Category: funding

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

Great progress in predicting impact of introduced forest insects

results of invasion by emerald ash borer (photo courtesy of Nathan Siegert, USFS ); one of the woodboring beetles found to be so damaging to hardwood trees

Over the last nine years scientists have made significant progress in identifying aspects of insect-plant host relationships that play important roles in determining how much damage an introduced, non-native pest is likely to cause within forest ecosystems in the United States. Predicting which introductions will probably cause the greatest damage is vitally important because scientists, phytosanitary officials, and resource managers cannot address all the hundreds of established insects, much less the thousands which might be introduced. This shortfall increases with each surge in import volumes (see my previous blogs about wood packaging by scrolling down the website below the “Archives” to “Categories”, then find “SWPM”), proliferation of goods types and source areas, and cutbacks in funding.

I hope USDA APHIS and Forest Service are adjusting their procedures to apply the scientists’ path-breaking findings.

Their progress will help protect our forests. I apologize if I seem ungrateful — but we need similar progress in managing plant pathogens. Consider the damage caused by chestnut blight, white pine blister rust, Dutch elm disease, sudden oak death, beech leaf disease … (All these and other pathogens are described briefly here.) Understanding the universe of introduced fungi, water molds, nematodes, viruses, etc., is per se much more challenging. Ashley Schulz points out that among the complications are pathogens’ complex life cycles, and possible new relationships with vectors.

Undertaking this analysis will be set back decades if agencies’ resources – funds and staffs – are decimated during the current “downsizing” of government. We must speak up!!

At least regarding non-native insects that attack North American tree species, scientists’ analyses promise a new ability to set priorities. This should improve the efficacy of phytosanitary programs – if government downsizing is not allowed to destroy USDA’s scientific, regulatory, and resource management programs.

We must speak up!!

What science tells us now

Schulz et al. (2025) summarize current findings. (Full citation to all references appear at the end of the blog.)

Earlier, scientists sought to find commonalities associated with introduced insects that caused high impacts on North American conifer trees [Mech et al. (2019)] and hardwoods (angiosperms) [Schulz et al. (2021)] (Full citations at the end of the blog; earlier blogs posted here and here.) Both studies found that the time elapsed since tree species in North America diverged from the host plants of the insects in their native range (i.e., host evolutionary history) is a diagnostic factor. This factor best predicted non-native insect impact compared to the other factors that were significant for conifer and hardwood specialists. For conifers, the other significant factors included the shade and drought tolerance of the North American host plants and whether there was a related insect native to North America on the same hosts that the non-native insect impacted. For hardwoods, another important factor explaining a specialist insect’s impact is if the insect is a wood borer, especially a scolytine beetle. The wood density of the North American host plant was also considered a significant factor when predicting impact of the non-native insect.

In 2022, Uden et al. applied the divergence time method to insect species not yet introduced to North America that might attack conifer species. They hoped to identify both insects posing the greatest hazard and tree species most vulnerable to introduced pests.

Now, a new team again led by Ashley Schulz and Angela Mech (see Schulz et al. 2025) has applied a similar approach to a more comprehensive range of pest-host relationships, including the pests that specialize on host plants and pests that feed on a broader array of hosts. Some feed on both conifers and hardwoods. They found that:

  • It is possible to quantify insect host breadth and identify the cutoff where “specialists” and “generalists” diverge. Specifically, the split occurs around 2,250 cumulative million years, where insects that feed on hosts that add up to less than that have narrow host breadth (i.e., “specialists”) and insects that feed on hosts that add up to more than that have broad host breadth (i.e., “generalists”). This technique also helps categorize insects that fall within the middle range of host breadth and are traditionally difficult to classify as either specialists or generalists based on differing qualitative definitions of the terms.
  • Insects that use more hosts in their native range also tend to use more hosts in the introduced range (North America). However, many of these insects utilized fewer hosts in the introduced range compared to the native range. This shrinkage was not universal, however; about 30% of insects increased their host breadth in the introduced range. Most of these fed on a single species in their native range but attacked additional species in the same family in North America. The corresponding i-Tree Pest Predictor tool uses the list of hosts in the insect’s native range and these models to determine the insect’s likelihood that it would cause high impact, as well as each North American tree species’ susceptibility to the insect entered into the tool.
  • Certain feeding guilds had – on average — a significantly narrower host breadth in North America than in their native ranges. These were gall makers (13 species analyzed); sap feeders (120 species); and wood borers (35 species). In contrast, host ranges did not differ for folivores (68 species), reproductive feeders (7 species), and root feeders (5 species). Still, we know that wood borers, as a group, have caused enormous damage to a range of North American tree taxa (see emerald ash borer, redbay ambrosia beetle, invasive shot hole borers (all described briefly here). Again, the i-Tree Pest Predictor tool can help identify the threat to particular tree species.

Of course, APHIS should not disregard pests with narrow host ranges; several have caused enormous damage.

red spruce (Pikea rubens) in Great Smoky Mountains National Park; photo by famartin via Wikipedia. Red spruce is the species found to be most vulnerable by the Uden et al. study

Schulz et al. (2025) developed models for three groups of introduced herbivorous insects that feed on trees:

1) conifer specialists (based on analysis of 69 species);

2) hardwood specialists (based on analysis of 141 species);

3) hardwood generalists (based on analysis of 30 species).

Because of their quantification of host breadth, they defined the “specialist” group more broadly than is commonly done, e.g., an insect that feeds on the three families Betulaceae, Fagaceae, and Juglandaceae would be considered “specialists” because all three host families are in the Fagales clade.

Tree relatedness was the only significant explanatory factor for all three host breadth categories. As determined in the previous studies, North American host tree species that were too closely or distantly related to the insect’s hosts in its native range were less impacted than hosts that diverged somewhere in the middle – the “Goldilocks” range. The divergence period differs among the three pest-risk categories: 3–4 million years ago for conifer specialists, 5–9 million years ago for hardwood specialists, ~1–2 million years ago for hardwood generalists. Schulz et al. suggest that the reason why the peak probability of high impact differs among these groups is that different feeding guilds cause the most damage to the specific host category, and each feeding guild is challenged by different tree host defenses. Bark and wood boring beetles (the hardwood specialists with the greatest impact) must overcome lethal constitutive and induced tree defenses in order to survive for long periods in the cambial layer. These insects have adapted the ability to locate and select poorly defended individuals in the host population. Folivores (i.e., the generalists with the highest impact) adapt to plant chemistry and trichomes (hair-like or scale-like outgrowths), or can avoid host defenses by moving off the foliage. Sap feeders (which include many high impact conifer specialists) are usually tolerated by trees, unless they stimulate hypersensitive reactions or vector pathogens.

Of course, scientists’ estimates of how long ago tree taxa diverged from common ancestors differ. Fortunately, Uden et al. (2022) found that these differences only rarely affect the predicted impact of a non-native insect – at least in the case of the 62 European insects and 47 North American conifer species they analyzed. In only 1.37% of the 2,914 pairs analyzed did the predicted risk differ depending on which source phylogeny was used. These cases were associated with 27 conifer-specialist insects and 9 conifer hosts. The article does not tell us which pest/host pairs these are but, overall, this paper demonstrates that the estimate differences in the phylogenetic trees does not differ enough to be problematic when forecasting insect impact.

Changes Needed in the Way Agencies Set Priorities

Schulz et al. (2025) urged agencies to stop relying only on insect traits as the basis for developing models & phytosanitary regulations. The only insect trait that predicted impact is the insect’s feeding guild. Considering hardwoods, they found that wood borers pose the greatest risk among specialists to hardwoods; folivores among generalists. While sap feeders do not cause statistically higher damage on hardwood tree species, four of the seven high-impact conifer specialists are sap feeders (hemlock woolly adelgid, balsam woolly adelgid, red pine scale, and spruce aphid). Therefore, the i-Tree Pest Predictor tool incorporates consideration of whether a pest of conifers is a sap feeder.

Schulz et al. (2025) also caution agencies against relying on just the number of hosts an insect might exploit. Assessors must consider the range of underlying plant chemistry / host defenses that the insect encounters. They found that hosts that are shade tolerant are more susceptible to high impact from conifer specialists and hosts that have intermediate to no shade tolerance are more susceptible to high impact from generalists.

Uden et al. (2022) identified a possible weakness in USDA efforts to prioritize pest prevention targets. They found that APHIS’ Prioritized Offshore Pest List included only 12 conifer specialists from Europe among the 150 species listed. They go on to note that while sap feeders constitute 53% of tree pest species established in the U.S., APHIS listed none. The models applied by Uden, Schulz, and Mech do not consider whether the insect is likely to become established. Improving our understanding of the many factors influencing an insect’s likelihood of being transported to North America or becoming established requires additional research. This might eventually lead to a usable tool for predicting this aspect of bioinvasion by forest pests.

There is an urgent need for such a tool. As Uden et al. noted, they found that 66% of the insect species they analyzed fell into the “high impact” category. This is a much higher proportion than estimates based on earlier studies, so identifying which of these insects are likely to establish versus not establish in North America can provide more resolution and help identify which insects are going to be most problematic.

Mature Fraser fir killed by balsam woolly adelgid; Clingman’s Dome; photo by Ben Ramsey via Flickr

Tree species at risk

The analysis undertaken by Uden et al. determined that three conifer species face a high level of hazard from European insects if they are introduced. They identified particularly high threats to two species, Fraser fir (Abies fraseri) and Carolina hemlock (Tsuga caroliniana). The fir is determined to be vulnerable to 17 insect species which are predicted to have high likelihood of a high impact. The hemlock is highly vulnerable to one of the insect species they sampled. They note that both of these conifers have a limited geographic range and ecological habitat, so they likely have a relatively narrow genetic pool. A third species said to be at elevated risk is red spruce (Picea rubens) – which, although more widespread, is also under attack by a non-native insect. All three species fit earlier finding by Mech et al. that conifer trees with high shade tolerance but low drought tolerance more vulnerable to non-native pests. In none of these cases do Uden et al. mention that the tree species have already been severely diminished by established non-native insects – i.e., balsam woolly adelgid on the fir (above), hemlock woolly adelgid on the Carolina hemlock. The Schulz/Mech team is working to refine methods for identifying tree species and regions at greatest risk.

Meanwhile, Uden et al. have suggested that phytosanitary authorities and forest managers apply their findings to identify the European herbivorous insects that pose the greatest threat to North American conifer species. They should identify Palearctic tree species that fall within the high-impact “Goldilocks” zone of divergence times in relation to specific North American tree species, then identify the insects that feed on those Palearctic trees. These insects would presumably pose the highest predicted hazard to those North American tree species. They suggest that species so identified should be added to the USFS’ list of species targetted by its wood borer early detection program. To address likelihood of introduction, they suggest incorporating data on insect species commonly intercepted at ports – an indication of high propagule pressure. There will always be exceptions though. For example, Ips typographus feeds on spruce and has been frequently detected at the ports, but it has not established in North America.

For those focused on identifying species or ecoregions at greatest risk, Uden et al. suggest scientists use several sources to identify vulnerable vegetation communities. Sources suggested include USFS Forest Inventory and Analysis (FIA) and NatureServe Explorer plant community descriptions) that have relatively high-value tree species predicted to be at risk from introduced species.

SOURCES

Aukema, J.E., D.G. McCullough, B. Von Holle, A.M. Liebhold, K. Britton, and S.J. Frankel. 2010. Historical Accumulation of Nonindigenous Forest Pests in the Continental United States. BioScience 60(11): 886-897. https://doi.org/10.1525/bio.2010.60.11.5

Mech,  A.M., K.A. Thomas, T.D. Marsico, D.A. Herms, C.R. Allen, M.P. Ayres, K.J. K. Gandhi, J. Gurevitch, N.P. Havill, R.A. Hufbauer, A.M. Liebhold, K.F. Raffa, A.N. Schulz, D.R. Uden, & P.C. Tobin. 2019. Evolutionary history predicts high-impact invasions by herbivorous insects. Ecology and Evolution 9(21): 12216–12230. https://doi.org/10.1002/ece3.5709

Schulz, A.N.,  A.M. Mech, M.P. Ayres, K. J. K. Gandhi, N.P. Havill, D.A. Herms, A.M. Hoover, R.A. Hufbauer, A.M. Liebhold, T.D. Marsico, K.F. Raffa, P.C. Tobin, D.R. Uden, K.A. Thomas. 2021. Predicting non-native insect impact: focusing on the trees to see the forest. Biological Invasions 23: 3921-3936. https://doi.org/10.1007/s10530-021-02621-5

Schulz, A.N., N.P. Havill, T.D. Marsico, M.P. Ayres, K.J.K. Gandhi, D.A. Herms, A.M. Hoover, R.A. Hufbauer, A.M. Liebhold, K.F. Raffa, K.A. Thomas, P.C. Tobin, D.R. Uden, A.M. Mech. 2025. What Is a Specialist? Quantifying Host Breadth Enables Impact Prediction for Invasive Herbivores

Ecology Letters 28: e70083. https://doi.org/10.1111/ele.70083

Uden, D.R., A.M. Mech, N.P. Havill, A.N. Schulz, M.P. Ayres, D.A. Herms, A.M. Hoover, K.J.K. Gandhi, R.A. Hufbauer, A.M. Liebhold, T.D. Marsico, K.F. Raffa, K.A. Thomas, P.C. Tobin, C.R. Allen. 2022. Phylogenetic risk assessment is robust for forecasting the impact of European insects on North American conifers. Ecological Applications 33(2): e2761. https://doi.org/10.1002/eap.2761

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

EAB biocontrol – evidence of impact

riparian ash killed by EAB; in this case, Mattawoman Creek in Maryland. Photo by Leslie A. Brice

Good news at the recent 33rd USDA Research Forum on Invasive Species. Scientists presented the first study that demonstrates significantly lower ash tree mortality in sites with high parasitism rates of two larval parasitoids, Tetrastichus planipennisi and Spathius galinae.

Their study area is the ash-dominated riparian area along the Connecticut River that flows north to south across the middle of Massachusetts. Knowing in advance that the emerald ash borer (Agrilus planipennis; EAB) would invade the area, scientists established monitoring plot that consisted of marked individual ash trees. EAB was first detected in the southern reach of the riparian area in 2015. It gradually moved north. By 2020 isolated mortality was observed at all sites. Meantime, they released three biocontrol agents – T. planipennis, S. galinae, and Oobius agrilii – early in the invasion at three of the six monitoring sites. These released occurred in 2018 – 2020 and again in 2022. 

In 2021 and 2025, the scientists counted the numbers of biocontrol agents in the marked trees or sentinel logs. Thus the first evaluation occurred six years after EAB arrived, three years after the first releases of biocontrol agents.

They found that at southern Massachusetts sites, where EAB density was higher at the time of the biocontrol agents’ initial release, remaining ash grew more slowly than in the North. They believe the trees’ growth rate was suppressed by the trees having fewer resources.  They also observed dieback. Smaller trees grew faster, perhaps responding to opening of the canopy as mature ash succumbed to EAB invasion.

The most important finding was that ash mortality at all sites was ~50% or less … not the 90% expected based on experience in the upper Midwest where the EAB invasion occurred before biocontrol agents were developed.

SOURCE

Ash survival and growth response to emerald ash borer invasion in Massachusetts riparian forests: impacts of biological control. Mitchell A. Reed, Jian Duan, Ryan S. Crandall, Roy G. van Driesche, Jeremy C. Anderson, Joseph S. Elkington. Presentation to the 33rd USDA Interagency Research Forum on Invasive Species, Annapolis, Maryland February 25-28, 2025  (The proceedings should be posted online before the end of the year.)

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

More pests in Europe & Mideast – hazard to North American trees

giant sequoia; photo by Matthew Dillon via Flickr

The pest alert system “PestLens” has again alerted us to plant pests in Europe or Asia that feed on species closely related to tree species native to North American forests.  Two of the insects named in the alert apparently pose a hazard to icons of the forests of America’s Pacific coast forests, giant sequoia and redwood.

I hope APHIS is using this information to alert port and on-the-ground staff and perhaps initiating more in-depth risk assessments.

The posting on February 27, 2025 reported that cotton jassid, Jacobiasca lybica (Hemiptera: Cicadellidae), affects not just cotton and citrus but also Cupressus sempervirens (Mediterranean cypress) [Cupressaceae]. More than a dozen North American trees species are in this family, including

  • Sequoiadendron giganteum or giant sequoia. Giant sequoia is listed as an endangered species by the IUCN with fewer than 80,000 remaining in its native California.
  • Chamaecyparis thyoides and C. lawsoniana (Port-Orford cedar). Port-Orford cedar has been decimated in its native range by an introduced pathogen, Phytopthora lateralis. A major breeding effort has developed trees that are resistant to the pathogen; they are now available for people to plant.
  • Thuja occidentalis, also known as northern white-cedar, eastern white-cedar, or arborvitae,
  • Taxodium ascendens, also known as pond cypress
  • several Juniperus
  • Hesperocyparis macrocarpa also known as Cupressus macrocarpa, or the Monterey cypress. NatureServe ranks the cypress as GI – critically imperiled.

Cotton jassid been reported from several countries in Europe, Africa, and the Middle East.

China has reported the existence of a previously unknown bark beetle species, Phloeosinus metasequoiae (Coleoptera: Curculionidae). It was found infesting Metasequoia glyptostroboides (dawn redwood) trees in China. Affected trees exhibited reddened leaves and holes and tunnels in branches.

China has also discovered a several new hosts utilized by the fungus Pestalotiopsis lushanensis (Sordariomycetes: Amphisphaeriales). Formerly known to infect tea (Camellia sinensis) and several other plant species, P. lushanensis has now been found shoot causing blight and leaf drop on a conifer, deodar cedar (Cedrus deodara) and leaf spots on an angiosperm with congeners in North America — the rare Chinese species, Magnolia decidua. There are eight species of Magnolia native to North America.

Magnolia grandiflora; photo by DavetheMage via Wikimedia

APHIS’ ability to respond to alerts remains uncertain.

The agency’s probationary employees have been fired – just as at other agencies. APHIS staff were prohibited from participating in last week’s annual USDA Invasive Species Research Forum – the 33rd such meeting. The bird flu emergency is demanding all the attention and funds.

So – how can the rest of us fill in?

At the USDA Research Forum I again presented a poster urging greater attention to tree-killing pathogens. Scientists have made considerable progress in identifying factors that indicate whether a non-native insect might pose a significant threat (see blogs on conifer and deciduous species; more to come!). However, USDA had not funded a similar effort to improve understanding of pathogens. The most promising strategy so far are sentinel plantings. However, these systems have weaknesses; I will blog in the near future about another analysis.

I propose that APHIS start by working with independent scientists to determine the actual, current level of pathogens associated with various types of incoming goods. Contact me directly if you wish to read the text of my poster.

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

APHIS funding for pests that kill trees (& cacti)

emerald ash borer; some of PPA grants are funding evaluation of biocontrol efficacy

USDA APHIS has released information about its most recent annual allocation of funds under the Plant Pest and Disease Management & Disaster Prevention Program under §7721 of the Plant Protection Act. (Also see Fading Forests II and III; links provided at the end of this blog.) These funds support both critical needs and opportunities to strengthen the nation’s infrastructure for pest detection, surveillance, identification, and threat mitigation. Since 2009, this USDA program has provided nearly $940 million to more than 5,890 projects.

For FY25 APHIS allocated $62.725 million to fund 339 projects, about 58% of the proposals submitted. About $10 million has reserved for responding to pest and plant health emergencies throughout the year.

According to APHIS’ press release, the highest amount of funds (almost $16 million) is allocated to the category “Enhanced Plant Pest/Disease Survey.” Projects on “Enhanced Mitigation Capabilities” received $13.6 million. “Targetting Domestic Inspection Efforts to Vulnerable Points” received nearly $6 million. “Improving Pest Identification and Detection Technology” was funded at $5 million. Outreach & education received $4 million.  I am not sure why these do not total $63 million.

Funding for States and Specific Pests

Wood-boring insects received about $2.3 million. These included more than $869,800 to assess the efficacy of biocontrol for controlling emerald ash borer (EAB) Agrilus planipennis, $687,410 was provided for various detection projects, and $450,000 for outreach efforts related to various pests. Ohio State received $93,000 to optimize traps for the detection of non-native scolytines (bark beetles).

Biocontrol efficacy will also be assessed for hemlock woolly adelgid, invasive shot hole borers, cactus moth, and several invasive plants (including Brazilian pepper). (Contact me to obtain a copy of CISP’s comments on this biocontrol program.)

Opuntia basilaris in Anza Boreggo; one of flat-padded Opuntia vulnerable to the cactus moth; photo by F.T. Campbell

Funding for other pests exceeded $1 million for spotted lanternfly (nearly $1.4 million), Asian defoliators ($1.2 million) and box tree moth (just over $1 million).

$630,000 was provided for detection surveys and studies of the sudden oak death pathogen Phytophthora ramorum, especially how it infects nursery stock. Nursery surveys are funded in Alabama, Louisiana, North Carolina, Ohio, Oklahoma, Pennsylvania, South Carolina, Tennessee, Virginia, and West Virginia. Most of these states are in regions considered most at risk to SOD infection of wildland plants.    

sudden oak mortality of tanoak trees in southern Oregon; photo by Oregon Department of Forestry

Oregon received much-deserved $41,000 to evaluate the threat of the NA2 and EU2 lineages of P. ramorum to nurseries and forests Oregon also received $104,000 to respond to the detection of Phytophthora austrocedri in nurseries in the state. The Oregon outbreak has been traced to Ohio, but I see no record of funds to assist that state in determining how it was introduced.

Asian defoliator (e.g., Lymantrid moths) surveys have been funded for several years. This year’s projects are in Alaska, Arkansas, California, Kentucky, Maryland, Massachusetts, Mississippi, Montana, Nevada, North Carolina, Oregon, Tennessee, Texas, Washington, and West Virginia. While I agree that the introduction risk is not limited to coastal states with maritime ports, I don’t what criteria were applied in choosing the non-coastal states which are funded to search for these insects

Spotted lanternfly surveys (including technological improvements) or related outreach are funded in Alabama, Connecticut, Delaware, Kentucky, New Hampshire, New Jersey, North Carolina, Oregon, Pennsylvania, and Tennessee. California’s project is focused on postharvest treatments.

The Don’t Move Firewood project continues to be funded by APHIS. Several states also direct attention specifically to the firewood pathway: Kentucky, Maine, and Michigan.

I applaud the precautionary funding of the Agriculture Research Service to generate of high-quality genomic resources for managing the causal agent of Japanese oak wilt Dryadomyces quercivorous

Florida Department of Agriculture, North Carolina State University, and West Virginia University each received more than $100,000 to improve detection and management of invasive hornets.

Tennessee State University got $100,000 to continue efforts to detect and understand Vascular Streak Dieback in redbud Cercis canadensis.

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

How beech leaf disease spreads in the forest

BLD symptoms; photo by Matt Borden, Bartlett Tree Experts

As beech leaf disease (BLD) is detected in an ever-expanding number of counties from Michigan to Maine south to Virginia, scientists are trying to clarify how the causal nematode — Litylenchus crenatae ssp. mccannii (Lcm) – spreads. One focus is on local spread from tree to tree. Mankanwal Goraya and colleagues set up an experiment in Stone Valley Forest, a recreation and research site managed by Penn State in Huntington County, Pennsylvania. BLD is present – although I have not been able to determine for how many years. [The full citation to Goraya et al. is provided at the end of this blog.]

Goraya et al. (2024) set up four stands, each bearing three funnels, at varying distances from naturally BLD-infected American beech (Fagus grandifolia) trees. Two stands were at 3.51 m from symptomatic trees of starkly different sizes: one of the trees had a dbh of 50 cm, the other of only 5.6 cm. A third close-up stand was set up at 2.20 m from another large tree, having a dbh of 46 cm. The fourth stand was set up at a significantly longer distance, 11.74 m from a symptomatic beech tree; this tree was also small, with a dbh of 5 cm. This arrangement allowed the scientists to detect influences of both distance from the source of infection and relative canopy size of the source tree. They consider dbh to be an adequate substitute for canopy size. There was apparently no other effort to determine or vary the height of “source” trees, although I think that might influence speed of the wind flowing through the canopy.

Goraya et al. also tested whether it is possible to detect the presence of Lcm in association with other invertebrates that live in beech forests. To do this, they counted numbers of nematodes in frass from six species of caterpillars that had been feeding on leaves of infected trees, and in two spider webs spun in the branches of symptomatic trees. They also determined whether these nematodes were alive (active) or inactive – presumably dead.

The study makes clear that Lcm’s life cycle and impact are not as surprising as initially thought. Several species in the family Anguinidae – to which Lcm belongs – are considered significant pests. These nematodes can parasitize aerial parts of the plants (leaves, stems, inflorescences and seeds), causing swellings and galls. Furthermore, they are migratory; they can move across the surface of host tissues using water films. Once they have penetrated the host tissues, they can induce host cell hyperplasia and hypertrophy, resulting in leaf or bulb deformities, shorter internodes, and neoplastic tissues. Furthermore, heavy rainfall and wind are known to play significant roles in the dissemination of plant-infecting nematodes. In their desiccated state on infected seeds, some species of this family can survive passage through animals’ gastrointestinal digestive tract (e.g., domestic livestock, insects, & birds).

A crucial factor is that Lcm can reach densities of thousands of nematodes per leaf by late summer or early fall, increasing the likelihood of their exposure to facilitating environmental conditions at the time they migrate from leaves to buds. And once established within the bud tissues, the nematodes feed on bud scales and newly forming leaves to develop & increase their pop #s. They also use the bud as protection from adverse environmental conditions.

Goraya and colleagues collected samples every other day from September 9 to November 23, 2023 – the period when Lcm migrate from highly infected leaves to newly forming buds. [I note that it in the mid-Atlantic – where Lcm is spreading – we had an extensive drought in autumn 2024 – more than 30 days without any rain from early October into November. I hope scientists are monitoring BLD spread sufficient closely to see whether this drought affected dispersal.]

Nematodes dispersal linked to weather

Goraya and colleagues collected 324 samples from the funnels. Eighty-two percent (n =266) of the samples had nematodes; up to 92% were identified as Lcm. Non-Lcm nematodes were distributed across different genera, mostly classified as free-living nematodes. While several hundred nematodes were found in the funnels on most days, numbers peaked noticeably on some days in September and October.   A startling 2,452 nematodes were recovered from a single funnel in October. Depending on the sample, up to 67% of Lcm recovered from the funnels were active.

Analysis of the environmental (weather) variables found that increases in wind speed, humidity, and precipitation (rainfall) coincided with higher numbers of Lcm being recovered from the funnels.  However, the effect of wind speed becomes less positive as precipitation increases or vice versa. Goraya et al. suggest a pronounced negative interaction between wind and rain. At low precipitation levels, increased wind speed might facilitate Lcm dispersal. As rainfall increases, higher wind speeds might carry the Lcm nematodes farther away. Support is seen in the fact that fewer nematodes were found in the funnels closer to the BLD-infected trees during these periods. Really heavy rain might push a significant preponderance of nematodes to the ground. The scientists point to a very complex interplay between weather patterns and Lcm population dynamics and dispersal.

BLD symptoms on beech tree in Fairfax County, Virginia – a dozen miles from known infestation; photo by F.T. Campbell

The model did not show any significant influence of maximum temperature on nematode numbers in autumn. Goraya et al. do not speculate on whether temperatures might play a role during summer, as distinct from cooler autumn periods.

Goraya et al.’s findings differ from those of previous studies. Earlier documentation of wind dispersal of nematodes concerned primarily free-living species. It was unexpected to find consistently much higher numbers of Lcm – especially because Lcm is a plant-parasitic nematode. Another surprise is the high proportion of nematodes that are active.

Goraya et al. conclude that because Lcm is actively migrating in large numbers during autumn months, it is primed to take advantage of favorable weather. This nematode will likely survive and thrive in the environmental conditions of beech forests in northeastern North America.

Considering the effect of distance, some findings fit expectations: significantly more Lcm were recovered from funnels placed near symptomatic “source” trees than from those farther away. However, this was not a simple relationship. For example, in two cases the scenarios seemed nearly alike: both “source” trees were large (dbh 46 or 50 cm) and symptoms were “medium-high” (more than half of leaves presenting dark-green interveinal bands). Distance of funnels from the “source” tree differed minimally: 2.2 m versus 3.51 m. Still, the number of nematodes retrieved from the two sets of funnels differed significantly: one set of funnels recovered the highest number of Lcm nematodes obtained during the entire experiment – 2,452; the second contained only up to 600 nematodes. The authors do not offer an explanation.

I am not surprised by the apparently strong correlation between numbers and proximity to the disease source (a symptomatic tree). Nor am I surprised that Lcm nematodes were also found in funnels 11 meters away. I do wonder, however, why they are certain that no source was closer. Detecting early stage infections is notoriously difficult.

beech with large canopy; photo by F.T. Campbell

Goraya et al. also evaluated the effect of size of the source tree. They used dbh a substitute for larger canopies. Trees with larger canopies can host more nematodes, so are likely to contribute more to dispersal events. Two sets of funnels were equidistant from separate “source” trees – 3.51 m. One tree was small – 5.6 cm dbh, 11% as large as the other tree (50 cm). They collected many fewer Lcm nematodes from the smaller tree – the maximum was only 132 compared to 600 (a decrease of 78%).

Still, small trees can apparently support spread of the nematode to a reasonable distance. The fourth set of funnels was set up more than three times farther away (11.74 m) from an infected tree of a similar size (dbh = 5 cm) but recovered almost the same number of Lcm nematodes (0 – 119).

I find it alarming that both small trees in this part of the experiment had low BLD symptoms – only a few leaves were banded. Yet they apparently are the source of Lcm spread. The alternative, as I noted above, is that other “source” trees were in the vicinity but were not detected, possibly because they did not yet display symptoms?

Goraya et al. conclude that “source” tree size directly impacts the number of recovered nematodes. In addition, wind plays a pivotal role in their local distribution. This suggests a complex dispersal pattern in which proximity to the source leads to higher numbers of nematodes but longer-distance spread is possible.

Tussock moth; photo by Jon Yuschock via Bugwood

 Nematodes’ association with other organisms

Goraya et al. (2024) collected one each of six caterpillar species from BLD-symptomatic trees. The frass of one – the tussock moth caterpillar (Halysidota tessellaris) — contained 12 nematode specimens — 10 of them Lcm. Two of the Lcm were alive and active. Their presence indicates that Lcm can survive passage through the caterpillar’s gastrointestinal tract. The authors conclude that caterpillars feeding on symptomatic leaves might contribute to local dispersal of Lcm.

Hundreds of Lcm were recovered from the two spider webs collected from the branches of a BLD-infected beech tree. From one web, 255 nematodes were captured; 58 were active. In the second web there were only 34 Lcm, but one-third — 10 – were active.

Goraya et al. (2024) hypothesized that any biotic form having the ability to move from a BLD-infected tree would be able to transport Lcm to other non-infected trees. Beyond caterpillars, they speculate that birds consuming these caterpillars might also disperse Lcm. Doug Tallamy has documented that many birds feed on caterpillars, link although he is focused on those that consume caterpillars in the spring, not the autumn. They note that others are studying that the bird species that feed on beech buds (e.g., finches) might transport nematodes. They note the need for additional research to clarify whether the nematode can survive birds’ digestive system.

Re: detection of live Lcm in spider webs, Goraya et al. suggest two possible interpretations: 1) this finding demonstrates that nematodes might fall from leaves, potentially spreading the infection to other trees beneath the canopy. (Supporting this idea is the fact that sub-canopy trees are often heavily infected with BLD and are frequently the first to exhibit BLD symptoms.) 2) Nematodes in spider webs are very likely to be transported by other “incidental organisms” (e.g., insects, birds, mammals) that feed on invertebrates trapped in webs — thereby potentially increasing the number and impact of nonspecific nematode vectors.

In conclusion, Goraya et al. found that many factors, e.g., distance & size of infected beech trees, wind speed, & humidity, contribute significantly to Lcm dispersal. The multitude of organisms interacting beneath the canopy also play a role.

They suggest that several major questions still need to be explored. These include how Lcm navigate environmental factors in their spread; and whether Lcm can survive – perhaps in a anhydrobioses state –transport over long distances, whether by abiotic or biotic vectors.

I remind my readers of the importance of beech in the hardwood forests in northeastern North America. Many wild animals, including squirrels, wild turkeys, white-tailed deer, and bears depend on beechnuts for fats and proteins. Moreover, some insects birds rely on beech tree canopies for shelter & nesting.

Other Hosts

Beech leaf disease attacks not just American beech (Fagus grandifolia). In North America, it has also attacked planted European beech(F. sylvatica), Chinese beech (F. engleriana), and Oriental beech (F. orientalis). Thus if it spreads it could have severe impacts across forests of much of the Northern Hemisphere.

range of European beech; from Royal Botanic Gardens, Kew

I appreciate that this project was funded by the USDA Forest Service International Program. I will pursue information concerning efforts by USFS Research and Development and the Forest Health Protection program.

SOURCE

Goraya, M., C. Kantor, P. Vieira, D. Martin, M. Kantor. 2024 Deciphering the vectors: Unveiling the local dispersal of Litylenchus crenatae ssp mccanni in the American beech (Fagus grandifolia) forest ecosystem  PLOS ONE |https://doi.org/10.1371/journal.pone.0311830 November 8, 2024 1 / 16

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

Hawaiian Efforts to Restore Threatened Trees

ʻŌhiʻa trees killed by ROD; photo by Richard Sniezko, USFS

Several Hawaiian tree species are at risk due to introduced forest pests. Two of the Islands’ most widespread species are among the at-risk taxa. Their continuing loss would expose watersheds on which human life and agriculture depend. Habitats for hundreds of other species – many endemic and already endangered – would lose their foundations. These trees also are of the greatest cultural importance to Native Hawaiians.

I am pleased to report that Hawaiian scientists and conservationists are trying to protect and restore them.

Other tree species enjoy less recognition … and efforts to protect them have struggled to obtain support.

1) koa (Acacia koa)

Koa is both a dominant canopy tree and the second-most abundant native tree species in Hawai`i in terms of areas covered. The species is endemic to the Hawaiian archipelago. Koa forests provide habitat for 30 of the islands’ remaining 35 native bird species, many of which are listed under the U.S. Endangered Species Act. Also dependent on koa forests are native plant and invertebrate species and the Islands’ only native terrestrial mammal, the Hawaiian hoary bat. Finally, koa forests protect watersheds, add nitrogen to degraded soils, and store carbon [Inman-Narahari et al.]

Koa forests once ranged from near sea level to above 7000 ft (2100 m) on both the wet and dry sides of all the large Hawaiian Islands. Conversion of forests to livestock grazing and row-crop agriculture has reduced koa’s range. Significant koa forests are now found on four islands – Hawai’i, Maui, O‘ahu, and Kauaʻi. More than 90% of the remaining koa forests occur on Hawai`i Island (the “Big Island) [Inman-Narahari et al.]

In addition to its fundamental environmental role, koa has immense cultural importance. Koa represents strength and the warrior spirit. The wood was used traditionally to make sea-going canoes. Now Koa is widely used for making musical instruments, especially guitars and ukuleles; furniture, surfboards, ornaments, and art [Inman-Narahari et al.]

Koa timber has the highest monetary value of any wood harvested on the Islands. However, supplies of commercial-quality trees are very limited (Dudley et al. 2020). Harvesting is entirely from old-growth forests on private land. [Inman-Narahari et al.]

Koa forests are under threat by a vascular wilt disease caused by Fusarium oxysporum f. sp. koae (FOXY). This disease can kill up to 90% of young trees and – sometimes — mature trees in native forests. The fungus is a soil-dwelling organism that spreads in soil and infects susceptible plants through the root system (Dudley et al. 2020).

Conservation and commercial considerations have converged to prompt efforts to breed koa resistant to FOXY. Conservationists hope to restore native forests on large areas where agriculture has declined. The forestry industry seeks to enhance supplies of the Islands’ most valuable wood. Finally, science indicated that a breeding program would probably be successful. Field trials in the 1990s demonstrated great differences in wilt-disease mortality among seed sources (the proportion of seedlings surviving inoculation ranged from 4% to 91.6%) [Sniezko 2003; Dudley et al. 2009].

In 2003, Dudley and Sniezko outlined a long-term strategy for exploring and utilizing genetic resistance in koa. Since then, a team of scientists and foresters has implemented different phases of the strategy and refined it further (Dudley et al. 2012, 2015, 2017; Sniezko et al. 2016]

First, scientists determined that the wilt disease is established on the four main islands. Having obtained more than 500 isolates of the pathogen from 386 trees sampled at 46 sites, scientists tested more than 700 koa families from 11 ecoregions for resistance against ten of the most highly virulent isolates (Dudley et al. 2020). 

The Hawaiian Agricultural Research Center (HARC), supported by public and private partners, has converted the field-testing facilities on Hawai`i, Maui, and Oahu into seed orchards. The best-performing tree families are being grown to maturity to produce seeds for planting. It is essential that the seedlings be not just resistant to FOXY but also adapted to the ecological conditions of the specific site where they are  to be planted [Dudley et al. 2020; Inman-Narahari et al. ] Locally adapted, wilt-resistant seed has been planted on Kauaʻi and Hawai`i. Preparations are being made to plant seed on Maui and O‘ahu also. Scientists are also exploring methods to scale up planting in both restoration and commercial forests [R. Hauff pers. comm.].  

koa; photo by David Eickhoff via Flickr

Restoration of koa on the approximately half of lands in the species’ former range that are privately owned will require that the trees provide superior timber. Private landowners might also need financial incentives since the rotation time for a koa plantation is thought to be 30-80 years. [Inman-Narahari et al.]

Plantings on both private and public lands will need to be protected from grazing by feral ungulates and encroachment by competing plants. These management actions are intensive, expensive, and must be maintained for years.

Some additional challenges are scientific: uncertainties about appropriate seed zones, efficacy of silvicultural approaches to managing the disease, and whether koa can be managed for sustainable harvests. Human considerations are also important: Hawai`i lacks sufficient professional tree improvement or silvicultural personnel, a functioning seed distribution and banking network — and supporting resources. Finally, some segments of the public oppose ungulate control programs. Inman-Narahari et al.

Finally, scientists must monitor seed orchards and field plantings for any signs of maladaptation to climate change. (Dudley et al. 2020).

2) ʻŌhiʻa Metrosideros polymorpha)   

ʻŌhiʻa  lehua is the most widespread tree on the Islands. It dominates approximately 80% the biomass of Hawaii’s remaining native forest, in both wet and dry habitats. ʻŌhiʻa illustrates adaptive radiation and appears to be undergoing incipient speciation. The multitude of ecological niches and their isolation on the separate islands has resulted in five recognized species in the genus Metrosideros. Even the species found throughout the state, Metrosideros polymorpha, has eight recognized varieties (Luiz et al. (2023) (some authorities say there are more).

Loss of this iconic species could result in significant changes to the structure, composition, and potentially, the function, of forests on a landscape level. High elevation ‘ohi‘a forests protect watersheds across the state. ʻŌhiʻa forests shelter the Islands’ one native terrestrial mammal (Hawaiian hoary bat), 30 species of forest birds, and more than 500 endemic arthropod species. Many species in all these taxa are endangered or threatened (Luiz et al. 2023). The increased light penetrating interior forests following canopy dieback facilitates invasion by light-loving non-native plant species, of which Hawai`i has dozens. There is perhaps no other species in the United States that supports more endangered taxa or that plays such a geographical dominant ecological keystone role [Luiz et al. 2023]

For many Native Hawaiians, ‘ōhi‘a is a physical manifestation of multiple Hawaiian deities and the subject of many Hawaiian proverbs, chants, and stories; and foundational to the scared practice of many hula. The wood has numerous uses. Flowers, shoots, and aerial roots are used medicinally and for making lei. The importance of the biocultural link between ‘ōhi‘a and the people of Hawai`i is described by Loope and LaRosa (2008) and Luiz et al. (2023).

In 2010 scientists detected rapid mortality affecting ‘ōhi‘a on Hawai‘i Island. Scientists determined that the disease is caused by two recently-described pathogenic fungi, Ceratocystis lukuohia and Ceratocystis huliohia. The two diseases, Ceratocystis wilt and Ceratocystis canker of ʻōhiʻa, are jointly called “rapid ‘ōhi‘a death”, or ROD. The more virulent species, C. lukuohia, has since spread across Hawai`i Island and been detected on Kaua‘i.  The less virulent C. huliohia  is established on Hawai`i and Kaua‘i and in about a dozen trees on  O‘ahu. One tree on Maui was infected; it was destroyed, and no new infection has been detected [M. Hughes pers. comm.] As of 2023, significant mortality has occurred on more than one third of the vulnerable forest on Hawai`i Island, although mortality is patchy.  

 [ʻŌhiʻa is also facing a separate  disease called myrtle rust caused by the fungus Austropuccinia psidii; to date this rust has caused less virulent infections on ‘ōhi‘a.]

rust-killed ‘ōhi‘a in 2016; photo by J.B. Friday

Because of the ecological importance of ‘ōhi‘a and the rapid spread of these lethal diseases, research into possible resistance to the more virulent pathogen, C. lukiohia began fairly quickly, in 2016. Some ‘ōhi‘a survive in forests on the Big Island in the presence of ROD, raising hopes that some trees might possess natural resistance. Scientists are collecting germplasm from these lightly impacted stands near high-mortality stands (Luiz et al. 2023). Five seedlings representing four varieties of M. polymorpha that survived several years’ exposure to the disease are being used to produce rooted cuttings and seeds for further evaluation of these genotypes.

ʻŌhiʻa flowers

Encouraged by these developments, and recognizing the scope of additional work needed, in 2018 stakeholders created a collaborative partnership that includes state, federal, and non-profit agencies and entities, ʻŌhiʻa Disease Resistance Program (‘ODRP) (Luiz et al. 2023). The partnership seeks to provide baseline information on genetic resistance present in all Hawaiian taxa in the genus Metrosideros. It aims further to develop sources of ROD-resistant germplasm for restoration intended to serve several purposes: cultural plantings, landscaping, and ecological restoration. ‘ODRP is pursuing screenings of seedlings and rooted cuttings sampled from native Metrosideros throughout Hawai`i while trying to improve screening and growing methods. Progress will depend on expanding these efforts to include field trials; research into environmental and genetic drivers of susceptibility and resistance; developing remote sensing and molecular methods to rapidly detect ROD-resistant individuals; and support already ongoing Metrosideros conservation. If levels of resistance in wild populations prove to be insufficient, the program will also undertake breeding (Luiz et al. 2023).

To be successful, ‘ODRP must surmount several challenges (Luiz et al. 2022):

  • increase capacity to screen seedlings from several hundred plants per year to several thousand;
  • optimize artificial inoculation methodologies;
  • determine the effects of temperature and season on infection rates and disease progression;
  • find ways to speed up seedlings’ attaining sufficient size for testing;
  • develop improved ways to propagate ʻōhiʻa from seed and rooted cuttings;
  • establish sites for field testing of putatively resistant trees across a wide range of climatic and edaphic conditions;
  • establish seed orchard, preferably on several islands;
  • establish systems for seed collection from the wide variety of subspecies/varieties;
  • if breeding to enhance resistance is appropriate, it will be useful to develop high-throughput phenotyping of the seed orchard plantings.

  [See DMF profile for more details.]

Developing ROD-resistant ‘ōhi‘a is only one part of a holistic conservation program. Luiz et al. (2023) reiterate the importance of quarantines and education to curtail movement of infected material and countering activities that injure the trees. Fencing to protect these forests from grazing by feral animals can drastically reduce the amount of disease. Finally, scientists must overcome the factors there caused the almost complete lack of natural regeneration of ‘ōhi‘a in lower elevation forests. Most important are competition by invasive plants, predation by feral ungulates, and the presence of other diseases, e.g., Austropuccinia psidii.

Hawaii’s dryland forests are highly endangered: more than 90% of dry forests are already lost due to habitat destruction and the spread of invasive plant and animal species. Two tree species are the focus of species-specific programs aimed at restoring them to remaining dryland forests. However, support for both programs seems precarious and requires stable long-term funding; disease resistance programs often necessitate decades-long endeavors.

naio in bloom; photo by Forrest & Kim Starr via Creative Commons

1) naio (Myoporum sandwicense)

Naio grows on all of the main Hawaiian Islands at elevations ranging from sea level to 3000 m. While it occurs in the full range of forest types from dry to wet, naio is one of two tree species that dominate upland dry forests. The other species is mamane, Sophora chrysophylla. Naio is a key forage tree for two endangered honeycreepers, palila (Loxioides bailleui) and `akiapola`au (Hemignathus munroi). The tree is also an important host of many species of native yellow-face bees (Hylaeus spp). Finally, loss of a native tree species in priority watersheds might lead to invasions by non-native plants that consume more water or increase runoff.

The invasive non-native Myoporum thrips, Klambothrips myopori, was detected on Hawai‘i Island in December 2008 (L. Kaufman website). In 2018 the thrips was found also on Oahu (work plan). The Myoporum thrips feeds on and causes galls on plants’ terminal growth. This can eventually lead to death of the plant.

Aware of thrips-caused death of plants in the Myoporum genus in California, the Hawaii Department of Lands and Natural Resources Division of Forestry and Wildlife and the University of Hawai‘i began efforts to determine the insect’s distribution and infestation rates, as well as the overall health of naio populations on the Big Island. This initiative began in September 2010, nearly two years after the thrips’ detection. Scientists monitored nine protected natural habitats for four years. This monitoring program was supported by the USFS Forest Health Protection program. This program is described by Kaufman.

naio monitoring sites from L. Kaufman article

The monitoring program determined that by 2013, the thrips has spread across most of Hawi`i Island, on its own and aided by human movement of landscaping plants. More than 60% of trees being monitored had died. Infestation and dieback levels had both increased, especially at medium elevation sites. The authors feared that mortality at high elevations would increase in the future. They found no evidence that natural enemies are effective controlling naio thrips populations on Hawai`i Island.

Kaufman was skeptical that biological control would be effective. She suggested, instead, a breeding program, including hybridizing M. sandwicensis with non-Hawaiian Myoporum species that appear to be resistant to thrips. Kaufman also called for additional programs: active monitoring to prevent thrips from establishing on neighboring islands; and collection and storage of naio seeds.

Ten years later, in February 2024, DLNR Division of Forestry and Wildlife adopted a draft work plan for exploring possible resistance to the Myoporum thrips. Early steps include establishing a database to record data needed to track parent trees, associated propagules, and the results of tests. These data are crucial to keeping track of which trees show the most promise. Other actions will aim to hone methods and processes. Among practical questions to be answered are a) whether scientists can grow even-aged stands of naio seedlings; b) identifying the most efficient resistance screening techniques; and c) whether K. myopori thrips are naturally present in sufficient numbers to be used in tests, or – alternatively – whether they must be augmented. [Plan]

Meanwhile, scientists have begun collecting seed from unaffected or lightly affected naio in hotspots where mortality is high. They have focused on the dry and mesic forests of the western side of Hawai`i (“Big”) Island, where the largest number of naio populations still occur and are at high risk. Unfortunately, these “lingering” trees remain vulnerable to other threats, such as browsing by feral ungulates, competition with invasive plants, drought, and reduced fecundity & regeneration.

Hawai`i DLNR has secured initial funding from the Department of Defense’s REPI program to begin a pest resistance project and is seeking a partnership with University of Hawai`i to carry out tests “challenging” different naio families’ resistance to the thrips [R. Hauff pers. comm.]

wiliwili; photo by Forrest & Kim Starr

2) wiliwili (Erythrina sandwicensis)

Efforts to protect the wiliwili have focused on biological control. The introduced Erythrina gall wasp, Quadrastichus erythrinae (EGW) was detected on the islands in 2005. It immediately caused considerable damage to the native tree and cultivated nonnative coral trees.

A parasitic wasp, Eurytoma erythrinae, was approved for release in November 2008 – only 3 ½ years after EGW was detected on O‘ahu. The parasitic wasp quickly suppressed the gall wasp’s impacts to both wiliwili trees and non-native Erythrina. By 2024, managers are once again planting the tree in restoration projects.

However, both the gall wasp and a second insect pest – a bruchid, Specularius impressithorax – can cause loss of more than 75% of the seed crop. This damage means that the tree cannot regenerate. By 2019, Hawaiian authorities began seeking permission to release a second biocontrol gent, Aprostocitus nites.Unfortunately, the Hawai’i Department of Agriculture still has not approved the release permit despite five years having passed. Once they have this approval, the scientists will then need to ask USDA Animal and Plant Health Inspection Service (APHIS) for its approval [R. Hauff, pers. comm.]

SOURCES

www.RapidOhiaDeath.org

Dudley, N., R. James, R. Sniezko, P. Cannon, A. Yeh, T. Jones, & Michael Kaufmann. 2009? Operational Disease Screening Program for Resistance to Wilt in Acacia koa in Hawai`i. Hawai`i Forestry Association Newsletter August 29 2009

Dudley, N., T. Jones, K. Gerber, A.L. Ross-Davis, R.A. Sniezko, P. Cannon & J. Dobbs. 2020. Establishment of a Genetically Diverse, Disease-Resistant Acacia koa Seed Orchard in Kokee, Kauai: Early Growth, Form, & Survival. Forests 2020, 11, 1276; doi:10.3390/f11121276 www.mdpi.com/journal/forests

Friday, J. B., L. Keith, and F. Hughes. 2015. Rapid ʻŌhiʻa Death (Ceratocystis Wilt of ʻŌhiʻa). PD-107, College of Tropical Agriculture and Human Resources, University of Hawai‘i, Honolulu, HI. URL: https://www.ctahr.HI.edu/oc/freepubs/pdf/PD-107.pdf  Accessed April 3, 2018.

Friday, J.B. 2018. Rapid ??hi?a Death Symposium -West Hawai`i (“West Side Symposium”) March 3rd 2018,  https://vimeo.com/258704469 Accessed April 4, 2018 (see also full video archive at https://vimeo.com/user10051674)

Inman-Narahari, F., R. Hauff, S.S. Mann, I. Sprecher, & L. Hadway. Koa Action Plan: Management & research priorities for Acacia koa forestry in Hawai`i. State of Hawai`i Department of Land & Natural Resources Division of Forestry & Wildlife no date

Kaufman, L.V, J. Yalemar, M.G. Wright. In press. Classical biological control of the erythrina gall wasp, Quadrastichus erythrinae, in Hawaii: Conserving an endangered habitat. Biological Control. Vol. 142, March 2020

Loope, L. and A.M. LaRosa. 2008. ‘Ohi’a Rust (Eucalyptus Rust) (Puccinia psidii Winter) Risk Assessment for Hawai‘i.

Luiz, B.C. 2017. Understanding Ceratocystis. sp A: Growth, morphology, and host resistance. MS thesis, University of Hawai‘i at Hilo.

Luiz, B.C., C.P. Giardina, L.M. Keith, D.F. Jacobs, R.A. Sniezko, M.A. Hughes, J.B. Friday, P. Cannon, R. Hauff, K. Francisco, M.M. Chau, N. Dudley, A. Yeh, G. Asner, R.E. Martin, R. Perroy, B.J. Tucker, A. Evangelista, V. Fernandez, C. Martins-Keli’iho.omalu, K. Santos, R. Ohara. 2023. A framework for establishlishing a rapid ‘Ohi‘a death resistance program  New Forests 54, 637–660. https://doi.org/10.1007/s11056-021-09896-5

Additional information on the koa resistance program is posted at http://www.harc-hspa.com/forestry.html 

Sniezko, R.A., N. Dudley, T. Jones, & P. Cannon. 2016. Koa wilt resistance & koa genetics – key to successful restoration & reforestation of koa (Acacia koa). Acacia koa in Hawai‘i: Facing the Future. Proceedings of the 2016 Symposium, Hilo, HI: www.TropHTIRC.org , www.ctahr.HI.edu/forestry 

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

Scientists: Introduced forest pest reshaping forests, with many bad consequences … will regulators step up?

Jarrah dieback in Western Australia

The number of introduced forest pathogens are increasing – creating a crisis that is recognized by more scientists. These experts say tree diseases are reshaping both native and planted forests around the globe. The diseases are threatening biodiversity, ecosystem services, provision of products, and related human wellbeing. Some suggest that bioinvasions might threaten forests as much as climate change, while also undermining forests’ role in carbon sequestration.

Unfortunately, I see little willingness within the plant health regulatory community to tackle improving programs to slow introductions. Even when the scientists documenting the damage work for the U.S. Department of Agriculture – usually the U.S. Forest Service — USDA policy-makers don’t act on their findings. [I tried to spur a conversation with USDA 2 years ago. So far, no response.]

counties where beech leaf disease has been detected

What the scientists say about these pests’ impacts

Andrew Gougherty (2023) – one of the researchers employed by the USDA Forest Service – says that emerging infectious tree diseases are reshaping forests around the globe. Furthermore, new diseases are likely to continue appearing in the future and threaten native and planted forests worldwide. [Full references are provided at the end of the blog.] Haoran Wu (2023/24) – a Master’s Degree student at Oxford University – agrees that arrival of previously unknown pathogens are likely to alter the structure and composition of forests worldwide. Weed, Ayers, and Hicke (2013) [academics] note that forest pests — native and introduced — are the dominant sources of disturbance to North American forests. They suggest that, globally, bioinvasions might be at least as important as climate change as threats to the sustainability of forest ecosystems. They are concerned that recurrent forest disturbances caused by pests might counteract carbon mitigation strategies. 

Scientists have proclaimed these warnings for years. Five years ago, Fei et al. (2019) reported that the 15 most damaging pests introduced to the United States — cumulatively — had already caused tree mortality to exceed background levels by 5.53 teragrams of carbon per year. As these 15 pests spread and invasions intensify, they threaten 41.1% of the total live forest biomass in the 48 coterminous states. Poland et al. (2019) (again – written by USFS employees) document the damage to America’s forest ecosystems caused by the full range of invasive species, terrestrial and aquatic.

Fei et al. and Weed, Ayers, and Hicke (2013) also support the finding that old, large trees are the most important trees with regard to carbon storage. This understanding leads them to conclude that the most damaging non-native pests are the emerald ash borer, Dutch elm disease fungi, beech bark disease, and hemlock woolly adelgid. As I pointed out in earlier blogs, other large trees, e.g., American chestnut and several of the white pines, were virtually eliminated from much of their historical ranges by non-native pathogens decades ago. These same large, old, trees also maintain important aspects of biological diversity.

It is true that not all tree species are killed by any particular pest. Some tree genera or species decrease while others thrive, thus altering the species composition of the affected stands (Weed, Ayers, and Hicke). This mode of protection is being undermined by the proliferation of insects and pathogens that cumulatively attack ever more tree taxa. And while it is true that some of the carbon storage capacity lost to pest attack will be restored by compensatory growth in unaffected trees, this faster growth is delayed by as much as two or more decades after pest invasions begin (Fei et al.).

ash forest after EAB infestation; Photo by Nate Siegert, USFS

Still, despite the rapid rise of destructive tree pests and disease outbreaks, scientists cannot yet resolve critical aspects of pathogens’ ecological impacts or relationship to climate change. Gougherty notes that numerous tree diseases have been linked to climate change or are predicted to be impacted by future changes in the climate. However, various studies’ findings on the effects of changes in moisture and precipitation are contradictory. Wu reports that his study of ash decline in a forest in Oxfordshire found that climate change will have a very small positive impact on disease severity through increased pathogen virulence. Weed, Ayers, and Hicke go farther, making the general statement that despite scientists’ broad knowledge of climate effects on insect and pathogen demography, they still lack the capacity to predict pest outbreaks under climate change. As a result, responses intended to maintain ecosystem productivity under changing climates are plagued by uncertainty.

Clarifying how disease systems are likely to interact with predicted changes in specific characteristics of climate is important — because maintaining carbon storage levels is important. Quirion et al. (2021) estimate that, nation-wide, native and non-native pests have decreased carbon sequestration by live forest trees by at least 12.83 teragrams carbon per year. This equals approximately 9% of the contiguous states’ total annual forest carbon sequestration and is equivalent to the CO2 emissions from more than 10 million passenger vehicles driven for one year. Continuing introductions of new pests, along with worsening effects of native pests associated with climate change, could cause about 30% less carbon sequestration in living trees. These impacts — combined with more frequent and severe fires and other forest disturbances — are likely to negate any efforts to improve forests’ capacity for storing carbon.

Understanding pathogens’ interaction with their hosts is intrinsically complicated. There are multiple biological and environmental factors. What’s more, each taxon adapts individually to the several environmental factors. Wu says there is no general agreement on the relative importance of the various environmental factors. The fact that most forest diseases are not detected until years after their introduction also complicates efforts to understand factors affecting infection and colonization.

The fungal-caused ash decline in Europe is a particularly alarming example of the possible extent of such delays. According to Wu, when the disease was first detected – in Poland in 1992 – it had already been present perhaps 30 years, since the 1960s.  Even then, the causal agent was not isolated until 2006 – or about 40 years after introduction. The disease had already spread through about half the European continent before plant health officials could even name the organism. The pathogen’s arrival in the United Kingdom was not detected until perhaps five years after its introduction – despite the country possessing some of the world’s premier forest pathologists who by then (2012) knew what they to look for. 

Clearly, improving scientific understanding of forest pathogens will be difficult. In addition, effective policy depends on understanding the social and economic drivers of trade, development, and political decisions are primary drivers of the movement of pathogens. Wu calls for collaboration of ecologists, geneticists, earth scientists, and social scientists to understand the complexity of the host-pathogen-surrounding system. Bringing about this new way of working and obtaining needed resources will take time – time that forests cannot afford.  

However, Earth’s forests are under severe threat now. Preventing their collapse depends on plant health officials integrating recognition of these difficulties into their policy formulation. It is time to be realistic: develop and implement policies that reflect the true level of threat and limits of current science.

Background: Rising Numbers of Introductions

Gougherty’s analysis of rising detections of emerging tree diseases found little evidence of saturation globally – in accord with the findings of Seebens et al. (2017) regarding all taxa. Relying on data for 24 tree genera, nearly all native to the Northern Hemisphere, Gougherty found that the number of new pests attacking these tree genera are doubling on average every 11.2 years. Disease accumulation is increasing rapidly in both regions where hosts are native and where they are introduced, but more rapidly in trees’ native ranges.This finding is consistent with most new diseases arise from introductions of pathogens to naïve hosts.

Gougherty says his estimates are almost certainly underestimates for a number of reasons. Countries differ in scientific resources and their scientists’ facility with English. Scientists are more likely to notice and report high-impact pathogens and those in high-visibility locations. Where national borders are closer, e.g., in Europe, a minor pest expansion can be reported as “new” in several countries.  New pathogens in North America appear to occur more slowly, possibly because the United States and Canada are very large. He suggests that another possible factor is the U.S. (I would add Canada) have adopted pest-prevention regulations that might be more effective than those in place in other regions. (See my blogs and the Fading Forest reports linked to below for my view of these measures’ effectiveness.)

ash dieback in the UK

Wu notes that reports of tree pathogens in Europe began rising suddenly after the 1980s. He cites the findings by Santini et al. (2012) that not only were twice as many pathogens detected in the period after 1950 than in the previous 40 years, the region of origin also changed. During the earlier period, two-thirds of the introduced pathogens came from temperate North America. After 1950, about one-third of previously unknown disease agents were from temperate North America. Another one-third was from Asia. By 2012, more than half of plant infectious diseases were caused by introduction of previously unknown pathogens.

What is to be done?

Most emerging disease agents do not have the same dramatic effects as chestnut blight in North America, ash dieback in Europe, or Jarrah dieback in Australia. Nevertheless, as Gougherty notes, their continued emergence in naïve biomes increases the likelihood of especially damaging diseases emerging and changing forest community composition.

Gougherty calls for policies intended to address both the agents being introduced through trade, etc., and those that emerge from shifts in virulence or host range of native pathogens or changing environmental conditions. In his view, stronger phytosanitary programs are not sufficient.

Wu recommends enhanced monitoring of key patterns of biodiversity and ecosystem functioning, He says these studies should focus on the net outcome of complex interactions. Wu also calls for increasing understanding of key “spillover” effects – outcomes that cannot be currently assessed but might impact the predicted outcome. He lists several examples:

  • the effects of drought–disease interactions  on tree health in southern Europe,
  • interaction between host density and pathogen virulence,
  • reproductive performance of trees experiencing disease,
  • effect of secondary infections,
  • potential for pathogens to gain increased virulence through hybridization.
  • potential for breeding resistant trees to create a population buffer for saving biological diversity. Wu says his study of ash decline in Oxfordshire demonstrates that maintaining a small proportion of resistant trees could help tree population recovery.

Quirion et al. provide separate recommendations with regard to native and introduced pests. To minimize damage from the former, they call for improved forest management – tailored to the target species and the environmental context. When confronting introduced pests, however, thinning is not effective. Instead, they recommend specific steps to minimize introductions via two principal pathways, wood packaging and imports of living plants. In addition, since even the most stringent prevention and enforcement will not eliminate all risk, Quirion et al. advocate increased funding for and research into improved strategies for inspection, early detection of new outbreaks, and strategic rapid response to newly detected incursions. Finally, to reduce impacts of established pests, they recommend providing increased and more stable funding for classical biocontrol, research into technologies such as sterile-insect release and gene drive, and host resistance breeding.

USDA HQ

Remember: reducing forest pest impacts can simultaneously serve several goals—carbon sequestration, biodiversity conservation, and perpetuating the myriad economic and societal benefits of forests. See Poland et al. and the recent IUCN report on threatened tree species.

SOURCES

Barrett, T.M. and G.C. Robertson, Editors. 2021. Disturbance and Sustainability in Forests of the Western United States. USDA Forest Service Pacific Northwest Research Station. General Technical Report PNW-GTR-992. March 2021

Clark, P.W. and A.W. D’Amato. 2021. Long-term development of transition hardwood and Pinus strobus – Quercus mixedwood forests with implications for future adaptation and mitigation potential. Forest Ecology and Management 501 (2021) 119654

Fei, S., R.S. Morin, C.M. Oswalt, and A.M. 2019. Biomass losses resulting from insect and disease invasions in United States forests. Proceedings of the National Academy of Sciences. www.pnas.org/cgi/doi/10.1073/pnas.1820601116  

Gougherty AV (2023) Emerging tree diseases are accumulating rapidly in the native and non-native ranges of Holarctic trees. NeoBiota 87: 143–160. https://doi.org/10.3897/neobiota.87.103525

Lovett, G.M., C.D. Canham, M.A. Arthur, K.C. Weathers, and R.D. Fitzhugh. 2006. Forest Ecosystem Responses to Exotic Pests and Pathogens in Eastern North America. BioScience Vol. 56 No. 5 May 2006

Lovett, G.M., M. Weiss, A.M. Liebhold, T.P. Holmes, B. Leung, K.F. Lambert, D.A. Orwig, F.T. Campbell, J. Rosenthal, D.G. MCCullough, R. Wildova, M.P. Ayres, C.D. Canham, D.R. Foster, S.L. Ladeau, and T. Weldy. 2016.  Nonnative forest insects and pathogens in the United States: Impacts and policy options.  Ecological Applications, 26(5), 2016, pp. 1437-1455

Poland, T.M., Patel-Weynand, T., Finch, D., Miniat, C. F., and Lopez, V. (Eds) (2019), Invasive Species in Forests and Grasslands of the United States: A Comprehensive Science Synthesis for the United States Forest Sector.  Springer Verlag.

Quirion, B.R., G.M. Domke, B.F. Walters, G.M. Lovett, J.E. Fargione, L. Greenwood, K. Serbesoff-King, J.M. Randall, and S. Fei. 2021 Insect and Disease Disturbance Correlate With Reduced Carbon Sequestration in Forests of the Contiguous US. Front. For. Glob. Change 4:716582.  [Volume 4 | Article 716582] doi: 10.3389/ffgc.2021.716582

Weed, A.S., M.P. Ayers, and J.A. Hicke. 2013. Consequences of climate change for biotic disturbances in North American forests. Ecological Monographs, 83(4), 2013, pp. 441–470

Wu, H. 2023/24. Modelling Tree Mortality Caused by Ash Dieback in a Changing World: A Complexity-based Approach MSc/MPhil Dissertation Submitted August 12, 2024. School of Geography and the Environment, Oxford University.

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

Phytophthoras – unsettling recent developments

tanoak killed by P. ramorum; photo by F.T. Campbell

I am belatedly catching up on the situation with regard to Phytophthora ramorum – sudden oak death – in the US and other countries.  

For a general factsheet on this plant disease, see profile here. Here, I’m summarizing more detailed information contained in the February, May, and August 2024 newsletters of the California Oak Mortality Task Force (COMTF) (Newsletters for earlier months are posted here.)

To obtain the most recent information, you can attend the Fall 2024 virtual meeting of the Task Force on Tuesday, October 29, 2024, from 1 pm to 3 pm PDT. Speakers will focus on the status of P. ramorum in California and Oregon wildlands.

On the next day, Wednesday, October 30, the Phytophthoras in Native Habitats Work Group will discuss “Threats to California Native Plants” including from viruses and excessive heat, along with other concerns.

Participation is free, but registration is required. Complete agendas and more information will be available soon here. Sessions will be recorded and posted to the same site. Questions? Contact Janice Alexander.


More in-depth information à Matteo Garbelotto’s UC Berkeley class, “Ecology and Impacts of Emergent Forest Diseases in California,” is now available free and online. Recommended reading, lecture recordings, slides, even essay topic suggestions are posted. Subjects covered include several high impact forest diseases, molecular diagnostics, disease control, and prevention.

I note that the recent detections of new outbreaks in forests and nurseries support the importance of weather in promoting or hindering establishment and spread of Phytophthora ramorum.

Phytophthora ramorum in North American Forests

In Oregon, P. ramorum continued to spread in 2023 and the first half of 2024.

These outbreaks were detected through extensive surveillance. Aerial monitoring (in cooperation with the USDA Forest Service) and high-resolution imagery covered more than half a million acres in Curry County — the region between the California border and the Coos County line. Ground surveys covered 860 acres. Sampling included 518 trees; 117 tested were positive for the fungus. Stream baits were deployed to 63 sites; 26 tested positive at least once (COMTF newsletter, February 2024; includes maps).

By summer 2024, 23 new P. ramorum infestations had been detected at or beyond the Generally Infested Area (GIA; the area where the pathogen is most commonly found) since 2021. Some of these involve one of the newly detected clonal lineages. Oregon officials are expecting to expand the state’s quarantine area to 901 square miles – 45% of Curry County. The designated GIA would also be enlarged to 178 square miles(COMTF newsletter, August 2024; contains maps).

Oregon continues trying to treat high-priority infestations. In 2023, the state treated 165 acres infested by one of the newly detected clonal lineages, NA2, in the Humbug Mountain area and 347 acres in the Port Orford infestation. Since 2001, Oregon’s Department of Forestry has completed eradication treatments on more than 9,000 acres at an estimated cost of over $37 million. Federal lands comprised 28% of treated acres; the remainder were private and state lands. Still, more than 1,000 high-priority acres have not been treated because neither state nor federal agencies could provide sufficient funds (COMTF newsletter, February 2024).

The stream baiting program in 64 stream drainages has – so far – detected six positive streams. Ground surveys are planned for the new positive drainages along the north bank of the Rogue River and a stream that drains into the Elk River east of Port Orford (COMTF newsletter, August 2024).

In California, recent wet winters have prompted several new detections. The first was in Del Norte County near previously detected sites. The UC Berkeley-coordinated “SOD Blitz” plans intensive surveys in this region in coming months (COMTF newsletter May 2024; contains map).

Somewhat later, new infestations were detected farther south, in Humboldt Redwoods State Park. The new sites were outside the formerly detected sites, on the north side of the creek and up to the top of the ridge (COMTF newsletter, August 2024).

Scientists have realized another concern: several other pathogens cause symptoms on bay laurel, tanoak, and madrone that are almost indistinguishable from SOD. This development will complicate monitoring (COMTF newsletter for August 2024; see below for more details).

Meanwhile, scientists determined that sites where the P. ramorum epidemic is driven by higher bay laurel (Umbellularia californica) densities sustained a higher genotypic diversity of P. ramorum. While tanoak (Notholithocarpus densiflorus) doesn’t contribute much to infection of true oaks (Quercus spp.) it can infect bay laurel, thus perpetuating the infection. Infected oaks and tanoaks maintain host-specific pathogen genotypes (Kozanitas et al. 2024)

The USDA Forest Service program that monitors streams in the East to detect P. ramorum placed baits in 63 streams in 10 eastern states: Alabama, Florida, Georgia, Illinois, Maryland, Mississippi, North Carolina, Pennsylvania, South Carolina, and Texas. In 2023, positive findings for P. ramorum were detected from two streams in Alabama, and one each in Mississippi and North Carolina. All sites are associated with nurseries that had previously tested positive for P. ramorum. Over the last five years – since 2019 – eight streams in four states have tested positive at least once: five in Alabama, and one each in Mississippi, North Carolina, and South Carolina. The detection in South Carolina is new. Vegetation in the watershed has been sampled multiple times; all samples collected so far — plant, soil, and run-off water – have been negative. The pathogen belongs to the NA1 lineage – the one established in forests in West Coast states. [COMTF newsletter February 2024]

from D.J. Haller & M.C. Wimberly. 2020

Situation in Europe

The February 2024, the COMTF newsletter summarized the situation in Great Britain. In England, aerial surveillance covered more than 31,000 ha of larch (Larix kaempferi)plantations. Follow-up investigations detected considerably fewer infested sites than the approximately 200 detected in 2022. Most remain in the southwest and northwest of the country. Weather conditions in 2023 were less conducive for sporulation in 2021 and 2022, which seemed to lead to a reduced level of disease in 2022 and 2023.

In Scotland, widespread aerial and ground surveillance detected a number of sites similar to those found since 2018. Scottish authorities note that where positive findings are not quickly followed by tree removal, localized spread occurred. 

In Wales, four helicopter surveillance flights identified around 150 sites deserving further investigation. About 60 of these sites held infected trees, mainly larch, but some noble fir (Abies procera). The COMTF newsletter contains a map showing infested locations. This year’s infection level might be less than in previous years, but this might reflect the fact that the infections are in smaller forest blocks. However, the wet and mild weather in autumn/winter 2023 provided optimal conditions for sporulation, so the scientist expected higher infection rates in 2024. The Welsh Government is working on a new strategy for managing P. ramorum.

In Northern Ireland, P. ramorum was described as still active and spreading. Only two surveys were flown. They identified 49 locations for follow-up, many in forests where the pathogen had been found previously. At two locations, follow-up inspections and sampling of larch confirmed infection by a different pathogen, Phytophthora pseudosyringae. So in 2024, larch samples will be tested for both P. ramorum and P. pseudosyringae.  

Other Phytopthoras in Europe

English scientists are trying to determine how damaging P. pseudosyringae is on larch. Infections have been observed at several locations in the north of England, as well as in Northern Ireland (COMTF newsletter February 2024).

Mullet et al. (2024) report that P. pseudosyringae is a self-fertile pathogen of woody plants, especially tree species in the genera Fagus, Notholithocarpus, Nothofagus and Quercus. It is found across Europe and in parts of North America and Chile. Genetic studies show that the North American population originated from Europe. P. pseudosyringae can infect roots; the stem collar region; bark; twigs and stems; as well as leaves. They report it is causing particular damage in Great Britain and western North America. Mullet et al. call for investigation of differences in life history traits between the two main population clusters, including their virulence and host ranges.

Nothofagus obliqua; photo by Line1 via Wikimedia

Chile (COMTF newsletter May 2024)

Concerned about decades of mortality of Nothofagus trees in native forests in Chile, González et al. 2024 sought to understand which other native plants might be reservoirs of inoculum of the pathogen Phytophthora pseudosyringae — which is a documented causal agent of partial defoliation and bleeding cankers on two native tree species, Nothofagus obliqua and N. alpina. P. pseudosyringae can sporulate on lesions on Cryptocarya alba, Nothofagus dombeyi and N. obliqua leaves. On Sophora macrocarpa, sporulation occurs on both asymptomatic tissues and on lesions. S. macrocarpa is a common understory species in Nothofagus forests, so it might be an inoculum reservoir for epidemic events in them.

Look-alikes on California Bay Laurel (COMTF newsletter May 2024)

Similar symptoms from a wide variety of pathogenic organisms were detected on bay laurels after last year’s wet winter. Among the pathogens — the list is not exhaustive — includes P. cinnamomi, Neofusicoccum nonquaesitum, Ganoderma brownie, P. pseudosyringae, P. nemorosa, Botryosphaeria dothidea, Armillaria gallica, Diplodia corticola, and others.  

Foliar symptoms tend to look identical on bay laurel leaves. Two foliar pathogens cause particular concern. The first is an “anthracnose” disease of bay laurel caused by a species of Kabatiella. Although known to be present for ~80 years, this organism did not seem to cause problems until 2023. In multiple locations around the San Francisco Bay area, it has caused extensive browning defoliation of bay laurel crowns. Whether the trees will die is uncertain.

The second focus is on a recently named species, Calonectria californiensis. This organism produces P. ramorum-like similar symptoms on a wide variety of native plants, including bay laurel, tanoak, salal, mock-orange, Oregon-grape, and rhododendron. On most of these plants this fungus causes black spots that can grow to kill entire leaves, but apparently C. californiensis is not a pathogen of woody plant parts. Initial symptoms of infection on bay laurel appear identical to those caused by the SOD pathogen (Phytopthora ramorum). C. californiensis does not appear (yet) to lead to lasting debilitating disease or tree mortality.

Nurseries and Managed Landscapes

In administering APHIS’ cooperative program aimed at minimizing spread of P. ramorum via interstate trade in plants, California’s Department of Agriculture (CDFA) relies – at least in part – on funds from USDA. CDFA received $1,308,771 from APHIS in 2023. More than 300 establishments in California are regulated under the program. They submitted ~ 7,400 P. ramorum regulatory samples to the CDFA in 2023. Seventy-eight of the samples were positive (COMTF newsletter February 2024).

At the end of 2023, seven California nurseries that had tested positive for the presence of P. ramorum were operating under the APHIS regulation governing positive nurseries. This was an increase over previous years; zero in 2022, three in 2021 (COMTF newsletter February 2024 Table 4). During 2024 five nurseries were confirmed as positive. Three of these had tested positive in previous years. Two retail nurseries were newly positive; one of these was apparently infected when it brought in plants from another nursery (COMTF newsletter August 2024). I wonder whether the very wet winters California has experienced lately have enhanced the pathogen’s ability to grow – and be detected.

In Oregon, in 2023 the Department of Agriculture regulated five interstate shippers under federal compliance agreements and a sixth intrastate shipper regulated under state requirements (COMTF newsletter February 2024). Spring compliance surveys tested 1,228 foliar samples; ten were positive. After this nursery incinerated all nearby plants, none of the 1,664 foliar samples tested in the fall was positive.

In 2023, the Washington State Department of Agriculture processed more than 300 plant, soil, and water samples; all were negative. Washington also inspected five of the nine nurseries that had ‘opted-out’ of the Federal program so they can no longer ship interstate. Host material appeared free of symptoms so no samples were collected (COMTF newsletter February 2024).

Washington nurseries and regulators frequently encounter the problem of infected plants being shipped into the state from outside. (P. ramorum has been found in 33 Washington nurseries since 2003.) During 2023, the Washington State Department of Agriculture conducted three trace-forward investigations. Fortunately no infestations were detected (COMTF newsletter February 2024). In March 2024, Washington faced another trace-forward involving plants sold to homeowners (COMTF newsletter May 2024). Thirteen tissue samples and two soil samples all tested negative (COMTF newsletter August 2024)

Finally, Washington conducted stream baiting. In 2023, none of the 66 samples was positive (COMTF newsletter February 2024)

Infested Plants

Most of the plant species on which P. ramorum was detected during these years are the usual ones: Rhododendron, Viburnum, Pieris, Arbutus, Prunus, Camellia, Loropetalum. I think the several Cornus species might be somewhat unusual. Disease was confirmed on a new Cornus species, C. capitata (evergreen dogwood). One taxon — Arbutus x ‘Marina’ — is not yet listed by APHIS as a host because Koch’s postulates have not been completed (COMTF newsletters for February 2024 and August 2024).

Research (summarized in the February 2024 newsletter)

Two studies found evidence of seasonal and weather factors influenced establishment of P. ramorum. One study found a clear seasonal pattern of pathogen incidence in the western US, plus a link to the El Niño-Southern Oscillation (ENSO) (Xuechung et al. 2024. The second study looked at a Japanese larch plantation in Scotland (Dun et al. 2024).

In both Scotland (above) and France (Beltran et al. 2024 2024), scientists demonstrated that prompt action helps to suppress P. ramorum establishment.

APHIS Updates its Regulations

In March 2024, APHIS revised the P. ramorum “Domestic Regulatory Program Manual.” The agency said it updated figures and definitions, clarified operational steps, and revised the Retail Nursery Dealer Protocol (COMTF newsletter for May 2024).

Funding

In Fiscal Year 2024, under the Plant Protection Act Section 7721 program, APHIS funded $1 million worth of projects focused on P. ramorum and related species. This was out of a total $62 million in funds dispersed for pest survey, research, mitigation, and outreach programs. This money funded nursery surveys in 11 states. Also, it paid for a project to evaluate the threat of the NA2 & EU2 lineages to nurseries and forests (COMTF newsletter May 2024).


SOURCES

Beltran, A.; Laubray, S.; Ioos, R.; Husson, C.; Marçais, B. 2024. Low persistence of Phytophthora ramorum  in western France after implementation of eradication measures. Annals of Forest Science. 81: 7. https://doi.org/10.1186/s13595-024-01222-1

Dun, H.F.; MacKay, J.J. & Green, S. 2024. Expansion of natural infection of Japanese larch by Phytophthora ramorum shows trends associated with seasonality & climate. Plant Pathology. 73(2): 419-430).

González, M.P.; Mizubuti, E.S.G.; Gonzalez, G.; Sanfuentes, E. 2024. Uncovering the hidden hosts: Identifying inoculum reservoirs for Phytophthora pseudosyringae in Nothofagus forests in Chile. Plant Pathology. 73(4): 937-947. https://doi.org/10.1111/ppa.13855. (Summarized in COMTF newsletter February 2024.)

Kozanitas, M.; Knaus, B.J.; Tabima, J.F.; Grünwald, N.J.; Garbelotto, M. 2024. Climatic variability, spatial heterogeneity & the presence of multiple hosts drive the population structure of the pathogen P ram & the epidemiology of Sudden Oak Death. Ecogeography. https://doi.org/10.1111/ecog.07012. (Summarized in COMTF newsletter May 2024.)

Mullet, M.S.; Harris, A.R.; Scanu, B. [and others]. 2024. Phylogeography, origin & population structure of the self-fertile emerging plant pathogen Phytophthora pseudosyringae. Molecular Plant Pathology. https://doi.org/10.1111/mpp.13450.  (Summarized in COMTF newsletter for May 2024.)

Xuechung, K.; Wei, C.; Siliang, L.; Tiejun, W.; Le, Y. & Singh, R. 2024. Spatiotemporal distribution of sudden oak death in the US & Europe. Agricultural & Forest Meteorology. 346: 109891)

Good News!!!! Treatments to Counter Beech Leaf Disease — at least for indidividual trees

beech leaf disease symptoms; photo by Matthew Borden via Flickr

Beech leaf disease (BLD) came to attention in 2012 near Cleveland. It has since spread to the Atlantic – Maine to New Jersey and northern Delaware; south into Virginia; north in Ontario; and west to eastern Michigan.

Scientists have scrambled to understand the disease – how it hijacks the tree’s metabolism;  & here its impacts on seedlings, saplings, and mature trees; how it spreads, locations at greatest risk.

(Maryland detections too recent to be shown)

Many of us have despaired.

Now Bartlett Tree Research Laboratories – the research arm of Bartlett Tree Experts – has announced development of Integrated Pest Management (IPM) strategies to treat individual trees – sadly not yet beech in the forest. The project is led by Dr. Andrew Loyd and Dr. Matthew Borden.

Seeing the disease’s impacts on a tree species with aesthetic and ecological values not easily replaced, and its rapid spread, scientists at Bartlett Tree Research Laboratories began testing fungicides and nematicides registered under the Federal Insecticide, Fungicide and Rodenticide Act (FIFRA) by the U.S. Environmental Protection Agency (EPA) to see whether they might be effective against the causal nematode Litylenchus crenatae ssp mccannii.

As Drs. Loyd and Borden note, managing BLD presents numerous challenges:

1. The disease was discovered recently, so there were many unknowns, including how it spreads and the causal organism’s novel life cycle.

2. The damage occurs in leaf buds during winter dormancy. There has been little previous research on such a system. It is difficult for chemicals to reach the tissues.

3. Mature trees are large, so reaching the vulnerable leaves in the canopy is difficult.

4. Treatment efficacy cannot be evaluated until nearly a year after application.

5. Few chemicals are registered for use against foliar nematodes or for trees in forest, nursery, or landscape settings.

6. Obtaining funding is difficult because protecting beech is a low priority among many of the usual sources.

Fortunately, the leadership at Bartlett – the company’s research department, the New England Division leadership, and especially Robert A. Bartlett, Jr. (head of the family-owned company) – saw the importance of protecting beech and have supported this research. The USDA Forest Service has also funded some of studies exploring soil drenches. Cameron McIntire reports that these studies do not yet have results.

Furthermore, Bartlett has chosen to make the science easily available to all interested parties. Three posters explaining experiments to date are available at ResearchGate. They have also published a study on the early tests of Fuopyram as a foliar spray. It is open-access. Additional publications presenting data on experiments with both spray (Fluopyram) and injection (Thiabendazole/Arbotect) are in preparation.

I summarize briefly here their findings as of August 2024.

In all the trials, the scientists judged efficacy of treatments by counting the number of viable nematodes in leaves, viable nematodes in overwintering buds, and BLD symptom severity at appropriate times before and after treatment (spray or injection).

Tests of foliar sprays on small to medium sized trees

The first tests of foliar applications that resulted in BLD suppression were carried out in Ohio starting in 2021, then expanded to other field sites in Ohio and several states in New England in 2022 and 2023 seasons. In early trials, trees were sprayed four times starting in mid to late July at 21-day intervals. The scientists say that recent trials focus on application timing and rate. They hope that optimizing these factors will help generate new recommendations that are more sustainable while maintaining efficacy.

At the annual meeting of the American Phytopathological Society in July 2023, Bartlett announced that Fluopyram is an effective management tool to combat BLD – on smaller trees that can be treated using foliar application. There are several EPA-registered products, though only one, Broadform, has been so far been granted a section 2(EE) recommendation “For Control of Beech Leaf Disease on Beech Trees.”

Treatments are less effective in situations where the inoculum load is very high (for example, a very dense stand of infected trees); or where mature, untreated canopies hang over treated understory beech.

They suggest that managers focus treatments on high-value specimen beech, collection preservation, and potentially uncrowded mixed natural stands.

Treatments should be made by certified pesticide applicators who are familiar with the disease and treatment specifications. For the injection treatment, technical training and specialized equipment is needed. Bartlett arborists and plant health care specialists in locations affected by BLD have all been trained to perform the treatments, and some other arborists are doing BLD treatments as well using the same products.

Soil drench

Matt Borden said that they tested drenches with three different chemicals. The approach did not reduce nemtatode numbers sufficiently. However, as noted above, the Forest Service is funding additional tests exploring possible combinations of drenches with other actions, such as thinning. Discovering management options across a range of application methods (e.g., foliar, injection, drench) and modes of action is vital for a disease that covers such a broad range of locations and tree sizes and forms.

a macroinjection demonstration; photo by Matthew Borden via Flickr

Injections

Scientists injected Thiabendazole (TBZ) into beech on private land in three locations in Ohio and New Jersey. They tested two application rates and three application timings. They have two years of follow-up data for one site, one year for the others.

Key findings:

  • nematode numbers in buds in late winter consistently reflected foliar symptoms when the leaves opened.
  • Injections made before mid-July provided the greatest reduction in nemtatode numbers and best canopy improvement. Trees injected late in the season (30 August), after the nematode has begun dispersing from leaves to buds, exhibited some BLD symptoms the next year, but suffered less canopy dieback than controls.

Margery Daughtrey of Cornell said during a discussion of these finding that the trees’ persistence suggests that trees can tolerate some level of symptoms. Among other things, it might be possible to treat the trees less frequently than annually.

  • TBZ appears to provide at least two seasons of nematode suppression

Bartlett continues to monitor these trees to see how long the injected chemical suppresses nematode numbers and how long the tree remains healthy. They are also establishing new field sites to further optimize rate and timing.

TBZ – in a product called Arbotect 20-S – has been used to manage Dutch elm disease and sycamore anthracnose since the 1970s. However, it is also a well-known nematicide, previously used as an anti-parasitic drug in human and veterinary medicine. Once injected, TBZ protects the tree for more than one season. The injection technology (MACRO-Injection) has also been used for decades. It infuses the chemical directly into the tree’s vascular system; it does not rely on root uptake. Matt says injection does require take technical skill and the right equipment. To minimize the risk of the wound cracking and weeping, the injection should be done low on the side of the root flare, not on top.

While Arbotect 20-S has been registered for use in 48 states for many years, new labeling is required for its use in beech trees and against BLD. Special Local Needs labels, 24(C)s, have been granted by eight states – Connecticut, Massachusetts, Maine, New Jersey, New York, Pennsylvania, and Virginia. Registration in a ninth – Maryland – is in progress and Bartlett scientists are prepared to apply for several more. The problem is that only a limited number of these “special needs” labels may be issued, and BLD has expanded so far, and so rapidly, that it is already infesting beech in more states than may be covered by 24(C)s. Furthermore, 24(C) labels expire if not renewed. Most current 24(C)s will be active through 2028 – not ideal for a disease that will likely be with us long into the future. The product manufacturer (Syngenta) and distributor (Rainbow Ecoscience) are drafting a change to the main Arbotect 20-S label to add beech and the new nematode pest, but warn that EPA review and approval of amendments can take a very long time. Until then, we must resort to limited special local needs labels, and some states will miss out.

contrasting canopy transparency in beech treated with TBZ v. untreated controls; photo by Matthew Borden

One of the key scientists who developed these treatments for Dutch elm disease, R. Jay Stipes, professor emeritus at Virginia Tech, is quoted by Bartlett rejoicing that his work might help protect another tree species.

Matt believes the treatments will be effective if applied every 2-3 years. This approach would also spread out the cost – which will depend on the arborist but Dave Anderson of Rainbow Ecoscience estimated to be about $25 / inch of dbh.

It is always best to obtain an accurate diagnosis before treatment. The next step is talking through your options with a certified arborist or tree disease specialist. The “good” thing about BLD is that it is a progressive disease and will not kill a tree in a single year. Therefore, waiting until you know the disease is present or active locally is generally recommended.

Tree injection is better than foliar application where the latter is impractical (e.g., the tree is tall) or to reduce runoff, particularly near streams. Bartlett recommends treating any beech larger than 10 cm dbh by injection; smaller trees by foliar spray.

Treated trees should be sound, without serious decay, girdling roots, or other conditions that curtail uptake. Based on research results to date, they recommend treating the tree before mid-July. Bartlett is testing the results of injecting the shortly after full leaf expansion – early to mid-June. Bartlett scientists are testing several application rates to determine how long a single injection will suppress BLD. So far they have had good results from both low and moderate label rates (0.4-1.6 fl oz/inch DBH).

All the technical information re: research into treatments and recommendations for applying either the foliar or injection treatments has been provided by Dr. Matthew Borden of Bartlett Tree Research Laboratories. He can be reached at

mborden@Bartlett.com
https://www.bartlett.com/staff/matthew-borden-dpm

Dr. Borden says he is immensely grateful for the support that allows him and Dr. Loyd to travel widely to establish the BLD research sites and spend weeks collecting data each year with their team. Company founder Francis A. Bartlett established the Bartlett Tree Research Laboratories as a separate entity within the company, where capital is reinvested directly into stable, long-term support of scientific tree research and preservation. The model is well-suited to provide the flexibility and freedom needed to rapidly respond to emerging invasive species issues.


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