulliensis.
Diaporthe inconspicua clade: D. inconspicua R.R. Gomes, Glienke & Crous was introduced by Gomes et al. (2013) for three endophytic isolates from the medicinal plants Maytenus ilicifolia and Spondias mombin in Brazil, based on the diagnosis of sequence data, since the isolates (including the ex-type strain CBS 133813) were sterile in culture; however, the morphological description of D. inconspicua was later emended by Bezerra et al. (2018) based on a set of endophytic isolates from Poincianella pyramidalis in Brazil phylogenetically related to D. inconspicua, and thus the description provided by Bezerra et al. (2018) was considered here. Similarly, the morphological description of D. isoberliniae Crous on Isoberlinia angolensis in Zambia (Crous et al. 2014b) was emended by Lambert et al. (2023) based on two strains on Pittosporum manii in Cameroon, which produced beta and gamma conidia, features that were not observed by Crous et al. (2014b) for the type specimen; the emended taxonomic description of D. isoberliniae was considered in this synopsis, along with its original description.
Diaporthe leucospermi clade: D. infecunda R.R. Gomes, Glienke & Crous was introduced by Gomes et al. (2013) for a set of eight isolates from leaves of medicinal plants growing in Brazil, such as Schinus terebinthifolius and Maytenus ilicifolia, based on the diagnosis of sequence data, since the isolates (including the ex-type strain CBS 133812) were sterile in culture; D. infecunda is synonymised here under D. leucospermi. D. australpacifica Y.P. Tan & R.G. Shivas was introduced by Tan & Shivas (2022) on a stem of Amaranthus blitum in Norfolk Island (Australia), based on the diagnosis of sequence data obtained apparently from the type specimen (BRIP 60163d), and no taxonomic description was provided; D. australpacifica is synonymised here under D. micheliae.
Diaporthe longicolla clade: D. breyniae Y. Marín & C. Lamb. Was introduced by Matio Kemkuignou et al. (2022) as an endophyte on leaves of Breynia oblongifolia in Cameroon, based on the diagnosis of sequence data, since no sporulation was observed for the ex-type strain CBS 148910 on different media. D. trevorrowii Y.P. Tan, Grice, Czislowski & R.G. Shivas was introduced by Tan & Shivas (2022) on stems of Cucumis melo in Queensland (Australia), based on the diagnosis of sequence data obtained apparently from the type specimen (BRIP 70737a), and no taxonomic description was provided.
Diaporthe rudis clade: D. asheicola L. Lombard & Crous was introduced by Lombard et al. (2014) on Vaccinium ashei in Chile, based on the diagnosis of sequence data, since the two isolates representing the species (including the ex-type strain CBS 136967) could not be induced to sporulate on different media or on sterilised V. myrtillus tissue placed on the media; however, a morphological description for D. asheicola was provided by Chethana et al. (2021b) for a Russian specimen of Diaporthe on a stem of Fraxinus pennsylvanica, phylogenetically related to D. asheicola, and thus the description provided by Chethana et al. (2021b) was considered here. D. cynaroidis Marinc., M.J. Wingf. & Crous was introduced by Marincowitz et al. (2008) on leaf litter of Protea cynaroides in South Africa, but only the sexual morph was reported associated with its type collection, and the asexual morph was regarded as “Phomopsis sp.”; however, a morphological description of the asexual morph of D. cynaroidis was provided by Hyde et al. (2020a) for an Italian saprophyte specimen of Diaporthe on a dead aerial stem of Eupatorium cannabinum, phylogenetically related to D. cynaroidis, and thus the description provided by Hyde et al. (2020a) was considered here. D. subcylindrospora S.K. Huang & K.D. Hyde was introduced by Hyde et al. (2018) as a saprophyte on a dead branch of Salix sp. in China, based on morpho-molecular analyses, but only the sexual morph was observed on the host tissue; D. subcylindrospora is synonymised here under D. cynaroidis. Similarly, D italiana Chethana, Camporesi & K.D. Hyde was introduced by Hyde et al. (2019) as a saprophyte on a dead, aerial branch of Morus alba, based on morpho-molecular analyses, but only the sexual morph was observed on the host tissue; D. italiana is synonymised here under D. rudis.