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Wood and bark borers comprise some of the most serious pests of forestry trees worldwide. These insects use the inside of bark and / or the wood to feed on and to make a home. Damage by these insects includes under bark girdling, extensive tunneling which weakens the tree, and / or the introduction of symbiotic fungi that weaken or kill the host. Although some wood boring beetles (such as Apate indistincta and Sinoxylon bellicosum) have been reported as minor pests of A. mearnsii, the current major wood and bark boring pests infest Eucalyptus and Pinus.

Wood borers of eucalypts

The cossid moth (Coryphodema tristis) is a major pest of Eucalyptus. This insect is reported to be native to South Africa with a wide range of native and introduced host plants, including grape vines (Vitis vinifera), quince (Cydonia oblonga) and bushwillows (Combretum sp.). It was first recorded infesting Eucalyptus in 2004. Strangely, despite its broad host range, the cossid moth has only been reported to infest E. nitens. No other Eucalyptus species has been infested, even when planted adjacent to highly infested E. nitens stands. The adult female cossid moth lays her eggs under the branches or in bark cracks. Emerging larvae first feed under the bark, but later instars bore into the sapwood. This insect is gregarious (feeds in groups) and causes extensive tunneling. Characteristic symptoms include large amounts of frass protruding from holes in the trunk, sawdust at the base of the trunk and a blackening of the trunk. The moths are also known as goat moths because of the unpleasant smell associated with their infestations. Trees often survive infestation by more than one generation of the cossid moth. But, in time trees weakened by the extensive tunneling are likely to be blown over by the wind. The tunneling also affects the quality and volume of the wood. The cossid moth has been reported to infest trees four years and older (Gebeyehu et al. 2004).

The Eucalyptus longhorn beetles (Phorocantha recurva and P. semipunctata) were accidentally introduced from Australia, and first recorded in South Africa in 1906. The adult female lays eggs under loose bark and the emerging larvae feed on the cambium and phloem layers. Fully grown larvae bore directly into the heartwood where they later pupate. The tunneling of the larvae can cause under bark girdling and reduce the value of the timber. However, these beetles are currently not considered major pests as they primarily infest dying trees.

Wood borers of pine

The Sirex woodwasp (Sirex noctilio) is one of the most serious pests of Pinus in South Africa (Hurley et al. 2008). This insect is native to Eurasia, but has been accidentally introduced to various southern hemisphere countries, and more recently to North America. In South Africa, the Sirex woodwasp was first detected in 1994 in Cape Town. It has since spread to the majority of pine growing areas in the country. The Sirex woodwasp has a symbiotic association with a fungus (Amylostereum areolatum). The adult female wasp places this fungus, together with its eggs and a toxic mucous, into the wood of pine trees. The fungus and mucous together overcome the defense of the tree and block the tracheids and thus nutrient transport. Attack by this insect usually results in tree death. Trees that survive the attack are usually attacked again the next year and killed. Importantly, the Sirex woodwasp primarily attacks stressed trees. Consequently, the most severe damage of this insect has been reported in areas where trees are stressed by factors such as drought and high stocking. The larvae tunnel in the wood, feeding on the fungus. Pupation occurs in the wood. The adult wasps do not feed and only live for one to two weeks.

The ambrosia beetles (Xyleborus and Xyleborinus spp.) also bore into the wood of Pinus. Unlike the Sirex woodwasp, these beetles are considered a minor pest. Infestations are often associated with cut or burnt trees. The beetles have a symbiotic association with fungi. The tunnels of these beetles and the staining of the wood from the fungi can make infested trees unsuitable for use as saw timber. Both the larvae and adults feed on the fungi.

Bark borers of pine

There are three species of bark beetles that are recorded to infest Pinus in South Africa. All three of these species have been accidentally introduced from the northern hemisphere. Bark beetles are considered as some of the most serious pest threats to forestry worldwide, but fortunately the three species currently in South Africa are only minor pests.

The Mediterranean pine engraver beetle (Orthotomicus erosus) feeds on the inner bark, generally on the main trunk. It attacks dead and dying trees, and can accelerate the death of dying trees by under bark girdling. It is also know to be associated with the fungus Ophiostoma ips that causes bluestain of the wood, thus decreasing its value as saw timber. The adults are dark brown and about 3 mm long. The pine bark beetle (Hylastes angustatus) feeds on the roots and stumps of dying trees. It is generally considered a secondary pest, although it has been known to kill seedlings by feeding on their roots and root-collars, thereby causing under bark girdling. In such cases, the pine bark beetle can become a serious pest. The adults are dark brown and about 4 mm long. The red-haired bark beetle (Hylurgus ligniperda) infests stumps or the base of weakened trees. The adults are dark brown and about 6 mm long (Tribe 1992).

Another bark borer on Pinus is the deodar weevil (Pissodes nemorensis). This insect breeds in dead or dying trees, but also infests the leaders of young healthy trees. The adult beetle lays its eggs under the bark and the larvae feed on the inner bark. When feeding occurs on the leaders of young trees, the leader is often killed from under bark girdling. This results in double leaders and malformation of the tree. It has been observed that such double leaders are more susceptible to infestation by the Sirex woodwasp. Pupation occurs in a chip-cocoon under the bark. Emerging adults are about 7 mm long with two creamy-white spots on their elytra (hind wings) (Gebeyehu and Wingfield 2003).

New Publications

Joubert M, van den Berg N, Theron J, Swart V. (2025) Small RNAs derived from avocado sunblotch viroid and their association with bleaching symptoms: implications for pathogenesis in avocado sunblotch disease. Archives of Virology 170(10):205. 10.1007/s00705-025-06360-z PDF
Mavima L, Steenkamp ET, Beukes CW, Palmer M, De Meyer SE, James EK, Venter SN, Coetzee MPA. (2025) Estimated timeline for the evolution of symbiotic nitrogen fixing Paraburkholderia. Molecular Phylogenetics and Evolution 213:108447. 10.1016/j.ympev.2025.108447
Pham NQ, Liu FF, Duong TA, Wingfield BD, Chen SF, Wingfield MJ. (2025) Genetic diversity of Calonectria reteaudii isolates from infected Eucalyptus leaves and associated soils indicates a phyllosphere origin of the pathogen. Forest Pathology 55:e70037. 10.1111/efp.70037
Schröder ML, Hurley BP, Wingfield MJ, Slippers B, Garnas JR. (2025) Thermal limitations to the biological control of Gonipterus sp. n. 2 (Coleoptera: Curculionidae) in South African Eucalyptus plantations. Agricultural and Forest Entomology 10.1111/afe.70002
Lynn KMT, Wingfield MJ, Tarigan M, Durán A, Santos SA, Nel WJ, Barnes I. (2025) Investigating bark, ambrosia and nitidulid beetle (Coleoptera: Scolytinae and Nitidulidae) communities and their potential role in the movement of Ceratocystis manginecans in commercial forestry plantations in Riau, Indonesia. Agricultural and Forest Entomology 10.1111/afe.12698
Solís M, Hammerbacher A, Wingfield MJ, Naidoo S. (2025) Transcriptional responses of Eucalyptus to infection by an aggressive leaf blight pathogen reveal the role of host secondary metabolites during pathogen germination. Plant Molecular Biology 115 10.1007/s11103-025-01625-2
Coertze S, Coetzee B, Basson E, de Villiers D, Makhura T, Moster D, Slippers B, Rose LJ, Visagie CM, Read D. (2025) First Report of Clavibacter nebraskensis Causing Goss’s Bacterial Leaf Blight on Maize (Zea mays) in South Africa. Plant Disease 109:1580. 10.1094/PDIS-01-25-0164-PDN
Overy DP, Frisvad JC, Witte TE, Hicks CL, Hermans A, Sproule A, Louis-Seize G, Seifert KA, Yilmaz N, Price J, van Vuuren NI, Visagie CM. (2025) Chemodiversity of Penicillium isolated from alpine and arctic environments, including ten new species. Studies in Mycology 112:75–116. 10.3114/sim.2025.112.03
Harris MA, Kemler M, Slippers B, Hassel N, Tsamba J, Arthan W, Kellogg EA, AuBuchon-Elder T, Vorontsova MS, Archibald S, Hempson GP, Lehmann CER, Besnard G, Bergerow D, Brachmann A, Solofondranohatra CL, Greve M. (2025) Productivity drives leaf mycobiome diversity patterns at global and continetal scales. Global Ecology and Biogeography 34:e70094. 10.1111/geb.70094
Gao M, Yan Z, Liu Z, Jiang Y, Liu T, Miao X, Dai M, Bose T, Chang R. (2025) A novel Arthrobotrys species: Taxonomic characterization, nematicidal activity, and multi-omics insights into nematode predation. Biological Control 208:105853. 10.1016/j.biocontrol.2025.105853
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
Crous PW, Catcheside DEA, Catcheside PS, Alfenas AC, Alfenas RF, Barreto RW, Lebel T, Balashov S, Broadbridge J, Jurjević Å, De la Peña-Lastra S, Hoffmann R, Mateos A, Riebesehl J, Shivas RG, Soliz Santander FF, Tan YP, Altés A, Bandini D, Carriconde F, Cazabonne J, Czachura P, Gryta H, Eyssartier G, Larsson E, Pereira OL, Rigueiro-Rodríguez A, Wingfield MJ, Ahmad W, Bibi S, Denman S, Esteve-Raventós F, Hussain S, Illescas T, Luangsa-ard JJ, Möller L, Mombert A, Noisripoom W, Olariaga I, Pancorbo F, Paz A, PiÄ…tek M, Polman-Short C, Suárez E, Afshan NS, Ali H, Arzanlou M, Ayer F, Barratt J, Bellanger J, Bidaud A, Bishop-Hurley SL, Bohm M, Bose T, Campo E, Chau NB, Çolak ÃF, Cordeiro TRL, Cruz MO, Custódio FA, Couceiro A, Darmostuk V, Dearnaley JDW, De Azevedo Santiago ALCM, De Freitas LWS, Yáñez-Morales MDJ, Domnauer C, Dentinger B, Dhileepan K, De Souza JT, Dovana F, Eberhardt U, Eisvand P, Erhard A, Fachada V, García-Martín A, Groenewald M, Hammerbacher A, Harms K, Haroon S, Haqnawaz M, Henriques S, Hernández AJ, Jacobus LM, Jaen-Contreras D, Jangsantear P, Kaygusuz O, Knoppersen R, Kumar TKA, Lynch MJ, Mahiques R, Maraia GL, Marbach PAS, Mehrabi-Koushki M, Miller PR, Mongkolsamrit S, Moreau P, Oberlies NH, Oliveira JA, Orlovich D, Pérez-Méndez AS, Pinto A, Raja HA, Ramírez GH, Raphael B, Rodrigues A, Rodrigues H, Ramos DO, Safi A, Sarwar S, Saar I, Sánchez RM, Santana JS, Scrace J, Sales LS, Silva LNP, Stryjak-Bogacka M, Tacconi A, Thanh VN, Thomas A, Thuy NT, Toome M, Valdez-Carrazco JM, Van Vuuren NI, Vasey J, Vauras J, Vila-Viçosa C, Villarreal M, Visagie CM, Vizzini A, Whiteside EJ, Groenewald JZ. (2025) Fungal Planet description sheets: 1781–1866. Persoonia 54:327–587. 10.3114/persoonia.2025.54.10
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
Queffelec J, Allison JD, Slippers B, Greeff JM. (2025) Determinants of mating success in a lek-mating species. Agricultural and Forest Entomology :1-10. 10.1111/afe.12692
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