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Diplodia pinea (Botryosphaeriaceae) is one of the most important pathogens of pines in South Africa. The fungus has been associated with a number of different disease symptoms, including shoot blight of seedlings and trees (die-back), stem cankers, root diseases and blue stain of timber (Wingfield and Knox-Davies 1980; Swart et al., 1987; Slippers and Wingfield 2007).

Diplodia pinea die-back following hail damage has been known in South Africa since the early 1900's. This serious disease, which accounts for the notoriety of the pathogen worldwide, has led to the restriction of the most susceptible species (Pinus patula, P. pinaster and P. radiata) to areas where hail is infrequent. Pinus patula is still planted in summer rainfall areas and severe losses commonly occur. Although less frequent, hailstorms do occur in areas where P. radiata is planted and these often also lead to substantial losses.

Diplodia pinea exists as a saprophyte on dead bark, cones and needles and is best known as an opportunist that infects wounds on susceptible pines. The fungus can, however, behave as a primary pathogen and infect young, unwounded pine shoots. Moisture is necessary for infection by D. pinea and young shoots become infected when rains coincide with warm temperatures, at the onset of growth. Once established in the shoots, D. pinea moves down the pith, where it can remain dormant. When pines are stressed, the fungus moves out of the pith and causes stem cankers.

A serious root disease of P. elliottii and P. taeda caused by D. pinea has been found in many parts of South Africa. Characteristic symptoms of this disease are dark-blue, radial lesions in young roots which extend to larger roots and into the trunk of diseased trees (Wingfield and Knox-Davies 1980). Needles become chlorotic and are shed. Pinus taeda is apparently most susceptible and the disease is always associated with stress due to factors such as overstocking, drought and plantings on poor sites.

Diplodia pinea (Botryosphaeriaceae) is one of the most important pathogens of pines in South Africa. The fungus has been associated with a number of different disease symptoms, including shoot blight of seedlings and trees (die-back), stem cankers, root diseases and blue stain of timber (Wingfield and Knox-Davies 1980; Swart et al., 1987; Slippers and Wingfield 2007).

Diplodia pinea die-back following hail damage has been known in South Africa since the early 1900's. This serious disease, which accounts for the notoriety of the pathogen worldwide, has led to the restriction of the most susceptible species (Pinus patula, P. pinaster and P. radiata) to areas where hail is infrequent. Pinus patula is still planted in summer rainfall areas and severe losses commonly occur. Although less frequent, hailstorms do occur in areas where P. radiata is planted and these often also lead to substantial losses.

Diplodia pinea exists as a saprophyte on dead bark, cones and needles and is best known as an opportunist that infects wounds on susceptible pines. The fungus can, however, behave as a primary pathogen and infect young, unwounded pine shoots. Moisture is necessary for infection by D. pinea and young shoots become infected when rains coincide with warm temperatures, at the onset of growth. Once established in the shoots, D. pinea moves down the pith, where it can remain dormant. When pines are stressed, the fungus moves out of the pith and causes stem cankers.

A serious root disease of P. elliottii and P. taeda caused by D. pinea has been found in many parts of South Africa. Characteristic symptoms of this disease are dark-blue, radial lesions in young roots which extend to larger roots and into the trunk of diseased trees (Wingfield and Knox-Davies 1980). Needles become chlorotic and are shed. Pinus taeda is apparently most susceptible and the disease is always associated with stress due to factors such as overstocking, drought and plantings on poor sites.

Disease name:

Diplodia diseases

Causal agents:

Diplodia pinea (Sphaeropsis sapinea)
Trees affected:

Pinus spp., especially P. patula, P. radiata

Tree part
affected:

Stems, branches, roots, sawn timber
Impact:

Tip and branch die-back, stem cankers, blue stain

Symptoms:

Sunken cankers on stems/branches, blue stain of affected parts, resin oozing from lesions, branch/tip death

 

New Publications

Esterhuizen HJ, Slippers B, Bosman AS, Roux J, Jones W, Bose T, Hammerbacher A. (2025) Early detection of Phytophthora root rot in Eucalyptus using hyperspectral reflectance and machine learning. Computers and Electronics in Agriculture 237:110761. 10.1016/j.compag.2025.110761
Pham NQ, Wingfield BD, Marincowitz S, Brawner JT, Hulcr J, Wingfield MJ. (2025) Cryphonectria canker on Eucalyptus in Florida reconsidered. Forest Pathology 55:e70031. 10.1111/efp.70031
Nzuza P, Schröder ML, Heim RJ, Daniels L, Slippers B, Hurley BP, Germishuizen I, Sivparsad B, Roux J, Maes WH. (2025) Assessing Gonipterus defoliation levels using multispectral unmanned aerial vehicle (UAV) data in Eucalyptus plantations. Ecological Informatics 90:103301. 10.1016/j.ecoinf.2025.103301
Kunene S, Mmushi TJ, Steenkamp E, Motaung T. (2025) Pinus-derived membrane vesicles disrupt pathogenic metabolism in fungi. plant biology 10.1111/plb.70069 PDF
Theron CA, Wingfield MJ, Ahumada R, Carnegie AJ, Fraser S, Rodas C, Barnes I. (2025) Diversity and distribution of Lophodermium species on non-native Pinus species in the southern hemisphere. Mycological Progress 24(44) 10.1007/s11557-025-02056-5
Msweli D, Geerts S, Nndanduleni M, Paap T. (2025) Evaluation of phosphite to protect a South African Proteaceae from Phytophthora root rot. Journal of Plant Pathology 10.1007/s42161-025-01945-8 PDF
Dewing C, Yilmaz N, Steenkamp ET, Wingfield BD, Visagie CM. (2025) Capturing the fungal diversity hidden in Eastern Cape dairy pastures. Mycological Progress 24(1):38. 10.1007/s11557-025-02059-2
Nel WJ, Duong TA, Fell S, Herron DA, Paap T, Wingfield MJ, de Beer ZW, Hulcr J, Johnson AJ. (2025) A checklist of South African bark and ambrosia beetles (Coleoptera: Curculionidae: Scolytinae, Platypodinae). Zootaxa 5648(1):1-101. 10.11646/zootaxa.5648.1.1
Dewing C, Yilmaz N, Steenkamp ET, Wingfield BD, Visagie CM. (2025) Capturing the fungal diversity hidden in Eastern Cape dairy pastures. Mycological Progress 24:38. 10.1007/s11557-025-02059-2 PDF
Chang R, Yan Z, Jiang J, Wang Y, Si H, Bose T, Miao C. (2025) Four novel endolichenic fungi from Usnea spp. (Lecanorales, Parmeliaceae) in Yunnan and Guizhou, China: Taxonomic description and preliminary assessment of bioactive potentials. MycoKeys 118:55–80. 10.3897/mycokeys.118.155248
Lötter A, Bruna T, Duong TA, Barry K, Lipzen A, Daum C, Yoshinaga Y, Grimwood J, Jenkins JW, Talag J, Borevitz J, Lovell JT, Schmutz J, Wegrzyn JL, Myburg AA. (2025) A haplotype-resolved reference genome for Eucalyptus grandis. G3 Genes|Genomes|Genetics 10.1093/g3journal/jkaf112
Wingfield MJ, Pham NQ, Marincowitz S, Wingfield BD. (2025) Cryphonectriaceae: Biodiverse and threatening tree pathogens in the tropics and southern hemisphere. Annual Review of Phytopathology 63 10.1146/annurev-phyto-121823-030316
Magagula P, Swart V, Fourie A, Vermeulen A, Nelson JH, van Rooyen Z, van den Berg N. (2025) Avocado rhizosphere community profiling: white root rot and its impact on microbial composition. Frontiers in Microbiology 16 10.3389/fmicb.2025.1583797
Marincowitz S, Pham NQ, Wingfield BD, Wingfield MJ. (2025) Microfungi associated with dying quiver trees (Aloidendron dichotomum) in South Africa. Fungal Systematics and Evolution 16:71–80. 10.3114/fuse.2025.16.5 PDF
Pham NQ, Marincowitz S, Crous PW, Wingfield MJ. (2025) Diversity of soil-borne Gliocladiopsis from Indonesia, Malaysia and Vietnam. Fungal Systematics and Evolution 16:81–92. 10.3114/fuse.2025.16.6 PDF
Tanney JB, Kemler M, Vivas M, Wingfield MJ, Slippers B. (2025) Silent invaders: The hidden threat of asymptomatic phytobiomes to forest biosecurity. New Phytologist 10.1111/nph.70209
Fick A, Swart V, Van den Berg N. (2025) In silico prediction method for plant Nucleotide-binding leucine-rich repeat- and pathogen effector interactions. The Plant Journal 122:e70169. 10.1111/tpj.70169
Bose T, Wingfield MJ, Brachmann A, Witfeld F, Begerow D, Kemler M, Dovey S, Roux J, Slippers B, Vivas M, Hammerbacher A. (2025) Removal of organic biomass in Eucalyptus plantations has a greater impact on fungal than on bacterial networks. Forest Ecology and Management 586:122734. 10.1016/j.foreco.2025.122734
Woodward S, Amin H, Mártin-Gárcia J, Solla A, Diaz-Vazquez R, Romeralo C, Alves A, Pinto G, Herron D, Fraser S, Zas R, Doğmuş-Lehtijärvi HT, Bonello P, Wingfield MJ, Witzell J, Diez JJ. (2025) Host-pathogen interactions in the Pine-Fusarium circinatum pathosystem and the potential for resistance deployment in the field. Forest Pathology 55(2):e70020. 10.1111/efp.70020
Maduke N, Slippers B, Van der Linde E, Wingfield M, Fourie G. (2025) Botryosphaeriaceae associated with racemes, fruits and leaves of macadamia in South Africa. Plant Pathology 0:1–15:1–15. 10.1111/ppa.14107