Natural and agroecosystems of the African continent are expected to be intensely vulnerable to climate change (Wheeler & Von Braun, ). This may impact particularly Sub‐Saharan countries, with negative cascading effects for land management and ecosystem health, food availability, and rural livelihoods (Müller, Waha, Bondeau, & Heinke, ; Schlenker & Lobell, ; Wheeler & Von Braun, ).
Trees, both in forests and on cropland in agroforestry settings, will play a pivotal role in the resilience and adaptation of African landscapes to these changes. Forests and tree cover on agricultural land have a vital function for the mitigation of climatic variations and carbon storage (Albrecht & Kandji, ; Bonan, ; Zomer et al., ). The overall forest cover in Africa is shrinking at the rate of almost 0.5% annually, due to deforestation of natural forests (FAO, ). Planted forests, which include production plantations, afforestation, and agroforestry, are however growing 1.3% annually, thus helping to partially reduce the overall loss of tree cover and carbon stock (FAO, ). The ecological and socioeconomic benefits from natural and planted forests will be increasingly crucial for Africa's capacity to face ecological and socioeconomic changes (Evans & Turnbull, ; Shackleton, Shackleton, Buiten, & Bird, ). In particular, agroforestry provides a variety of ecosystem services to smallholders in marginal lands. Planting trees moderates the effects of climatic extremes and plant pests on crops, reduces soil degradation and deforestation, and provides farmers with food, firewood, and timber (Mbow et al., ; Verchot et al., ).
In addition to trees in natural forests, both indigenous and introduced tree species are widely planted in forestry and agroforestry settings, and are crucial for the preservation of tree cover in Africa (Bennet & Kruger, ; Leakey et al., ). Eucalyptus, Pinus, Cupressus, and Acacia spp. are among the non‐indigenous trees dominating industrial plantation forestry across the continent (Evans & Turnbull, ), while the silk tree Grevillea robusta (Proteaceae) is an example of an important non‐indigenous tree used in small plantations and farms (Booth & Ekeleme, ). Indigenous African trees contribute immensely to the continent, and global, biodiversity. Africa counts some 4,500–6,000 tree species, of which 800 are documented to contribute significantly to food security (Linder, ; Slik et al., ; UNEP, ). The conservation of these resources will be crucial for Africa's future.
The introduction and establishment of non‐native invasive organisms are increasing globally, showing no saturation (Seebens et al., ), facilitated by accelerating global trade and amplified by climatic variations (Hellmann, Byers, Bierwagen, & Dukes, ; Meyerson & Mooney, ; Westphal, Browne, MacKinnon, & Noble, ). The spread of invasives in newly colonized regions reduces habitat biodiversity, disrupts ecosystem functioning, and harms economic development (Simberloff et al., ; Walsh, Carpenter, & Vander Zanden, ). Invasive plant pathogens and herbivorous arthropods in particular pose a devastating threat to the integrity of natural habitats, the productivity of agricultural commodities, and the sustainability of rural economies (Fisher et al., ; Lovett et al., ).
The global spread of tree pests and diseases of both natural and planted forests is also on the rise (Boyd, Freer‐Smith, Gilligan, & Godfray, ; Wingfield, Brockerhoff, Wingfield, & Slippers, ). In the United States, for instance, around 400 forest insect pests were detected during 1860 to 2006 (Aukema et al., ). In Europe, over 100 non‐native tree pathogens were introduced in the period 1800 to 2009 (Santini et al., ). These introductions have the potential to trigger deep effects on ecosystem functioning and services linked to tree‐based landscapes (Boyd et al., ; Ghelardini et al., ; Kenis et al., ). Major recent examples are the unprecedented devastation of ash trees in the North American natural and urban forests by the non‐native emerald ash borer Agrilus planipennis (Herms & McCullouhg, ), the widespread mortality of European ash Fraxinus excelsior by the ash dieback fungus Hymenoscyphus fraxineus, that is threatening to functionally remove the tree from landscapes (Burokiene et al., ), and the wave of native and non‐native arthropods and pathogens that are compromising the productivity of eucalypt plantations in its non‐native range, particularly in Africa (Burgess & Wingfield, ; Hurley et al., ; Wingfield et al., ).
Africa is increasingly susceptible to biological invasions (Paini et al., ; Pratt, Constantine, & Murphy, ). Due to vulnerable agroecosystems, weak cross border biosecurity, and limited intervention capacity, low‐income countries are more prone to suffering serious impacts from biological invasions (Early et al., ). The accelerating introduction and spread of non‐native and highly destructive arthropods and pathogens are triggering economic emergencies and local food crises. The newly introduced fall armyworm Spodoptera frugiperda (Lepidoptera: Noctuidae), for example, is devastating maize resources in numerous African countries just 2 years following detection (Nagoshi et al., ). The cumulative economic impact of invasives in Africa is expected to exceed 1.2 billion dollars per year (Pratt et al., ). Considering recent and imminent introductions this prediction may be underestimated, and the total invasion cost as proportion of gross domestic product (GDP) for many African countries is among the highest globally (Paini et al., ). This raises the stakes for developing locally appropriate management strategies across the continent.
Cultivation of important indigenous and introduced tree species in Africa is being increasingly targeted by new and old‐time invaders, which are locally disrupting the sustainability of plantation forestry, frustrating the benefits of agroforestry, and threatening the continent’s biodiversity (Crous et al., ; FAO, 2009a; Nair, ; Schroth, Krauss, Gasparotto, Aguilar, & Vohland, ; Speight, ; Wingfield et al., ). This highlights the urgency for coordinating efforts to limit accidental introduction of these organisms and mitigate their impact (Wingfield et al., ). We sought to provide an overview of emerging insects and pathogens targeting trees in Africa, discuss implications for further studies and management, and raise awareness about this threat for the conservation of indigenous and introduced trees in Africa.
Numerous native and non‐native species of herbivorous insects and pathogenic microorganisms are reported to be harming indigenous and exotic trees in plantations, natural forests, and agroforestry systems across Africa. The Food and Agriculture Organization of the United Nations (FAO) (, ) report approximately 100 species of insects and pathogens affecting trees in planted and natural forests across northern, western, eastern, central, and southern African countries (Ghana, Kenya, Malawi, Mauritius, Morocco, South Africa, Sudan). Only half of these species are identified as native organisms, while over one third are non‐native invaders, and 15% are of unknown origin. Non‐native species represent over one third of insects known to damage trees, while almost two thirds of pathogens are non‐native or of unknown origin (Figure ). Broadleaf trees are affected the most, with only one third of insect and pathogen species attacking conifers. This pattern reflects the composition of native flora, constituted for the majority of broadleaves and with numerous conifers introduced as exotic plantation trees (Craib, ). Introduced pests and diseases are targeting for the majority planted forests, with approximately 90% of pathogens of plantation forestry being non‐native or of uncertain origin. In the last few decades, new invaders have become established and spread across African landscapes, adding to the damage caused by old invaders and natives to natural and planted forests, and to indigenous and introduced tree species. The number of pests and diseases targeting plantation forestry is substantial. Over 47 native and 19 non‐native defoliators, sap‐feeders, wood, and shoot borers are harming Acacia mearnsii (Fabaceae), Eucalyptus spp. (Myrtaceae), Pinus spp. (Pinaceae) and teak tree, Tectona grandis (Lamiaceae), plantations (Hurley, Slippers, Sathyapala, & Wingfield, ), while 15 species of pathogens are described to cause major damage to eucalypts (Wingfield et al., ).
Overview of pests and diseases of natural and planted forests reported in Africa: (a) native and non‐native insects and pathogens; (b) native and non‐native insects and pathogens affecting conifer and broadleaf tree host; (c) native and non‐native insects; and (d) pathogens targeting natural or planted forests, or both types FAO (), FAO (). 1Includes pathogens of unknown origin. (Source: FAO (, ))
We collected information on native and non‐native insect pests and pathogens of trees reported in Africa using available reviews (FAO, 2009a, 2009b; Hurley et al., ; Nair, ; Roux et al., ; Wingfield et al., ), recent reports (Gichora, Kojwang, & Bosu, ), and invasive species compendiums to determine geographical distribution and to access additional literature (CABI, ; EPPO, ). We seek to present here a near‐exhaustive updated overview of highly significant arthropods and microorganisms affecting trees in Africa based on ecological or economic impact, widespread occurrence, or recent detection.
An updated list of relevant native insect pests reported on indigenous and exotic trees is presented in Table . Coleopteran stem and seed borers, lepidopteran defoliators, stem and shoot borers, and sap‐feeding hemipterans are the major groups of native pests, with several taxa affecting important indigenous trees. Among coleopterans, the seed borer Bruchidius uberatus (Coleoptera: Bruchidae) is a relevant pest of Vachellia (=Acacia) species (Fabaceae), and the stem borer Sphenoptera chalcichroa (Coleoptera: Buprestidae) is damaging Vachellia nilotica, an important tree of South African savannah (Atta, ; Delobel, ). The productivity of West African indigenous timber trees Triplochiton scleroxylon (Malvaceae), and African teak Milicia excelsa and M. regia (Moraceae), is affected by native psyllids Diclidophlebia eastopi, Phytolyma fusca (African teak gall bug), and P. lata (Iroko gall bug) (Hemiptera: Psyllidae), respectively (Bosu, Cobbinah, Nichols, Nkrumah, & Wagner, ; Ugwu & Omoloye, ; Wagner, Cobbinah, & Bosu, 2008a; Youmbi, Yana, & Tamesse, ). Among lepidopterans, the shoot borer Orygmophora mediofoveata (Lepidoptera: Noctuidae) is a significant pest that complicates cultivation of West African timber tree Nauclea diderrichii (Rubiaceae), targeting young trees and seedlings in nurseries (Bosu, Acquah, & Boamah, ). The defoliator Lamprosema lateritialis (Lepidoptera: Pyralidae) is a major forest pest in Ghana and Malawi, where it causes seedling mortality on Pericopsis elata (Fabaceae), an endangered tree species (Atuahene & Doppelreiter, ; IUCN, ; Wagner, Cobbinah, & Bosu, 2008b).
Native insect pests of indigenous and exotic trees in natural and planted forests (including agroforestry) reported in AfricaSpecies | Common name | Damage | Tree host | Host | Distribution |
Coleoptera | |||||
Bruchidius uberatus | Seed beetle | SE | I | Vachellia spp. | Widespread |
Sphenoptera chalcichroa | Silver tree borer | ST | I | Vachellia nilotica, V. arabica | SU |
Analeptes trifasciata | Long‐horned beetle | ST | I, N | Tectona grandis, Adansonia digitata, Eucalyptus spp. | W Africa |
Apate monachus | Black borer | ST | I, N | Azadirachta indica, Terminalia spp., others | Widespread |
Apate terebrans | Shot hole borer | ST | I, N | Tectona grandis, Terminalia, Khaya, Eucalyptus spp. | BE, GH, ZM |
Caryedon serratus | Tamarind seed beetle | SE | I, N | Vachellia, Acacia, Tamarindus spp., others | Widespread |
Ellimenistes laesicollis | (Weevil) | DE | I, N | Eucalyptus spp., Grevillea robusta, others | SA |
Hypopholis sommerii | Wattle chafer | DE | I, N | Acacia mearnsii, Eucalyptus, Pinus spp. | SA |
Platypus cylindrus | Cork oak ambr. beetle | ST | I, N | Quercus suber | AL |
Sphenoptera fulgens | Root‐boring beetle | ST | I, N | Prosopis chilensis, others | SU |
Chaetastus tuberculatus | (Ambrosia beetle) | ST | N | Eucalyptus spp. | GH |
Colasposoma spp. | (Leaf beetle) | D | N | Acacia mearnsii, Eucalyptus, Pinus spp. | SA |
Doliopygus spp. | (Ambrosia beetle) | ST | N | Tectona grandis, Eucalyptus spp. | GH |
Hypothenemus spp. | (Bark beetle) | ST | N | Tectona grandis | GH |
Monochelus calcaratus | Wattle chafer | DE | N | Acacia mearnsii | SA |
Oemida gahani | (Long‐horned beetle) | ST | N | Cupressus | W Africa, KE |
Platypus lintzi | (Ambrosia beetle) | ST | N | Eucalyptus spp. | GH |
Xyleborus perforans | Island pinhole borer | ST | N | Eucalyptus spp. | GH |
Hemiptera | |||||
Diclidophlebia eastopi | (Psyllid) | SP | I | Triplochiton scleroxylon | W Africa |
Phytolyma fusca | African teak gall bug | SP | I | Milicia excelsa | W Africa |
Phytolyma lata | Iroko gall bug | SP | I | Milicia regia | W Africa |
Helopeltis anacardii | (Mirid) | SP | N | Eucalyptus spp. | MW |
Lygidolon laevigatum | Black wattle mirid | SP | N | Acacia mearnsii | SA |
Parasaissetia nigra | Black scale | SP | N | Eucalyptus spp. | GH |
Planococcoides njalensis | Cocoa mealybug | SP | N | Tectona grandis | GH |
Saissetia coffeae | Hemispherical scale | SP | N | Eucalyptus spp. | GH |
Isoptera | |||||
Various Isoptera spp. | Termites | WO | I, N | Acacia, Eucalyptus, Cupressus spp. | SU, others |
Lepidoptera | |||||
Anaphe venata | African silk moth | DE | I | Triplochiton scleroxylon | GH, NI |
Lamprosema lateritialis | Leaf tying moth | DE | I | Pericopsis elata | GH, MW |
Operophtera brumata | Winter moth | DE | I | Quercus afares | AL, TU |
Orygmophora mediofoveata | Shoot borer | SH | I | Nauclea diderrichii | W Africa |
Diacrisia spp. | (Tiger moth) | DE | I, N | Tectona grandis, Eucalyptus spp., others | GH |
Gonometa podocarpi | Wild silkmoth | DE | I, N | Podocarpus, Cupressus, Pinus, Acacia, Eucalyptus | E Africa |
Hypsipyla robusta | Mahogany shoot borer | SH | I, N | Khaya, Entandrophragma, Eucalyptus spp. | E Africa, W Afr. |
Thaumetopoea pityocampa | Processionary moth | DE | I, N | Pinus spp. | N Africa |
Achaea lienardi | (Erebid moth) | DE | N | Acacia mearnsii | SA |
Ascotis selenaria | Giant looper | DE | N | Eucalyptus spp., Tectona grandis | GH, NI |
Biston (Buzura) spp. | (Looper) | DE | N | Eucalyptus spp. | S Africa |
Chaliopsis junodi | Wattle bagworm | DE | N | Acacia mearnsii | SA |
Cleora herbuloti | Pine looper | DE | N | Eucalyptus, Pinus spp. | SA |
Coryphodema tristis | Quince borer | ST | N | Eucalyptus nitens, Malus domestica, others | SA |
Euproctis spp. | (Tussock moth) | DE | N | Acacia mearnsii, Eucalyptus, Pinus spp. | GH, SA |
Gynanisa maia | Speckled emper. moth | DE | N | Acacia mearnsii | SA |
Holocerina smilax | (Emperor moth) | DE | N | Pinus spp. | SA |
Imbrasia spp. | (Emperor moth) | DE | N | Acacia mearnsii, Eucalyptus, Pinus spp. | SA |
Narosa viridana | (Slug caterpillar moth) | DE | N | Eucalyptus spp. | ZM |
Neocleosa spp. | (Looper) | DE | N | Eucalyptus spp. | S Africa |
Orgyia basali | (Tussock moth) | DE | N | Tectona grandis, Eucalyptus spp. | GH, NI |
Eutricha capensis | Cape lappet moth | DE | N | Acacia mearnsii, Eucalyptus, Pinus spp. | SA |
Pseudobunaea irius | (Emperor moth) | DE | N | Acacia mearnsii, Eucalyptus, Pinus spp. | SA |
Strepsicrathes rhothia | (Tortricid moth) | DE | N | Eucalyptus spp. | GH |
Thaumetopoea wilkinsoni | Processionary moth | DE | N | Pinus, Cedrus spp. | N Africa |
Xanthisthisa tarsispina | Pine looper | DE | N | Pinus spp. | MW |
Orthoptera | |||||
Anacridium melanorhoden | Sahelian tree locust | DE | I | Acacia senegal; Balanites aegyptiaca, others | SE |
Manowia spp. | (Eumastacidae grasshop.) | DE | N | Pinus spp. | MW |
Phymateus kazschi | (Milkweed locust) | DE | N | Eucalyptus spp. | GH, NI |
Species are arranged by insect order and origin of tree hosts (indigenous, introduced, or both). We included common name of insect species, when available, or common names of species’ taxonomic group (subfamily, family, or order), in parenthesis. Sources: Nair (), FAO (, ), Gichora et al. (), Hurley et al. (), and additional sources as included in the text.
2Damage: ST = stem borer, SE = seed borer, SP = sap feeder, DE = defoliator, SH = shoot borer, WO = wood feeder.
3Tree host: I = indigenous, N = introduced (exotic).
4Distribution: C Africa = Central Africa, E Africa = Eastern Africa, N Africa = Northern Africa, S Africa = Southern Africa, W Africa = Western Africa, widespread = present in Northern, Eastern, Western, Central and Southern Africa, AL = Algeria, BE = Benin, GH = Ghana,, MW = Malawi, NI = Nigeria, SA = South Africa, SE = Senegal, SU = Sudan, TU = Tunisia, ZM = Zambia.
Numerous native insect species known as pests of indigenous trees are reported to widen their host range and cause damage to exotic trees. Long‐horned beetles such as stem girdlers Analeptes and Paranaleptes spp. (Coleoptera: Cerambycidae) can cause severe damage to a wide range of indigenous trees including baobab Adansonia digitata and Bombax costatum (Malvaceae), as well as non‐indigenous teak tree T. grandis, eucalypts, and cashew, Anacardium occidentale (Anacardiaceae) (Asogwa, Ndubuaku, & Hassan, ; Jones, ; Lyimo, ). Another native coleopteran, Apate monachus (Coleoptera: Bostrichidae), is a common borer affecting indigenous Terminalia spp. (Combretaceae) and exotic neem tree Azadirachta indica (Meliaceae), while congeneric A. terebrans inflicts severe damage to African mahogany Khaya spp. (Meliaceae), and cultivated teak and eucalypts (Agboton et al., ; Becker, ). The quince borer Coryphodema tristis (Lepidoptera: Cossidae) is a wood borer with a wide range of native hosts, but has recently become a major pest of eucalypt plantations in South Africa (Adam, Mutanga, & Ismail, ). The wattle mirid Lygidolon laevigatum (Hemiptera: Miridae) is a major pest of the exotic black wattle, Acacia mearnsii (Fabaceae) in forestry plantations in South Africa, where it causes irregular branching and defoliation (Govender, ; Ingham, Samways, & Govender, ). Termites feed on wood within the wood‐soil interface, and various species can locally cause severe damage to young plantings of several indigenous and exotic trees (Ambele, Bisseleua Daghela, Babalola, & Ekesi, ).
Numerous non‐native tree pests of plantation forestry trees have invaded Africa in the past 100 years, and the accumulation of invaders has progressively increased in the last few decades (Table ). Eucalyptus long‐horned borers Phoracantha semipunctata and Phoracantha recurva (Coleoptera: Cerambycidae) are two stem borers introduced in the early 1900s in South Africa, and currently impacting eucalypt production in northern and southern African countries (Paine, Steinbauer, & Lawson, ). The Eucalyptus snout beetle Gonipterus scutellatus, the deodar weevil Pissodes nemorensis (Coleoptera: Curculionidae), and the teak defoliator Hyblaea puera (Lepidoptera: Hyblaeidae) are also historic invaders; detected in South Africa in the first half of the 20th century quickly established as important pests for eucalypts, pines, and teak, respectively (Gebeyehu & Wingfield, ; Hurley et al., ; Newete, Oberprieler, & Byrne, ). Non‐native aphids are major pests of exotic conifers in Africa (Hemiptera: Aphididae). The pine woolly aphid Pineus pini and the pine needle aphid Eulachnus rileyi where introduced several decades ago and then spread to most regions of the continent, while the distribution of black pine aphid Cinara cronartii is still limited to southern Africa (Day et al., ; Odendaal, ; Zwolinski, ). The cypress aphid Cinara cupressi was introduced some 30 years ago and currently occurs in all the main cypress‐growing areas, reducing the productivity of exotic cypress plantations, but also affecting native African cedar Juniperus procera (Cupressaceae), which natural populations in native range are declining (IUCN, ; Watson, Voegtlin, Murphy, & Foottit, ).
Non‐native insect pests of indigenous and exotic trees in natural and planted forests (including agroforestry) reported in AfricaSpecies | Common name | Damage | Year detection | Tree host | Host | Distribution |
Coleoptera | ||||||
Hylurgus ligniperda | Red‐haired p. bark beetle | ST | 1885 | N | Pinus spp. | SA |
Phoracantha semipunctata | Eucalyptus long‐horn. bor. | ST | 1906 | N | Eucalyptus spp. | N Africa, S Africa |
Phoracantha recurva | Lesser Euc. long‐horn. bor. | ST | 1906 | N | Eucalyptus spp. | N Africa, S Africa |
Gonipterus scutellatus | Eucalyptus snout beetle | DE | 1916 | N | Eucalyptus spp. | E Africa, S Africa |
Hylastes angustatus | Pine bark beetle | ST | 1930 | N | Pinus spp. | SA |
Pissodes nemorensis | Deodar Weevil | DE | 1942 | N | Pinus spp. | SA |
Orthotomicus erosus | Mediterr. pine engraver | ST | 1968 | N | Pinus spp. | SA |
Trachymela tincticollis | Eucalyptus tortoise beetle | DE | 1982 | N | Eucalyptus spp. | SA |
Hemiptera | ||||||
Ctenarytaina eucalypti | Blue gum psyllid | SP | 1958 | N | Eucalyptus spp. | KE, SA |
Pineus pini | Pine woolly aphid | SP | 1960s | N | Pinus spp. | E, N, S Africa |
Pineus boerneri | Pine woolly aphid | SP | 1960s | N | Pinus spp. | E Africa, S Africa |
Eulachnus rileyi | Pine needle aphid | SP | 1970s | N | Pinus spp. | C, E, N, S Africa |
Cinara cronartii | Black pine aphid | SP | 1974 | N | Pinus spp. | SA |
Aonidiella orientalis | Oriental yellow scale | SP | 1985 | N | Azadirachta indica | W Africa |
Cinara cupressi sensu lato | Cypress aphid | SP | 1986 | I, N | Cupressus, Juniperus spp. | C, E, N, S Africa |
Heteropsylla cubana | Leucaena psyllid | SP | 1992 | N | Leucaena, Mimosa spp. | E, N, S, W Africa |
Thaumastocoris peregrinus | Bronze Bug | SP | 2003 | N | Eucalyptus spp. | E, S Africa |
Blastopsylla occidentalis | Eucalyptus psyllid | SP | 2006 | N | Eucalyptus spp. | SA |
Glycaspis brimblecombei | Red gum lerp psyllid | SP | 2012 | N | Eucalyptus spp. | N, S Africa |
Spondyliaspis cf. plicatuloides | Shell lerp psyllid | SP | 2014 | N | Eucalyptus spp. | SA |
Hymenoptera | ||||||
Sirex noctilio | Sirex Woodwasp | WB | 1994 | N | Pinus spp. | N Africa, S Africa |
Leptocybe invasa | Blue gum chalcid | GM | 2000 | N | Eucalyptus spp. | E, N, S Africa |
Ophelimus maskelli | Eucalyptus gall wasp | GM | 2002 | N | Eucalyptus spp. | N, S Africa |
Lepidoptera | ||||||
Hyblaea puera | Teak defoliator | DE | Old invader | N | Tectona grandis | E Africa, S Africa |
Species are arranged by insect order and then chronologically by year of detection. Sources: Nair (), Wingfield et al. (), FAO (, ), Gichora et al. (), Hurley et al. (), CABI () and EPPO (), and additional sources as included in the text.
6Damage: ST = stem borer, SE = seed borer, SP = sap feeder, DE = defoliator, WB = wood borer, GM = gall maker.
7Tree host: I = indigenous, N = introduced (exotic).
8Distribution: C Africa = Central Africa, E Africa = Eastern Africa, N Africa = Northern Africa, S Africa = Southern Africa, W Africa = Western Africa, SA = South Africa.
The wood borer Sirex noctilio (Hymenoptera: Siricidae), a global pest of Pinus spp. native to Europe, Asia, and Mediterranean Africa, was accidentally introduced and detected in South Africa in 1994, where it caused a major outbreak and tree mortality in pine plantations (Tribe & Cillié, ). Five new non‐native pests feeding on eucalypt leaves, which included three hemipterans and two hymenopteran gall makers, were introduced from Australia to South Africa since 2002 (Bush et al., ). The shell lerp psyllid Spondyliaspis cf. plicatuloides (Hemiptera: Psyllidae) is the most recent of those invaders, and is currently reported in other countries (Bush et al., ). Following detection, the red gum lerp psyllid Glycaspis brimblecombei and the bronze bug Thaumastocoris peregrinus (Hemiptera: Thaumastocoridae) spread quickly, colonizing other countries in southern and northern Africa the former, and in southern and Eastern Africa the latter (Attia & Rapisarda, ; Ndela, Manyangadze, Sachisuko, Lingen, & Makowe, ; Saavedra, Avila, Withers, & Holwell, ). A similar pattern of invasion is observed for the gall makers blue gum chalcid Leptocybe invasa and Eucalyptus gall wasp Ophelimus maskelli (Hymenoptera: Eulophidae). Within a few years from first introduction to the continent, O. maskelli was detected in Algeria, Morocco, and Tunisia, and L. invasa spread to several countries in northern and Eastern Africa (Asfaw, ; Nyeko, Mutitu, Otieno, Ngae, & Day, ).
Microbial pathogens of trees are increasingly affecting the health of natural and planted forests in the continent, with well‐known diseases and multiple recent detections of new species in the continent (Table ). While in many cases it is not always possible to determine the geographic origin of these organisms due to their cryptic nature, non‐native pathogens have a long history in the continent. Armillaria root rot pathogens were introduced by early settlers in South Africa with potted plants from Europe in the 1600s (Coetzee et al., ). The disease was first observed decimating planted pine and eucalypt in the early 1900s and later in Eastern Africa, but is now impacting native plants in woody landscapes in South Africa and Ethiopia (Coetzee, Wingfield, & Wingfield, ; Gezahgne, Coetzee, Wingfield, Wingfield, & Roux, ; Gibson, ). Eucalypts are hosts of several global plant pathogens. Anthracnose caused by Colletotrichum spp., including widespread C. gloeosporioides, are a problem in eucalypt plantations and nurseries as they have wide host ranges including several fruit trees for which they are known to cause post harvest disease (Mangwende, Aveling, & Chirwa, ). Root rots and blights caused by Phytophthora spp. are an important group of emerging pathogens, as they are one of the major sources of damage to plantations and can affect indigenous trees. Phytophthora cinnamomi causes root rot of eucalypts in South Africa and Kenya, and basal canker of A. mearnsii in South Africa, but also impacts natural vegetation, such as native Proteaceae of South Africa (Brasier, ; Nagel, Gryzenhout, Slippers, & Wingfield, ). Recent surveys show an incredible diversity of Phytophthora taxa in the country, suggesting an imminent threat to natural ecosystems (Oh, Gryzenhout, Wingfield, Wingfield, & Burgess, ).
Pathogens of indigenous and exotic trees in natural and planted forests (including agroforestry) reported in AfricaSpecies | Common name | Damage | Year detection | Tree Host | Host species | Distribution |
Ascomycota | ||||||
Lasiodiplodia theobromae | ‐ | SB, CA | ‐ | I | Boswellia, Eucalyptus spp., other | ET, SA, UG |
Diplodia sapinea | Sphaeropsis blight | FD, SB, CA | 1912 | N | Pinus spp. | E, S Africa |
Aulographina eucalypti | Corky Leaf Spot | FD | 1928 | N | Eucalyptus spp. | KE, SA, ZM |
Fairmaniella leprosa | Fairmaniella leaf spot | FD | 1928 | N | Eucalyptus spp. | SA |
Mycosphaerella spp. | Mycosphaerella leaf blotch | FD | 1935 | N | Eucalyptus spp. | E, S Africa |
Kirramyces epicoccoides | Phaeophleospora leaf spot | FD | 1988 | N | Eucalyptus spp. | KE, SA |
Teratosphaeria zuluense | Coniothyrium stem canker | CA | 1988 | N | Eucalyptus spp. | ET, MA, MZ, SA, UG |
Chrysoporthe spp. | Chrysoporthe canker | CA | 1989? | I, N | Eucalyptus spp, Syzygium cordatum | KE, MA, MZ, SA |
Colletotrichum spp. | Anthracnose | FD | 1980s | I, N | Eucalyptus spp., Proteaceae, other | ET, SA |
Fusarium circinatum | Pitch canker | CA, RR | 1990 | N | Pinus spp. | SA |
Cylindrocladium spp. | Cylindrocladium leaf blight | FD | 1991 | N | Eucalyptus spp. | KE, CO, SA |
Botryosphaeriaceae spp. | Euc. Botryosphaeria canker | CA | 1994 | N | Eucalyptus spp. | ET, KE, SA, UG |
Holocryphia eucalypti | Endothia canker | CA | 1993 | N | Eucalyptus spp. | SA, UG |
Ceratocystis fimbriata | Ceratocystis wilt | CA, WI | 1998 | N | Eucalyptus spp. | CO, CT, SA, UG |
Ceratocystis spp. | Wattle wilt | CA, WI | 1990s | I, N | Eucalyptus spp., Acacia mearnsii | CO, E, S Africa |
Botryosphaeriaceae spp. | Botryosphaeria cankers | CA | 2000s | I, N | Pinus, Acacia spp. | SA |
Botryosphaeriaceae spp. | Grevillea stem canker | CA | 2001 | N | Grevillea robusta | KE, UG |
Teratosphaeria gauchensis | Eucalyptus stem canker | CA | 2013 | N | Eucalyptus spp. | KE |
Basidiomycota | ||||||
Armillaria spp., A. mellea | Armillaria root rot | RR | 1900s | I, N | Eucalyptus, Pinus spp., other | ET, KE, MA, SA, TA |
Erythricium salmonicolor | Pink disease | CA | 1993 | I, N | Eucalyptus, Acacia, Podocarpus | ET, SA |
Quambalaria eucalypti | Quambalaria blight | FD, SB | 1993 | N | Eucalyptus spp. | SA |
Amylostereum areolatum | (symbiont of Sirex noctilio) | WR | 1994 | N | Pinus spp. | SA |
Phakopsora myrtacearum | Eucalyptus rust | FD | 2009 | N | Eucalyptus spp. | KE, MZ, SA |
Puccinia psidii | Eucalyptus rust | FD | 2013 | N | Eucalyptus spp., Myrtaceae | KE |
Oomycota | ||||||
Phytophthora cinnamomi | Phytophthora root rot | RR | 1980 | I, N | A. mearnsii, Eucalyptus, Proteaceae | KE, SA |
Pythium splendens | Pythium root rot | RR | Native | N | Eucalyptus spp. | SA |
Proteobacteria | ||||||
Ralstonia solanacearum | Bacterial canker | CA | 2000 | N | Eucalyptus spp. | SA |
Pantoea spp. | Bacterial canker | CA | 2001 | N | Eucalyptus spp. | SA |
Organisms are arranged by taxonomic group and then chronologically by year of detection. Sources: Roux et al. (), Wingfield et al. (), FAO (2009a, 2009b), Gichora et al. (), CABI () and EPPO (), and additional sources as included in the text.
10Damage: CA = canker, DI = dieback, FD = foliar disease (leaf spot, foliar blight, blotch or rust), SB = shoot blight, RR = root rot, WI = wilt, WR = white rot.
11Tree host: I = indigenous, N = introduced (exotic).
12Distribution: C Africa = Central Africa, E Africa = Eastern Africa, N Africa = Northern Africa, S Africa = Southern Africa, W Africa = Western Africa, widespread = present in Northern, Eastern, Western, Central and Southern Africa, CO = Republic of Congo, CT = Côte d'Ivoire, ET = Ethiopia, KE = Kenya, MA = Madagascar, MZ = Mozambique, SA = South Africa, TA = Tanzania, UG = Uganda, ZM = Zambia.
13Detected in 1994.
Following a similar trend to the one described for some insect pests, many pathogens of Eucalyptus spp. are discovered and described in important eucalypt producing countries, then are later found in other African countries. The canker causing pathogen Teratosphaeria zuluense was detected in South Africa and later reported also from East Africa (Gezahgne, Cortinas, Wingfield, & Roux, ). The agent of pink disease Erythricium salmonicolor was first described in Ethiopia on Eucalypt, then appeared in South Africa where it is now infecting indigenous forest trees including native conifer Podocarpus spp. (Podocarpaceae), and Ekebergia capensis (Meliaceae) (Roux & Coetzee, ). Similarly, the canker pathogen Chrysoporthe spp. was first reported on Eucalyptus in South Africa, now are occurring in many countries, also affecting indigenous Syzygium trees (Nakabonge, Roux, Gryzenhout, & Wingfield, ).
Africa is also affected by global pathogens of Pinus spp. (Burgess & Wingfield, ). The agent of Sphaeropsis blight and cankers Diplodia sapinea was reported some 100 years ago, but is still a major threat to pine health, and able to infect other Cupressus spp. (Bihon, Slippers, Burgess, Wingfield, & Wingfield, ; Linde, Kemp, & Wingfield, ; Swart, Knox‐Davies, & Wingfield, ). The agent of pitch canker Fusarium circinatum is among the recent invaders: detected in South Africa in 1990 affecting pine seedlings in nurseries, it caused an outbreak in pine plantation 10 years ago, and is now spreading in the country (Coutinho, Steenkamp, Mongwaketsi, Wilmot, & Wingfield, ). The white rot fungus Amylostereum areolatum is a symbiont of the wood wasp S. noctilio, and was introduced with its insect vector to South Africa, where it causes extensive damage to pine stands in combination with the wood wasp (Slippers, Wingfield, Coutinho, & Wingfield, ).
The ascomycete family Botryosphaeriaceae contains a group of relevant emerging diseases in the continent, with several species involved in novel disease complexes. Lasiodiplodia theobromae is a long‐time known native pathogen, producing cankers on many indigenous species and eucalypts (Mohali, Burgess, & Wingfield, ; Roux, Coutinho, Byabashaija, & Wingfield, ). Non‐native Botryosphaeriaceae species are causing stem cankers of Eucalyptus (Gezahgne, Roux, Slippers, Wingfield, & Hare, ; Roux et al., ; Slippers et al., ) and two other species are associated with stem cankers and major dieback to the silk tree G. robusta in East Africa (Njuguna et al., 2011). Some Botryosphaeriaceae species are latent pathogens infecting a wide range of hosts from planted Pinus spp. to indigenous Acacia and others, thus raising concerns on imminent diseases of important indigenous species caused by Botryosphaeriaceae (Jami, Slippers, Wingfield, & Gryzenhout, ; Jami, Wingfield, Gryzenhout, & Slippers, ). Dieback of large baobab trees was recently reported from southern Africa: various microorganisms were described to be associated with symptoms, but the causes are still uncertain (Cruywagen, Crous, Roux, Slippers, & Wingfield, ; Cruywagen, Slippers, Roux, & Wingfield, ).
Indigenous and exotic trees in Africa are affected by a multitude of native and non‐native insect pests and microbial pathogens, with detrimental consequences for African natural and planted forests, agroecosystems, and rural communities (Crous et al., ; FAO, 2009a; Gichora et al., ; Hurley et al., ; Roux et al., ; Wingfield et al., ). The rate of introduction of non‐natives is increasing (Figure ). This should be considered as an emergency that adds to the effects of climate change on the continent, and calls for strategies that provide smallholders and land managers with tools to mitigate such impact quickly, and ultimately preserve the productivity of natural resources (Challinor, Wheeler, Garforth, Craufurd, & Kassam, ; Lobell et al., ). The effects of climate change on non‐natives’ introduction and spread, pests and disease ecology, and ecosystem vulnerability will challenge the ability to predict their impact and implement management programs on the continent (Allen et al., ; Anderson et al., ; Dukes et al., ; Ramsfield, Bentz, Faccoli, Jactel, & Brockerhoff, ).
Cumulative detections of established non‐native pests and diseases (and both) of natural and planted forests in Africa for the years 1900–2013. We considered detections of non‐native species (or species of unknown origin) presented in Tables and
Invasion pathways are shaping the pattern of introduction and spread on the continent and determining taxonomy of plant hosts affected by non‐native organisms. South Africa is a major port of entry for many arthropods and pathogens targeting exotic Eucalyptus, Pinus, and Acacia spp. in planted forests. Some non‐native Eucalyptus pests are initially established in the southern and then northern part of Africa, but are now colonizing other regions as a result of accidental intracontinental introductions and spread. For instance, the number of Eucalyptus pests introduced to South Africa from other biogeographic regions surpasses the number of Eucalyptus pests introduced elsewhere in Africa (Faulkner, Hurley, Robertson, Rouget, & Wilson, ). Faulkner et al. () found that eucalypt pests introduced to South Africa and then spread elsewhere in the continent are more numerous than predicted, and significantly more numerous compared to the number of pests introduced elsewhere in Africa which then spread to South Africa.
The geographic distribution of non‐native pests and pathogens detection (Figure ) may be explained by two main factors. First, the higher capacity of some country‐level national plant protection organizations to detect introductions and track the spread of invasives. Secondly, the activity of local plantation forestry sectors might facilitate introductions of pests and diseases of non‐indigenous trees through international exchange of improved plant material. This highlights the risk of introducing invasives through forestry and the consequences for management (Burgess & Wingfield, ; Wingfield et al., ; Wingfield, Roux, Coutinho, Govender, & Wingfield, ; Wingfield, Slippers, Roux, & Wingfield, ).
Geographic distribution of detections of non‐native pests and diseases invading natural and planted forests in Africa. We considered first detections in the African continent of non‐native species (or unknown origin) presented in Tables and . (Satellite image: Africa vegetation map 2004, https://www.earthobservatory.nasa.gov)
Local economic growth and increasing global trade with African countries will likely accelerate the rate of invasions further, while climate change could exacerbate invasibility and impact (Hulme, ; Paini et al., ). In this scenario, we emphasize the urgent need for improving plant biosecurity in Africa and developing effective control options for managing invasives, but efforts require coordination at regional and international level (Burgess, Crous, Slippers, Hantula, & Wingfield, ; Wingfield et al., ). The reinforcement of phytosanitary barriers at country and regional level through improved diagnostic tools, updated plant exchange regulations, and renewed trade policies will be the key in reducing accidental introduction and spread of invasives, (Mumford, Macarthur, & Boonham, ; Robert, Orden, & Josling, ; Roy et al., ; Wingfield et al., ). Because of their cryptic nature and variable lag times, and the limited detection capacity of some countries, numerous non‐native pathogenic microorganisms may have been introduced and established without discovery.
Highly efficient and long‐term effective management options such as biological control, innovative silviculture practices, and selection of resistant trees could be the answer for mitigating the impact of biotic threats (Garnas, Hurley, Slippers, & Wingfield, ; Sollars et al., ; Wingfield et al., ; Wingfield & Swart, ). Biological control has been used successfully against several non‐native insects (Garnas et al., ), and development of resistant exotic tree clones for forest plantations is promising (Oates, Külheim, Myburg, Slippers, & Naidoo, ; Wingfield et al., ). Furthermore, the opportunity for managing resistance of indigenous African tree species is worthy of attention. Relevant programs for the conservation of tree germplasm and domestication of indigenous species in Africa have been implemented, and numerous field gene banks of high‐priority indigenous trees have been deployed across African eco‐regions (Dawson et al., ; ICRAF, ). Such programs offer the opportunity to evaluate the susceptibility of multiple provenances of indigenous taxa to pests and pathogens, and represent a very valuable resource for selecting resistant trees. As domestication of indigenous trees for use in agroforestry progresses, resistant varieties could be the right tool to manage emerging pests and pathogens in small plantings and farm settings.
The invasion of African natural and planted forests by biotic threats is a growing emergency of continental scale, with pervasive and long‐lasting harmful effects on livelihoods and ecosystems. This is calling for action. There is a compelling need for coordinated responses at continent and international level that aim to reduce the gap in intervention capacity among African countries, consider region‐specific ecological differences, and integrate innovative policy, management, and knowledge dissemination tools.
We thank Simon Kang'ethe, Zakayo Kinyanjui, and Ramni Jamnadass for providing information and advice, and Lynne Rieske‐Kinney for kindly reviewing this manuscript.
I.G. planned and designed the manuscript, prepared tables and images, and led the manuscript preparation, I.G., M.T., J.K. and A.M provided information included in the manuscript and contributed to writing.
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Abstract
An increasing multitude of insect pests and pathogens is targeting indigenous trees of natural forests, agroforestry systems, and exotic trees in planted forests in Africa. This is raising major concerns for a continent already challenged by adaptations to climate change, as it threatens a vital resource for food security of rural communities, economic growth, and ecosystem conservation. The accidental introduction through trade of non‐native species in particular is accelerating, and it adds to the damage to tree‐based landscapes by native pests and diseases. Old‐time and new invaders heavily impact planted forests of exotic eucalypts, pines, and acacias, and are spreading quickly across African regions. But many non‐native pathogens are recently found affecting important indigenous trees. We describe the threat to African trees by providing an overview of highly relevant insect pests and diseases of indigenous and exotic trees in Africa, and discuss implications for management and future research. The implementation of an integrated and globally coordinated approach based on improved biosecurity, biological control, and tree resistance would contribute to mitigate the potentially devastating impact of these invasions on African natural resources.
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1 World Agroforestry Centre, Nairobi, Kenya; Department of Entomology, University of Kentucky, Lexington, Kentucky, USA
2 Zambia Agriculture Research Institute, Lusaka, Zambia
3 Institute of Agricultural Research for Development, Yaoundé, Cameroon
4 World Agroforestry Centre, Nairobi, Kenya