Pest Threats to Plantations: Will At-Risk Countries Demand Improvements to IPPC?

pines in a plantation in Argentina killed by *Sirex noctilio*; photo by J. Villacide

A decade ago, Payn et al. (2015) compiled studies from around the globe to evaluate threats to widespread tree plantations. At that time, they said climate change posed the greatest threat to plantation forestry globally, in the forms of storm and flood damage and simultaneous warming and drying trends with extreme temperatures.

Still, the authors warned that forest health would be an increasingly important constraint to plantation productivity. They were optimistic, however, that modern breeding and other technologies could offset losses.

What is the current situation? The countries that depend on these plantations for fiber production are not demanding that leaders of the international phytosanitary structure build a more effective system to protect their investments. Instead, individual scientists struggle to better understand threats. Mostly, they propose expanded research.

Economic Importance of these Species

Eucalypts

“Eucalypts” comprises three genera in the family Myrtaceae: Angophora, Corymbia and Eucalyptus. These include more than 700 tree species native primarily to Australia. A few species are native to Indonesia, New Guinea and the Philippines (Paine et al. 2011; Crous et al. 2019). Some of these species have been extensively planted outside their native ranges for more than 100 years. These plantations have expanded rapidly in recent decades, especially in Southeast Asia and the Southern Hemisphere (Crous et al. 2019). Eucalypts are now the most widely planted hardwood timber in the world (Paine et al. 2011).

Eucalypt plantation in Brazil; photo by Jonathan Wilken via Wikimedia

Eucalypts’ popularity has been driven chiefly by their rapid growth; short rotation times including through coppicing; and adaptability to a very wide variety of sites and climatic conditions (Paine et al. 2011; Crous et al. 2019). Also, these trees are an important source of the short-fiber pulp required for production of high-quality paper used in modern office copiers and printers (Paine et al. 2011). Plantations are increasing even in Australia, where harvesting of native forests is increasingly being restricted (Paine et al. 2011).

Pines

Pines – a genus restricted naturally to the Northern Hemisphere – is second in global popularity. South America hosts 4.6 million hectares of pine plantations (Lantschner and Villacide 2025). South America is more dependent on forestry plantations for wood production than any other region. In 2012, 88% of its industrial roundwood was produced by non-native plantations. This far exceeded the global proportion of approximately 19%.

These intensively managed plantations have enabled Brazil and Chile to become “planted forest powerhouses.” Uruguay and, more slowly, Argentina are following the same path (Payn et al. 2015).

Documentation of the Damage

Euclaypts

The highly diverse eucalypts host an even greater diversity of fungi. As of 30 years ago, scientists were aware of more than 500 species of just one type, the leaf-infecting fungi. Additional fungi are associated with seeds, capsules, twigs, branches, and stems. Little is known about the vast majority of these fungi. Even species considered causal agents of important diseases have not yet been confirmed using Koch’s Postulates. Areas of origin for most is also unknown (Crous et al. 2019).

Crous et al. (2019) compiled information on 110 genera of fungi found on eucalypt foliage. Some genera include well-recognized primary pathogens. They name Austropuccinia and Calonectria, Coniella, Elsinoe, Pseudocercospora, Quambalaria and Teratosphaeria. Other genera are thought to include species that are opportunists that develop on stressed or dying tissues. Many other leaf fungi are putative pathogens, but unstudied. Additional fungi cause vascular wilts (e.g. Ceratocystidaceae), stem canker diseases (Cryphonectriaceae, Botryosphaeriaceae) and root diseases (e.g. Armillaria, Ganoderma) of eucalypts.

Crous et al. (2019) state that the rust Austropuccinia psidii is one of the most damaging of the foliage fungal pathogens. They consider it to be a greater threat to eucalypt plantations outside the trees’ native ranges. (The Myrtaceous species in Australia most damaged by A. psidii are in other genera.)

Two families of leaf fungi – Mycosphaerellaceae and Teratosphaeriaceae – include species that cause serious diseases. Pérez, et al. report a study in plantation in Uruguay that detected six new species. They also discovered new hosts for some known species. (Such initial detections of new fungal species in out-of-native-range plantations is a usual occurrence.)

Over the 100-year history of planting eucalyptus outside Australasia, dozens of leaf pathogens have been transported to novel regions. Crous et al. 2019 report the wide geographic breadth of many of these introductions. For example, Mycosphaerella heimii is crippling plantation forestry in five global regions – South America (Brazil and Venezuela); Asia (Indonesia and Thailand); Africa (Madagascar), Europe (Portugal); and in its presumably native Australia. A second species, M. marksii, has a similarly wide introduced range: Portugal, China and Indonesia, South Africa, Ethiopia, and Uruguay. Pérez et al. calls Mycosphaerella leaf diseases one of the most important impediments to Eucalyptus plantation forestry in Uruguay.

Although Crous et al. do not provide dates of detection, it appears that many of these leaf pathogens were introduced outside Australasia before the mid-990s, when the World Trade Organization (WTO) and International Plant Protection Convention (IPPC) came into force. Together, these agreements govern what actions phytosanitary officials may take to curtail international movement of plant pests. (To see my critique of the WTO/IPPC system, visit here.) The possible exception might be Kirramyces gauchensis, a well-known pathogen of Eucalyptus grandis in South America (Argentina and Uruguay), Hawai`i, and Africa (Uganda and Ethiopia) (Pérez, et al. 2009). Crous et al. (2019) expect another genus, Quambalaria species, to become a threat to eucalypt plantation forestry globally in the future.

*Phoracantha semipunctata*; photo by Umo Schmidt via Flickr

Arthropod pests have also been spread to many Eucalyptus-growing regions in North and South America, Europe and Africa since the 1980s. Some species have colonized virtually all eucalypt-growing regions, e.g., Phoracantha semipunctata. Some have – so far – appeared on only one continent.

In an effort to determine how many of these introductions have occurred after adoption of the WTO/ IPPC system, I Googled the species named by Paine et al. (2011). I used the year 2000 as the cutoff date, to allow for detection lag. Among the insect species that fit this criterion are a lerp psyllid, a leaf beetle, and two gall wasps detected in North America; a true bug, two galling insects, and a leaf beetle in South Africa; and three psyllids in Europe.

Asia stands out as having very few introduced Australian insects plaguing eucalyptus plantations. Only one insect of Australian origin is causing significant damage in this region, Leptocybe invasa. It was detected after 2000, so it might have been introduced under the WTO/IPPC regime. Many widespread species, e.g., Phoracantha semipunctata, are notably absent. Instead, large numbers of endemic insects use these trees. This contrasts with the situation in the Southern Hemisphere, where few of the numerous native insects have shifted onto eucalypts.

New Zealand has detected only two new species of Australian origin since 1999 — two psyllids. This is despite the two nations’ proximity, the large volume of trade that passes between them, and the likelihood that at least some small sap-suckers might be introduced via aerial dispersal. New Zealand is famous for its strict phytosanitary (and sanitary) policies and programs.

Eucalyptus plantation in Kwa-Zulu, South Africa

Plantations’ vulnerability has been increased by expanding reliance on clonal, artificially-induced hybridization. Developers’ goals – and initial results – are enhanced adaptation to specific environments, desired fiber characteristics, and hybrid vigor. However, these vast areas planted in genetically identical trees are sitting ducks. An insect or pathogen that overcomes the host’s defenses can spread rapidly across the entire planting.

These hybrids also can act as “bridges,” facilitating spread of fungi to formerly resistant host species. Crous et al. (2019) fear that this process will undermine resistance in Eucalyptus pellita to the pathogen Teratosphaeria destructans. Plantations in Southeast Asia and South Africa now comprise hybrids between this resistant species and the highly susceptible Eucalyptus brassiana.

Pines

As with the eucalypts, the intensively managed pine plantations are comprised of fast-growing exotic species, all at the same developmental stage, and with minimal genetic diversity, planted to maximize wood production. These practices again lead to biological homogenization and reduced resilience to pests (Villacide and Fuetealba, 2025)

In the Southern Hemisphere, Sirex noctilio has become the most significant economic pest of Pinus species. These attacks can cause up to 80% mortality. Several other Sirex species have also been introduced, all apparently in the 1980s or earlier (Wilcken et al., 2025) – before adoption of the current international phytosanitary regime. However, in 2023, a new species, Sirex obesus, was discovered causing tree mortality in pine plantations in southeastern Brazil. This species is indigenous to the United States and Mexico.

Stazione et al. (2026) discuss two other non-native pine pests that established recently in South America.

Analysis of mitochondrial DNA of Orthotomicus erosus points to a western Eurasian lineage. The low genetic diversity of the introduced population in Argentina and Uruguay suggests a single or limited introduction event followed by regional spread.

The source region of Cyrtogenius luteus is more difficult to determine but is probably somewhere in China. The higher haplotype diversity might reflect multiple introductions. Again, shared haplotypes between Argentina and Uruguay countries indicates a contiguous regional spread, possibly driven by extensive pine plantations & intra-regional trade (Stazione et al. 2026)

Policy Aspects

Some scientists express concern about the failure of international phytosanitary measures. But are their countries speaking up in regulatory bodies, especially the International Plant Protection Convention?

Studies by Crous et al. (2019) and Pérez et al. (2009) clearly show that pathogens from Australia continue to be transported to regions where eucalypt plantations are grown. This happens despite most of the movement of genetic material being in the form of seeds – which should be less likely to transport pathogens than trade in plants. Pérez et al. (2009) explicitly raise concerns about the effectiveness of current quarantine procedures. Crous et al. (2019) state that quarantines continue to fail in many parts of the world.

Burgess and Wingfield (2017) list pathogens that have spread widely since the beginning of the 21st Century: Austropuccinia psidii, Calonectria (= Cylindrocladium) eudonaviculata (=Cylindrocladium buxicola), Ceratocystis lukuohia and C. huliohia introduced to Hawai`i. I add that insect-vectored diseases such as Euwallacea species carryingFusarium fungi have also experienced a burst of introductions around the globe since 2000.

Crous et al. (2019) attribute this failure partially to the enormous difficulty of applying effective quarantine to the huge volumes of planting material traded globally. Another factor is undoubtedly the poor understanding of microbial species, their pathogenicity, hosts, pathways of spread, even taxonomies. Some genera cannot be grown in culture.

Furthermore, pathogens’ impacts vary, possibly due to environmental conditions of the location or differing virulence on different hosts. Finally, with so many fungi and so little knowledge, it is difficult to separate true disease agents from multiple secondary infections.

Crous et al. (2019) express the hope that increased recognition of the importance of pathogens, along with improved detection and identification tools, will clarify patterns of spread. But is that enough? Are there no policy changes needed?

Crous et al. (2019) also warn us about additional pathways for spreading pathogens. Some potential pathogens of eucalypts have been moved on plants of other, related genera. Furthermore, Botryosphaeriaceae have been detected in the skins of mangoes (Mangifera indica) and avocados (Persea americana). Both of these fruits move globally in large volumes.

mangoes; photo by Obsidian Soul via Wikimedia

Regarding insects, Paine et al. (2011) focus on a concern that species native to the plantation countries and generalist herbivores from other parts of world will invade Australia and threaten eualypts in their native ranges. See other blog They also call for research to understand international pathways, develop detection methods, improve understanding of patterns of host suitability, susceptibility, and selection.

Villacide and Fuetealba (2025) note that while the introductory pathway for that new species, Sirex obesus, has not been determined, they suspect it might have been wood packaging materials. Villacide and another colleague (Lantschner and Villacide 2025) suggest an initial step would be for Argentina and other countries in the region to negotiate with Brazil to adopt more protective protocols governing trade in wood products, including wood packaging.

I have repeatedly advocated strengthening regulation of wood packaging. Such measures could improve protection of Earth’s forests from pests that use a well-documented high-risk introductory pathway. To see my arguments and underlying data, scoll down below the “archives” to “Categories” and click on “wood packaging”.

SOURCES

Burgess, T.I. and M.J. Wingfield. 2017. Pathogens on the Move: A 100-Year Global Experiment with Planted Eucalypts. Bioscience. Volume 67, Issue 1, January 2017. https://doi.org/10.1093/biosci/biw146

Crous, P.W., M.J. Wingfield, R. Cheewangkoon, A.J. Carnegie, T.I. Burgess, B.A. Summerell, J. Edwards, P.W.J. Taylor, and J.Z. Groenewald. 2019. Folia pathogens o eucalypts. Studies in Mycology 94:125-298 (2019).

Lantschner, V. and J. Villacide. 2025. Invasion Potential of the Recently Established Woodwasp Sirex obesus. Neotropical Entomology. (2025) 54:117 https://doi.org/10.1007/s13744-025-01347-6

Paine, T.D., M.J. Steinbauer, and S.A. Lawson. 2011. Native and Exotic Pests of Eucalyptus: A Worldwide Perspective. Annu. Rev. Entomol. 2011. 56:181-201

Payn, T., J-M. Carnus, P. Freer-Smith, M. Kimberley, W. Kollert, S. Liu, C. Orazio, L. Rodriguez, L. Neves Silva, M.J. Wingfield. 2015. Changes in planted forests and future global implications. Forest Ecology and Management 352 (2015)

Pérez,, C.A., M.J. Wingfield, N.A. Altier, and R.A. Blanchette. 2009. Mycosphaerellaceae and Teratosphaeriaceae associated with Eucalyptus leaf diseases and stem cankers in Uruguay For. Path. 39 (2009) 349–360 doi: 10.1111/j.1439-0329.2009.00598.x www3.interscience.wiley.com

Stazione, L., Soliani, C., Cognato, A. et al. Reconstructing the invasion history of the bark beetles Orthotomicus erosus & Cyrtogenius luteus (Coleoptera, Curculionidae, Scolytinae) in South America. Biol Invasions 28, 49 (2026). https://doi.org/10.1007/s10530-026-03779-6

Villacide, J. and A. Fuetealba. 2025. Pests in plantations: Challenging traditional productive paradigms in the Southern Cone of America. Forest Ecology and Management 597 (2025) 123127

Wilcken, C.F., T.A. da Mota, C.H. de Oliveir, V.R. de Carvalho, L.A. Benso, J.A. Gabia, S.R.S. Wilcken, E.L. Furtado, N.M. Schiff, M.B. de Camargo, M.F. Ribeiro. 2025. Sirex obesus (Hymenoptera: Siricidae) as invasive pest in pine plantations in Brazil. Scientific Reports. 2025. 15:22522 https://doi.org/10.1038/541598-025-06418-7

Posted by Faith Campbell

We welcome comments that supplement or correct factual information, suggest new approaches, or promote thoughtful consideration. We post comments that disagree with us — but not those we judge to be not civil or inflammatory.

For a detailed discussion of the policies and practices that have allowed these pests to enter and spread – and that do not promote effective restoration strategies – review the Fading Forests report at http://treeimprovement.utk.edu/FadingForests.htm

https://fadingforests.org

Threat to Native Myrtaceae in South America

*Blepharocalyx salicifolius –* a tree in the Myrtaceae native to South America on which found symptoms similar to those caused by Mycosphaerellaceae or Teratosphaeriaceae; photo by Pablo di Flores via Wikimedia

Pests that have followed their hosts to plantations outside the trees’ native ranges might threaten native plants in their new, introduced ranges. That is, the countries where the plantations are located.

Eucalypts

Eucalypts are now the most widely planted hardwood timber taxon in the world (Paine et al 2011). The 700 – 800 species in the three genera considered “eucalypts” (Angophora, Corymbia, and Eucalyptus) host a highly diverse fungal community — more than 500 species have been identified of just one type, leaf-infecting fungi (Crous et al. 2019).

As I described in a related blog, link dozens of leaf pathogens have been transported to countries hosting eucalypt plantations. Among them, two families – Mycosphaerellaceae and Teratosphaeriaceae – are prominent in both numbers of introductions and potential to cause serious diseases.

Pérez et al. (2009) reported that a relatively large number of Mycosphaerellaceae and Teratosphaeriaceae are found on Eucalyptusin Uruguay. The authors cite one troubling case of host shifting: Mycosphaerella lateralis is causing leaf disease on a Musa cultivar (banana!) which is not in the Myrtaceae.

A follow-up study by the same authors (Pérez et al. 2013) surveyed several native forests, paying special attention to those located close to Eucalyptus plantations. They found five species belonging to the Mycosphaerellaceae and Teratosphaeriaceae clades on native Myrtaceous trees; three of these had previously been reported on Eucalyptus in Uruguay. Those occurring on both Eucalyptus and native Myrtaceae included Pallidocercospora heimii, Pseudocercospora norchiensis, and Teratosphaeria aurantia. A fourth species, Mycosphaerella yunnanensis, not previously recorded in Uruguay, was found on the leaves of two native Myrtaceous hosts. Pérez et al. (2013) believe circumstances indicate that all these fungi have been introduced. They warn that these apparent jumps to new hosts have the potential to result in serious disease problems and they should be carefully monitored. This finding is more than a decade old; I have not found a more recent report.

On the global level, Pérez et al. (2013) report, at least 23 species of Mycosphaerellaceae and Teratosphaeriaceae have been found on non-Eucalyptus species in the Myrtaceae. These hosts are in several plant orders, including Myrtales, Proteales, Fabaes and Apiales. The authors express “considerable concern” about the apparent ease of movement in these fungi between hosts. I have been unable to learn more details about these introductions.

Arthropod pests have also been spread to many Eucalyptus-growing regions in North and South America, Europe, and Africa since the 1980s – but not to Asia or New Zealand (Paine et al. 2011). blog

*Myrrhinium atropurpureum* – another South American plant in the Myrtaceae on which symptoms found; photo by Prof. Atilio L, Botanical Garden of Uruguay

Pines

Pines – a genus restricted naturally to the Northern Hemisphere – is second in popularity for intensively managed plantations. South America has 4.6 million hectares of pine plantations (Lantschner and Villacide 2025). Most are in Brazil, Chile, Uruguay, and Argentina (Payn et al. 2015).

*Cinara cupressi;* photo by LBM via Wikimedia

As I reported in an earlier blog, some of the insect pests that followed pines to South America have entered native forests. The most alarming of which I am aware is the aphid Cinara cupressi. It attacks the native conifer Austrocedrus chilensis, which forms pure and mixed stands with southern hemisphere beech (Nothofagus spp.) across approximately 160,000 hectares (Villacide and Fuetealba 2025). Cordilleran cypress is also under attack by the oomycete Phytophthora austrocedri, an oomycete of unknown origin.

Some scientists express concern about phytosanitary measures … but are their countries speaking up in meetings of the International Plant Protection Convention?

Studies by Crous et al. and Pérez et al. clearly show that pathogens from Australia continue to be transported to regions where eucalypt plantations are grown – despite the fact that most of the movement of tree genetic material is in the form of seeds – which should be less likely to transport pathogens than trade in plants. Pérez et al. (2009) explicitly raise concerns about the effectiveness of current quarantine procedures. Crous et al. (2019) state that the quarantines continue to fail in many parts of the world.

See my critique of the international phytosanitary system under the IPPC by visiting the Fading Forest II report (see link below) and reading other blogs under the categories “invasive species policy” and “plants as vectors of pests”.

SOURCES

Crous, P.W., M.J. Wingfield, R. Cheewangkoon, A.J. Carnegie, T.I. Burgess, B.A. Summerell, J. Edwards, P.W.J. Taylor, and J.Z. Groenewald. 2019. Foliar pathogens of eucalypts. Studies in Mycology 94:125-298 (2019)

Lantschner, V. and J. Villacide. 2025. Invasion Potential of the Recently Established Woodwasp Sirex obesus. Neotropical Entomology. (2025) 54:117 https://doi.org/10.1007/s13744-025-01347-6

Paine, T.D., M.J. Steinbauer, and S.A. Lawson. 2011. Native & Exotic Pests of Eucalyptus: A Worldwide Perspective. Annu. Rev. Entomol. 2011. 56:181-201

Payn, T., J-M. Carnus, P. Freer-Smith, M. Kimberley, W. Kollert, S. Liu, C. Orazio, L. Rodriguez, L. Neves Silva, M.J. Wingfield. 2015. Changes in planted forests & future global implications. Forest Ecology and Management 352 (2015)

Pérez, C.A., M.J. Wingfield, N.A. Altier, and R.A. Blanchette. 2009. Mycosphaerellaceae & Teratosphaeriaceae associated with Eucalyptus leaf diseases & stem cankers in Uruguay For. Path. 39 (2009) 349–360 doi: 10.1111/j.1439-0329.2009.00598.x www3.interscience.wiley.com

Pérez, C.A., M.J. Wingfield, N. Altier, and R.A. Blanchette. 2013. Species of Mycosphaerellaceae and Teratosphaeriaceae on native Myrtaceae in Uruguay: evidence of fungal host jumps. Fungal Biology Volume 117, Issue 2, February 2013.

Villacide, J. and A. Fuetealba. 2025. Pests in plantations: Challenging traditional productive paradigms in the Southern Cone of America. Forest Ecology and Management 597 (2025) 123127

Posted by Faith Campbell

https://fadingforests.org

Pest Threats to Eucalypts and Australia

*Chilecomadia valdiviana* – one of the South American moths that attack Eucalyptus; photo by Natural History Museum of London via Wikimedia

Fifteen years ago, Paine, Steinbauer, and Lawson (2011) worried that insects in South America, Africa, Asia, and Europe that adapt to attacking Eucayptus trees planted there might be introduced to Australasia and threaten the genus in its native range. Their analysis applies to species in all three genera considered to be “eucalypts” — Angophora, Corymbia and Eucalyptus.

Some insects native to those continents have made this host shift already. Paine, Steinbauer, and Lawson reported that such host switching was especially prevalent among lepidopterans. They name several from Brazil, the Chilean cossid moth, Chilecomadia valdiviana, and southern African Coryphodema tristis. In their view, Brazilian eucalypt plantations’ proximity to native vegetation facilitates host-switching. Still, at that time they thought that there were no established pathways for introduction of the South American moths to Australia.

Host-switching is exceptionally common in Asia. Paine, Steinbauer, and Lawson (2011) thought the risk was greatest from insects on native eucalypts in near-neighbors Papua New Guinea, Timor, and The Philippines. An earlier risk assessment evaluating 10 insect species from the region concluded that most are polyphagous and probably switched to eucalypts. Two woodborers – Agrilus opulentus and A. sexsignatus –seem to have coevolved with Eucalyptus deglupta in New Guinea and The Philippines.

According to the same authors, most of the insects that have switched hosts are either polyphagous or normally feed on other myrtaceous species native to these regions. Thus, the Brazilian moth Thyrinteina arnobia feeds on Psidium guajava and several other Myrtaceae. Sarsina violascens is also a pest of Psidium species, as well as species in the Asteraceae, and Oleaceae. And the foliar rust Austropuccinia psidii was first described from Psidium guajava in Brazil and boasts a wide host range in the Myrtaceae in South America. It has been introduced to many regions with plants in the Myrtaceae, notably Hawai`i, Australia, South Africa, New Caledonia, and New Zealand. At least 15 Myrtaceae species in Australia are threatened with extinction.

Still, few non-native insects were damaging eucalypts in Australia’s native forests or plantations as of 2011. Those few are highly polyphagous. Several, if not most, were introduced in the first half of the 20^th Century.

Why so few? Paine, Steinbauer, and Lawson (2011) suggest three possibilities: (a) Australia’s diverse endemic insects already occupy most niches, so they exclude new, foreign competitors; (b) most introduced insects were not previously exposed to Myrtaceae in their native range; and (c) Australia has strong quarantine procedures aiming to limit introductions of non-native herbivores.

The fact that none of the introduced insects has adapted to feed significantly on mature eucalypts’ above-ground tissues seems to me to point to protection provided by the adult trees’ phytochemicals and leaf structure. Paine, Steinbauer, and Lawson (2011) discuss some aspects of leaf structure and wax coatings.

As to Australia’s quarantine procedures, as I reported before, the country has been much less proactive regarding plant pests and diseases that threaten tree species rather than agricultural crops. Significant new programs were established only after 2000, when Plant Health Australia (PHA) was incorporated. The PHA is supposed to facilitate preparedness and response arrangements between governments and industry for plant pests (once an alien pest has become established, management becomes responsibility of the land manager). In 2005, federal, state, and territorial governments and plant industry bodies signed a legally-binding agreement — the Emergency Plant Pest Response Deed (EPPRD). As of 2022, 38 were engaged. It sets up a process to implement management and funding of agreed responses to the detection of exotic plant pests – including cost-sharing and owner reimbursement.

Still, studies documented significant gaps in post-border forest biosecurity systems and the country’s response to the anticipated introduction of the foliar rust Austropuccinia psidii was disappointing. This prompted yet another initiative: development of the National Forest Biosecurity Surveillance Strategy (NFBSS) in 2018. The strategy was; accompanied by an Implementation Plan and appointment of a National Forest Biosecurity Coordinator. The forest sector fund a significant proportion of the proposed activities for the first five years. Still, Drs. Carnegie and Nahrung thought that in-country forest pest surveillance was still too fragmented.

Paine, Steinbauer, and Lawson (2011) consider the Asian spongy moths Lymantria dispar and Orgyia thyellina to pose serious threats. Five eucalypt species were assessed to be at risk of attack as are two preferred host oaks in Europe, Quercus pubescens and Q. robur. They note high volumes of imports from East Asia of containers, vehicles, and machinery, which are known to transport spongy moth egg-masses. It is not known whether the numerous natural enemies of Australia’s diverse lymantriid fauna [which includes four in the genus Lymantria] might provide some protection. These experts also worried that the highly polyphagous Asian longhorned beetle (Anoplophora glabripennis) might arrive in Australia. Eucalypts are not recognized as hosts.

Australia has adopted an enhanced surveillance program for ships arriving from Asian and European Lymantria ranges during female flight periods. Described here. Nahrung and Carnegie (2021) though that the high priority assigned to Lepidoptera exceeded the actual risk; only two non-native species had established in Australia over 130 years.

Paine, Steinbauer, and Lawson (2011) suggest several research topics aimed at reducing the risk to eucalypts in Australia. These include interactions between these insects and mechanisms by which insects adapt to new hosts; host chemistry and resistance mechanisms), chemical ecology (including host selection), population and community dynamics, including possible biocontrol agents, and pathway and risk analysis.

On the other hand, Carnegie and Nahrung (2019) called for developing more effective methods of detection, especially of Hemiptera and pathogens. They also promoted national standardization of data collection. Finally, they advocated inclusion of technical experts from state governments, research organizations and industry in developing and implementing responses to pest incursions. They noted that surveillance and management programs must expect and be prepared to respond to introductions of unanticipated species. They had found that 85% of the pests detected over the last 20 years—and 75% of subsequently mid-to high-impact species established—were not on high-priority pest list.

SOURCES

Carnegie A.J. and H.F. Nahrung. 2019. Post-Border Forest Biosecurity in AU: Response to Recent Exotic Detections, Current Surveillance and Ongoing Needs. Forests 2019, 10, 336; doi:10.3390/f10040336 www.mdpi.com/journal/forests

Nahrung, H.F. and A.J. Carnegie. 2021. Border interceptions of forest insects established in Australia: intercepted invaders travel early and often. NeoBiota 64: 69–86. https://doi.org/10.3897/neobiota.64.60424

Paine, T.D., M.J. Steinbauer, and S.A. Lawson. 2011. Native & Exotic Pests of Eucalyptus: A Worldwide Perspective. Annu. Rev. Entomol. 2011. 56:181-201

Native & Exotic Pests of Eucalyptus: A Worldwide Perspective

Posted by Faith Campbell

https://fadingforests.org

Bird nesting habitats – why no mention of invasive species or deer?

ovenbird (*Seiurus aurocapilla*); photo by Rhododentrities via Wikimedia

Studies of forest ecosystems in eastern North America that claim to be comprehensive still too often make no reference to invasive species – pests, earthworms, or plants. I try here to bridge these gaps.

Akresh et al. (2023) conducted a meta-analysis of bird species’ use of forests as nesting habitat. They applied the Partners-in-Flight to evaluate the community-wide bird conservation values of unmanaged forests compared to various levels of tree removal by harvest. Because of the decline of many bird species that prefer shrubland or early-successional stands, their process gave highest ranks to management approaches that retained 40%–70% of the canopy trees.

Their study notes that habitats for shrubland birds comprise only about 6% of forests in the eastern U.S. They don’t provide data for southeastern Canada. But hasn’t this scarcity of open upland, non-wetland, habitats in this region been true for thousands of years?

The type of forest that undoubtedly has shrunk significantly in recent centuries is “virgin” (or old-growth or late-seral) forests. As Akresh et al. (2023) report, contemporary closed-canopy forests in eastern North America are predominantly structurally homogeneous, mid-seral, even-aged, stands that have regenerated on land previously cleared for either agriculture or timber. These forests are much younger from a forest developmental perspective than precolonial forests; they lack the latter’s range of tree fall gap sizes and multiple age-classes. The tiny fraction of eastern forests that are in the late-seral stage might have higher species richness and conservation value for birds, but since they are usually not under management, Akresh et al. (2023) did not include that question in their analysis.

Akresh et al. (2023) list the bird species whose density appears to be closely linked to various tree canopy densities. For example, ovenbirds and brown creepers promptly decline in abundance in response to any amount of tree harvesting. Two other species — wood thrush and cerulean warbler — have declined steeply range-wide in recent decades. Nesting densities of three of these four species (excluding the warbler) are significantly higher in areas harvested in ways that retain a greater percentage of trees. Densities of another five bird species (Acadian flycatcher, hermit thrush, black-throated green warbler, and red-breasted nuthatch) are also higher in areas with a greater proportion of trees retained.

Another nine species had a more complex relationship with tree densities but still had lower densities in stands with low tree retention. These were blue-gray gnatcatcher, blue-headed vireo, blackburnian warbler, black-throated blue warbler, eastern wood-pewee, least flycatcher, red-eyed vireo, scarlet tanager, and yellow-bellied sapsucker. They found little relationship between bird density and tree retention for five putative mature-forest species (American redstart, great-crested flycatcher, hooded warbler, veery, and yellow-rumped warbler).

scarlet tanager (*Piranga olivacea*); photographed in scrub at Edwin B. Forsythe (Brigantine) NWR by F.T. Campbell

Akresh et al. (2023) claim that silviculture approaches can be used to restore aspects of the structural and compositional conditions found in old-growth forests to second-growth systems, providing a potential pathway for rapidly increasing the conservation value of these areas for bird species. They advocate reducing canopies moderately via variable retention harvests, shelterwood establishment harvests, and irregular shelterwood systems. This strategy can increase understory vegetation density, which they assert can then increase foraging and nesting opportunities for both many mature-forest bird species and many shrubland birds.

I am skeptical; it is much easier to create openings in the canopy than to “create” large trees supporting cavities and associated fauna and flora utilized by some bird species. The authors do advise managers that late-seral, unharvested stands can provide important habitat for old-growth-dependent taxa and any intensive forestry should also take into account other factors.

old-growth hemlock stand in Cook Forest State Forest, Pennsylvania; photo by F.T. Campbell

In addition, often the understory vegetation that responds to the more open environment will be invasive non-native plants. Already about half of eastern U.S. forests have been invaded by non-native plants (Oswalt et al. 2016; Kurtz 2023). Many of these are shrubs: honeysuckles, privets, roses, buckthorn. Management of these plants is difficult – especially when opening the canopy to allow light to reach the forest floor. (at www.nivemnic.us, scroll down to “categories”, click on “invasive plants”.) So the question arises, do the non-native plant species adequately substitute for native shrubs in providing resources needed by those birds?

Maybe. Gleditsch and Carlo (2014) found that a shrub layer dominated by non-native honeysuckle shrubs (Lonicera species) does support nesting populations of several common species, especially catbird (Dumetella carolinensis), American robin (Turdus migratorius ), and northern cardinal (Cardinalis cardinalis). However, they did not consider the species of concern to Akresh et al. (2023) – the rare species that prefer open-canopy, early-successional communities. So they do not inform us whether these high-priority species can utilize shrublands dominated by non-native species. Gleditsch and Carlo (2014) apparently did not find nests of several species considered to be associated with mature forests. So, again, these forests’ value for conservation remains unclear. Gleditsch and Carlo (2014) do counter earlier fears that these non-native shrubs are “traps” for nesting passerine birds. (The concern was that the plants’ structure facilitated nest raiding by predators.) They say, instead, that these plants’ effects are species-specific, context-dependent, and often a mix of both positive and negative outcomes.

invasive shrub honeysuckle; photo by Kevin Casper via public.domain.pictures.net

Akresh et al. (2023) also do not address the impact of browsing by super-abundant deer. Others (at www.nivemnic.us, scroll down to “categories”, click on “deer”.) have demonstrated that interactions of deer predation with invasive plants is especially damaging to native flora. Considering forests from Virginia to Maine, Miller et al. (2023) advise opening the canopy or subcanopy of forests to promote tree regeneration where deer and invasive shrubs overlap only where deer are controlled.

I have seen no recent analyses of the impact of widespread pest-caused tree mortality beyond some early efforts focused on eastern hemlocks and on high-altitude whitebark pines.

SOURCES

Akresh, M.E., D.I. King, S.L. McInvale, J.L. Larkin, and A.W. D’Amato. 2023. “Effects of Forest Management on the Conservation of Bird Communities in E North America: A Meta-Analysis.” Ecosphere 14(1):e4315. https://doi.org/10.1002/ecs2.4315

Gleditsch, J.M. and T.A. Carlo. 2014. Living with Aliens: Effects of Invasive Honeysuckles on Avian Nesting. PLOS One. September 2014. Volume Nine Issue Nine. E107120

Miller, K.M., S.J. Perles, J.P. Schmit, E.R. Matthews, M.R. Marshall. 2023. Overabundant deer and invasive plants drive widespread regeneration debt in eastern United States national parks. Ecological Applications. 2023;33:e2837. https://onlinelibrary.wiley.com/r/eap

Oswalt, C.M., S. Fei, Q. Guo, B.V. Iannone III, S.N. Oswalt, B.C. Pijanowski, K.M. Potter. 2016. A subcontinental view of forest plant invasions. NeoBiota. 24:49-54 http://www.srs.fs.usda.gov/pubs/48489

Posted by Faith Campbell

https://fadingforests.org

A New Year …Will there be a new priority on countering invasive species?

Alaska yellow cedar (*Chamaecyparis nootkatensis*); one of the species vulnerable to *Phytophthora austrocedri*; APHIS has determined it is too late to try to slow its spread. Photo by Nucatum amygdalarum via Wikimedia

On 30 December 2025, US Department of Agriculture Secretary Brooke L. Rollins issued a Secretary’s Memorandum setting five new priorities for research and development. One is to protect agriculture from invasive species. Another is to resolve longstanding trade barriers due to sanitary and phytosanitary concerns.

The Secretary’s intention is to strengthen US agriculture to benefit both farmers and consumers. He justifies the action by claiming that President Lincoln’s original purpose in establishing USDA was to acquire and diffuse useful information on subjects connected with agriculture. According to this interpretation, Lincoln recognized that working to improve agriculture and secure the nation’s food supply would benefit everyone. The emphasis on research and development was reiterated by the almost simultaneous adoption of the Morrill Act of 1862, which created the system of land-grant universities and development of the Cooperative Extension System via the Smith-Lever Act of 1914.

The memorandum specifies five priority areas of research to be pursued by all USDA agencies and offices – to the maximum extent permitted by law and in accordance with any applicable regulations and procedural requirements.

Increasing Profitability of Farmers & Ranchers — especially reducing volatility in profitability. Goals include reducing inputs or increasing mechanization and automation.
Expanding Markets for US agricultural products. Two approaches are mentioned: generating science and data to resolve longstanding sanitary and phytosanitary trade barriers; and expanding use of agricultural commodities in novel biobased products and bioenergy.
Protecting the Integrity of American agriculture from Invasive Species. The memorandum lists four examples of current invasive pest and pathogen threats: new world screwworm in Mexico; continued westward expansion of spotted lanternfly; persistence of highly pathogenic avian influenza in poultry flocks; and citrus greening. It notes that invasive species threaten both agriculture and natural resources. The research is to focus on new and effective methods for preventing, detecting, controlling,and eradicating these threats.
Promoting Soil Health to Regenerate Long-Term Productivity of Land. The research is to promote soil health practices, increase water-use efficiency, & reduce the need for inputs.
Improving Human Health through Precision Nutrition and Food Quality. Research on “precision nutrition” is said to improve understanding of how healthy dietary patterns impact individuals. Research will also focus on increasing foods’ nutritional content and quality.

*Vaccinium myrtillus* (photo by Anneli Salo via WikiMedia); one of several species in genera shared with North America that are infected by *Phytophthora* spp in the Italian alps

The memorandum also instructs USDA’s Office of the Chief Scientist (that is, the Under Secretary for Research, Education, & Economics) to coordinate these priorities within USDA and among key partners in other federal agencies.

Does This Policy Mean Substantially Stronger USDA Efforts to Counter Bioinvasions?

Can we expect new energy in USDA’s programs aimed at managing non-native forest pests and invasive plants that damage forests, wetlands, grasslands, and other natural systems? The first paragraph of the memorandum states that it is USDA policy to reaffirm a focus on the Department’s original objectives of maximizing and promoting American agriculture; ensuring a safe, nutritious, and secure food supply; enhancing rural prosperity; and protecting our National Forests & Grasslands. That is promising.

The explicit recognition that invasive species pose severe threats to both agriculture and natural resources is also promising. I welcome the inclusion of two plant pests among the examples. Livestock diseases usually receive far more attention in USDA pronouncements.

I note three caveats:

The prominence of enhancing markets for US agricultural exports (# 2). In the past, this longstanding emphasis has led to undercutting phytosanitary agencies’ ability to counter suspected — but incompletely understood — pest risks. I discussed the impracticality of determining a newly detected species’ probable impacts in Chapter 3 of my report, Fading Forests II.
The memorandum makes no reference to implementing stronger sanitary or phytosanitary policies. In my view, the Animal and Plant Health Inspection Service has sufficient knowledge to support adoption of a more assertive regulatory stance with regard to both new introductions and spread within the country? Does the memorandum signal support for such a stance by high-ranking USDA officials?

These officials have often reminded APHIS that it is not a research agency. However, its staff do “methods development” and it funds considerable research through the Plant Pest and Disease Management and Disaster Prevention Programs – Section 7721 of the Plant Protection Act and a matching program for animal diseases.

The US Forest Service does have a research division – although the Trump Administration proposed its virtual elimination in early 2025. The Congressional appropriators have provided funding for USFS R&D – but those bills have not yet been enacted into law. I have complained for years that USFS R&D allocates too few resources (about 1% of the total budget) to research on introduced pests and disease pathogens. Might this new directive help fix this problem?

I hope the emphasis on protecting National Forests & Grasslands does not result in narrowing the types of invasive pests addressed.

Posted by Faith Campbell

https://fadingforests.org

It Zigs, We Zag: Following the Invasion of Elm Zigzag Sawfly in North America

elm zigzag sawfly larvae feeding on an elm leaf; photo by Delaney Serpan

As one of the newest – and most unique – invasive insects, elm zigzag sawfly (EZS; Aproceros leucopoda) has been making headlines across the eastern U.S. and Canada since 2020. The defoliating pest was first confirmed in North America in Québec, Canada and has since spread rapidly across many states and provinces. As its name suggests, EZS larvae feed primarily on elm in a distinctive zigzag pattern. Moving inwards from the leaf edge, the larvae can eventually consume nearly the entire leaf, leaving nothing but the midrib and a few lateral veins behind. Defoliation from EZS can range from nearly undetectable to 100% canopy defoliation of a mature tree.

(See earlier blog here.)

adult zigzag sawfly; photo by Delaney Serpan

Elm zigzag sawfly biology

EZS is a multivoltine insect, meaning it can have multiple generations in a single growing season. In Europe, where EZS has been invasive since 2003, 1 to 4 generations are common though up to 6 generations have been recorded. In the U.S., many regions document up to 5 generations per year.

In the early spring, EZS emerges from the soil where it has overwintered. They reproduce parthenogenetically- a form of asexual reproduction- allowing them to lay eggs immediately following adult emergence. Each individual is able to lay up to 49 eggs, drastically increasing EZS reproductive potential. Once the eggs hatch, the larvae begin feeding on the foliage until they are ready to pupate. At that point, the larva may build a summer cocoon, attached to a nearby object such as a branch or fence post. Four to 7 days later, an adult will emerge. The entire life cycle only takes 3 to 6 weeks. Alternatively, the larva could drop to the soil beneath the tree’s canopy where it will build its winter cocoon and overwinter, waiting to repeat the cycle the following spring. A small portion of each generation create overwintering cocoons.

EZS summer cocoons attached to the underside of a leaf with evidence of larval feeding; photo by Delaney Serpan

Where is EZS now?

As of the end of 2025, EZS can be found in 15 states and 4 provinces as far west as Minnesota and Manitoba and as far south as North Carolina and Tennessee.

map of states/provinces with official EZS detections;

Invasion pathways in North America are currently unknown; however, EZS has been documented attaching its summer cocoons to truck wheel wells and other objects which may be moved. The subsequent movement of these objects can potentially contribute to EZS spread. It has also been suggested that infested elm nursery stock or potted soil of any plants could be a potential pathway for EZS, but more research is needed to fully understand this.

EZS cocoons on truck – under side mirror & wheel well; photos by Jared Beach, adapted from Oten et al. 2025

How does EZS affect the trees?

Defoliating pests typically decrease the aesthetic value of trees but leave the host largely unharmed. Across Europe and its native range of eastern Asia, EZS defoliation is relatively minimal, with the occasional severe outbreak resulting in total defoliation of a tree. Resulting branch dieback is even more uncommon.

When EZS was first found in North America, particularly North Carolina and Virginia, there were initial concerns about the implications of a warmer climate accelerating development. Like most insects, EZS development is related to temperature; a warmer climate allows for faster insect development. It was hypothesized that a longer growing season could allow for faster population growth and potentially more damage to host trees. At this point, it is still unclear if this will consistently occur in the southern extent of the range. In North Carolina, reported damage has varied widely since it was found there in 2023. Some trees have been 75% defoliated or more multiple years in a row and are exhibiting upwards of 20% branch dieback after just 3 years. However, trees with less than 10% defoliation and no branch dieback have also been recorded.

Since its first detection in North America, researchers have been working to better understand how this pest will affect stakeholders. They’ve been conducting research on the phenology and voltinism of EZS, exploring novel host associations, and evaluating management techniques. Here’s what they’ve learned so far.

A severely defoliated American elm in Surry County, N.C. Photo by Delaney Serpan

First, the bad news.

Elm zigzag sawfly has recently been found to feed on Japanese zelkova (Zelkova serrata), another common ornamental planting within the Ulmaceae family. However, it is important to note that Japanese zelkova is likely not a preferred host. It is suggested that while EZS can complete its life cycle on Japanese zelkova, it will do so only when no other suitable host is present. Researchers are continuing to explore this novel host association.

But help is on the way! There are management recommendations to control elm zigzag sawfly.

Research conducted at North Carolina State University has determined that soil injections of imidacloprid or dinotefuran at label rate are effective methods to significantly reduce larval populations on infested trees. Both active ingredients are easily accessible to landowners and can provide at least one year of protection against EZS. There is ongoing research to explore more treatment options, including augmentative biocontrol.

What can you do about elm zigzag sawfly?

If you are in an EZS-infested region, check vehicles or outdoor items before moving them.

And if you find EZS, report it! To best manage and prevent the spread of EZS, forest health professionals need to know where it is. Elm zigzag sawfly is the only insect that feeds in the unique zigzag pattern on elm trees. If you see the diagnostic feeding pattern, take a picture of it and contact your county’s local Extension agent or state forestry agency to report it.

Invited blog posted by Delaney Serpan

Delaney Serpan is a second-year Ph.D. student in the Forest Health Lab at NC State University, where she studies elm zigzag sawfly biology and management. She first began working with elm zigzag sawfly as an undergraduate researcher shortly after it was detected in North Carolina for the first time. Working with a novel invasive species on the leading edge of its invasion has been incredibly rewarding. Her work aims to provide accessible management techniques to stakeholders while also protecting elms, an already imperiled species, from further damage.

CISP welcomes comments that supplement or correct factual information, suggest new approaches, or promote thoughtful consideration. We post comments that disagree with us — but not those we judge to be not civil or inflammatory.

https://fadingforests.org

US imports continue falling … expected to sink further in 2026

Kevin Saville reports for the Journal of Commerce that containerized imports in 2025 are expected to be only 25.2 million TEUs, a decrease of 1.4% from 2024.

Declines are particularly large in the final months of 2025 since importers frontloaded their purchases to try to get ahead of the Trump Administration’s new tariffs. Imports for the first half of the year were up 3.6% compared with 2024 at 12.53 million TEUs. Thus, Saville’s sources expect November import levels to be 11.6% lower than in November 2024; December’s to be almost 13% lower.

Analysts expect the steeper decline to continue into the new year. Ben Hackett, of Hackett Associates, expects import volumes in the first four months of 2026 to be 10.3%, 8.5%, 16.8% , and 11% lower than the corresponding months a year earlier. The data source covers the ports of Los Angeles/Long Beach, Oakland, & Seattle & Tacoma on the West Coast; New York/New Jersey, the Port of Virginia, Charleston, Savannah, Port Everglades, Miami & Jacksonville on the East Coast; & Houston on the Gulf Coast. These are not all the maritime ports, but they are the major ones.

Another JOC reporter, Michael Angell, quoted several sources as saying they expect import volumes for all of 2026 to be flat or down 2% from 2025. Illustrating the reversal from past trends, The Port Authority of New York and New Jersey expects total container volumes in 2026 to be 8.5 million TEUs, a decline of about 2% from 2024. Since 2016, NY-NJ port container volumes have grown at an annual average of 4.2%.

As I have blogged before — see here and here — these swings in import volumes threaten to undermine programs intended to prevent introductions of wood-boring insects hitching rides in wood packaging material. While the higher volumes arriving from Asia in the first half of 2025 pose the most obvious risk, falling volumes reduce fee-based funding that support port inspectors. Another factor is the shift to suppliers other than China – primarily countries in Southeast Asia. Two beneficiaries of this shift are Vietnam and – at least initially – India. They have much better records of compliance with ISPM#15-mandated treatments for wood packaging link than does China.

A third JOC source reports that while US and European imports are down, trade volumes in Asia, Africa, the Middle East and Latin America are rising. I expect this growing trade to facilitate new pest introductions, although we will have to wait several years to see any data.

Posted by Faith Campbell

https://fadingforests.org

New Sirex established in South America … threat to pine plantations + threat to native conifer from North American aphid

pine plantation near Buenos Aires; photo by Biologicadero via Wikimedia

I have learned about the introduction of a North American woodwasp, Sirex obesus, in Brazil. Forestry interests in South America are worried that this woodwasp will cause significant damage to the pine plantations occupying 4.6 million hectares on the continent.

In July 2023, experts at the Estação Experimental de Ciências Florestais at ESALQ/USP in Itatinga, São Paulo, Brazil, investigated dead and symptomatic trees of several Pinus species and subspecies. They expected the causal agent to be Sirex noctilio – a woodwasp native to Europe and North Africa that has caused considerable damage to South American pine plantations since the 1980s (Wilcken et al.).

However, the pine species attacked were not typical hosts for S. noctilio (in Brazil, loblolly pine Pinus taeda). Instead, the infected trees were Caribbean pines, i.e., Pinus caribaea hondurensis, P. caribaea bahamensis, P. caribaea caribaea, P. maximinoi, P. tecunumani. The responsible woodwasp was identified as Sirex obesus. This species is native to the southwestern United States and northern and central Mexico (Wilcken et al.). This species is closely related to S. californicus (Wilcken et al.).

A second outbreak was found in November ~ 130 km away (still in São Paulo state). Scientists have not determined whether the two São Paulo outbreaks are related. Dr. Villacide reports (pers. comm.) that the two populations genetics have been compared, but he does not have the results.

A third population has been detected in a second, neighboring, state, Minas Gerais (Wilcken to Lantschner and Villacide).

This is the first record of S. obesus outside of North America (Wilckens et al.).

Little is known yet about this woodwasp’s probable impact. It is clear that it can oviposit in a wide range of pines. In its native range, S. obesus has been reported on three host species: Pinus ponderosa, P. teocote (twisted-leaf pine), and P. leiophylla (no common name; native to Chihuahua – mostly in Mexico, and border areas of New Mexico and Arizona]. In Brazil, as noted, it has been recorded on other species as well as the hybrids P. caribaea x P. elliottii and P. caribaea x P. tecunumanii (Wilcken et al.).

So for purposes of their risk assessment, Lantschner and Villacide assumed that S. obesus can affect any of the species commonly planted in the region: P. taeda, P. elliottii, P. ponderosa, P. contorta, P. caribaea, P. oocarpa, P. patula, P. radiata, and P. tecunumanii (Lantschner and Villacide).

The risk assessment predicts suitable climatic conditions for invasion by S. obesus in 48% of the areas where South American pine plantation occur, particularly in montane and high-altitude regions along the Andean corridor and central-eastern Brazil. Incorporating other factors – host distribution, proximity to invaded areas, and volume of wood imports from Brazil – identified the most vulnerable areas as in southern Brazil, northeast Argentina, the Argentine Patagonia, and central Chile (Lantschner and Villacide).

pine plantation in Argentina; photo by Tomas Asurmendi via pexels

Preliminary sampling (Wilcken et al.) indicates the impacts could be severe. Mortality varies by species: in the worst cases average mortality approached 43% on P. caribaea hondurensis but only 11% on loblolly pine (P. taeda). They expect mortality rates to increase. Another 30% of P.c. hondurensis trees are dripping resin, a sign of woodwasp oviposition. If these eggs hatch, those larvae will probably kill the affected trees. Such a result would increase total mortality of P.c. hondurensis from 43% to ~ 73%. For P. taeda, the current mortality rate of 11% could rise to 49% as an additional 38% of trees succumb. Following this logic, these areas could experience complete tree mortality within a few years. Given the extent of pine plantations, and possible mortality rates, even a partial spread of S. obesus could lead to significant econ losses.

As second factor is the number of generations per year; the higher the number, the faster woodwasp populations can increase. Wilckens et al. report that adult emergence in Pinus logs maintained in cages indicates that S. obesus could have two or three generations per year.

S. obesus seems to prefer a different climate than S. noctilio. As noted, S. obesus seems to prefer montane and high-altitude climates. S. noctilio is concentrated in lowland temperate and humid regions (Lantschner and Villacide). The newly introduced species might substantially broaden the geographic area where pine plantations might be at risk – although further research is needed to clarify this point.

S. obesus also appears to be spreading at a rapid rate — ~46 km / year. At this rate, Lantschner and Villacide say it could spread throughout all major pine plantation areas in Brazil in less than years.

Sirex woodwasps kill trees by injecting a symbiotic wood decay fungus and a phytotoxic mucus into the tree when ovipositing. The toxin weakens the tree, allowing the fungus to spread, typically killing the tree in as little as three–four months. In North America S. obesus is associated with Amylostereum chailletti. While this species has not yet been confirmed in Brazil, (Wilckens et al.). Brazilian scientists are exploring whether S. obesus might adopt the fungus already present, Amylostereum areolatum, which is associated with S. noctilio.

Two insect species known to feed on woodwasps have emerged from logs infested with S. obesus: Ibalia leucospoides (Hymenoptera: Ibaliidae) and a species of Schlettererius (Hymenoptera: Stephanidae). While these two predators have not proved to be effective controls of woodwasps by themselves, they might become part of a control program. The parasitic nematode, Deladenus siricidicola (Nematoda: Neotylenchidae) used successfully in several South Hemisphere countries to control S. noctilio has not been found in Brazil (Wilckens et al.).

Scientists don’t know the pathway by which S. obesus entered Brazil. Wilckens believes it was via wood packaging; technicians from the Ministry of Agriculture have found some pallets associated with imports that lacked the ISPM#15 mark (Wilckens et al.).

Both Lantschner and Villacide and Wilcken et al. stress the vulnerability of South American pine plantations to introduction of damaging pests. The plantations are reportedly intensively managed, even-aged, regularly spaced monocultures. These conditions can facilitate invasive species establishment and spread by providing abundant host resources and reduced natural enemy pressure. Lantschner and Villacide cite Michael Wingfield that in plantation forestry, introduction of a single pest species can damage large areas of valuable timber.

mortality caused by *Sirex noctilio* in a pine plantation in Argentina; photo courtesy of Jose Villacide

The family Siricidae contains more than 120 species distributed across the forests of the Northern Hemisphere. In their native ranges they are typically minor or secondary pests (Wilckens et al.). Woodwasps have demonstrated that they can be transported in international commerce – S. noctilio alone has invaded pine stands (native or exotic) in nine countries in Oceania, Africa, and South and North America. Three other species in the family — Urocerus gigas, Urocerus flavicornis and Tremex fuscicornis – have been detected in South America (Wilckens et al.). If each represents a unique threat, countries with widespread pine plantations should enhance their phytosanitary programs. Exporting parties, e.g., the United States and European Union, should assist in efforts to prevent spread of these wood borers. One major step would be to strengthen regulations governing wood packaging material. [To see my criticisms of shortfalls of the ISPM#15 system, scroll down the list of blogs to “Categories” and click on “wood packaging”.]

Lantschner and Villacide cautionthat their assessment is based on a limited record of S. obesus occurrences in its native range. This range might be restricted by factors other than climate, including geographic barriers or biotic interactions (natural enemy pressure or interspecific competition). If so, the species’ potential invasive range might be larger than the climate-based models predict.

Recommendations for management strategies

I applaud Lantschner and Villacide for proposing immediate steps to improve management of the threat posed by introduction of S. obesus. These recommendations should prioritize enhanced phytosanitary inspections of wood products moving between high-risk regions and other South American countries. They suggest that Brazil adopt bilateral agreements with its major trading partners which would specify protocols for woodwaspdetection and quarantines. [Since many of these countries already have established populations of S. noctilio they probably do not have strong phytosanitary measures targeting wood borers at present.] Lantschner and Villacide advise creation of targeted surveillance programs in southern Brazil, northeastern Argentina, Argentine Patagonia, and central Chile. They should focus on sites near major transportation hubs and border crossings. Less intense surveillance should be instituted in regions they classified as medium risk. Again, the focus should be on major points of entry for imported goods and on plantations located near the Brazilian border. They note that preventing spread of S. obesus into new areas will require not only national efforts but also regionally coordinated monitoring, research, and forest health policies.

Lantschner and Villacide also identify priority areas for future research. These include clarifying S. obesus’shost range, the environmental conditions that enable the woodwasp to establish and persist beyond its native range, dispersal rates, and whether S. obesus exhibits pulse-like pop dynamics[long periods of low density interrupted by sudden outbreaks] seen in S. noctilio.

Dr. Villacide (pers. comm.) reports that Brazilian scientists are trying to delimit the extent of the outbreaks. Public and private scientists in other countries with pine plantations have begun developing responses. Dr. Villacide has posted a video from a recent online seminar sponsored by the Southern Cone Forest Health Group. Go to https://youtu.be/uVU6CpFNhlQ?si=lqXtwJTtz5rKXfL3 or
https://sanidadforestalconosur.org/

A wider prespective

Dr. Villacide’s attention to Sirex obesus is part of his broader work on pest issues in South America’s commercial plantations. In another publication (Villacide and Fuetealba 2025; full citation at the end of this blog), he explores how to make these plantations sustainable in the face of rising threats from pests – both introduced and native to the region. Dr. Villacide and Alvaro Fuetealba report that every year 1.2 million hectares of plantations in the Southern Cone are affected by pests. Their vulnerability of will be worsened by the extreme weather events expected under climate change.

These plantations present vast areas of homogeneous stands: ~97% of the Southern Cone planted area consists of exotic tree species – mainly Pinus and Eucalyptus. Typical plantations are high density and managed intensively – including thinning, pruning, and fertilizing – to prompt rapid growth. As Villacide and Fuetealba point out, while these practices maximize wood production efficiency, they also lead to biological homogenization and reduced resilience to pests.

They report that pine plantations are under attack by wood and bark borers that have followed pines to the region, including Sirex noctilio, Orthotomicus erosus, and Cyrtogenius luteus; and now the newly detected Sirex obesus (above). At least two fungal pathogens — Fusarium circinatum and Dothistroma septosporum – have also been introduced. The principal threat to pine plantations from native pests comes from leaf-cutting ants (Atta and Acromyrmex).Eucalyptus plantations are plagued by several insects that have arrived from Australia, including Phoracantha semipunctata, Thaumastocoris peregrinus, and Leptocybe invasa. Pests native to the region that attack Eucalyptus are the Chilean carpenter worm (Chilecomadia valdiviana) and the leaf-cutting ants.

Cordilleran cypress; photo by LBM 1948 via Wikimedia

Threat to native conifer

More worrying to me is that introduced pests have entered native forests. Villacide and Fuetealba report that the aphid Cinara cupressi is attacking the native conifer Austrocedrus chilensis. Cordilleran cypress, also called Chilean or Patagonian cedar, is an endemic, monospecific tree in the Cupressaceae family. In southern Argentina and Chile the species forms pure and mixed stands with southern hemisphere beech (Nothofagus spp.) across ~ 160,000 ha. The profile Cinara cupressi on the Global Invasive Species Database is unclear about how many species are in the species complex and their places of origin.

Cordilleran cypress is also under attack by the oomycete Phytophthora austrocedri, an oomycete of unknown origin. This pathogen is of unknown origin. It is now thought to have been present in Argentina since at least the 1960s. P. austrocedri has also been ntroduced to Europe, western Asia, and North America.

Villacide and Fuetealba advocate several actions to might diversify tree species in the plantations to reduce their vulnerability to pests. They note that this recommendation builds on foundational ecological theory, including the resource concentration and natural enemy hypotheses. Diversity-promoting actions should reach beyond any plantation to the landscape level. Managers should consider connectivity of susceptible stands, the number of nutritionally optimal host trees in the landscape, and the availability and quality of hosts in adjacent stands.

Villacide and Fuetealba say mixed plantations can provide additional ecological and economic benefits, such as enhanced stand-level productivity; production of a wider range of commercial and subsistence products; and greater resistance and resilience to natural disturbances, e.g., extreme weather events.

They warn that designing and implementing mixed plantations must reflect ecological interactions and pest dynamics as well as management. There is need for regionally coordinated experimental plantations where scientist could test how variables such as tree species composition, density and spatial arrangement, and silvicultural practices influence pest dynamics, forest productivity, and ecosystem resilience under local conditions. They suggest incorporating sentinel plantings both early-warning systems and decision-support tools at plot and regional scales. Researchers should evaluate pest-specific responses, productivity trade-offs, long-term forest health outcomes under different scenarios.

Since the plantations extend across a multinational region with few natural barriers and uniform silvicultural practices, as well as high levels of trade, so do the pest problems. Therefore, the response must also be regional – e.g., regional experimental plantations and living laboratories. A collaborative approach linking researchers, forest managers, and policymakers is essential to translate experimental findings into practice and develop adaptive, ecol grounded silvicultural strategies. Long-term ecological trials must be embedded in operational contexts and aligned across countries.

SOURCES

Lantschner, V. and J. Villacide. 2025. Invasion Potential of the Recently Established Woodwasp Sirex obesus. Neotropical Entomology. (2025) 54:117 https://doi.org/10.1007/s13744-025-01347-6

Villacide, J. and A. Fuetealba. 2025. Pests in plantations: Challenging traditional productive paradigms in the Southern Cone of America. Forest Ecology and Management 597 (2025) 123127

Posted by Faith Campbell

https://fadingforests.org

Welcome high-level attention to bioinvasions – although key issues remain unresolved

Japanese knotweed (*Reynoutria japonica*) – one of the worst invaders around globe. Photo by Will Parson, Chesapeake Bay Program via Flickr

On 23 October, Science published a five-page, data-packed analysis of bioinvasion impacts on terrestrial ecosystems!!!

Thakur, Gu, van Kleunen, and Zhou (full citation at end of this blog) analyzed 775 studies with the goal of improving understanding of factors contributing to invasions’ impacts – as distinct from “invasibility” (ability to establish). This knowledge is essential to assessing the risk posed by introduced species and setting priorities for management. They analyzed five ecological contexts—diversity of native species and introduced species in the recipient systems, latitude, invader residence time, and invader traits.

They concluded that ecological factors commonly used to explain invasion success do not consistently translate into strong predictors of invasion impacts. Impacts vary in response to the context of the invasion.

[In January 2026, the authors announced changes in details of the article due to some errors in the database and their understanding of it. (Science 8 Jan 2026 Vol. 391 Issue 6781) They conclude that the corrected analysis did not alter the trends described or the overall conclusions.]

limber pine (*Pinus flexilis*) – one of the species killed by *Cronartium ribicoli*; photo by F.T. Campbell

Among the studies available for analysis, reports on plants dominated: 605 focused on plant invasions, 114 on animal invasions, and only 56 on microbial invasions. Among the animals were one study of Adelges tsugae (hemlock woolly adelgid), two studies of Agrilus planipennis (emerald ash borer) and one study each of Lymantria dispar (spongy moth), and Ips pini (North American pine engraver). Studies also addressed earthworms, ants, rats, and feral hogs. Microorganisms included Cronartium ribicoli (white pine blister rust) and several Phytophthora species, including P. agathidicida (kauri dieback), P. alni (affects alders), and P. ramorum (sudden oak death).

Thakur et al. note the skewed taxonomic coverage and say that the low number and narrow taxonomic/ecological variety in the animals and microorganisms probably limit their ability to reach robust conclusions about the impacts of such invasions.

The most consistent negative impact they found is reductions in native plant diversity. While this is not surprising given the studies analyzed, I think it is still important since it counters the widespread sense that plant invasions are somehow less deserving of a robust response.

The authors also detected some broader ecosystem impacts of plant invasions. Plant invasions increased soil organic carbon; soil nitrogen (ammonium and nitrate), and available phosphorus; soil moisture, litter biomass; and emissions of carbon dioxide (CO₂), nitrous oxide (N₂O), and methane (CH₄). The changes in biogeochemical properties might reinforce impacts on native plant communities. The reported increase in greenhouse gas emissions might reflect a bias in the studies so Thakur et al. call for more research to solidify this finding.

High native plant species richness had only a weak overall effect on ecosystem-level impacts. While plant invasions often resulted in higher overall plant species richness, when considering only native community responses, the gain in species numbers did not necessarily indicate conservation benefits. Native plants’ biomass increased after invasion. This might reflect short-term increases in productivity in response to altered resource conditions or structural facilitation, rather than a long-term reversal of competitive exclusion. Finally, the longer the invasive [plant] species had been present, the greater the negative effects on native diversity. However, soil abiotic property impacts weakened over time. In fact, the initial increase in soil organic carbon and total nitrogen disappeared after 6 to 10 years. This development might reflect fertilization of ecosystems by long-established nitrogen-fixing invaders such as non-native legumes.

Traits of non-native plant species related to growth and resource acquisition were overall weak predictors of ecosystem impacts. Thakur et al. consider that this finding reflects the relatively narrow range of specific leaf area exhibited by the plant species studied most commonly.

Consequently, Thakur et al. urge managers to focus on containment and impact mitigation, and to prioritize persistent losses of native plant diversity. When considering abiotic responses that might lessen over time, managers should apply “adaptive monitoring” (which is not defined).

Thakur et al. had greater difficulty determining the impacts of animal and microorganism invasions because of the smaller number of studies. They could not determine the effect of native species richness. The observed decline in soil organic carbon they thought was attributable to the large proportion of studies (9 out of 114) that focused on introduced earthworms. Earthworms reduce organic matter by consuming litter. Mammals were also found to reduce soil organic carbon. Introduced insects had no significant ecosystem effects on soil organic carbon. Non-native animals also increased soil emissions of carbon dioxide and nitrous oxide. The microorganisms included in reviewed studies decreased soil ammonium and increased nitrate, consistent with elevated nitrification. While data on body size of invasive animals were sparse, the authors could determine that larger-bodied species tended to increase soil nitrate while reducing effects on total soil N.

Applying the Results

Thakur et al. report that residence time outperformed other factors as a predictor of invasion impacts. The authors regret the scarcity of long-term studies, especially in the Global South, that could increase our understanding of whether these impacts persist or shift under sustained invasion pressure.

How can scientists apply this information in risk assessments evaluating not-yet introduced species or in deciding what is the appropriate intensity of immediate response to newly detected incursions. Should they give greater weight to others’ studies that focus on long-established invasions by the species in question? Otherwise, this finding seems to largely duplicate the long-established “invasion curve”.

I hope scientists will note that observational studies generally showed stronger impacts than experimental ones, particularly in the case of plant invasions. Perhaps this is true because observational studies better incorporate environmental heterogeneity and longer time spans.

Agrostis stolonifera – one of the plants invading on Prince Edward Island, an Antarctic region island under South African jurisdiction. Photo by Stefan Iefnaer via Wikimedia

Thakur et al. note that one factor they analyzed, “latitude”, incorporates several ecological and anthropogenic components relevant to invasion impacts. One element is the greater native bioidiversity in warmer, lower-latitude, regions. According to the “biotic resistance” hypothesis, greater diversity might make these systems more resistant to bioinvasion. However, the situation is complicated by the fact that temperate regions have also often experienced longstanding and intensive land-use modifications — which are believed to facilitate invasive species establishment and spread. I regret that the authors make no attempt to separate the effects of factors that are anthropogenic from those arising from immutable conditions, e.g., latitude, topography, weather patterns, etc.

Thakur et al. call for more studies that cover a wider geographic range. In addition, the studies should include more experimental designs and explore the relationship between invaders’ traits and impacts — especially regarding animals and microbes.

SOURCE

Thakur, M.P., Z. Gu, M. van Kleunen, X. Zhou. 2025. Invasion impacts in terrestrial ecosystems: Global patterns and predictors. Science 23 October 2025

Posted by Faith Campbell

https://fadingforests.org

Actions USDA Could Take to Better Protect Our Forests

ohia trees killed by ROD near Pahoa, Hawai`i; with JB Friday; photo by F.T Campbell … APHIS has not applied NAPPRA to this pathogen

As I have documented numerous times in these blogs, [see here, here, here, here, here, here, here and here] forests throughout the world are being reshaped by rising numbers of introduced, non-native pathogens. Once established, these diseases are nearly impossible to contain, much less eradicate.

While the worst effect of such bioinvasions is widespread mortality of host species, even “lesser” results produce significant changes in the impacted ecosystems.

I believe that the international phytosanitary “system” adopted by the World Trade Organization (WTO) and amended by the International Plant Protection Convention (IPPC) in the mid-1990s impedes efforts to prevent introductions of pathogens. These rules require unattainable levels of certainty about an organism’s impacts before it can be restricted. Scientists such as Haoran Wu and Kenneth Raffa have called for phytosanitary approaches that will be more effective because they are realistic, reflect the true level of threat, and the limits of current science. I agree and have repeated their calls.

How Well Is This “System” Keeping Pathogens At Bay?

If the world’s phytosanitary system worked well, we should be seeing fewer high-risk forest pathogens being introduced to new countries. Instead, examples abound of pests invading new ecosystems in the post-WTO/IPPC era: Austropuccinia psdii — detected in Hawai`i in 2005, Japan in 2009, Australia in 2010, China in 2011, New Caledonia and South Africa in 2013, Indonesia and Singapore in 2016, and New Zealand in 2017.
Phytophthora ramorum – 8 to 14 additional introductions to California after its initial detection.
Fusarium disease vectored by beetles in the Euwallaceae genus:
- Euwallacea fornicatus s.s.— detected in southern California in 2003, Hawai`i in 2007, Israel in 2009, in South Africa in 2012, in Australia in 2021, and in Argentina and Uruguay in 2023 and 2024 . The haplotype detected in South America and several European greenhouses differs from that established elsewhere.
- E. kuroshio detected in southern California in 2013; has spread to nearby Mexico
- E. interjectus detected in central California in 2024.
Boxwood blight fungus Calonectria pseudonaviculata — first detected in the Caucuses in 2010 and the US in 2011. Now established in at least 24 countries in three geographic areas: Europe and western Asia; New Zealand; and North America. Boxwood blight has caused rapid and intensive defoliation of native stands of Buxus sempervirens. Although disease was detected in United Kingdom in the mid-1990s, the causal agent was not determined until 2002.
Beech leaf disease caused by the nematode Litylenchus crenatae subsp. mccannii — detected near Cleveland, Ohio, in 2012. Has since spread east to the Atlantic Ocean, south to Virginia, north into Ottawa.
Phytophthora austrocedrii — detected in nurseries in Ohio and Oregon in 2024. Previously known from Argentina and in England and Scotland. At the latter location it is causing mortality of native Juniperus and introduced Cupressaceae. See here and here.

Most of these pathogens were unknown at the time they were discovered – because they were causing disease in the invaded ecosystems.

beech leaf disease symptoms in northern Virginia; photo by F.T. Campbell

In the Face of International Failures, How Can USDA’s APHIS Succeed?

When countries choose to prioritize preventing bioinvasions, they can impose more restrictive controls than those implemented by the WTO/IPPC system.

I urge USDA to more proactively use its authority to protect America’s plant resources. In particular, I urge USDA leaders to use the NAPPRA authority more effectively and quickly. This allows the agency to temporarily prohibit importation of plants that host potentially damaging pathogens. ). https://www.aphis.usda.gov/plant-imports/nappra

We Americans can’t protect our forests from pathogens without APHIS responding more promptly to recent detections of pathogens in North America and on Pacific islands. Recent events are not encouraging.

The agency did undertake an analysis of Phytophthora austrocedrii after it was detected in nurseries in two states. Unfortunately, in my view, APHIS and the states decided the pathogen was too widespread so they dropped any idea of regulating it. This was despite the apparent threat to junipers across the country. See here and here. P. austrocedri also attacks cypress trees, including Port-Orford cedar, Chamaecyparis lawsoniana. USFS scientists recently announced success in breeding POC trees resistant to a different pathogen.

There are no indications that APHIS will respond to detection of a new pathogen causing wilt disease in elms (Plenodomus tracheiphilus) recently discovered in Alberta, Canada. The pathogen is spread primarily through movement of infected plant material, including on asymptomatic material. Current U.S. regulations do not prohibit importation of plants or cut greenery in the Ulmus genus from Canada. Beyond the risk associated with elm material, I think it is probable that this pathogen also survives on plants in additional taxa, since it was formerly known for causing disease on citrus trees.

Although APHIS has classified Leptosillia pistaciae as a federal quarantine pest, I have learned of no response to detection of the pathogen on the native California shrub, lemonade berry (Rhus integrifolia), in 2019.

Rhus integrifolia – host of *Leptosillia pistaciae*

Has APHIS Changed its Practices in Response to Recent Detections?

We’ve known about gaps and weaknesses in APHIS’ approach for a long time. Here are specifics.

Has APHIS upgraded its attention to nematodes – as should have been prompted by detection of the beech leaf disease nematode (above) and as recommended by Kantor et al.?

Has APHIS changed any of its practices or policies in response to detection of plant and human pathogens associated with wooden handicrafts from countries other than China? Or wood pieces used for unanticipated purposes, e.g., to decorate aquaria? All 31 fungal taxa detected by one of these studies were viable despite having been subjected to various phytosanitary requirements.

USDA has no authority to regulate organisms that pose a risk to non-plant hosts, like us humans! Has APHIS contacted officials at the relevant agency?

Does APHIS respond to detections abroad when pests attack congeners of North American trees? I have blogged about several — see here, here, here and here — detected in Europe or Asia that attack cypress, magnolia, dogwood, Persea, and oaks. PestLens — an alert system created by APHIS — reported these.

How has APHIS incorporated the findings at various “sentinel garden” projects? And the wider implications of findings by Eliana Torres Bedoya and Enrico Bonello regarding findings on asymptomatic plants?

How is APHIS applying the impact assessment tools developed (for insects) by Ashley Schulz and Angela Mech? Has APHIS incorporated Kenneth Raffa’s advice about the strengths and weaknesses of various prediction tools?

I wonder whether APHIS has responded in any way to the rash of woodborer introductions on the west coast, including three species in the invasive shot hole borer complex and the Mediterranean oak borer. Has the agency explored the threat that the spotted poplar borer (Agrilus fleischeri) – another wood-boring beetle native to northern Asia – might pose to North American Populus species? Canada has twice intercepted the species on solid wood packaging material .

USDA APHIS is explicitly not a research agency. However, it claims that its decisions are science-based. In my view, this means APHIS has a responsibility to respond to scientific findings (such as those above) and to bring about research aimed at answering pertinent questions, e.g., those related to risks of pest introduction and establishment, effective detection and management technologies, etc.

APHIS has occasionally done this:

It established the NORS-DUC research facility to study what aspects of nursery management facilitate establishment of Phytophthora ramorum.
It enabled and participated in several studies of wood-borer introduction via wood packaging, including those by Robert Haack and colleagues (see blogs on this website under the category “wood packaging”).
It enabled and participated in a study of introduction pathways that included plants-for-planting – relying on 2009 data. (Liebhold et al. 2012)
Did APHIS support the study by Li et al. to evaluate the vulnerability of two oak and two pine species to 111 fungi associated with Old World bark and ambrosia beetles?

APHIS could do much more to determine whether North American trees are vulnerable to pathogens and arthropods detected on the congeners in trade partner countries. Opportunities include:

studying which North American species might be vulnerable to the growing number of the 38 new Phytophthora species detected overseas. This would be a monumental task: 216 species have been recognized in the genus. I have focused specifically on the 38 species detected by Jung, Brasier, and others in Vietnam and now the 18 Phytophthora species detected in the Alps. (I have already noted that APHIS and the states dropped any idea of regulating one of those species, P. austrocedrii).
Regarding P. ramorum specifically, scientists now recognize 12 genetic strains; 8 are in Southeast Asia, a ninth (EU2) in Europe. How likely is it that some of these will be introduced to the U.S.? Three strains are known to be established in western North American forests – NA1, NA2, and EU1.

In addition, new hosts continue to be identified. APHIS has pledged to update the host list annually. In the past I have criticized APHIS for not accepting hosts identified in the United Kingdom.

While APHIS is not well-funded, it has largely escaped budget slashing by “DOGE,” other Trump Administration cuts, and congressional decreases. Scientific expertise at the USDA Forest Service has been shrinking for decades (see Chapter 6). Now, loss of expertise has reached crisis levels. The result will be less capacity to assist APHIS in evaluating pest risks and research needs.

Earlier, I noted the importance of APHIS using its full NAPPRA authority. Unfortunately, the record is not encouraging here, either.

Since the agency gained this authority in 2011, it has adopted lists of species temporarily prohibited for importation only three times – in 2013, 2017, and 2021. I complained that the last action was tardy and provided insufficient protection to Hawai’i’s unique flora arising from multiple strains of the ‘ōhi‘a rust pathogen Austropuccinia psidii and here. Even worse, four years after promising to close the loophole that allowed continued imports of cut flowers and foliage – the most likely pathway by which the rust was introduced to Hawai`i, APHIS has not proposed the necessary rule.

Pathogens are more difficult to detect and manage than invasive insects. The “disease triangle” is complex! Numerous pathways are involved! But they also get less attention – and this reflects unwise decisions by agency leaders. I suggest that they should respond to this complexity by adding resources. Voglmayr et al. (full reference at the end of this blog) also called for more attention to pathogens. Kantor et al. noted that nematodes are also neglected.

Of course, I have repeatedly urged APHIS leadership to enhance enforcement of regulations governing imports of wood packaging. One suggestion is that it prohibit importation of Chinese wood packaging because of its 25-year record of not complying with – first – U.S. and Canadian regulations and – later – the international regulation known as ISPM#15.

Information Gaps Impede APHIS’ Domestic Program

I have criticized APHIS’ failure to find answers to several questions important to managing the sudden oak death pathogen, Phytophthora ramorum. Like the many questions listed earlier, these also need priority attention.

APHIS has regulated interstate movement of nursery stock to contain P. ramorum for over 20 years. I appreciate its creation of NORS-DUC. But it is also responsible for protecting natural systems in regions not yet invaded, e.g, in the East. APHIS should have studied these issues years ago, given the frequency with which pests spread nationwide via the nursery trade.

Other pathogen systems also have genetic variation that might be important in determining pest-host relationships. As of 2022, scientists had identified 43 haplotypes (genetic variants) of E. fornicatus s.s. worldwide, with the greatest diversity in several Asian countries (P. Rugman-Jones, pers. comm). Other species of plant pathogens also have several haplotypes.

Forests At Risk Outside of North America

North American forests are not alone in being besieged by non-native pathogens. Their numbers have been rising also in Europe and Oceania. The record is less clear in Africa, South America, and Asia.

Reports of tree pathogens in Europe began rising suddenly after the 1980s – admittedly 15 years before the WTO took effect. By 2012, more than half of infectious plant diseases in Europe were caused by introduction of previously unknown pathogens https://www.nivemnic.us/?p=5164

Antonelli et al. (full citation at the end of this blog) report that three previously undetected species of Phytophthora have been detected in European nurseries since 2016. Voglmayr et al. reported that the number of alien fungi in Austria increased 4.6-fold over 20 years. Eighty percent were plant pathogens. The introductory pathway was unclear for the vast majority. They note that differences in research efforts probably explain some discrepancies.

The ash decline pathogen, Hymenoscyphus fraxineus, has apparently been present in eastern Europe since the 1980s, so its spread has probably not been facilitated by the downsides of the WTO/IPPC system.

Other sources report recent introductions of insects to Europe. Musolin et al. reported that 192 species of phytophagous non-native insects had been documented in European Russia as of 2011. They included the emerald ash borer detected in Moscow in 2003. Some of these insects were probably introduced to Europe (outside Russia) before the WTO/IPPC system came into effect. Examples are two insects from North America that were detected in 1999 and 2000, respectively – the western coniferous seed bug, Leptoglossus occidentalis, which vectors a pathogenic fungus Sphaeropsis sapinea (=Diplodia pinea); and the oak lace bug, Corythucha arcuata.

Australia was slow to respond to detection of myrtle rust, Austropuccina psidii. Few federal resources were made available to study its impacts – although the Australian flora includes at least 1,500 species in the vulnerable plant family. Carnegie and Pegg said this experience demonstrated the need to integrate the work of agencies responsible for conservation of natural ecosystems with those determining and implementing phytosanitary policy. New Zealand initially responded more assertively, but also found little funding to support resistance breeding or even to track the rust’s spread.

The record is less clear regarding Africa, South America, and Asia.

Africa

Sitzia et al. expressed concern that bark and ambrosia beetles threaten to cause significant damage to tropical forests. Several factors contribute to these threats: the long history of plant movement between tropical regions; conversion of tropical forests that disturbs canopies, understory plant communities, and soils; and, generally, regions with fewer resources to prevent or respond to invasions.

In Africa, Graziosi et al. reported on the cumulative economic impact of invasive species and the continent’s limited capacity to prevent or respond to introductions. They don’t discuss whether pests attacking plantations of non-native trees followed those trees from their point of origin. They found that some introduced insects pose significant threats to native tree species. They mentioned the Cypress aphid, Cinara cupressi, which was attacking both native African cedar, Juniperus procera, and exotic cypress plantations. All the examples appear to have been introduced before the WTO/IPPC system took effect. All the examples appear to have been introduced before the WTO/IPPC system took effect.

*Cinara cupressi*; photo by Blackman & Eastop via Wikimedia

Graziosi et al. point out that South Africa plays a central role because it imports significant volumes of goods that can transport pests. At most immediate risk is South Africa’s highly diverse and endemic flora. For example Phytophthora cinnamomi is attacking native Proteaceae, which are important components of the unique Cape Floral Kingdom. Other pathogens are attacking native conifers in the Podocarpus genus, Ekebergia capensis (Meliaceae), and Syzygium trees. However, pests first introduced to South Africa often spread. Graziosi et al. name several insects and pathogens of Eucalyptus and the wood-boring pest of pine Sirex noctilio.

Pests in Asia

Available information about China is not definitive. The FAO reports that half of the most damaging forest pests are non-indigenous. They were estimated to occur over an area of 1.3 million ha and to kill over 10 million trees per year. However, the three tree-killing pests which receive the most attention are the pinewood nematode (Bursaphelenchus xylophilus), red turpentine beetle (Dendroctonus valens), and fall webworm (Hyphantria cunea). These were all introduced before the World Trade Organization was founded.

The FAO notes several non-native insects that attack native trees in India, but all were introduced decades before the World Trade Organization began. There is no discussion of tree pathogens.

Thu et al. report a growing number of pest outbreaks damaging plantations of non-indigenous trees in Vietnam. In most cases the pests are indigenous to the country. They report that almost nothing is known about pests that attack species in the highly diverse native forests.

The September 2025 meeting of the International Forest Quarantine Research Group (IFQRG) had a session devoted to the topic “Risk of international trade in plants for planting”. The specific presentations are titled

“Using molecular tools to elucidate the pathways of cryptic pests on plants for planting”
“Risk-based approach to the movement of germplasm into Australia: the luxury afforded to an affluent continent” (note my earlier blog criticizing Australian efforts re forest pests)
“Challenges in the validation of methods for detection of quarantine pathogen – P. ramorum”
“Challenges in surveillance and detection of quarantine fungal tree pathogens in European Union”
“Pathogens in trade and the risk of establishment – update”

I hope that some of these discussions begin to tackle the crucial questions I raised in this blog and earlier. Also, I hope IFQRG continues to explore these important questions.

As Wu and Raffa et al. have said, Earth’s forests cannot afford delay in finding solutions to the challenges posed by introductions of novel pathogens to naïve systems.

SOURCES

Antonelli, C.; Biscontri, M.; Tabet, D.; Vettraino, A.M. 2023. The Never-Ending Presence of

Phytoph Spp in Italian Nurseries. Pathogens 2023, 12, 15. https://doi.org/10.3390/pathogens12010015

Voglmayr, H., A. Schertler, F. Essl, I. Krisai-Greilhuber. 2023. Alien and cryptogenic fungi and oomycetes in Austria: an annotated checklist (2nd edition). Biol Invasions (2023) 25:27–38 https://doi.org/10.1007/s10530-022-02896-2

Posted by Faith Campbell

https://fadingforests.org