Category: forest pathogens

Tree deaths in a National Park – what I saw

In June I visited Shenandoah National Park (SHNP) (above) for the first time in years. The Park’s forests are mostly mature secondary forests, having recovered over the 90 years since establishment from earlier logging and clearing for small-scale farms and pasture.

While I loved the forest and the vistas, I was aware of which species are missing …

Five years ago I blogged about a study by Anderson-Teixeira et al. (full citation at the end of this blog) that reported on the changes in the forests of SHNP and the neighboring Smithsonian Conservation Biology Institute (SCBI). This is important because, as Fei et al. (2019) (full citation at the end of this blog) documented, nine of the 15 most damaging introduced forest pests grow in eastern forests. In fact, the greatest increase in biomass loss has occurred in Eastern forests. Seven are found specifically in SHNP (Potter et al. 2019; full citation at the end of the blog).

Anderson-Teixeira et al. report that non-native forest pests caused a loss of about a quarter of ecosystem above-ground biomass between 1991 and  2013 across 66 sites. These invasions occurred after the worst impacts of chestnut blight, which entered the country ~120 years ago – before “modern” phytosanitary programs were instituted. Still, total above-ground biomass has largely recovered through germination and growth by trees in other genera. Greatest increases have been by tulip poplar (Liriodendron); oaks (Quercus); ash (Fraxinus) – but see below; birch (Betula); and maples (Acer). And while several taxa were lost from monitoring plots in SHNP and SCBI, a-diversity also remained steady.

So what does that look like on the ground?

American chestnut used to dominate many Eastern forests, composing more than one-third of the pollen assemblage in some stands (Fei et al.) According to Anderson-Teixeira et al., chestnut trees larger than 10 cm DBH disappeared by 1910, killed by chestnut blight. In past decades I frequently saw chestnut root sprouts when hiking. The National Park Service now urges visitors to hike to low elevation sections of the South River Trail to see such sprouts.

In the 1980’s, groves of eastern hemlocks occupied about 9,800 acres in SHNP, primarily in shaded valleys and along streams. Invasion by the hemlock woolly adelgid killed 95% of these hemlocks. Anderson-Teixeira et al. document the species’ disappearance from their study plots by 2007. Park staff treated more than 20,000 hemlocks using injections of imidacloprid. In 2015, the Park began partnering with Virginia Polytechnic Institute and State University in releasing predatory biocontrol beetles (Laricobius spp.)  While the beetles have shown promising establishment and spread, it is now recognized that additional biocontrol agents will be needed to suppress the adelgid. The Park plans to allow releases of predatory silver flies (Leucotaraxis spp.) in remaining hemlock sites and will begin to phase out the imidacloprid treatments.

I remember the hemlocks! But this year, at least in the creek valleys where I hiked, I saw almost no remnants – not even fallen logs.

fallen hemlock; all photos by F.T. Campbell in Shenandoah NP in June 2025

And I remember the flowering dogwoods. They are almost gone now from the Appalachian chain, killed by dogwood anthracnose. Their status in SHNP is unclear. Anderson-Teixeira et al. report flowering dogwoods only from the Smithsonian property. There, they declined by almost 90% from the study plots from 2008 to 2019. The Park’s list of tree and shrub species reports that flowering dogwood is still “abundant”; my visit was too late in the season to observe how visible flowering dogwoods still are. Certainly the species survives the disease better in open settings, e.g., meadows and roadsides. I don’t know how the three other native Cornus species were affected.

Dead ash are still visible. Ash trees made up about 5% of the Park’s forest cover. Anderson-Teixeira et al. report that ash aboveground biomass was increasing in SHNP and stable on the SBCI property before arrival of the emerald ash borer (EAB). EAB-caused mortality was first detected in 2016. In just three years — by 2019 – 28% of green, white, and black ash had died; this meant a loss of 30% of ashes’ aboveground biomass. Ninety-five percent of remaining live trees were described as “unhealthy’’. In an effort to retain ash trees for visitor enjoyment, reduce threats to visitors from hazard trees, and to preserve a portion of the park’s ash tree communities until host-specific biological controls become available, SHNP staff – supported by specially trained volunteers and interns, Virginia Department of Forestry and Fairfax County – began treating high-value ash with emamectin benzoate. They began at Loft Mountain Campground, a location (elevation 3,300 feet) where ash trees make up most of the forest. Three hundred forty three trees were treated there — exceeding expectations for what could be accomplished in a single year. The park hopes to treat an additional 200-400 trees. They will target ash trees around campgrounds, picnic areas, overlooks and other areas frequently used by visitors. These efforts were supported by the Shenandoah National Park Trust and here.

I saw many dead oaks – probably the result primarily of repeated attacks by the spongy moth link beginning in 1982. Oak-dominated study plots in SHNP lost on average 25% of individuals and 15% of above-ground biomass. After 1995, when spraying of Bacillus thuringiensis var. curstaki improved control efforts (at the expense of native moths), oak aboveground biomass increased gradually, driven by individual tree growth rather than recruitment. Oak abundance continues to decline due to oak decline and absence of management actions to promote regeneration (Anderson-Teixeira et al.).  These authors do not mention oak wilt although a decade-old map shows the disease to be present just to the west of the Blue Ridge (visible here).

Fortunately Shenandoah National Park has relatively few American beech, so it will be less affected by beech leaf disease (BLD). The Blue Ridge is also far from large waterbodies — which promote the disease. However, I did see some beech sprouting in creek valleys – probably in gaps opened when the hemlocks died. These valleys with higher humidity are the type of ecosystem most conducive to the disease! Anderson-Teixeira et al. note that they did not analyze the impact of beech bark disease – which was the disease of concern before arrival of BLD and continues to be present.

They also did not evaluate the impacts of balsam woolly adelgid, described as having decimated high-elevation populations of firs (Abies balsamea); white pine blister rust on eastern white pine; or EAB on fringetree (Chionanthus virginicus) in SCBI. Nor did they document the impact of thousand cankers disease (TCD) on walnuts or butternuts. This concerns me because they report that the disease “appears to be affecting Juglans spp. in our plots.” Furthermore, butternut (J. cinera) had been ‘‘common’’ in 1939, but had disappeared from SHNP by 1987. On the Smithsonian property, the four individuals found originally had declined by half – to two living individuals. Butternut has suffered high levels of mortality throughout its range from butternut canker.

The understory tree redbud (Cercis canadensis) also declined precipitously – by almost76% from 1995 to 2018 in SCBI plots. While Anderson-Teixeira et al. do not speculate why, a few years ago a wider decline was reported.

Of course, Shenandoah also has been invaded by non-native plants! So I saw some plants that should not be there. At least the mid- and high-elevations that I visited appear to be much less abundant in the Park than in coastal and piedmont regions of Virgina. Ailanthus is listed as “common” in the Park. I didn’t see Japanese stiltgrass but it is clearly present at lower elevations. I was particularly disturbed to see oriental bittersweet along trails located in all three sections of the Park.

The Blue Ridge PRISM is targeting 12 species: autumn olive, garlic mustard, Japanese honeysuckle, Japanese stiltgrass, kudzu, mile-a-minute, multiflora rose, oriental bittersweet, porcelainberry, privet, tree of heaven, and wavyleaf grass. 

SOURCES

Anderson-Teixeira, K.J., V. Herrmann, W.B. Cass, A.B. Williams, S.J. Paull, E.B. Gonzalez-Akre, R. Helcoski, A.J. Tepley, N.A. Bourg, C.T. Cosma, A.E. Ferson, C. Kittle, V. Meakem, I.R. McGregor, M. N. Prestipino, M.K. Scott, A.R. Terrell, A. Alonso, F. Dallmeier, & W.J. McShea. 2021. Long-Term Impacts of Invasive Insects & Pathogens on Composition, Biomass, & Diversity of Forests in Virginia’s Blue Ridge Mountains. Ecosystems

Fei, S., R.S. Morin, C.M. Oswalt, & A.M. Liebhold. 2019. Biomass losses resulting from insect & disease invasions in United States forests. Proceedings of the National academy of Sciences.

Potter, K.M., M.E. Escanferla, R.M. Jetton, G. Man, & B.S. Crane. 2019. Prioritizing the conservation needs of United States tree spp: Evaluating vulnerability to forest insect & disease threats. Global Ecology & Conservation.

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

Or

https://fadingforests.org

Call for new approach to biological conservation – integrating bioinvasion

whitebark pine in Glacier National Park killed by white pine blister rust

The Kunming-Montreal Global Biodiversity Framework (KMGBF) is a major global policy driver around the world for more effective action to preserve biodiversity from current and future threats. (However, the United States has not joined the underlying treaty, the Convention on Biological Diversity (CBD). So its importance is probably less in the United States than in countries that take part.) This relatively new Framework was adopted at the 15th Conference of the Parties (COP) of the CBD in December 2022 after four years of negotiations. However, cynics note that the 196 countries that are parties to the CBD have rarely met previous ambitious goals set at earlier COP.

Hulme et al. have just published a paper [full reference at the end of this blog] addressing how invasive species and this Framework’s target may interact. They note that conserving biodiversity costs money. Many of the countries hosting diverse and relatively intact ecosystems lack sufficient resources, capability, or robust governance structures for this conservation.

The Kunming-Montreal Global Biodiversity Framework sets out ambitious global targets to reduce biodiversity loss by 2030 so as to maintain the integrity of ecosystems and their constituent species. Of the 23 targets, one – Target 6 – addresses bioinvasion. Countries endorsing the CBD have committed to eliminating, minimizing, reducing and/or mitigating invasive species’ impacts on biodiversity and ecosystem services. This is to be accomplished by identifying and managing introduction pathways; preventing introduction and establishment of priority invasive species; reducing rates of introduction and establishment of known or potential invasive species by at least 50% by 2030; and eradicating or controlling invasive species, especially in priority sites.

I rejoice that the CBD parties have recognized invasive species as a major driver of biodiversity loss in terrestrial and marine ecosystems. I wish conservation organizations’ and funders’ activities clearly reflect this finding.

This is the challenge raised by Hulme et al.: countries must integrate efforts to counter bioinvasions into overall conservation programs. Success in curbing bioinvasion depends upon achieving almost all other KMGBF targets. And this is a two-way street: the more holistic approach offers greater likelihood of successful biodiversity conservation.

The same authors point out that some of the 22 other targets address rapidly evolving introductory pathways e.g.,

  • Target 15 – increasing international and domestic tourism;
  • Target 12 – encroachment of urban areas near protected areas;
  • Target 10 – development of intensive agriculture or aquaculture systems near protected areas;
  •  Target 7 – species rafting on plastic marine pollutants; and
  • Target 8 – growing risk from species shifting ranges in response to climate change.  
pallet graveyard behind camp store & snack bar art Lake MacDonald, Glacier National Park; photo by F.T. Campbell

Other targets relate to management of established invasive species, e.g.,

  • Target 1 – planning and priority-setting for allocation of limited resources among the various threats to biodiversity;
  • Identifying factors that pose risks to highly-valued species, e.g., threatened species (Target 4) and species that provide important ecosystem services (Target 11);
  • Target 19—obtaining necessary financial resources.  

A final group of targets are intended to guide all conservation efforts. These goals include integrating biodiversity concerns in decision-making at every level (Target 14); reducing harmful economic incentives and promoting positive incentives (Target 18); and several targets addressing issues of equity, benefit sharing, and access to information.  Hulme et al. assert that the threat posed by bioinvasions must be incorporated into policies, regulations, planning and development processes and environmental impact assessments across all levels of government.

Hulme et al. decry an imbalance as to which KMGBF targets have been the focus of attention from governments, conservation organizations, and media. These stakeholders have concentrated on

  • Target 3, which calls for extending legal protection to 30% of lands and waters by 2030;
  • Target 4, which promotes maintaining genetic diversity within and among populations of all species;
  • Target 7,  which encourages reducing harmful pollution;
  • Target 15, which urges businesses to decrease biodiversity risks arising from their operations; and
  • Target 21, which advocates ensuring equitable and effective biodiversity decision-making.

Even when stakeholders have looked at Target 6, they have focused primarily on how to quantify the numbers of species being introduced to novel ecosystems. Hulme et al. argue that conservationists should instead concentrate on the challenge of achieving the target. They note that bioinvasion is worsening despite implementation of many long-term management programs. As they note, numbers of introduced species globally have increased, these species are occupying larger geographic areas, and the species’ measured impacts have risen to astounding levels (see my previous blog about new cost estimates). This same point was made two years ago by Fenn-Moltu et al. (2023) [full citation at the end of this blog]; they found that the number of invasive species-related legislation and treaties to which a country adheres did not relate to either the number of insect species detected at that country’s border or the number of insect species that had established in that country’s ecosystems.

As conservationists, Hulme et al. remind us that not all damages are monetary: invasive species threaten more than half of all UNESCO World Heritage Sites.

Hulme et al. say achieving Target 6 presents several scientific challenges – most of which have been discussed by numerous other authors. Introduction pathways are changing rapidly. There is great uncertainty regarding current and especially future propagule pressures associated with various pathways. Information about particular species’ impacts and where they are most likely to be introduced is insufficient. Management costs are routinely underestimated. Perhaps most challenging is the need to judge programs’ effectiveness based not simply on outputs (e.g., number of acres cleared of weeds) but on outcomes in relation to reducing the subsequent impact on biodiversity and ecosystem services.

I note that several environmental organizations endorsed a “platform” that discussed this last point a decade ago. [I have rescued the NECIS document from a non-secure website; if you wish to obtain a copy, contact me directly through the “comment” option or my email.] Unfortunately, the coalition that prepared this document no longer exists. Even when conservation organizations have invasive species efforts, they are no longer attempting to coordinate their work.

APHIS inspecting imported plants

I greatly regret that Hulme et al. continue a long-standing misrepresentation of international border biosecurity controls as consisting primarily of inspections — of imported commodities, travellers, and associated transport conveyances. I have argued for decades that inspections are not effective in preventing introductions. See Fading Forests II Chapter 3 (published in 2003); Fading Forests III Chapter 5 (published in 2014); “briefs” describing pathways of introduction prepared for the Continental Dialogue on Non-Native Forest Insects and Diseases – in 2014 and in 2018.    

 The weaknesses of visual inspection are especially glaring when trying to prevent introductions via wood packaging material and living plants — also here.

Hulme et al. propose a politically astute approach to finding the resources to strengthen countries’ efforts to curtail invasive species’ spread within their borders.  Recognizing that no country has unlimited resources to allocate to managing invasive species, they suggest concentrating slow-the-spread efforts on preventing damage to legally protected areas. Furthermore, authorities should avoid designating as new “protected areas” places that are already heavily invaded – or at risk of soon becoming so. As they note, programs aimed at protecting these areas often engage conservation stakeholders, decision-makers, even potential non-governmental donors. In other words, there is a foundation on which to build.

To buttress their argument, Hulme et al. cite evidence that bioinvasions threaten these areas’ integrity. For example, Cadotte et al. (2024) found that bioinvasion is one of most frequently identified threats identified in a survey of 230 World Heritage sites; and that they pose a greater degree of concern than other threats to biodiversity. They reiterate that managing invasive species is one of the most effective interventions aimed at protecting biodiversity.

The task remains complex. Hulme et al. note that accurate information about pressure caused by invasive species is not easily quantified using remote sensing. It requires expensive on-the-ground data collection. Even current methods for ranking invasive species have crucial gaps regarding species’ potential impact and the feasibility of their control. Choosing management strategies also requires assessing potential unintended effects on biodiversity and other GBF Targets, e.g., pollution from pesticides (Target 7).

Still, the context remains: successful management of bioinvasions to support the integrity of protected areas depends on the integrative approach described above.

Hulme et al. note a contradiction within the Kunming-Montreal Global Biodiversity Framework: Target 10 calls for the agriculture, aquaculture, and forestry industries to adopt sustainable practices, but doesn’t raise the issue of these sectors’ role in the introduction and spread of invasive species. They say guidelines have been developed for sustainable forestry production. These guidelines recommend that commercial plantation forests not plant non-native tree species within 10 km of a protected area. Hulme et al. also suggest applying a “polluter pays” fine or bond to forestry businesses that use invasive species without sufficient safeguards to prevent escape. These funds could be accessed to support invasive species management in protected areas, particularly surveillance. (Target 19 mandates obtaining more funds for this purpose).  They add that these aquaculture, agriculture, horticulture and forestry sectors should take action to prevent the local feralization of alien crops and livestock.

Target 8 calls for minimizing the impacts of climate change on biodiversity. Hulme et al. note numerous scientific challenges here, including understanding how specific ecosystems’ and native species’ are vulnerable to altered climates, along with how specific invasive species’ are responding to an altered climate regime.

These same authors provide specific recommendations to the global conservation community to put in place a more holistic perspective. Some recommendations deal with data integration. Others call for major undertakings: i.e., developing a protected area management toolkit at a global scale. This action will require significant investment in capacity-building of protected area managers plus international cooperation and technology transfer (Target 20). Hulme et al. suggest funding this effort should be a priority for any resources leveraged from international finance (Target 19).

Hulme et al. also propose changes in the conservation approaches advocated by the CBD and IUCN. Specifically, they call for more explicit consideration of current and future impacts of bioinvasions and their management — on protected areas. The needed activities fall into six areas:

(1) reduce risks associated with various pathways;                                 

(2) plan for range-shifting invasive species;

(3) mitigate invasive species’ impacts on biodiversity and (4) on ecosystem services;

(5) ensure new protected areas (including urban green spaces and infrastructure corridors) are largely free of established (“legacy”) invasive species; and

(6) provide managers sufficient resources to take effective action.

SOURCES

Fenn-Moltu, G., S. Ollier, O.K. Bates, A.M. Liebhold, H.F. Nahrung, D.S. Pureswaran, T. Yamanaka, C. Bertelsmeier. 2023. Global flows of insect transport & establishment: The role of biogeography, trade & regulations. Diversity & Distributions DOI: 10.1111/ddi.13772

Hulme, P.E., Lieurance, D., Richardson, D.M., Robinson, T.B. 2025 Multiple targets of Global Biodiversity Framework must be addressed to manage invasive species in protected areas. NeoBiota 99: 149–170. https://doi.org/10.3897/neobiota.99.152680

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

Or

https://fadingforests.org

Invasive shot hole borers – global travellers

Erythrina caffra (native tree in South Africa) infested by PSHB; photo by J. Paap

A complex of closely related ambrosia beetles continues to be introduced to new places and cause increasing damage. The most widespread is the polyphagous shot hole borer (PSHB) Euwallacea fornicatus ss. Other members of the complex include the Kuroshio shot hole borer (KSHB) E. kuroshio and a third species, E. interjectus. Each beetle harbors its own plant-pathogenic fungus – all in the Fusarium genus.

Places invaded and impacts

The PSHB is established in the U.S. (southern and central California), Israel, South Africa, & Australia. The outbreak in South Africa covers the largest geographic area; the PSHB-Fusarium disease has been found in eight of the country’s nine provinces (every province except Limpopo) (Bierman et al. 2022). The South Africa outbreak is the most extensive geographically of all of them (Mudede et al. 2025).

The KSHB is established in southern California, from where it has spread to neighboring Mexico. E. interjectus is established in Santa Cruz County in California. 

A fourth member of the species complex, E. perbrevis, has been established for decades on several Hawaiian islands and for at least 20 years in Florida. E. perbrevis has also been detected in nurseries in the Netherlands, but authorities reported it has been eradicated. E. perbrevis has long been known to be present in northern Queensland; this region might be part of its native range.

South America

In 2023 PSHB had been detected in Argentina – reported as E. fornicatus. A few weeks ago it was reported in neighboring Uruguay (PestLens for June 26, 2025). The beetle in South America is a different haplotype (genetic strain) than that introduced in South Africa, Israel, and California. It is more similar to specimens found in European greenhouses (Ceriani-Nakamurakare & others) As of 2022, scientists had identified 43 haplotypes (genetic variants) of E. fornicatus s.s. identified around the world; the greatest diversity is in several Asian countries  (P. Rugman-Jones, pers. comm). The other species also comprise several haplotypes.

In South America the beetle has been observed attacking several new hosts. The most frequently attacked hosts are are Acer japonicum (Japanese maple) and a Ficus sp. Other hosts that support the full life cycle of the beetle and its associated fungus are Bauhinia forficata (cow’s foot), Ceiba speciosa (floss silk tree), Diospyros inconstans (jacuiba), Ficus aspera (mosaic fig), Fraxinus excelsior (European ash), Gardenia thunbergia (white gardenia), Geoffroea decorticans (chañar), Myrsine laetevirens, and Neltuma (Prosopis) caldenia (caldén) plants (PestLens June 26, 2025).

Ceiba speciosa A.St.-Hil. via Flickr

South Africa

The beetle and disease have been present since 2012 or earlier although it was not detected until 2017 (Winzer et al.). (This delay in detection is typical; in California PSHB was present for probably nine years before it was detected.) Winzer et al. decry the communication failure that resulted in the delayed official detection in South Africa and propose a system to correct the breakdown.

The haplotype (genetic strain) is the same as that found in Vietnam and introduced in California and other sites (Mudede et al.).

The South Africa outbreak is the most extensive geographically of all the outbreaks globally; within five years of its official detection, the PSHB-Fusarium disease was confirmed to be present in eight of the country’s nine provinces (every province except Limpopo) (Bierman et al. 2022).

More than 100 tree species – native and exotic – have been confirmed as hosts. Sources differ on the specific number: Mudede et al. report 130 species; Townsend et al. 2025 report 162. Both figures include both hosts that support reproduction of the insect and those that do not.

Mudebe et al. cite other studies that project the Fusarium disease will cause a decline in tree populations over a 10-year period of between 3.5% and 15.5%. They estimate the cost of removing urban trees killed by the disease will be $USD18.45 billion.

The impact in South Africa might differ from other invaded areas. Mudebe et al. report that over the five years of the study none of the Platanus species or A. buergerianum was dying despite being heavily infested. They say this suggests that trees can survive for more than 5 years.

Townsend et al. present a more disturbing picture. Their study examined PSHB impacts in plots in native forests in two provinces — KNZ (where PSHB first detected) and Western Cape. Over five years, PSHB invaded seven forest types; the only forest type not invaded was mangroves. PSHB colonization was detected on 43 native tree species. Eighteen species were recorded as competent hosts (able to support PSHB reproduction), eight as kill-competent hosts (can be killed by PSHB).

Over the five years 11 individual trees belonging to seven species died as a result of PSHB infestations.  Some died very rapidly (within 2–5 years of first infestation); some died after apparently minor levels of infestation.

Each year of the study trees had a 7.5% increased chance of PSHB infestations; the number of entrance holes rose by over 10%. This means – no surprise – that the longer PSHB is active in the enviro the more trees it will infest, the higher its impact will be on hosts, & the higher the # of dispersing individuals produced. This will substantially increase the chances & rates of additional areas becoming infested, especially in areas close to infestation borders. Townsend et al. state that PSHB populations might be increasing exponentially – as occurred in California and Israel.

Townsend et al. discuss factors that might explain differing levels of infestation. Currently, a higher proportion of trees in the study plots in KwaZulu-Natal were infested than in the plots in Western Cape. The most likely explanation is that PSHB established there first – before 2012 compared to possibly five years later in the Western Cape. Other factors might be that source populations in the Western Cape were often found in alien tree species in urban areas distant from the study plots, while in KwaZulu-Natal, the beetles were frequently found in indigenous trees within monitoring plots. Forests in KZN are also fragmented, unlike the nearly contiguous woodlands in the Western Cape, and closer to urban areas with high PSHB infestation levels.

Although the PSHB’s spread into natural forests seems to be slow, Townsend et al. warn that they expect an increase in the rate of infestations as progressively more competent host individuals are infested. They fear severe ecological effects from rapid mortality of some key tree species, especially those sensitive to comparatively few attacks. They mention the native Erythrina caffra (coral tree), which is an important component of coastal forest ecosystems, especially in KwaZulu-Natal.

Other native trees at particular risk of PSHB infestations are Diospyros glabra, Ficus, Sparmannia africana, Trichelia emetic, and Vepris lanceolata. Townsend et al. remind us that each native tree species has a specific role in normal ecosystem functioning and supports a unique suite of species. Even if attacked trees do not die, Fusarium infection might weaken them, thereby increasing their susceptibility to other pathogens and pests, decreasing their longevity, or reducing their ability to produce fruits and flowers which can have long-term direct & indirect effects on normal ecosystem functioning & resilience.

Remember, South Africa is a biodiversity hotspot, home to its own Floral Kingdom!

The South Africans are trying to find more efficient methods for tracking spread of PSHB. Mudede et al. 2025 tested whether Google street view (GSV) images can be used to monitor its spread in urban forests. The test took place in Johannesburg. The test demonstrated that GSV images can be useful for mapping and monitoring PSHB-FD infestation on Platanus trees – but not on trees with rougher bark, e.g., Acer.  While there were no false positives for any host species, most of the maple trees were misclassified as non-infested (false negatives).

Vietnam

Even in its native range, PSHB is a threat – in this case, to plantations utilizing non-native or exotic tree species. Thu et al. describe a growing number of pests threatening reforestation efforts in Vietnam. Surveys over the period 2011 to 2020 revealed outbreaks by 14 new insect species and 2 pathogens. Only two of the trouble-causing species are themselves non-native to Vietnam. One of these is PSHB. Thu et al. report the species’ range has spread rapidly in the country.

Thu et al. inform us that Vietnam has a high diversity of forest trees – and that almost nothing is known about pests that attack these trees.

Neolamarkia cadamba – native tree in Vietnam that might be resistant to PSHB; via Flickr

I welcome their call for higher investment in selection and breeding of hosts resistant to the various pests.  The limited effort so far has identified provences of Neolamarckia cadamba and Nauclea orientalis that display some resistance to PSHB. Thu et al. advocate breeding programs to address the main biotic threats. They also recommend several actions to improve biosecurity, including enhanced hygiene in tree nurseries; improved silvicultural practices to minimize damage to trees; diversification of tree species being grown; and strengthening biosecurity and quarantine programs. They note that early detection of pest outbreaks is critical, so the country should develop forest health monitoring protocols for extensive forest reserves – sentinel plantings and remote sensing to detect trees under stress.

On a personal level, I found it interesting that Mudede et al. report that Google street view imagery determined that the invasive tree Ailanthus altissima dominates the street tree population in Istanbul – despite not having been intentionally planted. I visited Istanbul in April – and saw evidence of invasive vines and possibly the North American tree Cercis canadensis.

SOURCES

Ceriani-Nakamurakare, E., A.J. Johnson, D.F. Gomez. 2023. Uncharted Territories: First report of Euwallacea fornicates (Eichhoff) in South America with new reproductive host records. Zootaxa, 5325 (2), 289-297. https://doi.org/10.11646/zootaxa.5325.10

Mudede, M.F., S.W. Newete, K. Abutaleb, M.J. Byrn. 2025 Monitoring a polyphagous shot hole borer infestation in an urban forest using Google street view in the City of Johannasburg, South Africa Biol Invasions (2025) 27:144         https://doi.org/10.1007/s10530-025-03595-4

Thu, P.Q., D.N. Quang, N.M. Chi, T.X. Hung, L.V. Binh, B. Dell. 2021. New and Emerging Insect Pest and Disease Threats to Forest Plantations in Vietnam. Forests 2021, 12, 1301. https://doi.org/10.3390/f12101301

Townsend, G., M. Hill, B.P. Hurley, and F. Roets. 2025 Escalating threat: increasing impact of the polyphagous shot hole borer beetle, Euwallacea fornicatus, in nearly all major South African forest types. Biol Invasions (2025) 27:88 https://doi.org/10.1007/s10530-025-03551-2

Winzer, L.F, K.T. Faulkner, T. Paap, and J.R.U. Wilson. Preprint. From detection to action—a proposed workflow to ensure first reports of alien spp from molecular analyses are acted upon DOI: https://doi.org/10.3897/arphapreprints.e162421

Pest-lens link:  https://pestlens.info/

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

Or

https://fadingforests.org

Update: pests spreading … funding stalled …

Oregon ash in swamp in Ankey National Wildlife Refuge, Willamette Valley, Oregon; photo by Wyatt Williams, Oregon Department of Forestry

1) Funds still not released

As of the end of June, the Office of Management and Budget has not released funds to programs under the USDA Forest Service’ State, Private, and Tribal section. This includes many programs – grants, etc. – that support state and other entities’ efforts and operation of the Forest Health Protection program. Meanwhile, tree-killing insects, pathogens, and nematodes pursue their lives … killing trees in the process.

Congress has not yet acted on legislation that will determine the funding level for USFS FHP and Research programs in Fiscal Year 2026, which begins on October 1. I remind you that the Administration has proposed 0 funds for these programs. Take advantage of the Congressional delay – contact your Member of the House and Senators.

2) the Mediterranean oak beetle (MOB) Xyleborus monographus has now been detected in nine California counties, including Napa, Sonoma, Lake, Sacramento, El Dorado, Yolo, Mendocino, and as of last month, Marin. MOB is also present in Oregon – in Multnomah, Clakamass, Marion and Washington counties.

There is no treatment for infected trees. California authorities urge landowners to search for the insect and remove infected trees – and to avoid moving infested wood.

3) Oregon Department of Forestry has announced that thousand canker disease (TCD) of walnut is killing trees of the Juglans genus in the Willamette Valley. Where the insect has been found in traps, the majority of black walnut trees have since died. Black walnut (Juglans nigra) is not native in Oregon; its range east of the Great Plains. Apparently the range of northern California black walnut (Juglans hindsii) also does not extend into Oregon.

Cities in Oregon are preparing for the inevitable arrival of the emerald ash borer (EAB) (Agrilus planipennis) which was detected in Forest Grove in June 2022. The City of Salem inventoried all of its street & park trees in the last 5 years. It plans to inject a systemic pesticide into at least 550 trees this year and a similar number next year. These trees have been judged to be in good condition. Ash trees in poor condition along streets or in parks are gradually being removed and replaced.

Salem also plans to inventory Oregon ash growing in the city’s natural areas so as to understand where they will need to plant other native species. I blogged earlier about the threat EAB and MOB pose to western Oregon’s wetlands and oak savannahs.

4) Ann Hajek of Cornell and colleagues haves published a review of 20 years of research on entomopathogens that might contribute to control efforts targetting the Asian longhorned beetle (ALB) (Anoplophora glabripennis). The authors call for renewed efforts to find appropriate control agents and techniques. They conclude that various pathogens – especially fungi – can support ALB eradication efforts. They would be particularly helpful if ALB populations spread – or a new outbreak is detected. (Remember, ALB has been detected in seven locations in North America – some the result of more than one introduction; and nine locations in Europe.)

The article is open access!! See

Ann E. Hajek, A.E., E.H. Clifton, and L.F. Solter. 2025. Entomopathogens for control of Asian longhorned beetles (Coleoptera: Cerambycidae). Environmental Entomology, XX(XX), 2025, 1–10 https://doi.org/10.1093/ee/nvaf016

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

New way to learn what others are doing … & tell them about your work!

field surveys; photo by F.T. Campbell

Several bioinvasion scientists have announced launch of a bi-annual Invasions Newsletter.  It will be an open-access digital magazine intended to meet the growing need for effective communication across the diverse community of researchers, practitioners, & policymakers. It will offer accessible insights into current research; communication & management strategies; novel technologies; research centers, groups, journals, networks, projects & resources; emerging policy trends; & past & upcoming meetings & events.

The initial issue is available here Among the topics addressed:  

  • invasive plant biocontrol efforts in Zimbabwe,
  • setting national-level invasive species priorities in Chile,
  • conservation actions to recover invaded endemic forests in Galápagos Islands,
  • protecting ground-nesting birds from introduced predators,
  • IUCN ISSG’s assistance in tackling invasive species in Europe.

The organizers — Ana Novoa, Susan Canavan, Katelyn T. Faulkner, Piero Genovesi,  Deah Lieurance, Dan Simberloff, Hsiao-Hsuan Wang, Tsungai Zengeya, & Laura A. Meyerson – invite us to contribute to future editions. Inform your global colleagues about your efforts and findings: fieldwork, model development, designing or implementing management interventions at a local, national or continental scale, or crafting policy frameworks.

outreach

To submit a contribution, contact any of the organizers.

Let’s ensure that tree-killing critters (with or without legs) get the attention they deserve!

Faith Campbell

Sentinel Gardens – useful tool if microbes scrutinized sufficiently

Northern red oak – one of the species planted in Europe & China as part of sentinel garden project; photo by F.T. Campbell

During the USDA Interagency Forum on Invasive Species, Dr. Eliana Torres Bedoya, from the Bonello lab at Ohio State, provided insights gained from a sentinel garden project operating for the last five years.

The gardens were established in six locations: two in China in the Nanjing area, one each in Italy, Sweden, Ohio, and New Hampshire. The network required collaboration among scientists in several countries, a difficult task in itself. (Jiri Hulcr of the University of Florida has also stressed the importance of mutually beneficial collaborations.)

The focus was on detecting and identifying novel fungal pathogens abroad before they ever enter a country, in an approach called ex patria sentinel plantings. Altogether, 32 tree species were planted in at least one location. For example, Chinese and European tree species were planted in the U.S. to identify potential threats to China and Europe. Conversely, North American species were planted in Europe and China to detect potential threats to the U.S. As noted, the reciprocity is crucial to establishing and maintaining a long-term relationship.

Key information gained to date:

  • While the scientists isolated several potential pathogens from symptomatic plants, analysis of all plants’ leaf microbiomes showed that asymptomatic plants harbored many more potential pathogens that had not been isolated.

Healthy plants tend to harbor larger and often more diverse microbial communities. This study found that asymptomatic plants supported a significantly more abundant, richer, and taxonomically diverse leaf-associated fungal community than symptomatic plants. Importantly, this pattern pertains also to the subset of taxa classified as potential plant pathogens.

  • Detection of the full range of fungal pathogens requires that samples must be collected both early and mid-to-late in the growing season because microbes present differ.
  • Core leaf microbiomes were associated with specific tree species, no matter where they were planted. However, the constituents of the core microbiome were outnumbered by other organisms driven primarily by the location of the planting. This had been expected.

Other contributing factors – in declining order – were geographic location, tree species, season, and host health status. In other words, the phylogenetic relationship.

The drivers of fungal community composition interact in complex ways. For instance, the effect of the plant’s health on pathogenic fungal communities might depend on the host species. This relationship can be further modulated by seasonal variation and geographic context.

European & Asian trees planted in Ohio as part of the sentinel garden program; photo by P (E) Bonello

Implications:

  • Sentinel gardens can facilitate identification of novel host-pathogen interactions in symptomatic and asymptomatic plants, so they should be adopted / supported by governmental and regional phytosanitary agencies.
  • The findings demonstrate the need to expand surveillance beyond symptomatic plants – at both sentinel gardens and plant health border inspection stations. Phytosanitary agencies should employ both full microbial community molecular characterization to detect threats in asymptomatic plants and traditional symptom-based approaches. These modern approaches are described in Munck and Bonello 2018 (full reference at end of the blog).
  • Enrico Bonello (pers. comm.) thinks it is likely that similar context-dependent interactions among host and fungus species, season, and geography also drive disease infection and virulence.

Eliana Torres Bedoya (pers. comm.) clarifies that the leaf microbiome is the community of microorganisms living on and within tree leaves. These microbes can contribute to protecting trees against pathogens, enhance tolerance to environmental stressors such as drought or pollution, and influence how trees interact with their surroundings. Because the composition of the leaf microbiome responds to changes in climate, location, and tree species, it also serves as a valuable indicator of forest health and environmental change.

There are several approaches to studying microbial communities in leaves. One is the traditional, culture-based method, which relies on isolating and cultivating microorganisms on nutrient media. While this approach is effective for recovering fast-growing and easily culturable taxa, it has a major limitation: the vast majority of environmental microbes are not readily culturable under standard laboratory conditions. As a result, full understanding requires use of culture-independent methods. One technique widely used is metabarcoding. This technique involves extracting total DNA from leaf tissue and amplifying a phylogenetically informative genetic marker specific to the microbial group of interest (for example, the internal transcribed spacer (ITS) region for fungi or the 16S rRNA gene for bacteria). The amplified regions are then sequenced using high-throughput sequencing platforms. After a series of processing steps, the sequences are clustered into Amplicon Sequence Variants (ASVs), which represent unique DNA sequences that can be used as proxies for microbial taxa present in the sample. Torres Bedoya and Bonello used the ASVs for comparative analysis.

Tilia cordata (linden) via Picaryl (seed wings make a great tea!)

In her presentation, Torres Bedoya provided examples of the complexities arising when trying to detect fungi associated with trees. Eleven potentially pathogenic fungal genera were found to be more abundant in asymptomatic Northern red oak (Quercus rubra) trees (a North American species) planted in both Europe and China. Five ASVs were more abundant in asymptomatic Fraxinus mandshurica trees (an Asian species) planted in Sweden. In this case, the season when the leaves were sampled explained a higher proportion of the variance in the community composition than did the health status of the host. Molecular methods detected 10 genera not revealed through isolation from little-leaf linden species (Tilia cordata) trees (a European species) planted in China and the US.

This “proof of concept” study considered only fungi associated with leaves. As shown above, learning the true plant health risk associated with any tree taxon’s leaves is already complicated and resource-demanding. To fully exploit the power of the ex patria sentinel plantings approach, phytosanitary officials must provide additional resources (land, people, equipment, money) to enable screening of all plant parts, above and below-ground, and all potentially pathogenic taxa, including nematodes, phytoplasmas, and viruses. These systems must be maintained over years.

Reference

Munck, I.A., Bonello, P. 2018. Modern approaches for early detection of forest pathogens are sorely needed in the United States. Forest Pathology 48 (5). doi:10.1111/efp.1445

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  https://treeimprovement.tennessee.edu/

or

www.fadingforests.org

USFS programs “0’d out” in Administration’s budget – please help!

please – this should be you!!!!

In early May I posted a blog about the Trump Administration’s proposed budget – saying that it would eliminate funding for nearly all  USFS research & Forest Health Protection.

I can now provide some additional information.

The Administration has released a supplemental document providing a few details about the severe cuts it is proposing for USFS programs vital to countering bioinvasion in the coming fiscal year (FY2026), which starts October 1st. You can download this document at https://www.whitehouse.gov/wp-content/uploads/2025/05/appendix_fy2026.pdf

Congress has the final say on appropriations – so please!!! inform your representative & senators about why these cuts are disastrous.

USFS [See pages 162-168 of the Appendix]

Research & Development

The Administration requests $0 for R&D. It says it will strategically use existing carryover balances to responsibly terminate research programs & close research stations. Thus, funding for R&D will decrease from the $301 million in FY24 to $44 million in FY26. The Forest Inventory & Analysis will be shifted to the National Forest System and funded at $21.5 million – less than program supporters are seeking.

The proposal does contain an “additional amount” of $26 million for dealing with the consequences of wildfires, hurricanes & other natural disasters that occurred in calendar years 2022, 2023, and 2024. I am confused about this funding.

 State, Private, and Tribal Forests

The Administration requests $0 for S,P&T.  Again, the proposal says the agency will use existing carryover balances to effectively & responsibly terminate these programs. The number of employees would be cut from 520 employees in FY24 to 37.

Again, the proposal contains an “additional amount” of $208 million for Forest Health Management to deal with the consequences of wildfires, hurricanes & other natural disasters that occurred in calendar years 2022, 2023, and 2024.  $14 million of this sum is earmarked for assistance to states in the Northeast that are anticipating an outbreak of eastern spruce budworm (which has been spreading from Canada).  In a highly unusual move, the proposal says this funding is not subject to a requirement that grant recipients provide matching funds from non-federal sources. [Is it a coincidence that Maine Senator Susan Collins chairs the Senate Appropriations Committee?]

National Forest System

Total funding for NFS would be $1.5 billion. This includes an “additional amount” of nearly $2.5 billion for expenses related to the consequences of wildfires, hurricanes & other natural disasters that occurred in calendar years 2022, 2023, and 2024. $75 million of this amount is earmarked for construction or maintenance of shaded fuel breaks in the Pacific Northwest.

As I noted above, the Forest Inventory and Analysis program would be placed under the NFS.

I am particularly concerned that the budget proposal provides explicitly for $20 million to improve or maintain landscape & watershed conditions by preventing invasive plant infestations and installing aquatic organism passages, etc. There is no mention of programs intended to address damage caused by non-native insects and pathogens.  It appears that the Administration proposes to drop all programs re: these organisms.

The overall objective of NFS programs is defined as managing the forests for productive use & resilience to catastrophic wildfire & provide broad range of ecosystem services. The budget allegedly prioritizes funding of programs designed to increase health & resilience of National Forests & Grasslands – including meeting multiple use requirements for resources on these lands.

The prose no longer says that timber production is the sole purpose of Nation forests – as the original budget stated.

APHIS appears to have survived – although the supplement provides minimal information (on pp. 85 – 87 of the Appendix).

The supplement contains a lengthy description of APHIS’ purpose — to protect America’s agricultural and natural resources from introduced pests.  It requests $1.1 billion for FY2026. The only plant pest listed as a priority is exotic fruit flies. Personnel would be cut from 6,142 in FY24 to 5,092. I could find no specifics regarding funding for programs of interest – tree & wood pests, specialty crops, pest detection, and methods development.

Implications for Non-native Insects and Pathogens

Remember that USFS’s research and development program is intended to improve forest managers’ understanding of ecosystems, including human interactions and influences, thereby enabling improvements to the health and use of our Nation’s forests and grasslands. Most importantly to me, this program provides foundational knowledge needed to develop effective programs to prevent, suppress, mitigate, and eradicate the approximately 500 non-native insects and pathogens that are killing America’s trees.

The Forest Health Program provides technical and financial assistance to the states and other forest-management partners to carry out projects (designed based on the above research) intended to prevent, suppress, mitigate, and eradicate those non-native insects and pathogens. The program’s work on non-federal lands is crucial because introduced pests usually start their incursions near cities that receive imports (often transported in crates, pallets, or imported plants).

[FIA might inform all about where such pests are found — but it doesn’t address how to contain their spread, suppress their impacts, or restore the affected tree species.]

Eliminating either or both programs will allow these pests to cause even more damage to forest resources – including timber.

Both supporting research and on-the-ground management must address pest threats across all U.S. forests, including the more than 69% that are located on lands managed by others than the USFS. Already, the 15 most damaging of these pests threaten destruction of 41% of forest biomass in the “lower 48” states. This is a rate similar in magnitude to that attributed to fire (Fei et al. 2019). [This estimate does not include loss of beech beech leaf disease.] It is ironic that the Administration considers the fire threat to be so severe that it has proposed restructuring the government’s fire management structure.

I remind you that the existing USFS R&D budget allocates less than 1% of the total appropriation to studying a few of the dozens of highly damaging non-native pests. I have argued that this program should be expanded, not eliminated. Adequate funding might allow the USFS to design successful pest-management programs for additional pests (as suggested by Coleman et al.).

As a new international report (FAO 2025) notes, genetic resources underpin forests’ resilience, adaptability, and productivity. Funding shortfalls already undercut efforts to breed trees able to thrive despite introduced pests and climate change (the latter threat is still real, although the Administration disregards it). I have frequently urged the Congress to increase funding for USFS programs – which are sponsored primarily by the National Forest System and State, Private, and Tribal, although some are under the R&D program.

I repeat: Please ask your Member of Congress and Senators to oppose these proposed cuts. Ask them to support continued funding for both USFS R&D and its State, Private, and Tribal Programs targetting non-native insects and pathogens. America’s forests provide resources to all Americans – well beyond only timber production and they deserve protection.

Contacting your Representative and Senators is particularly important if they serve on the Appropriations committees.

House Appropriations Committee members:

Republicans: AL: Robert Aderholt, Dale Strong; AR: Steve Womack; AZ: Juan Ciscomani; CA: Ken Calvert, David Valadao, Norma Torres; FL: Mario Diaz-Balart, John Rutherford, Scott Franklin; GA: Andrew Clyde; ID: Michael Simpson; IA: Ashley Hinson; KY: Harold Rogers; LA: Julia Letlow; MD: Andy Harris; MI: John Moolenaar; MO: Mark Alford; MS: Michael Guest;  MT: Ryan Zinke; NC: Chuck Edwards; NV: Mark Amodei; NY: Nick LaLota; OH: David Joyce; OK: Tom Cole, Stephanie Bice; PA: Guy Reschenthaler TX: John Carter, Chuck Fleishmann, Tony Gonzales, Michael Cloud, Jake Ellzey; UT: Celeste Maloy; VA: Ben Cline; WA: Dan Newhouse; WV: Riley Moore

Democrats: CA: Pete Aguilar, Josh Harder, Mike Levin; CT: Rosa DeLauro; FL: Debbie Wasserman Schultz, Lois Frankel; GA: Sanford Bishop; HI: Ed Case IL: Mike Quigley, Lauren Underwood; IN: Frank Mrvan; MD: Steny Hoyer, Glenn Ivey; ME: Chellie Pingree; MN: Betty McCollum; NJ: Bonnie Watson Coleman NY: Grace Meng, Adriano Espaillat, Joseph Morelle; NV: Susie Lee;  OH: Marcy Kaptur;  PA: Madeleine Dean; SC: James Clyburn;  TX: Henry Cuellar, Veronica Escobar; WA: Marie Gluesenkamp Perez; WI: Mark Pocan

Senate Appropriations Committee members:

Republicans: AK: Lisa Murkowski; AL: Katie Britt; AR: John Boozman (AR); KS: Jerry Moran; KY: Mitch McConnell; LA: John Kennedy; ME: Susan Collins; MS: Cindy Hyde-Smith; ND: John Hoeven; NE: Deb Fischer; OK: Markwayne Mullin; SC: Lindsey Graham; SD: Mike Rounds TN: Bill Hagerty; WV: Shelley Moore Capito;

Democrats: CT: Chris Murphy; DE: Chris Coons; GA: Jon Ossof; HI: Brian Schatz; IL: Richard Durbin; MD: Chris van Hollen; MI: Gary Peters; NH: Jeanne Shaheen; NM: Martin Heinrich; NY: Kirsten Gillibrand; OR: Jeff Merkley; RI: Jack Reed; WA: Patty Murray; WI: Tammy Baldwin

Addendum

Maintaining the USFS State, Private, and Tribal (SPT) programs is essential to

  • complying with laws adopted by the Congress (see second page).
  • meeting the USFS mission of sustaining “the health, diversity, and productivity of the nation’s forests and grasslands to meet the needs of present and future generations.”
  • ensuring future economic and ecological benefits to Americans.

More than two-thirds of U.S. forests are privately owned or managed by state, local, or tribal governments. These forests provide many benefits, including 89% of America’s timber harvest.[i] SPT is the only federal program providing technical, financial, & educational assistance to these non-federal landowners.

Among the many threats to American forests, the Center for Invasive Species Prevention (CISP) focuses on the threat from insects and pathogens introduced from abroad. More than 41% of forest biomass in the “lower 48” states is at risk to non-native pests already established in the country.[ii] From 2011 to 2020, sap feeders, e.g., hemlock woolly adelgid, killed trees on 635,000 acres; foliage feeders, e.g., spongy moth, killed trees on 948,884 acres.[iii] Additional pests will be introduced and kill more trees.

Non-native pests are introduced primarily in crates, pallets or other packaging made of wood; and in imported plants. These imports – and the pests – usually land in cities or suburbs and establish there. Initially they cause widespread death of urban trees and impose high costs on local governments and property owners who must remove dying trees. The pests also spread. Hemlock woolly adelgid, emerald ash borer, polyphagous and Kuroshio shot hole borers, goldspotted oak borer, sudden oak death, and beech leaf disease have all spread to National forests from cities or suburbs.

The most effective way to protect America’s forests is to find and kill the pests where they first appear – usually in city trees. Waiting to act until a pest reaches National Forest boundaries means failure. Instead, we should expand the Forest Health Management (FHM) Cooperative Lands program to quickly detect, contain, and – if possible – eradicate the pests. With higher appropriations, the STP FHM program could tackle more of the 53 tree species under threat. At present, only four of these species benefit from 95% of FHM projects – eastern oaks, loblolly and ponderosa pines, and hemlocks.[iv]

USFS Research and Development (R&D) program

FHM adopts strategies based on knowledge of pests’ life histories and traits gained through research conducted or sponsored by the USFS R&D program. CISP urges you to support continued funding for the USFS Research and Development (R&D) program. However, we advocate a realignment: raise the proportion of research funding allocated to invasive species from the current paltry level of 1% to 5%. Funding for studying non-native pests has decreased 70% since FY2010 despite new pests attacking our forests. As a result, the Forest Service is hampered from developing effective programs to prevent, suppress, and eradicate most non-native pests.

Another crucial strategy for reducing loss of tree species to non-native pests is breeding trees able to thrive despite introduced pests. Currently these projects are supported – inadequately – by all three USFS divisions: R&D, SPT, and National Forest System (NFS).

The model program is the Dorena Genetic Resource Center. The Center has bred Western white pine and Port-Orford-cedar trees resistant to introduced pathogens; these trees are now being planted. Promising projects target the pathogens killing whitebark pine, American chestnut, American elm, and Hawaiian koa. Projects at earlier stages address ash, beech, and ʻōhiʻa.

Lesson: federal dollars, wisely invested, can mitigate the damage caused by invasive species. CISP asks you to support continuing these programs so that America can restore threatened trees to our forests.

Complying with the Law

The Cooperative Forestry Assistance Act of 1974

Section 2 (a) Findings …—

(1) most of the productive forest land of the United States is in private, State, and local governmental ownership, and the capacity of the United States to produce renewable forest resources is significantly dependent on such non-Federal forest lands;

(b) Purpose.—… authorize[s] the Secretary …, with respect to non-Federal forest lands … to assist in—

…

(3) the prevention and control of insects and diseases affecting trees and forests;

(c) Priorities.—In allocating funds … , the Secretary shall focus on the following national private forest conservation priorities, …:

…

(2) Protecting forests from threats, including … invasive species, insect or disease outbreak, … and restoring appropriate forest types in response to such threats.

(e) Policy. …  it is in the national interest for the Secretary to work through and in cooperation with State foresters, or equivalent State officials, nongovernmental organizations, and the private sector …

Healthy Forests Restoration Act of 2003

Sec. 401(a) FINDINGS.—(1) high levels of tree mortality resulting from insect infestation (including the interaction between insects and diseases) may result in — (A) increased fire risk; … (E) degraded watershed conditions; (F) increased potential for damage from other agents of disturbance, including exotic, invasive species; and (G) decreased timber values;

…

(3) the hemlock woolly adelgid is— (A) destroying streamside forests throughout the midAtlantic and Appalachian regions; (B) threatening water quality and sensitive aquatic species; and (C) posing a potential threat to valuable commercial timber land in northern New England;

(4)(A) the emerald ash borer …  has quickly become a major threat to hardwood forests …; and (B) … threatens to destroy more than 692,000,000 ash trees in forests in Michigan and Ohio alone, and between 5 and 10 percent of urban street trees in the Upper Midwest;

…

(11)(A) often, there are significant interactions between insects and diseases; (B) many diseases (such as white pine blister rust, beech bark disease, and many other diseases) can weaken trees and forest stands and predispose trees and forest stands to insect attack; and (C) certain diseases are spread using insects as vectors (including Dutch elm disease and pine pitch canker); …

(b) … The purposes of this title are— (1) to require the Secretary to develop an accelerated basic and applied assessment program to combat infestations by forest-damaging insects and associated diseases; (2) to enlist the assistance of colleges and universities …, State agencies, and private landowners to carry out the program; and (3) to carry out applied silvicultural assessments.

Sec. 402 Definitions

…

 (3) FOREST-DAMAGING INSECT. … means … (D) a gypsy moth; (E) a hemlock woolly adelgid; (F) an emerald ash borer; … and (I) such other insects … identified by the Secretary.

[i] Oswalt, S.N., .W.B. Smith, P.D. Miles, & S.A. Pugh. Forest Resources of the United States, 2017  Uport WO-97SDA Forest Service Gen. Tech. Report WO-97. March 2019

[ii] Fei, S., R.S. Morin, C.M. Oswalt, and A.M. 2019. Biomass losses resulting from insect and disease invasions in United States forests. PNAS August 27, 2019. Vol. 116 No. 35  17371–17376

[iii] Coleman, T.W, A.D. Graves, B.W. Oblinger, R.W. Flowers, J.J. Jacobs, B.D. Moltzan, S.S. Stephens, R.J. Rabaglia. 2023. Evaluating a decade (2011–2020) of integrated forest pest management in the United States. Journal of Integrated Pest Management, (2023) 14(1): 23; 1–17

[iv] Ibid.

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  https://treeimprovement.tennessee.edu/

or

www.fadingforests.org

Act Now!!! Administration Proposes to “0 out” key USFS Programs

The Trump Administration’s budget for Fiscal Year 2026 [which begins at the end of September 2025] proposes to eliminate funding for nearly all  USFS research & Forest Health Protection.

Proposed Cuts to USFS Research: Timber the Sole Aim

 In a letter from Office of Management and Budget (OMB) to Senate Appropriations Committee Chair Susan Collins (R-Maine, Director Russell Vought says the Administration wants to manage National forests “for their intended purpose of producing timber” and that the research and development program “is out of step with the practical needs of forest management for timber production.” The Administration proposes to eliminate funding for USFS research projects other than the small portion covering Forest Inventory and Analysis.

I understand that the USFS Chief told various NGOs that his job is to run the National Forest System, increase timber production by 40%, and do nothing else.

This single aim conflicts with the 1897 legislation founding and authorizing the USFS. It also violates provisions of subsequent legislation such as the Multiple-Use Sustained-Yield Act of 1960 and the National Forest Management Act of 1976. It also departs from long-standing US Forest Service policy – which is the intention. 

The “intended purpose” of establishing “forest reserves” [which were later renamed National forests] has never been solely for timber production. The “Organic Act” of 1897 provided that any new forest reserves would have to meet the criteria of forest protection, watershed protection, and timber production.

Specifically, the ORGANIC ACT OF 1897 [PUBLIC–No.2.] says:

“[All public lands heretofore designated and reserved by the President of the US under the provisions of the Act [of] March 3rd 1891, the orders for which shall be and remains in full force and effect, unsuspended and unrevoked, and all public lands that may hereafter be set aside as public forest reserves under said act, [these were the “forest reserves,”predecessors of “National Forests]” shall be as far as practicable controlled and administered in accordance with the following provisions:

“No public forest reservation shall be established, except to improve and protect the forest within the reservation, or for the purpose of securing favorable conditions of water flows, and to furnish a continuous supply of timber for the use and necessities of [US] citizens; but it is not the purpose or intent of these provisions, or of the Act providing for such reservations, to authorize the inclusion therein of lands more valuable for the mineral therein, or for agricultural purposes, than for forest purposes.”

The Department of the Interior, which then managed these forest reserves, promptly issued implementing regulations. The regulations stated that the “object” of forest reservations was:

“2. Public forest reservations are established to protect and improve the forests for the purpose of securing a permanent supply of timber for the people and insuring conditions favorable to continuous water flow.”

Therefore, I think the Administration has exaggerated the emphasis on timber production by calling it “the” intended purpose of the original establishment of National forests. The Administration has also chosen to ignore subsequent legislation, such as the Multiple-Use Sustained-Yield Act of 1960 and the National Forest Management Act of 1976.

Sec. 13 of the NFMA limits the sale of timber from each national forest to a quantity equal to or less than a quantity which can be removed from such forest annually in perpetuity on a sustained-yield basis. This limit might be exceeded under certain circumstances, but such excess must still be consistent with the multiple-use management objectives of the land management plan. Further, Sec. 14 requires public input into any decision to raise timber allowances.

During his period as Chief (1905 – 1910), Gifford Pinchot invented and applied the concept of “conservation” of natural resources. As a result “wise use” became accepted as the national goal.

Culminating more than a century of legislation and informed policy, the mission of the USDA Forest Service is to “sustain the health, diversity, and productivity of the nation’s forests and grasslands to meet the needs of present and future generations.”

Proposed Cuts to State, Private, and Tribal Forests

The budget also cuts $303 million from the State, Private, and Tribal Forests program. (I understand this zeroes out the entire program). The OMB Director alleges that the program has been “plagued by oversight issues, including allegation of impropriety by both the Agency and State governments.” I understand that this would eliminate the cooperative projects managed by the Forest Health Protection program, too.

Implications for Non-native Insects and Pathogens

Remember that USFS’s research and development program is intended to improve forest managers’ understanding of ecosystems, including human interactions and influences, thereby enabling improvements to the health and use of our Nation’s forests and grasslands. Most importantly to me, this program provides foundational knowledge needed to develop effective programs to prevent, suppress, mitigate, and eradicate the approximately 500 non-native insects and pathogens that are killing America’s trees.

The Forest Health Program provides technical and financial assistance to the states and other forest-management partners to carry out projects (designed based on the above research) intended to prevent, suppress, mitigate, and eradicate those non-native insects and pathogens. The program’s work on non-federal lands is crucial because introduced pests usually start their incursions near cities that receive imports (often transported in crates, pallets, or imported plants).

Eliminating either or both programs will allow these pests to cause even more damage to forest resources – including timber.

Both supporting research and on-the-ground management must address pest threats across all U.S. forests, including the more than 69% that are located on lands managed by others than the USFS. Already, the 15 most damaging of these pests threaten destruction of 41% of forest biomass in the “lower 48” states. This is a rate similar in magnitude to that attributed to fire (Fei et al. 2019). It is ironic that the Administration considers the fire threat to be so severe that it has proposed restructuring the government’s fire management structure.

I remind you that the existing USFS R&D budget allocates less than 1% of the total appropriation to studying a few of the dozens of highly damaging non-native pests. I have argued that this program should be expanded, not eliminated. Adequate funding might allow the USFS to design successful pest-management programs for additional pests (as suggested by Coleman et al.).

As a new international report (FAO 2025) notes, genetic resources underpin forests’ resilience, adaptability, and productivity. Funding shortfalls already undercut efforts to breed trees able to thrive despite introduced pests and climate change (the latter threat is still real, although the Administration disregards it). I have frequently urged the Congress to increase funding for USFS programs – which are sponsored primarily by the National Forest System and State, Private, and Tribal, although some are under the R&D program.

Please ask your Member of Congress and Senators to oppose these proposed cuts. Ask them to support continued funding for both USFS R&D and its State, Private, and Tribal Programs targetting non-native insects and pathogens. America’s forests provide resources to all Americans – well beyond only timber production and they deserve protection.

Contacting your Representative and Senators is particularly important if they serve on the Appropriations committees.

House Appropriations Committee members:

Republicans: AL: Robert Aderholt, Dale Strong; AR: Steve Womack; AZ: Juan Ciscomani; CA: Ken Calvert, David Valadao, Norma Torres; FL: Mario Diaz-Balart, John Rutherford, Scott Franklin; GA: Andrew Clyde; ID: Michael Simpson; IA: Ashley Hinson; KY: Harold Rogers; LA: Julia Letlow; MD: Andy Harris; MI: John Moolenaar; MO: Mark Alford; MS: Michael Guest;  MT: Ryan Zinke; NC: Chuck Edwards; NV: Mark Amodei; NY: Nick LaLota; OH: David Joyce; OK: Tom Cole, Stephanie Bice; PA: Guy Reschenthaler TX: John Carter, Chuck Fleishmann, Tony Gonzales, Michael Cloud, Jake Ellzey; UT: Celeste Maloy; VA: Ben Cline; WA: Dan Newhouse; WV: Riley Moore

Democrats: CA: Pete Aguilar, Josh Harder, Mike Levin; CT: Rosa DeLauro; FL: Debbie Wasserman Schultz, Lois Frankel; GA: Sanford Bishop; HI: Ed Case IL: Mike Quigley, Lauren Underwood; IN: Frank Mrvan; MD: Steny Hoyer, Glenn Ivey; ME: Chellie Pingree; MN: Betty McCollum; NJ: Bonnie Watson Coleman NY: Grace Meng, Adriano Espaillat, Joseph Morelle; NV: Susie Lee;  OH: Marcy Kaptur;  PA: Madeleine Dean; SC: James Clyburn;  TX: Henry Cuellar, Veronica Escobar; WA: Marie Gluesenkamp Perez; WI: Mark Pocan

Senate Appropriations Committee members:

Republicans: AK: Lisa Murkowski; AL: Katie Britt; AR: John Boozman (AR); KS: Jerry Moran; KY: Mitch McConnell; LA: John Kennedy; ME: Susan Collins; MS: Cindy Hyde-Smith; ND: John Hoeven; NE: Deb Fischer; OK: Markwayne Mullin; SC: Lindsey Graham; SD: Mike Rounds TN: Bill Hagerty; WV: Shelley Moore Capito;

Democrats: CT: Chris Murphy; DE: Chris Coons; GA: Jon Ossof; HI: Brian Schatz; IL: Richard Durbin; MD: Chris van Hollen; MI: Gary Peters; NH: Jeanne Shaheen; NM: Martin Heinrich; NY: Kirsten Gillibrand; OR: Jeff Merkley; RI: Jack Reed; WA: Patty Murray; WI: Tammy Baldwin

SOURCES

Coleman, T.W, A.D. Graves, B.W. Oblinger, R.W. Flowers, J.J. Jacobs, B.D. Moltzan, S.S. Stephens, R.J. Rabaglia. 2023. Evaluating a decade (2011–2020) of integrated forest pest management in the United States. Journal of Integrated Pest Management, (2023) 14(1): 23; 1–17

FAO. 2025. The Second Report on the State of the World’s Forest Genetic Resources. FAO Commission on Genetic Resources for Food and Agriculture Assessments, 2025. Rome.

Fei, S., R.S. Morin, C.M. Oswalt, and A.M. 2019. Biomass losses resulting from insect and disease invasions in United States forests. PNAS August 27, 2019. Vol. 116 No. 35  17371–17376

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  https://treeimprovement.tennessee.edu/

or

www.fadingforests.org

Shothole borer & associated fungus – demonstrating threat in South Africa & possibly beyond

Erythrina caffra one of the native tree species in South Africa killed by PSHB. photo by Coana/Riti via Flickr

Introductions of bark and ambrosia beetles (Coleoptera: Curculionidae, Scolytinae) have significantly increased over the past century. Surveys conducted at borders and ports of entry around the world have shown the majority of beetles intercepted were scolytines. These insects are highly destructive on their own. Also, they can carry pathogenic fungal symbionts that can have devastating effects on the trees they attack.

One or more species in a complex in the Euwallacea genus have become established in countries around the world.  One of these, the polyphagous shot hole borer (Euwallacea fornicatus; PSHB) and its associated fungus (renamed from Fusarium euwallaceae to Neocosmospora euwallaceae) is threatening havoc in South Africa about a decade after its establishment (Townsend, Hill, Hurley, and Roets. 2025).

Over this brief period PSHB/Fusarium disease has spread from two introduction sites – Pietermaritzburg, in KwaZulu-Natal Province, and Cape Town, in Western Cape Province – to all but one of the country’s nine provinces. It has become established in four of five forest types studied – Afrotemperate, coastal, sand, and swamp forests. It has not established in mangrove forests. (The Western Cape Province is home to its own “floral kingdom”. The kingdom’s charactersitic fynbos flora is a heathland habitat, not a forest one.)

Townsend and colleagues established a network of 78 monitoring plots in the Western Cape and KwaZulu-Natal provinces. The sites reflected a variety of natural and human impacts.

tree infested by PSHB/Fusarium disease in KwaZulu-Natal Botanical Garden, Pietermaritzburg. Photo from website of Greenpop.org

By monitoring these plots over five years (2019 – 2024), Townsend and colleagues have demonstrated that the beetle/fungus complex and resulting “Fusarium disease” is spreading and intensifying. The number of infected trees rose from 100 to 176 over the five years – a mean increase of 0.6% per year. The number of PSHB entry holes increased by over 10% annually. The number of plots containing infected trees roughly doubled from 23 in 2019 (29% of the 78 plots) to 48 (60%) in 2023.

By the end of the study, 29% of the 148 species sampled had been infected. This represented 43 species and 7 unidentified trees infected. Trees of eight native species died, , although one — Diospyros glabra (Ebenaceae) – resprouted after the main bole died.

In addition to the eight species known to suffer mortality, another 18 species were found to be able to support PSHB reproduction. Townsend and colleagues worry that, as the infestation spreads and intensifies, some of these species might also succumb. They mention specifically Erythrina caffra (coral tree), which is prevalent in coastal forest ecosystems across South Africa.

Most of the hosts are in the same families as those identified earlier by Lynch et al. (2021), e.g., Ebenaceae, Fagaceae, Fabaceae, Malvaceae, Podocarpaceae, Rutaceae, Sapindaceae and Stilbaceae.

Disease progress, speed of death, and visibility of symptoms varied not only between species, but sometimes among individuals of the same species. Some trees died rapidly. Townsend and colleagues say it is impossible to predict which individuals will succumb to infection.

There is, though, a clear frequency-dependent relationship between trees and beetles. Sites with higher relative abundance of host trees also had a higher proportion of infected trees, on average. The number of PSHB holes per species and per plot both increased to a larger extent at these same sites.

Individual trees’ traits influenced the severity of infestations (measured by the number of PSHB entry holes). Larger trees, those with a less healthy canopy, and those farther from a water source suffered more attacks. (This last finding differs from others’; Townsend et al. speculate that in the absence of flood-stressed trees, drought-stressed trees might be more attractive to ambrosia beetles.)

native tree in Tsitsikama National Park; photo by F.T. Campbell

Characteristics of the monitoring plots also affected disease progression. Higher proportions of trees became infected when they grew in plots that were closer to source populations, or that contained a higher proportion of host species as distinct from non-host species. The proportion of trees infected decreased in plots with higher tree densities or tree species richness.

As of 2023, “Fusarium disease” is more widespread and intense in KwaZulu-Natal than in the Western Cape. In KwaZulu-Natal 0.11% of monitored trees are infected compared to 0.06% in the Western Cape. The number of infected trees rose twice as fast over the five years in KwaZulu-Natal – ~6%, than in Western Cape – 3%. While all KwaZulu-Natal plots contained infected trees, three of 11 monitoring sites in the Western Cape did not. Townsend and colleagues believe that the most likely explanation is that PSHB arrived in KwaZulu-Natal earlier (as far back as 2012 as opposed to 2017 in Western Cape). Another possible factor is that source populations of infected trees are indigenous trees within the forest in KwaZulu-Natal whereas, in the Western Cape, they are often non-native trees planted in urban areas far from the study plots. Also, forests in KwaZulu-Natal are fragmented while, in Western Cape, the study forests are nearly contiguous. Townsend et al. conclude that the disease will spread and intensify in Western Cape as additional source populations become established in the forest.

locations of PHSB/Fusarium disease in Cape Town, South Africa – West of the study sites; map from City of Cape Town

As of 2023, the proportion of trees infected appears to be small — 7.6% of the 2,313 trees monitored. Only 11 trees in the monitored plots have died. However, the longer PSHB is active in the environment the more trees it will infest, the higher its impact will be on hosts, and the higher the number of dispersing individuals produced. This will substantially increase the chances and rates of additional areas becoming infected, especially in areas close to infestations – e.g., cities. They fear that in the future impacts will increase as progressively more competent host individuals are infected. Therefore, they emphasize the importance of mitigating PSHB increase in natural ecosystems, even in already infected areas.

Townsend and colleagues urge phytosanitary officials and resource managers to prioritize surveillance and management on the families containing several host species (above) and within plant communities in which they predominate. Managers must also be alert to new reproductive hosts for the beetle that appear as the infestation spreads and intensifies.

The situation could be worse than described; the Townsend et al. study did not examine how the invasion might affect eco-regions outside these two provinces. Because the PSHB has such a broad host range, hosts can die quickly, and South Africa provides ideal climatic conditions, this bioinvader could cause severe ecological effects on most indigenous forest types as well as agriculture and urban trees throughout Africa.

SOURCES

Lynch, S.C., A. Escalen, and G.S. Gilbert. 2021. Host evolutionary relationships explain tree mortality caused by a generalist pest-pathogen complex. Evol Appl 14:1083 – 1094. https://doi.org/10.1111/eva.13182

Townsend, G., M. Hill, B.P. Hurley, and F. Roets 2025. Escalating threat: increasing impact of the polyphagous shot hole borer beetle, Euwallacea fornicatus, in nearly all major South African forest types. Biol Invasions (2025) 27:88 https://doi.org/10.1007/s10530-025-03551-2  

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  https://treeimprovement.tennessee.edu/

or

www.fadingforests.org

“Ecological memory” determines a forest’s resilience — implications of bioinvasion to New Zealand’s unique flora

kauri dieback

Scientists in New Zealand are saying explicitly that a forest’s unique mixture of species matters when considering the future. This mixture is the result of the forest’s evolutionary history. Losing members of the biological community reduces the forest’s ability to respond to current and future stresses – its resilience.

New Zealand’s forests are part of the broader legacy of the ancient supercontinent of Gondwanaland – the island nation’s plants have close relatives in South America, the Pacific Ocean islands, and Australia. Still, these forests are unique: 80% of New Zealand’s plant species are endemic. The forests are also species-rich. The warm temperate evergreen rain forests of the North Island are home to at least 66 woody plant species that can reach that reach heights above six meters (Simpkins et al. 2024).

These forests have been severely changed by human activity. In just ~ 750 years people have cut down approximately 80% of the original forest cover! (Simpkins et al. 2024) Of the eight million hectares of surviving native forest, a little over five million hectares is managed for the conservation of biodiversity, heritage, and recreation.  Another 2 million hectares are plantations of non-native species.

sites in New Zealand where pine plantations are “wilding”

All these forests are challenged by introduced mammals – from European deer to Australian possums. Climate change is expected to cause further disturbance, both directly (through e.g., drought, extreme weather) and indirectly (e.g., by facilitating weed invasion and shifting fire regimes) (Simpkins et al. 2024).

Pathogen threats are also common threats to the native trees of the Pacific’s biologically unique island systems. For example, Ceratocystis lukuohia and C. huliohia (rapid ‘ōhi‘a death, or ROD). The latter is killing ‘ōhi‘a (Metrosideros polymorpha) on the Hawaiian Islands. More than 40% of native plant species in Western Australia are susceptible to Phytophthora cinnamomi. Here I focus on two pathogens, kauri dieback and myrtle rust, now ravaging New Zealand’s native flora. No landscape-level treatment is available for either pathogen.

When considering this suite of challenges, Simpkins et al. focus on these two pathogens’ probable impact on forest carbon sequestration. They worry in particular about erosion of the forests’ resilience due to loss of “ecological memory” – the life-history traits of the species (e.g., soil seed banks) and the structures left behind after individual disturbances.

one of the largest remaining kauri trees, “Tane Mahuta”, in Waipoua Kauri Forest; photo by F.T. Campbell

Kauri Dieback

The causal agent of Kauri dieback, Phytophthora agathidicida, is a soil-borne pathogen that spreads slowly in the absence of animal or human vectors. The disease affects a single species, Agathis australis (kauri, Araucariaceae). However, kauri is a long-lived, large tree that is a significant carbon sink. It probably modifies local soil conditions, nutrient and water cycles, and associated vegetation. Also, kauri has immense cultural significance.

Simpkins et al. note that kauri dieback threatens stand-level loss of A. australis – that is, local extinctions. In the absence of disturbance Kauri trees can grow to awe-inspiring size. In the 19th Century, before widespread logging, some were measured at 20 meters or more in circumference. Consequently, kauri dieback might cause a decline in aboveground live carbon storage of up to 55%. This loss would occur over a period of hundreds of years, not immediately.

Huge kauri are not likely to be replaced by other long-lived emergent conifers (based on an analysis of one species, Dacrydium cupressinum). Instead, kauri are probably going to be replaced by late-successional angiosperms. The authors discuss the ecological implications for levels of carbon storage and proportions of trees composed of Myrtaceae – exacerbating damage caused by myrtle rust (see below).

The expectation of Simpkins et al. that kauri will suffer at least local extinctions is based on an assumption that no kauri trees are resistant to the pathogen. Fortunately, this might not be true: different Agathis populations show various levels of tolerance to Agathis dieback. Identification and promotion of some levels of resistance could enable A. australis to retain a diminished presence in the landscape.

However, Lantham, et al. make clear that containing kauri dieback remains “challenging,” despite its discovery nearly 20 years ago (in 2006). Scientists and land managers have little information on the distribution of symptomatic trees, much less of the pathogen itself. This means they don’t know where infection foci are or how fast the disease is spreading.

As is often true, the pathogen is probably present in a stand for years, possibly a decade or more, before symptoms are noticed. This means that the current reliance on public reports of diseased trees, or targetting surveillance on easy-to-access sites (e.g., park entrances and along existing track networks), or at highly impacted areas readily identified through aerial methods, fails to detect early stages of infection. Indeed, it seems probable that P. agathidicida had been present in New Zealand’s ecosystems for decades before its formal identification.

The Waipoua forest is one of the largest areas of forest with old kauri stands in the country. A new analysis of aerial surveys done between 1950 and 2019, shows how the forest is changing. The number of dead trees increased more than four-fold and the number of unhealthy-looking trees increased 16-fold over these 70 years. Kauri dieback is now widespread in this forest, especially in areas near human activities like clearing for pasture or planting commercial pine plantations).

Lantham et al. have developed a model which they believe will help identify areas of higher risk so as to prioritize surveillance and inform responses. These could delimit the disease front and help implement quarantines or other measures aimed at limiting the spread of P. agathidicida to uninfected neighboring sites.

I hope New Zealand devotes sufficient resources to expand surveillance and management to levels commensurate with the threat to this ecologically and culturally important tree species.

Leptospermum scoparia; photo by Brian Gatwicke via Flickr

Myrtle Rust

Myrtle rust is a wind-borne disease that affecting numerous species in the Myrtaceae, including some of the dominant early successional species (e.g., Leptospermum spp.). Simpkins et al. expect that myrtle rust might hasten the decline of two such tree species (L. scoparium and Kunzea ericoides). However, these trees’ small size and rapid replacement by other species during succession minimizes the effect of their demise on carbon storage.

Because I am concerned about the irreplaceable loss to biodiversity, I note that Simpkins et al. also feared immediate threats to some trees in the host Myrtaceae family, specifically highly susceptible species such as Leptospermum bullata.

As I reported in a recent blog, a second group of scientists (McCarthy et al.) explored the threat from myrtle rust more broadly. Austropuccinia psidii has spread through Myrtaceae-dominated forests of the Pacific islands for about 20 years.

Trees in the vulnerable plant family, Myrtaceae, are second in importance (based on density and cover) in New Zealand’s forests. Successional shrub communities dominated by the two species named above, Kunzea ericoides and Leptospermum scoparium, are widespread in the northern and central regions of the North Island and in northeastern and interior parts of the South Island. These regions’ vulnerability is exacerbated by the area’s climate, which is highly suitable for A. psidii infection (Simpkins et al. 2024).

McCarthy et al. concluded that if Leptospermum scoparium and Kunzea ericoides prove to be vulnerable to myrtle rust, their loss would cause considerable change in stand-level functional composition across these large areas. They probably would be replaced by non-native shrubs, which are already common on the islands. Any resulting forest will differ from that formed via Leptospermeae succession.

These authors also worry that the risk to native ecosystems would increase if more virulent strains of the myrtle rust pathogen were introduced or evolved. They note that A. psidii is known to have many strains and that these strains attack different host species.

SOURCES

Latham, M.C., A. Lustig, N.M. Williams, A. McDonald, T. Patuawa, J. Chetham, S. Johnson, A. Carrington, W. Wood, and D.P. Anderson. 2025.  Design of risk-based surveillance to demonstrate absence of Phytophthora agathidicida in New Zealand kauri forests. Biol. Invasions (2025) 27, no. 26

McCarthy, J.K., S.J. Richardson, I. Jo, S.K. Wiser, T.A. Easdale, J.D. Shepherd, P.J. Bellingham. 2024. A Functional Assessment of Community Vulnerability to the Loss of Myrtaceae from Myrtle Rust. Diversity and Distributions, https://doi.org/10.1111/ddi.13928

Simpkins, C.E., P.J. Bellingham, K. Reihana, J.M.R. Brock, G.L.W. Perry. 2024. Evaluating the effects of two newly emerging plant pathogens on North Aotearoa-New Zealand forests using an individual-based model.  Ecological Modelling, www.elsevier.com/locate/ecolmodel

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  https://treeimprovement.tennessee.edu/

or

www.fadingforests.org