Category: invasive species policy

“Year of Plant Health” – Opportunity to Review International Phytosanitary Programs’ Effectiveness

Rome – site of the FAO

The U.N. Food and Agriculture Organization has declared 2020 to be  the International Year of Plant Health. APHIS, U.N. FAO, and others planned celebratory events — most now postponed.

The designation prompts consideration of whether the current global phytosanitary system – created in 1995 – is succeeding in preventing movement of invasive plant pests and invasive plants. Join me in this evaluation!

I focus on evaluating the most widespread invasive pests killing trees – and the pathways on which they travel. Some of the most damaging tree pests, of course, were moved around the world decades ago. But too many have been transported after the modern plant health system was developed in the mid-20th Century with the adoption of the original International Plant Protection Convention (IPPC) in 1951.

Of course, this is also the period when trade volume exploded, resulting in new source countries, new products, and new technologies that facilitated newly rapid movement of goods and accompanying pests. See my earlier blog here and the book by Marc Levinson, The Box: How the Shipping Container Made the World Smaller and the World Economy Bigger. It is well-documented that rising trade volumes, new trade connections, new products have and will continue to exacerbate unintended movement of species (Seebens et al., 2018). 

The phytosanitary regime was massively revised in the mid-1990s through adoption of the World Trade Organization and the Agreement on Sanitary and Phytosanitary Standards (SPS Agreement). Two principal changes were to constrain individual countries’ freedom to establish their own phytosanitary regulations and to require evidence of risk rather than allowing action on the basis of “if in doubt, keep it out”. I have written a critique of the new system in Fading Forests II. See Chapter 3, available here.

USDA officials burn infested cherry trees – gifts from Japan
Washington, D.C. 1912

Has the new regime allowed spread of pests, as I predicted in my critique?

Of course, the explosion of global trade has made prevention of species introductions far more difficult. So the rising numbers of introductions cannot be blamed entirely on the SPS Agreement. Still, it is vital to review pest status in order to see whether the SPS Agreement is succeeding in protecting Earth’s flora. Here, I am looking at only one type of bioinvader. Many more types need to be evaluated, even among plants and plant pests. Nor do I pretend that my list is comprehensive even in the category I focus on – tree-killing insects, nematodes, and pathogens.

My definition of “global invader” is an insect, pathogen, or nematode that has been moved from its known or probable place of origin to at least two novel continents or widespread island groups.

Before the SPS Agreement

Of course, many highly damaging forest insects and pathogens spread widely before the eruption of global trade in the second half of the 20th Century. Examples include several pathogens:

American chestnut bred to be resistant to blight
photo by F.T. Campbell
  • Phytophthora cinnamomi – Europe, North America, Oceania, South America
  • Cryphonectria parasitica – Europe and North America; Oceania probably much later
  • Dutch elm disease causal agents Ophiostoma ulmi & novo-ulmi (the vectors are sometimes native insects) – Europe, North America, Oceania;

And some insects:

  •  Hylastes ater – Oceania, South America, Africa
  • Scolytus multistriatus (Dutch elm disease vector) – North America 1909; later to Oceania; mid-20th Century to Africa

There have also been initial introductions of some organisms that would become “global” later:

  • Phytophthora lateralis – North America before 1950

During the period 1950 – 1995 –when trade began exploding and countries were adopting their own phytosanitary regulations as allowed under the original IPPC – the following pests were introduced “globally”:

P. ramorum in Big Sur, California
photo by Matteo Garbelotto
  • Phytophthora ramorum was introduced from Southeast Asia to Europe and North America.
  • Hylurgus ligniperda – Oceania, South America, Africa, Asia after 1950; North America before 1995
  • Phoracantha recurva – detected in various geographies after 1995, but almost certainly introduced to North America, South America, Europe, Africa, and Oceania before that date
  • Palm pests – red palm weevil (Rhynchophorus ferrugineus) to most areas of the Old World and Oceania where palms grow; coconut rhinoceros beetle (Oryctes rhinoceros) around Africa, Mauritius, Reunion; Oceania;

Again, there were initial introductions of numerous insects in wood packaging and on “plants for planting” that would expand to “global” ranges after 1995:

Anoplophora glabripennis
  • To North America: Anoplophora glabripennis;, Agrilus planipennis; Austropuccinia psidii; Phoracantha recurve; Glycaspis brimblecombei
  • To Asia: Pine wood nematode Bursaphelenchus xylophilus
  • To Oceania, South America – Sirex noctillio;

After the SPS Agreement

There has been an apparent explosion of spread since adoption of SPS Agreement in 1995. No doubt these introductions were made possible by the concurrent explosion of trade volumes and more pest-friendly shipping practices (e.g., use of shipping containers and more rapid transportation). The principal vector appears to be plants for planting. About 50% of new plant pathogen invasions are associated with plants for planting (Jimu et al. 2016). Wood packaging is a strong second vector.

Tree-killing pests of which I am aware that have apparently spread globally after 1995 include:

Insects

Aulacaspis ysumatsui – North America, Caribbean, Pacific Ocean islands, Oceania, Africa, Europe, various islands off Southeast Asia that are probably outside original range

Erythrina humeana in the Manie van der Schijff Botanical Garden, Pretoria
vulnerable to Euwallacea / Fusarium complex

Quadrastichus erythrinae – North America, Southeast Asia, islands in the Indian and Pacific oceans 

Euwallacea fornicatus complex, esp. Euwallacea whitfordiodendrus and E. kuroshio and their Fusarium symbionts Fusarium euwallaceae, Graphium euwallaceae, & Paracremonium pembeum – North America, Africa 

Several insects that attack Eucalyptus have been widely introduced to areas where plantations of these species have been planted, e.g.,

  • Blue gum chalcid wasp or eucalyptus gall wasp Leptocybe invasa –   throughout Africa, the Middle East, Asia, the Pacific Region, Europe, South America, Mexico, and the United States [CABI]
  • Red gum lerp psyllid (Glycaspis brimblecombei) Europe 2009 [EPPO]
  • Eucalyptus snout beetles Gonipterus spp complex à two species introduced to five continents (Schroder et al. 2019).
  • Eucalyptus gall wasp(Ophelimus maskelli) – Mediterranean Region, the Middle East, South Africa, Europe, U.S., New Zealand [CABI]  

Continued spread of species that had been introduced to a single new continent before 1995:

  • Pine wood nematode Bursaphelenchus xylophilus – to Europe
  • Phytophthora lateralis – to Europe and South America
  • Myrtle rust Austropuccinia psidii – to Pacific oceanic islands and Oceania
  • Anoplophora glabripennis and A. chinensis – to Europe
  • Sirex noctillio – to North America  
  • Agrilus planipennis – to Russia and western Europe
  • Red palm weevil (Rhynchophorus ferrugineus) – to North America (California- eradicated)
  • Coconut rhinoceros beetle (Oryctes rhinoceros) – to Pacific islands, e.g.,  Guam and Hawai`i

I note that several studies have identified large numbers of introduced species in certain categories, although the dates of introduction are uncertain. Some were probably introduced before 1995. Here I cite the following:

  • Jung et al. (2015) found 59 putative Phytophthora taxa in forest and landscape planting sites in Europe; none had been detected by inspectors at the European Union borders.
  • Jimu et al. (2019) report global spread of Eucalyptus pathogens carried by the trade in seed and cuttings to support establishment of new plantations and breeding programs. 
  • Numerous species of Phytophthora across North America – about 60 species in California native plant nurseries; eleven species in Minnesota (both from Swiecki et al. 2018); Parke et al. (2014) identified 28 Phytophthora taxa in four Oregon nurseries.
  • Nine species of Phytophthora associated in urban streetscapes, parks, gardens, and remnant native vegetation in urban settings in Western Australia (Barber et al. 2013).

So What’s the Bigger Picture?

I have blogged frequently about the weaknesses of the international standard governing wood packaging; go here.

Clearly the weaknesses of the international phytosanitary system are not limited to the wood packaging pathway. And I repeat that the phytosanitary system is under severe challenge by trade volumes and practices – at least before the Covid-19 pandemic. Still, it is clear that the international phytosanitary system has failed in achieving its purpose: to provide adequate protection in response to this challenge.

I have two suggestions:

1) I hope that the most affected countries will take action per their authority under Section 5.7 of the SPS Agreement. This allows emergency action to prevent further introductions via the principal pathways and from the geographic origins posing the greatest threats (e.g., China for wood packaging, Southeast Asia for Phytophthora pathogens).

2) I hope further that all the nearly 200 countries that are parties to the SPS Agreement and the IPPC will rapidly institute an analysis of the current phytosanitary system to quickly identify amendments to the agreements that would better enable countries to protect their plants from non-native pests.

SOURCES

Barber, P.A., T. Paap, T.I. Burgess, W. Dunstan, G.E.St.J. Hardy. 2013. A diverse range of Phytophthora species are associated with dying urban trees. Urban Forestry & Urban Greening 12 (2013) 569-575

Jimu, L., M. Kemler, M.J. Wingfield, E. Mwenje, and J. Roux. 2016. The Eucalyptus stem canker pathogen Teratosphaeria zuluensis detected in seed samples. Forestry 2016 89 316-324 https://academic.oup.com/forestry/article/89/3/316/1749105

Jung, T., L. Orlikowski, B. Henricot, P. Abad‐Campos, A. G. Aday. O. Aguín Casal, J. Bakonyi, S. O. Cacciola, T. Cech, D. Chavarriaga, T. Corcobado, A. Cravador, T. Decourcelle, G. Denton, S. Diamandis, H. T. Doğmuş‐Lehtijärvi, A. Franceschini, B. Ginetti, S. Green, M. Glavendekić, J. Hantula, G. Hartmann, M. Herrero, D. Ivic, M. Horta Jung, N. Keca, V. Kramarets, A. Lyubenova, H. Machado, G. Magnano di San Lio, P. J. Mansilla Vázquez, B. Marçais, I. Matsiakh, I. Milenkovic, S. Moricca, Z. Á. Nagy, J. Nechwatal, C. Olsson, T. Oszako, A. Pane, E. J. Paplomatas, C. Pintos Varela, S. Prospero, C. Rial Martínez, D. Rigling, C. Robin, A. Rytkönen,  M. E. Sánchez, A. V. Sanz Ros, B. Scanu, A. Schlenzig, J. Schumacher, S. Slavov, A. Solla, E. Sousa, J. Stenlid,  V. Talgø, Z. Tomic, P. Tsopelas, A. Vannini, A. M. Vettraino, M. Wenneker, S. Woodward, A. Peréz‐Sierra. 2016. Widespread Phytophthora infestations in European nurseries put forest, semi-natural and horticultural ecosystems at high risk of Phytophthora disease. Forest Pathology. November 2015.

Levinson, M. The Box: How the Shipping Container Made the World Smaller and the World Economy Bigger Princeton University Press 2008

Schroder, M. Slippers, B., Wingfield, M.J., Hurley, B.P, Invasion history and management of Eucalyptus snout beetles in the Gopterus scutellatus species complex. 2019. Journal of Pest Science

Parke, J.L., B.J. Knaus, V.J. Fieland, C.Lewis, and N.J. Grünwald. 2014.  Phytophthora Community Structure Analyses in Oregon Nurseries Inform Systems Approaches to Disease Management. Phytopathology Vol. 104, No 10.

Schroder, M. Slippers, B., Wingfield, M.J.,Hurley, B.P, Invasion history and managementof Eucalyptus snout beetles in the Gopterus scutellatus species complex. 2019. Journal of Pest Science

Seebens, H., T.M. Blackburn, E.E. Dyer, P. Genovesi, P.E. Hulme, J.M. Jeschke, S. Pagad, P. Pyse, M. van Kleunen, M. Winter, M. Ansong, M. Arianoutsou, S. Bacher, B. Blasius, E.G. Brockerhoff, G. Brundu, C. Capinha, C.E. Causton, L. Celesti-Grapow, W. Dawson, S. Dullinger, E.P. Economo, N. Fuentes, B. Guénard, H. Jäger, J. Kartesz, M. Kenis, I. Kühn, B. Lenzner, A.M. Liebhold, A. Mosen, D. Moser, W. Nentwig, M. Nishino, D. Pearman, J. Pergl, W. Rabitsch, J. Rojas-Sandoval, A. Roques, S. Rorke, S. Rossinelli, H.E. Roy, R. Scalera, S. Schindler, K. Stajerová, B. Tokarska-Guzik, K. Walker, D.F. Ward, T. Yamanaka, and F. Essl. 2018. Global rise in emerging alien species results from increased accessibility of new source pools. PNAS Plus. Available at http://www.nature.com/articles/ncomms14435

Swiecki, T.J., E.A. Bernhardt, and S.J. Frankel. 2018. Phytophthoraroot disease and the need for clean nursery stock in urban forests: Part 1 Phytophthora invasions in the urban forest and beyond. Western Arborist Fall 2018.

Wondafrash, M., B. Slippers, A. Nambazimana, I. Kayumba, S. Nibouche, S. van der Lingen, B.A. Asfaw, H. Jenya, E.K. Mutitu, I.A. Makowe, D. Chungu, P. Kiwuso, E. Kulimushi, A. Razafindrakotomamonjy, P.P. Bosu, P. Sookar & B.P. Hurley. 2020.  Distribution and genetic diversity of five invasive pests of Eucalyptus in sub-Saharan Africa. Biological Invasions Vo. 22, pp. 2205-2221 (2020) 

Coconut rhinoceros beetle – https://www.cabi.org/isc/datasheet/37974 + websites for Guam and Hawai`i

Red palm weevil – https://cisr.ucr.edu/invasive-species/red-palm-weevil

Posted by Faith Campbell

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

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

Why such scattershot responses to myrtle rust?

myrtle rust infestation;
source: New Zealand Department of Agriculture alert May 2017

Pacific countries’ policy and management responses to the spread of the myrtle rust pathogen, Austropuccinia psidii (formerly Puccinia psidii), has had puzzling – even infuriating – gaps … which perhaps have contributed to its spread and damage.

Reminder: ‘ōhi‘a or myrtle rust attacks species in the Myrtaceae – a family now said to include 5,600 species (Stewart et al. 2018). Ten percent of Australia’s native flora is in the family – or about 1,300 species. New Zealand is home to 27 native plants in the Myrtaceae family (Bereford et al. 2019) and the Hawaiian Islands to eight (JB Friday pers. comm.).  See a writeup about the disease here.

Austropuccinia psidii is one of the global invaders: it has invaded 27 countries on several continents. It is apparently native to parts of the American tropics.

Levels of worry rose considerably with the pathogen’s spread across the Pacific beginning with the detection in Hawai‘i in spring 2005. Additional introductions in the region were Japan in 2009; China in 2011; Australia, New Caledonia, and South Africa in 2013; and New Zealand in 2017.

The known host range currently exceeds 500 species in 86 genera – all in the Myrtaceae family. The pathogen has several strains or biotypes; the impact of the various biotypes on the various host species differs. Environmental factors also apparently affect disease.

[For my earlier discussions of threats to the unique Hawaiian flora, go here for dryland flora, here and here for more general discussions. I discuss National Park Service efforts – including in Hawai`i – here.]

There are several factors that militate against a political entity choosing to act:

1) Inherent Difficulty in Controlling Wind-Borne pathogen

In both Hawai`i and Australia, the rust spread rapidly once it was established outside of nurseries. In Hawai`i, it had spread to all the islands within a few months of its detection in spring 2005 (Loope and La Rosa 2008). In Australia, the rust was established in natural ecosystems throughout coastal New South Wales and to far northern Queensland by mid-2012 – less than two years after detection (Carnegie et al. 2016). The number of host species also expanded rapidly – from 214 native plants in 2016 (Carnegie et al. 2016) to 393 species by 2019 (Winzer et al. 2019). Myrtle rust is believed to have been carried to Australia and New Caledonia on imported plants or cut vegetation; then to New Zealand by winds from Australia across the Tasman Sea (Toome-Heller et al. 2020).

2) Lack of Clarity About Probable Impacts

Austropuccinia psidii had been introduced fairly widely before 2000, and some biotypes had caused significant damage on introduced species within both the native and introduced ranges of the rust – e.g., Eucalyptus in Brazil, allspice (Pimento doica) in Jamaica, rose apple (Syzygium jambos) in Hawai`i.  However, the rust had had little impact on native floras in introduced ranges, especially not on widespread species (Carnegie et al. 2016).

However, concerns existed in the Pacific region because of:

  • Its wide host range (before the introduction to Australia, the known host range was “only” 129 species in 33 genera Carnegie et al. 2016).
  • The severe damage to Australian genera growing outside their native range, e.g., nurseries and plantations of Eucalyptus in South America and Melaleuca quinquenervia and Rhodomyrtus tomentosa in Florida (Carnegie et al. 2016)

In Hawai`i, ‘ōhi‘a rust caused little damage to the dominant tree species in Hawaiian forests, ‘ōhi‘a lehua for the first 10 years after its introduction. The rust did cause severe damage to the invasive alien shrub rose apple and several native plants, especially the endangered Eugenia koolauensis. A more damaging outbreak in ‘ōhi‘a lehua trees in 2017 has increased concern.

ohia rust on E. kooaulensis
photo by Edward Eickhoff via Flickr

So – while Austropuccinia psidii has an extremely wide host range, its impact in naïve ecosystems to which it might be introduced is unclear.

In most cases, lack of knowledge about a pest’s impacts on naïve hosts in new ranges is almost inevitable – unless scientists undertake host vulnerability tests. Such tests are rarely done in advance of an introduction. One exception is European scientists evaluating European trees’ vulnerability to a suite of newly discovered Phytophthora species in Vietnam and elsewhere.  (I am unaware that U.S. scientists are carrying out parallel studies.)

Still, environmental and other factors play important roles and might counter expectations raised by lab experiments or experience of hosts planted in non-native sites. In Australia, McRae (2013) noted that the “mycological firestorm” predicted by environmentalists to result from introduction of the rust had not occurred. This at least partly explained waning interest in combatting the pathogen (Carnegie et al. 2016).

In my view, the swings in perceptions of the risk reflected more flaws in understanding than actual risk. Impacts can take time to manifest – especially when, as with Austropuccinia psidii – the pathogen is known to affect primarily new growth and fruit and flowers (Carnegie et al. 2016). The impact might be greatest in the form of suppressing regeneration rather than by killing mature trees right away. [See beech leaf disease as another possible example of this phenomenon.]

Questions hampering predictions of impact were further confused by taxonomic questions (Carnegie et al. 2016). Austropuccinia psidii has at least nine genetically distinct clusters. So far, two have been introduced outside South/Central America. One strain – called the “pandemic biotype” – has been found at all introduction sites in Florida, Hawai‘i, Asia, and the Pacific – Australia, New Zealand, New Caledonia (Stewart et al. 2018). This biotype is not known to be present in Brazil (Toome-Heller et al. 2020). A second biotype has been introduced to South Africa; it has been shown to be able to infect some Myrtaceae in New Zealand (Toome-Heller et al. 2020). See especially Stewart et al. 2017, full citation below.

3) Policy Barriers Created by Phytosanitary Regulations

In the U.S., the pathogen has been established in one state – Florida – since 1977. There, it is not considered to be causing damage to important species. Under U.S. regulations – reflecting the international trade rules – an organism that is already in the country cannot be treated as a “quarantine pest” unless there is an “official control program” targeting the pest. (For a discussion of this issue, see the analysis of the SPS Agreement in Chapter 3 and Appendix 3 of Fading Forests II). For this reason, when ‘ōhi‘a rust was detected in Hawai`i in 2005, USDA’s Animal and Plant Health Inspection Service (APHIS) was unable to adopt regulations governing imports or interstate movement of vectors (i.e., cuttings or nursery stock of plant species in the Myrtaceae).  

The State responded to the initial detection by adopting an emergency order two years later, in August 2007. This prohibited importation of plants in the myrtle family from “infested areas”- specified as South America, Florida, and California. This state rule expired in August 2008.

It became apparent that USDA APHIS would not take action to assist Hawai`i unless APHIS accepted  scientific findings as proving that additional biotypes of the rust existed that could pose a more severe threat to plants on the Islands. Such studies were undertaken, some funded by the USDA Forest Service.  This process took years. During this period, Hawai`i developed a permanent rule which was adopted in May 2020. This regulation restricts the importation to Hawai`i of plants in the Myrtaceae, including live plants and foliage used in cut flower arrangements. Dried, non-living plant parts, seeds that are surface sterilized, and tissue cultured plants in sterile media and containers are exempted from the ban. Other importations may be done by permit.

Meanwhile, in 2019, APHIS proposed to include all taxa in the Myrtaceae destined for Hawai`i in an existing regulatory category of “plants for planting” not authorized for importation pending pest risk assessment (NAPPRA). The intent was to reduce the probability of introduction of additional strains of Austropuccinia psidii to the Islands. This proposal appeared 14 years after the rust was first detected in Hawai`i. And the proposal has not yet taken effect. Therefore, imports of most living plants and cut foliage are still subject only to inspection (7 Code of Federal Regulations 319.37). The tiny size of the rust spores makes detection during inspection unlikely unless the plant is displaying symptoms of the disease.

Imports of logs and lumber involving tropical hardwood species (including Eucalyptus) into Hawai`i are regulated under separate provisions which have been in effect since 1995. The wood must be debarked or fumigated [Code of Federal Regulations – 7 CFR 319.40-5(c)]. Incoming wood packaging is regulated under ISPM#15; I think it unlikely that the treatments prescribed therein would kill any rust spores present.

Policy Responses in Other Vulnerable Countries

Australia

Austropuccinia psidii had been recognized as a potentially serious biosecurity threat to Australia as early as 1985 (publications cited by Carnegie et al. (2016). The introduction of ‘ōhi‘a rust to Hawai`i so alarmed plant health and conservation officials in Australia and New Zealand that they sent representatives half way around the world to participate in the North American Plant Protection Organization’s annual meeting in Newfoundland, Canada, in October 2007! Yet interest in Australia waned when large scale tree mortality and major impacts on industries did not immediately occur (Carnegie et al. 2016).  The state of New South Wales listed the rust as a Key Threatening Process to the Natural Environment, but the federal agencies rejected a petition to do the same at a national level (Carnegie et al. 2016).

Groups of scientists are carrying out research with the goal of demonstrating that the rust is already having severe effects on key species in natural ecosystems, and probably significantly affecting a wider range of species (Carnegie et al. 2016; Winzer et al. 2019; Winzer et al. 2020)

In 2018 a scientist affiliated with the Australian Network for Plant Conservation published a draft conservation plan.  Its development had input from staff at the Plant Biosecurity Cooperative Research Centre and the Australian Government Department of the Environment and Energy. The goal was to help direct and stimulate further research on critical questions and build awareness of the potentially devastating effects myrtle rust might have if it remains unchecked. As of April 2020, no funding had yet become available to finalize and implement the report (Dr Michael Robinson, Managing Director, Plant Biosecurity Science Foundation).

New Zealand

New Zealand has been more aggressive in its policy approach. It adopted a strategy when Australia announced arrival of the rust in 2010. The islands had bad luck – myrtle rust is believed to have been carried to New Zealand by wind from Australia across the Tasman Sea.

As soon as the rust was first detected in 2017, two government agencies initiated broad surveys of Myrtaceae across natural and urban areas, with active outreach to citizens (Toome-Heller et al. 2020).  By April 2018, it was recognized that the pathogen was too widespread to be eradicated. Significant finds were made on the western side of the North Island and at the very northern tip of the South Island (see map in Beresford et al. 2019). At that point, the government changed its focus to long-term management of the disease.

A. psidii is still very much a focus for Maori (indigenous) groups, central and local government, community groups, Myrtaceae-based industries, and research institutions.

Several research programmes are currently looking for management options, including resistance breeding (Toome-Heller et al. 2020). See research plan and reports of results to date here. However, which plant species can become infected, and under what environmental conditions, remain unclear.

New Zealand researchers have made some findings that should be of concern to forest pathologists working with all Myrtaceae:

  • A. psidii can overwinter as a latent infection without reproducing.
  • A. psidii can reproduce sexually, although the importance of the sexual cycle in seasonal epidemic development is not yet understood and teliospores have only infrequently been found in New Zealand (Bereford et al. 2019).
  • the unique biotype found in South Africa has already been found to be pathogenic towards some New Zealand native Myrtaceae  (Toome-Heller et al. 2020).

We can expect these finding to have implications for elsewhere, including in Hawaii.

Pathways of Introduction

It is thought probable that the rust was introduced to Hawai`i on cut foliage imported from Florida. The first Australian detection was at a cut flower facility (Australian Invasive Species Council).

CABI considers plants and plant parts (including cuttings, flowers, and germplasm) to be the principal pathway. Other pathways appear to be contaminated plant waste, timber, wood packaging and dunnage; and – over short distances – contaminated equipment and tools and clothing, shoes and other personal effects.

Conclusions

The saga of myrtle rust demonstrates both the biological and technical difficulties of controlling an airborne pathogen and the inability of the existing phytosanitary system to respond to new situations. Regulatory officials are obligated to demand levels of knowledge and certainty that just are not realistic. The gap is especially great at the crucial time – before an invasion or at its earliest stage — when phytosanitary actions might be most effective.

This saga also demonstrates that efforts often wane at the management and restoration stages. At least in Hawai`i and New Zealand, government resources are still being allocated to research possible resistance breeding or other possible long-term approaches. I refer you to the article by Enrico Bonello, me, and others about the need to provide sufficient resources to such efforts in the U.S.

Sources

Australian Invasive Species Council.2011. www.invasives.org.au Environmental impacts of myrtle rust Fact Sheet February 2011

Beresford, R., G. Smith, B. Ganley and R. Campbell. 2019. Impacts of myrtle rust in NZ since its arrival in 2017. 2019. New Zealand Garden Journal 2019, Vo. 22 (2).  https://www.myrtlerust.org.nz/assets/news/NZ-Garden-Journal-Dec-2019-p5-10.pdf

Bonello, P. , F.T. Campbell, D. Cipollini, A.O. Conrad, C. Farinas, K.J.K. Gandhi, F.P. Hain, D. Parry, D.N. Showalter, C. Villari, and K.F. Wallin. 2019.  Invasive tree pests devastate ecosystems – A proposed new response framework. Frontiers  http://journal.frontiersin.org/article/10.3389/ffgc.2020.00002/full?&utm_source=Email_to_authors_&utm_medium=Email&utm_content=T1_11.5e1_author&utm_campaign=Email_publication&field=&journalName=Frontiers_in_Forests_and_Global_Change&id=510318

Carnegie, A.J., A. Kathuria, G.S. Pegg, P. Entwistle, M. Nagel, F.R. Giblin. 2016. Impact of the invasive rust Puccinia psidii (myrtle rust) on native Myrtaceae in natural ecosystems in Australia. Biological Invasions (2016) 18:127–144

Code of Federal Regulations. January 1, 2005 (Title 7, Volume 5). 7 CFR319.40-5: Logs, lumber, and other unmanufactured wood articles – importation and entry requirements for specified articles. (available by using search engines/retrieval services at http://www.gpoaccess.gov/fr/index.html).

Code of Federal Regulations. January 1, 2005 (Title 7, Volume 5). 7 CFR319.37: Nursery stock, plants, roots, bulbs, seeds, and other plant products – prohibitions and restrictions on importation: disposal of articles refused importation. (available by using search engines/retrieval services at http://www.gpoaccess.gov/fr/index.html).

Loope, L. and A.M. La Rosa. 2008. An Analysis of the Risk of Introduction of Additional Strains of the Rust Puccinia psidii Winter (`Ohi`a Rust) to Hawa`i.  Pacific Island Ecosystems Research Center

Stewart, J. E., A. L. Ross-Davis, R. N. Graça, A. C. Alfenas, T. L. Peever, J. W. Hanna, J. Y. Uchida, R. D. Hauff, C. Y. Kadooka, M.-S. Kim, P. G. Cannon, S. Namba, S. Simeto, C. A. Pérez, M. B. Rayamajhi, D. J. Lodge, M. Agruedas, R. Medel-Ortiz, M. A. López-Ramirez, P. Tennant, M. Glen, P. S. Machado, A. R. McTaggart, A. J. Carnegie, and N. B. Klopfenstein. 2018. Genetic diversity of the myrtle rust pathogen (Austropuccinia psidii) in the Americas and Hawaii: Global implications for invasive threat assessments. Forest Pathology 48(1): 1-13. https://doi.org/10.1111/efp.12378

Toome-Heller, M. W.W.H. Ho, R.J. Ganley, C.E.A. Elliott, B. Quinn,  H.G. Pearson, B.J.R. Alexander. 2020. Chasing myrtle rust in New Zealand: host range and distribution over the first year after invasion. Australasian Plant Pathology

Winzer, L.F., K.A. Berthon, A.J. Carnegie, G.S. Pegg, M.R. Leishman. 2019. Austropuccinia psidii on the move: survey based insights to its geographical distribution, host species, impacts and management in Australia. Biological Invasions April 2019, Volume 21, Issue 4, pp 1215–1225

Winzer, L.F., K.A. Berthon, P. Entwistle, A. Manea, N. Winzer, G.S. Pegg, A.J. Carnegie, M.R. Leishman. 2020. Direct and indirect community effects of the invasive plant pathogen Austropuccinia psidii (myrtle rust) in eastern Australian rainforests. Biological Invasions. Volume 22, pages2357–2369 (2020)

Outrageous – Asian longhorned beetle Appears Again – Will US Respond Appropriately?

Here we go again … another Asian longhorned beetle population established in the U.S.

For the ninth time in 24 years, the Asian longhorned beetle (ALB) has been found in North America – this time in South Carolina.

This means thousands – perhaps tens of thousands – of trees will be removed. Thousands more will be injected with imadacloprid. Millions of dollars will be spent. There will be uncounted aesthetic and spiritual losses. There will be unmeasured damage to at least the local environment – which probably includes bottomland hardwood forests – protection of which South Carolina has declared to be a conservation priority. All this destruction is necessitated by the need to prevent catastrophic damage to North America’s hardwood forests by the ALB.

By early August I have learned that the South Carolina outbreak has been present for seven years or longer, and that it might be related to the Ohio outbreak (which was detected in 2011 but was probably introduced at least four years earlier). APHIS reports that, as of the end of July, nearly 1,300 infested trees had been detected. The area around the neighborhood where the detection was made is swampy – complicating search and removal operations and probably home to many box elder and willows – preferred hosts for the ALB.

Why did we let this happen? Why do we persist with a policy that has allowed repeated introductions of this pest via the well-documented wood packaging pathway? After all, we learned about this risk 22 years ago – after the ALB introductions to New York and Chicago. We have had plenty of evidence that the policy is failing. We know how to stop this. Why do we – through our elected and appointed government officials – not act to prevent it?

What We Need: a New, Protective Policy

With live pests continuing to be present in wood packaging 14 years after the U.S. and Canada imposed the treatment requirements in ISPM#15 – and 21 years after we required China to treat its wood packaging – we urgently need better federal policy. I have long advocated:

  • USDA APHIS join Bureau of Customs and Border Protection in penalizing violators for each violation; stop allowing five violations over a 12-month period before applying a penalty.
  • APHIS and the Canadian Food Inspection Agency (CFIA) should apply their rights under Section 5.7 of the World Trade Organization Sanitary and Phytosanitary Agreement to immediately prohibit China from packaging its exports in wood. China can use crates and pallets made from such alternative materials as plastic, metal, or oriented strand board.
  • APHIS and CFIA should being the process of supporting permanent application of this policy to China and other trade partners with poor compliance records. This step would require that they cite the need for setting a higher “level of protection” and then prepare a risk assessment to justify adopting more restrictive regulations.
  • USDA Foreign Agriculture Service (FAS) should assist U.S. importers to determine which suppliers reliably provide wood packaging that complies with ISPM#15 requirements.
  • USDA FAS and APHIS should help importers convey their complaints about specific shipments to the exporting countries’ National Plant Protection Organizations (NPPOs; departments of agriculture).
  • APHIS should increase pressure on foreign NPPOs and the International Plant Protection Convention more generally to ascertain the reasons ISPM#15 is failing and to fix the problems.
  • APHIS should fund more studies and audits of wood packaging to document the current efficacy of the standard, especially
    • Update the Haack study of pest approach rate.
    • Determine whether high rates of pest infestation of wood bearing the ISPM#15 mark results from fraud or failures of treatment – and whether any failures are due to mistakes/misapplication or shortcomings in the treatment themselves.
    • Allocate the risk among the three major types of wood packaging: pallets, crates, and dunnage. 

These folks work for us – tell them to protect our forests!

See also the recommendations of the Tree-Smart Trade program at www.tree-smart-trade.org

Tree-Smart also has a Twitter account: @treeSMARTtrade

Justification

The ALB poses a threat to 10% of US forests and nearly all of Canada’s hardwoods, so eradication of the South Carolina outbreak is essential. For a longer discussion of ALB introduction history, the threat, and eradication efforts to date, visit here. https://www.dontmovefirewood.org/pest_pathogen/asian-long-horned-beetle-html/).

Another ALB Outbreak in the US: No Surprise

This Chinese insect is a world traveler. It has been detected 36 times outside its natural range: in North America, Europe, and Japan. Seventeen of these outbreaks have been detected since 2012 (Eyre & Haack 2017). These 17 introduction have occurred six years or later after the 2006 implementation of the International Standard for Phytosanitary Measures (ISPM) #15 – which was intended to reduce the likelihood of such introductions. .Ten of the outbreaks have been eradicated (Eyre & Haack 2017; APHIS press release October 2019).  This includes four in the United States and Canada; see here.

Despite U.S. and international efforts, ALB and related pests have been detected continuously in imported goods. U.S. and European data (Eyre and Haack 2017) document rising numbers of Cerambycids detected in wood packaging in recent years. (For a description of pest prevention efforts, see Fading Forests II and III here and this blog).

It is also not surprising that the newly introduced pest is from China. It has long been among countries with the worst records on implementing ISPM#15. 

The APHIS-CBP joint study of pest interceptions over the period 2012 – 2017 (Krishnankutty et al. 2020b) found the highest numbers of interceptions came from Mexico, China, and Turkey. During the period 2011 – 2016, China accounted for 11% of interceptions (APHIS interception database – pers. comm. January 2017).

These numbers reflect in part the huge volumes of goods imported from China. But China’s poor performance has continued, perhaps even increased in recent years. For example, consider the choice of wood used to manufacture packaging. Authorities recognized by the late 1990s that wood from plantations of Populus from northern China was highly likely to be infested by the Asian longhorned beetle. Yet, more than a dozen years later, this high-risk wood was still being used: between 2012 and 2017, the ALB was intercepted six times in wood packaging made of Populus wood – each time originating from a single wood-treatment facility in China (Krishnankutty et al. 2020b).

The location just outside Charleston also is not a surprise. Charleston ranked seventh in receipt of incoming shipping containers in 2018. Charleston received 1,022,000 containers, or TEUs measured as 20-foot equivalents, in 2018 (DOT report). This was a 14% increase over the 894,000 TEUs in 2017 http://www.marad.dot.gov/MARAD_statistics/index.html – click on “trade statistics”, then “US Waterborne trade” (1st bullet).  I expect decreased import volumes in 2019 and 2020 due to the tariffs/trade war and the 2020 economic crash linked to the Covid-19 virus.

Why US and International Policy Still Fails

Leung et al. (2014) estimated that implementation of the International Standard of Phytosanitary Measures (ISPM)#15 resulted in only a 52% reduction in pest interceptions. They concluded that continued implementation at the 2009 level of efficacy could triple the number of wood borers established (not just intercepted) in the U.S. by 2050.

Since 2010 the Department of Homeland Security’s Bureau of Customs and Border Protection (CBP) has found an average of 794 shipments infested by pests each year (Harriger). In 2019 specifically, live pests were found in 747 shipments (Stephen Brady, CBP, April 2020). These violations were occurring four to 13 years after the U.S. began implementing ISPM#15 in 2006. According to my calculations, based on estimates of pest approach rates by Haack et al. (2014), these detections probably represented about eight percent of the total number of infested shipments entering the country each year.

And there are good reasons to think this estimate is low. First, Haack et al. (2014) did not include imports from China, Canada, or Mexico in their calculations. Both China and Mexico rank high among countries with poor compliance records. Second, Haack and Meissner based their calculations on 2009 data – 11 years out of date. Since 2009, ISPM#15 has been amended to make it more effective. The most important change was restricting the size of bark remnants that may remain on wood. Also, countries and trading companies have 11 more years of implementation – so they might have improved their performance. I have asked several times that APHIS commission a new analysis of Agriculture Quarantine Inspection Monitoring data. We all need an up-to-date determination of the pest approach rate, not only before but also after the CBP action. Without it, there’s no evidence whether the more aggressive enforcement stance CBP adopted in 2017 (see below) has led to reductions in non-compliant shipments at the border.

Another demonstration of the failure of ISPM#15 is the repeated presence of the velvet longhorned beetle (Trichoferus (=Hesperophanes) campestris) in wood packaging and its establishment in at least three states (Krishnankutty, et al. 2020a; also see the discussion in my recent blog here).

Astoundingly, data indicate that 97% of wood packaging infested with pests bears the stamp certifying that the wood has been treated according to the requirements of ISPM#15 – and hence should be pest-free (Eyre et al. 2018; CBP interception data). In other words, the presence of the stamp is not a reliable indicator of whether the wood has indeed been treated nor that it is pest-free. Scientists have speculated for years why this is the case. ALB’s new arrival provides an impetus to finally answer this question and to ensure policy reflects the answer.

What Federal Agencies Are Doing to Better Prevent Introductions

In contrast to such a comprehensive approach, this is what changes are under way.

CBP strengthened its enforcement in November 2017. The agency’s total “enforcement actions” increased by 400% from 2017 to 2018 (Sagle, pers. comm). The 2019 data show decreases, in absolute numbers, from earlier years in all categories: a 19% decrease below 2010-2018 in average number of shipments intercepted; a 13% decrease in number of shipments intercepted because the wood packaging lacked the ISPM#15 mark; and a decrease of 6% in the number of shipments intercepted that had a quarantine pest (Stephen Brady, CBP, April 2020). However, one year of interception data do not provide a basis for saying whether CBP’s stronger enforcement has resulted in a lower number of shipments in violation of ISPM#15 approaching our shores. Again, I call for APHIS to repeat Haack et al. (2014) study.

Harriger reported that CBP is also trying harder to educate importers, trade brokers, affiliated associations, CBP employees, and international partners about ISPM#15 requirements. CBP wants to encourage them to take actions to reduce all types of non-compliance: lack of documentation, pest presence in both wood packaging and shipping containers, etc.

APHIS has not altered its long-standing policy of allowing an importer to rack up five violations over a 12-month period before imposing a penalty. Instead, APHIS has focused on “educating” trade partners to encourage better compliance. For example, APHIS worked with Canada and Mexico – through the North American Plant Protection Organization — to sponsor workshops for agricultural agencies and exporters in Asia and the Americas

APHIS also planned to host international symposia on wood packaging issues as part of events recognizing 2020 as the International Year of Plant Health. These symposia have been postponed by travel and other restrictions arising from the coronavirus pandemic.

The Broader Significance of Continuing Wood Packaging Problems

The premise of the international phytosanitary system – the Agreement on the Application of Sanitary and Phytosanitary Standards (SPS Agreement) and the International Plant Protection Convention (IPPC) – is that importing countries should rely on exporting countries to take the actions necessary to meet the importing countries’ plant health goals. The ISPM#15 experience undermines the very premise of these international agreements.

If we cannot clean up the wood packaging pathway – which involves boards or logs that are, after all, already dead – it bodes poorly for limiting pests imported with other commodities that are pathways for tree-killing pests – especially living plants (plants for planting). Living plants are much more easily damaged or killed by phytosanitary measures, so ensuring pest-free status of a shipment is even more difficult.  (A longer discussion of the SPS Agreement and IPPC is found in Chapter III of Fading Forests II, available here.

SOURCES

Eyre, D., R. Macarthur, R.A. Haack, Y. Lu, and H. Krehan. 2018. Variation in Inspection Efficacy by Member States of SWPM Entering EU. Journal of Economic Entomology, 111(2), 2018, 707–715)

Haack RA, Britton KO, Brockerhoff EG, Cavey JF, Garrett LJ, et al. (2014) Effectiveness of the International Phytosanitary Standard ISPM No. 15 on Reducing Wood Borer Infestation Rates in Wood Packaging Material Entering the US. PLoS ONE 9(5): e96611.

Kevin Harriger, US CBP. Presentations to the annual meetings of the Continental Dialogue on Non-Native Forest Insects and Diseases over appropriate years. See, e.g., https://continentalforestdialogue.org/continental-dialogue-meeting-november-2018/

Krishnankutty, S.M., K. Bigsby, J. Hastings, Y. Takeuchi, Y. Wu, S.W. Lingafelter, H. Nadel, S.W. Myers, and A.M. Ray. 2020a. Predicting Establishment Potential of an Invasive Wood-Boring Beetle, Trichoferus campestris (Coleoptera:) in the United States. Annals of the Entomological Society of America, XX(X), 2020, 1–12

Krishnankutty,  S., H. Nadel, A.M. Taylor, M.C. Wiemann, Y. Wu, S.W. Lingafelter, S.W. Myers, and A.M. Ray. 2020b. Identification of Tree Genera Used in the Construction of Solid Wood-Packaging Materials That Arrived at U.S. Ports Infested With Live Wood-Boring Insects. Commodity Treatment and Quarantine Entomology

Leung, B., M.R. Springborn, J.A. Turner, E.G. Brockerhoff. 2014. Pathway-level risk analysis: the net present value of an invasive species policy in the US. The Ecological Society of America. Frontiers of Ecology.org

Meissner, H., A. Lemay, C. Bertone, K. Schwartzburg, L. Ferguson, L. Newton. 2009. Evaluation of Pathways for Exotic Plant Pest Movement into and within the Greater Caribbean Region. Caribbean Invasive Species Working Group (CISWG) and USDA APHIS Plant Epidemiology and Risk Analysis Laboratory

USDA APHIS interception database – pers. comm. January 2017.

USDA APHIS press release dated September 12, 2018

U.S. Department of Agriculture, Press Release No. 0133.20, January 27, 2020

U.S. Department of Transportation, Maritime Administration, U.S. Waterborne Foreign Container Trade by U.S. Customs Ports (2000 – 2017) Imports in Twenty-Foot Equivalent Units (TEUs) – Loaded Containers Only at https://ops.fhwa.dot.gov/freight/freight_analysis/nat_freight_stats/docs/06factsfigures/fig2_9.htm and

US Department of Transportation. Port Performance Freight Statistics in 2018 Annual Report to Congress 2019  https://rosap.ntl.bts.gov/view/dot/43525

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.

Calamity in Pacific Island Forests

Cycas micronesica
photo by A. Gawel

We know the dire threats to Hawaiian forests from pathogens. Some threaten the most widespread tree – ohia. Others are insects threatening trees and shrubs in the remnant dryland forests.

The forests of smaller islands of the Pacific also appear to be facing severe threats – although I have been unable to find information on the current situation.

Guam and its Neighbors

The forests of Guam, Palau, and others in the Western Pacific are among those threatened.

They are geographically isolated and hard to reach, but that distance has not protected them from biological invaders. Their predicament illustrates the dominant role of global movement and trade in spreading pests. In this case, it’s mostly trade in ornamental plants.

These islands have unique flora and fauna. And true to invasive species experts’ expectations, they are vulnerable to bioinvaders. Guam’s most famous invasive species is the brown tree snake (Boiga irregularis), which over a few decades eradicated many bird species and the only native terrestrial mammal, the fruit bat.  

Less known, but equally damaging, have been a group of insects that are decimating Guam’s native forest flora.

The most widespread arboreal species in the forests of Guam and neighboring islands is the Micronesian cycad, Cycas micronesica. Its range is Micronesia, the Marianas Group including Guam and Rota Islands; and several of the western Caroline Islands, e.g., Palau and Yap (Marler, Haynes, and Lindstrom 2010).

These forests have already absorbed severe habitat destruction as the sites of fierce fighting in World War II and – in some cases – construction of large military bases. Still, cycads were the most common species in the forest as late as 2002 (Moore, A., T. Marler, R. Miller, and L. Yudin. Date uncertain).

The Worst Pest: Asian Cycad Scale

The most severe current threat to the cycads are introduced insects, especially the Asian cycad scale Aulacaspis ysumatsui.

The cycad scale is native to Southeast Asia. It was first detected on Guam in 2003, when officials noticed that cycads planted near hotels had begun to die. However, this scale had already been spreading thanks to the trade in ornamental cycads. It was detected in Florida in 1996, on Hawai`i in 1998. It continued to spread rapidly in the western Pacific: to Rota in 2007, Palau in 2008 (University of Guam 2012). By late 2019, the scale had spread globally – numerous islands and neighboring mainland areas in the Caribbean (including Puerto Rico and US Virgin Islands), several US states in the Southeast,  California, and Taiwan (Moore, Marler, Miller, and Yudin. Date uncertain.) and South Africa.  (van­Wilgen, et. al. 2020) Also, see the map prepared by CABI.

In every case, the scale has apparently been spread on nursery stock. It is difficult to contain by standard phytosanitary measures – visual inspection – because the scale is tiny and hides deep in the base of the plant’s stiff leaves and other crevices. (Marler and Moore 2010)

By 2005 the scale was killing the native cycad on Guam. Within four years, the millions of C. micronesica on Guam were reduced by more than 90% (Marler, T.E. and K.J. Niklas. 2011). The last time cycads on Guam reproduced in any significant number was in 2004 (Marler and Niklas 2018).

The severe impact of the scale was so rapid that the International Union for Conservation of Nature and Natural Resources (IUCN) changed its listing of C. micronesica from “near threatened” in 2003 to “endangered” in 2006. (IUCN Red List of Threatened Species Online 2008).

Scientists have made several attempts to introduce a biocontrol agent. However, the most promising – the lady beetle Rhyzobius lophanthae – has failed to control the scale, despite having become virtually ubiquitous on Guam. The beetle is too big to reach the significant proportion of scale insects living in small cracks and voids within the plant structures. Evidence from another cycad species indicates that the beetles also don’t prey on scale insects living beneath trichomes (fine hairlike structures on the leaves) or on parts of the plant close to the ground. (Moore, Marler, Miller, and Yudin. Date uncertain.).

Attempts to introduce a second biocontrol organism – the parasitoid wasp Aphytis lignanensis – were stymied by the presence of R. lophanthae (Moore, Marler, Miller, and Yudin. Date uncertain).

Micronesian cycad
photo by Lauren Gutierrez

Other Invasive Species Attacking Cycads

The cycad blue butterfly (Chilades pandava) was detected in 2005 and spread throughout Guam within months (IUCN 2009). Also, it’s been found on Saipan (1996) and Rota (2006). The butterfly is native to southern Asia from Sri Lanka to Thailand and Indonesia. High populations can cause complete defoliation of new foliage. Repeated defoliations can kill the plant. Cycads on Guam are particularly vulnerable because the scale has already caused loss of most of their leaves. Butterfly larvae are often protected by ants (Anonymous).

On cultivated plants the butterfly can be controlled by microbial insecticides containing Bacillus thuringiensis kurstaki (Moore). Scientists at the University of Guam are exploring use of injected insecticides (Moore). They have found an egg parasite, but parasitism levels are low. Any biocontrol agent targetting larvae would have to contend with the ants (Anonymous).

A longhorned beetle (Dihammus (Acalolepta) marianarum) and a snail (Satsuma mercatorius) are also feeding on the cycads (Marler 2010).

The Indo-Malayan termite Schedorhinotermes longirostris was detected in 2011. The termites weaken the cycad stems, which are then toppled by feeding by introduced deer. The termites are also damaging the cycad’s reproductive structures (megastrobili). Termite attacks on cycads surprised scientists since cycads do not form true wood. The termite had probably been introduced recently because, as of 2011, it had been detected only near the Andersen Air Force Base airport (Marler, Yudin, and Moore 2011).

More Isolated – but Still Overrun

Scattered across the Pacific are groups of atolls, including Palmyra and Rose.

Despite their distance from other islands, they have all been visited by mariners for centuries. As a result, they have non-native species, including insects that attack trees.

Pisonia tree forest – Wikimedia

The tree most affected is pisonia – Pisonia grandis. 

The principal insect is another scale, Pulvinaria urbicola. There are some reports that the scale is farmed by ants; species mentioned include several introduced species such as the yellow crazy ant, Paratrechina longicornis.

The scale is probably from the West Indies. Once it reached the Pacific, it might have been distributed to additional islands on seabirds, which travel long distances between the atolls.

The scale’s impact is unclear.

At first, in the mid-2000s, impacts seemed dire. It was reported to be causing widespread tree death on Palmyra and Rose atolls, islands around northeastern Australia, in the Seychelles, and possibly in Tonga.

However, in 2018, scientists reported that eradication of rats on Palmyra Atoll had resulted in an immediate spurt of reproduction of a tree. Numbers of “native, locally rare tree” seedlings (possibly but not explicitly said to be Pisonia grandis) jumped from 140 pre-eradication to 7,756 post-eradication (in 2016). The study made no mention of the scale.

Rose Atoll has only one small island (6.6 ha) with vegetation. Before 1970, it was dominated by Pisonia grandis, but by 2012, there were only seven trees on the island. Several possible causes of this decline have been suggested. Other than the scale, suggested causes include storms, drought, rising sea level / saltwater incursion, and imbalance of bird guano-derived nutrients in the soil. [All information about Rose Atoll is from Peck et al., 2014)

A survey carried out in April 2012 and November 2013 detected 73 species of arthropods from 20 orders on Rose Island, including nine ant species (all but one non-native). Two of these ants – Tetramorium bicarinatum and T. simillimum – were detected tending the scales on Pisonia.

The survey found no evidence of natural enemies of the Pulvinaria scales.

The scientists tested treatment of Pisonia with the systemic insecticide imidacloprid. This treatment apparently reduced scale populations considerably for several months, but then they began to build up again.

In contrast to Palmyra, Polynesian rats (Rattus exulans) were eliminated from Rose Atoll in 1990–1991 – so their role in destroying the trees had ended 20 years before the study. What does the continued decline of the Pisonia trees in subsequent decades suggest for the future of Pisonia trees on Palmyra?

I have sought updates on the tree-pest situations on Guam and the other Pacific islands, but my queries have not received a reply.

SOURCES

Anonymous. 2015. Cycad blue butterfly fact sheet.

Brooke, USFWS, pers. comm. June 3, 2005

CABI November 2019. Aulacaspis yasumatsui (cycad aulacaspis scale (CAS)) or the Asian cycad scale. https://www.cabi.org/isc/datasheet/18756   (was formerly Commonwealth Agricultural Bureaux (CAB) International; now apparently just uses acronym)

Marler, T.E. pers. comm. August 15, 2012

Marler, T.E. 2010. Cycad mutualist offers more than pollen transport. American Journal of Botany, 2010; 97 (5): 841. Viewed as materials provided by University of Guam, via EurekAlert; accessed 6 August, 2012.

Marler, T., Haynes, J. & Lindstrom, A. 2010. Cycas micronesica. The IUCN Red List of Threatened Species 2010: e.T61316A12462113. http://dx.doi.org/10.2305/IUCN.UK.2010-3.RLTS.T61316A12462113.en Accessed 22 April, 2020.

Marler, T.E., and A. Moore. 2010. Cryptic Scale Infestations on Cycas revoluta Facilitate Scale Invasions. HortScience. 2010; 45 837-839. Retrieved August 6, 2012 from www.eurekalert.org

Marler, T.E., L.S. Yudin, A. Moore. 1 September 2011. Schedorhinotermes longirostris (Isoptera: Rhinotermitidae) on Guam Adds to Assault on the Endemic Cycas micronesica.   https://bioone.org/journals/florida-entomologist/volume-94/issue-3/024.094.0339/Schedorhinotermes-longirostris-Isoptera–Rhinotermitidae-on-Guam-Adds-to-Assault/10.1653/024.094.0339.full

Marler, T.E. and K.J. Niklas. 2011. Reproductive Effort and Success of Cycas micronesica K.D. Hill Are Affected by Habitat. International Journal of Plant Sciences, 2011; 172 (5): 700. Viewed as materials provided by University of Guam, via EurekAlert; accessed 6 August, 2012.

Moore, A. Cycad blue butterfly fact sheet. http://www.guaminsects.net/gisac2015/index.php?title=Cycad_blue_butterfly_fact_sheet accessed 20-4/24

Moore, A., T. Marler, R. Miller, and L. Yudin. Date? Biological Control of Cycad Scale, Aulacaspis yasumatsui, Attacking Guam’s Endemic Cycad, Cycas micronesica. Western Pacific Tropical Research Center University of Guam. Powerpoint  http://guaminsects.myspecies.info/sites/guaminsects.myspecies.info/files/CycadScaleBiocontrolAustin.pdf

Peck, R., P. Banko, F. Pendleton, M. Schmaedick, and K. Ernsberger. 2014. Arthropods of Rose Atoll with Special Reference to Ants and Pulvinaria urbicola scales (Hemiptera: Coccidae) on Pisonia grandis trees. Hawaii Cooperative Studies Unit. University of Hawaii. Technical Report HCSU-057 December 2014

University of Guam (2012, August 2). Invasive insects cause staggering impact on native tree. ScienceDaily. Retrieved August 6, 2012, from www.sciencedaily.com-/releases/2012/08/120803094527.htm).

 van­Wilgen, B.W.,J. ­Measey, D.­M. ­Richardson, J.R. ­Wilson,  T.A. Zengeya­. Editors. 2020. Bioinvasions in South Africa. Invading Nature. Springer Series in Invasion Ecology 14.

Posted by Faith Campbell

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

For a detailed discussion of the policies and practices that have allowed these pests to enter and spread – and that do not promote effective restoration strategies – review the Fading Forests report at http://treeimprovement.utk.edu/FadingForests.htm These reports do not include details on the pest situation on the Pacific islands (including Hawai`i).

Serious Invasive Species Damage to High-Elevation Sites in the West

Dream Lake, Rocky Mountain National Park, with limber pine
photo by F.T. Campbell

In this blog, I summarize two pest threats to the unique ecosystems on high-elevation mountain ridges in the West. At risk are several keystone tree species: the five-needle pines growing at high elevations (“high-five” pines) and subalpine fir. The invasive species causing this damage – white pine blister rust (WPBR; Cronartium ribicola) and balsam woolly adelgid (BWA; Adelges piceae) – are two of the most widespread non-native species threatening North American trees and affecting the highest proportion of host volumes (Morin).

The pines being killed by white pine blister rust are whitebark pine (Pinus albicaulis), limber pine (P. flexilis), Rocky Mountain bristlecone pine (P. aristata), foxtail pine (P. balfouriana), and southwestern white pine (P. flexilis var. reflexa). As of 2010, infestations had not been reported on Great Basin bristlecone pine (P. longaeva) and the Mexican white pine species. [Unless otherwise indicated, information on white pine blister rust is from a comprehensive review and synthesis published in the August 2010 issue of Forest Pathology (Vol. 40:3-4).]

As noted above, sub-alpine fir (Abies lasiocarpa) is also being affected – although less uniformly than the pines – by the balsam woolly adelgid.

Both of these pests arrived approximately a century ago, but they are still spreading and causing additional damage. White pine blister rust had spread widely throughout the West within 40 years of its introduction. Meanwhile, BWA spread among lowland and subalpine firs along the Pacific coast from California to British Columbia within 30 years of its first detection. Its spread eastward was slower, but relentless. It reached Idaho, Montana, Utah and interior British Columbia within 50 years.  Also, BWA reached Alaska within 90 years of its introduction in California. These pests are perfect examples of how invasive species introduced long ago are dreaded “gifts that keep on giving”.

For a detailed discussion of these pests’ impacts, see the descriptions posted here. To summarize, though, WPBR is present in the ranges of eight of the nine vulnerable western white pines and has caused severe mortality to some species (Sniezko et. al. 2011). For example, 88% of the limber pine range in Alberta is affected (Dawe et al. 2020). WPBR is generally causing more damage to its hosts’ northern populations. Impact of the BWA are more subtle than WPBR. Also, impacts’ severity is linked to climatic conditions. For example, measurable decline on the Olympic Peninsula was greater on south-facing slopes. However, the study did not determine whether this reflected heat-loading and tree stress or more abundant subalpine fir on these slopes. An estimated 19-53% (average 37%) of subalpine fir trees had died on sample plots on one ridge over the 19 years since BWA was first detected there. Overall forest growth after 2007 could indicate partial recovery, a momentary pause in BWA invasion, or tree growth after severe weather events (Hutton 2015).

Ranges of Trees at Risk

Many of the host trees of these two pests are widespread; others are more narrowly endemic.

Limber pine reaches from Alberta and British Columbia south to mountain peaks in Arizona and New Mexico. Whitebark pine is found from Alberta and British Columbia to California and Nevada (USDA Plants database. Subalpine fir stretches from southeast Alaska along the Canadian Rockies coast into Washington, Oregon, east into Idaho, Montana, Wyoming, Colorado, Utah, even into scattered mountain ranges of Nevada and New Mexico (Hutton 2015).

Limber pine and subalpine fir are also found in a wide range of ecosystems within these ranges. Limber pine is found at both upper and lower tree lines in grassy, open forests; on exposed rocky slopes; and in dense, mixed-conifer stands. Subalpine fir is a pioneer species on ridges, alpine meadows, avalanche chutes, and lava beds (Ragenovich and Mitchell, 2006).

Before arrival of non-native pests or pathogens, these tree species have persisted for thousands of years under harsh conditions (Hutton 2015). Many of the individual trees were long-lived; some five-needle pines, e.g., bristlecone pines, have famously live for thousands of years. Core studies demonstrated that subalpine firs trees could live 272 years in the forests of Olympic National Park and 240 years in Glacier National Park (Hutton 2015). Surely loss of these trees – or even their conversion from large and old to small and short-lived – will result in significant destruction of these unique biomes.

All these trees play important roles in high altitude, unique ecosystems (Pederson et al. no date; Dawe 2020; Hutton 2015):

  • They retain ground water, slow the rate of snow melt, and maintain stream flow characteristics and water quality;
  • They curtail soil erosion and maintain slope stability; and
  • They provide high-value food and shelter to wildlife.

Whitebark and limber pines are famous for providing critical food for many wildlife species at high elevations —notably bears and nutcrackers (Compendium and Dawe 2020).   

More Pest Threats

Other diseases, insects, and disturbances also pose serious threats to these tree species. The threats vary by region and age of the stand. They include – for the pines — mountain pine beetle (Dendroctonus ponderosae), dwarf mistletoe (Arceuthobium spp.), and various shoot, cone or foliage insects and pathogens. For subalpine fir, threats include western balsam bark beetle (Dryocoetes confusus), fir engraver (Scolytus ventralis), and the fir root bark beetle (Pseudohylesinus granulatus) (Hutton 2015). Trees are also damaged by bear and deer, seed predation by squirrels, wildfire, and biotic succession.

On Washington’s Olympic Peninsula, BWA initiates or predisposes subalpine fir for a novel disturbance complex. BWA-caused stress makes the trees more susceptible to moisture stress and endemic bark beetle attack. Surviving trees are subsequently subject to toppling by wind. A tree can die in a few years, survive with insects for up to 20 years, or recover, depending on duration, severity, and location of infestation, and local environmental conditions (Hutton 2015).

BWA study plots in the Cascade Range experienced subalpine fir mortality ranging from 7 to 79% (measured as stem counts, not basal area) over a 19 to 38 years study period. Higher mortality occurred at low-elevation, mesic sites. One stand experienced 40% mortality in 19 years, but lost the remaining 60% during a subsequent spruce budworm infestation. Most plots continued to show sporadic signs of adelgid presence and continued tree mortality. However, 41-69% of trees survived stem infestations (Hutton 2015).

How to Protect These Ecosystems

The seeds of both whitebark and limber pines are dispersed to newly disturbed, open areas by Clark’s nutcracker (Nucifraga columbiana). Furthermore, whitebark cones open to release seeds only after fire. This had led to expectations that prescribed fire could promote regeneration of these species. However, studies by Dawe (2020) and other have found that nutcracker seed caching behavior and seedling establishment are complex. Fire management might have to vary among regions, demanding consideration of stand characteristics,like openness and the presence of other tree species. For example, in the Colorado Front Range, limber pine can be replaced by subalpine fir when fire-free intervals are long. On the other hand, in Alberta, fire appeared to boost regeneration of the dominant tree species in the stands pre-fire. In the study areas, these were white spruce (Picea glauca) and lodgepole pine (Pinus contorta) (Dawe 2020).  Dawe recommends protecting existing stands of limber pine through fire mitigation efforts, e.g., thinning and other fuel treatments, and supplementary planting of seedlings.

Efforts to find biocontrol agents to target the balsam woolly adelgid began in 1957; the original focus was on the insects’ damage to Fraser fir (Abies fraseri) in the southern Appalachians.  More than 25 predatory species have been introduced from Europe and Asia. There was simultaneous research on native predators. None has had an impact on BWA populations in either the East or the West.

Neither white pine blister rust nor balsam woolly adelgid is considered a quarantine pest by federal officials, so there is no attempt to prevent their movement via interstate trade in Christmas trees, timber, or nursery stock. Hutton (2015) hypothesizes that the absence of regulatory measures targetting BWA arises from the pest’s gradual effect and the hosts’ not being commercially important as timber species (although several firs are important in horticulture and as Christmas trees). I think another factor is that the pests were introduced so long ago and are now widespread.

Efforts are under way to detect resistant genotypes to be used in breeding programs. Several of the lower-elevation five-needle pines vulnerable to WPBR have benefitted from extensive breeding efforts Whitebark pine has more recently been added to programs.

The eastern Fraser fir is the target of breeding – primarily for Christmas trees (APS). However, at least small-scale volunteer efforts have been carried forward by the Alliance for Saving Threatened Forests.

Hutton (2015) expresses hope that evolutionary pressure by BWA might enhance survival of more resistant forms of subalpine fir and lead to their gradual takeover. However, I ask, why leave it to chance?

In this context, I remind you of my involvement with a group (see Bonello et al. 2019) proposing creation of a federal Center for Forest Pest Control and Prevention to implement end-to-end responses to forest pest invasions – including overcoming the currently inadequate focus on detection, development and deployment of genetic resistance using modern techniques that allow for much faster breeding cycles.

I am puzzled that the Project CAPTURE places whitebark pine and subalpine fir only in Class A4.2, not among the highest priority species (Potter et al. 2019). As I blogged last spring, Project CAPTURE is part of a multi-partner effort to categorize and prioritize US tree species for conservation actions based on the threats and the trees’ ability to adapt to those threats. I find it puzzling because I am not sure I agree that these two species have a moderately high mean pest severity score – as required by the category. I am less puzzled by the assignment of a low adaptive capacity score.

Limber pine apparently ranks even lower in the Project CAPTURE priority process.

Posted by Faith Campbell

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

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

SOURCES

A comprehensive review and synthesis of the history, ecology, and management of white pines threatened by white pine blister rust see the August 2010 issue of Forest Pathology (Vol. 40:3-4).

American Phytopathological Society. Science Daily. December 9, 2019 https://www.sciencedaily.com/releases/2019/12/191209161314.htm?utm_source=feedburner&utm_medium=email&utm_campaign=Feed%3A+sciencedaily%2Fplants_animals%2Finvasive_species+%28Invasive+Species+News+–+ScienceDaily%29

Bonello, P. , F.T. Campbell, D. Cipollini, A.O. Conrad, C. Farinas, K.J.K. Gandhi, F.P. Hain, D. Parry, D.N. Showalter, C. Villari, and K.F. Wallin. 2019.  Invasive tree pests devastate ecosystems – A proposed new response framework. Frontiers 

Dawe, D.A., V.S. Peters, M.D. Flannigan. 2020. Post-fire regeneration of endangered limber pine (Pinus flexilis) at the Northern extent of its range. Forest Ecology and Management 457 (2020) 117725

Hutton, K.M. 2015. A dissertation submitted in partial fulfillment of the requirements for the degree of Doctor of Philosophy. University of Washington. Available here

Morin, R. Presentation to the 81st Northeastern Forest Pest Council Northeastern states forst agencies, Philadelphia, Pennsylvania, March 2019.

Potter, K.M., Escanferla, M.E., Jetton, R.M., Man, G., Crane, B.S. 2019. Prioritizing the conservation needs of US tree spp: Evaluating vulnerability to forest P&P threats, Global Ecology and Conservation (2019), doi: https://doi.org/10.1016/

Ragenovich, I.R. and R.G. Mitchell. 2006. Forest Insect and Disease Leaflet (FIDL) #118. http://www.na.fs.fed.us/pubs/fidls/bwa.pdf

Sniezko, R.A., M.F. Mahalovich, A.W. Schoettle, D.R. Vogler. 2011. Past and Current Investigations of the Genetic Resistance to Cronartium ribicola in High-elevation Five-needle Pines. In Keane, R.F., D.F. Tomback, M.P. Murray, and C.M Smith, eds. 2011. The future of high-elevation, five-needle white pines in Western North America. Proceedings of the High Five Symposium. 28-30 June, 2010. Missoula, MT.

International Year of Plant Health: Time to Admit that the International Phytosanitary System is Failing

As I noted last November, the premise of the international phytosanitary system – the Agreement on the Application of Sanitary and Phytosanitary Standards (SPS Agreement) and the International Plant Protection Convention (IPPC) – is that importing countries should, and can, rely on exporting countries to take the actions necessary to meet the importing countries’ plant health goals. However, the experience with the International Standard on Phytosanitary Measures (ISPM) #15 and wood packaging casts doubt on this premise.

Exporters are not reliably ensuring the cleanliness of their wood packaging, putting American forests at risk. Indeed, some experts have concluded that continuing to implement ISPM#15 at current levels could triple the number of non-native wood-boring insects introduced into the U.S. by 2050 (Leung et al. 2014).

Too many shipments carry wood packaging that bears no ISPM#15 stamp. And too many pieces of wood packaging arrive with the ISPM#15 stamp, yet are not reliably pest-free. If we cannot clean up this pathway – which involves boards or even logs that are, after all, already dead — it bodes poorly for limiting pests imported with other commodities that are pathways for tree-killing pests – especially living plants (plants for planting). Living plants are much more easily damaged or killed by treatments than the dead wood used in packaging – so ensuring pest-free status of a shipment is even more difficult.  (A longer discussion of the SPS Agreement and IPPC is found in Chapter III of Fading Forests II, available here.

Here are the problems – and the latest evidence.

ALB larva in piece of wood packaging material

Too Many Shipments with Pest-Infested Wood Packaging Are Reaching the Country

My information on Customs and Border Protection (CBP) interceptions comes primarily from Kevin Harriger (see full reference at end of the blog). I will note when it comes from other sources.

In November 2019, Kevin Harriger reported that over the past three years, CBP detected a regulated pest, on average, in 30% of the wood packaging the agency intercepted because it was not compliant with ISPM#15. Non-compliance is defined as wood packaging that either lacks an official mark or is infested by a quarantine pest, or both.

From this and previous reports, I have 10 years of CBP interception data – from 2020 – 2019. These data thus begin four years after the U.S. began implementing ISPM#15 (in 2006) and 11 years after the U.S. began requiring China to treat wood packaging accompanying its exports (in 1999).

Over the period 2010 – 2018, CBP intercepted an average of 3,183 shipments with non-compliant wood packaging each year. On average, 2,100 (66%) of these shipments lacked the required ISPM#15 mark. A live quarantine pest was found in an average of 794 (25%) shipments. (There was some overlap in the categories).

In 2019, CBP intercepted a total of 2,572 non-compliant shipments (Stephen Brady, CBP, April 2020). Those lacking the ISPM#15 mark number 1,825 (71%). Shipments in which a live pest was found numbered 747 (29%).

The 2019 data show decreases, in absolute numbers, from earlier years in all categories: a 19% decrease below 1010-2018 average of shipments intercepted; a 13% decrease in number of shipments intercepted because the wood packaging lacked the ISPM#15 mark; a decrease of 6% in the number of shipments intercepted that had a quarantine pest. It is too early to say whether CBP’s stronger enforcement approach launched in November 2017 has resulted in a lower number of shipments in violation of ISPM#15 approaching our shores.

There has been a dispute about which categories of packaging are most likely to be infested. The categories are pallets, crates, spools for cable, and dunnage (wood used to brace cargo and prevent it from shifting). The CBP data available to me and the study by Krishnankutty et al. (2020b – see full reference at the end of this blog) shed no light on that issue.  

What is the actual number of infested containers approaching our shores? We know that CBP inspects, on average, 2% of incoming containers – so the above interception data reflect a small percentage of probable true approach rate.

The first issue is, how many containers arrive here?

I have been unable to find data for 2019 – much less 2020, when the media report that import volumes have crashed. Until recently, import volumes had been rising. According to a U.S. DOT report to Congress (see reference at the end of this blog), 25 U.S. maritime ports received 24,789,000 loaded shipping containers (measured as TEU – 20-foot equivalent) in 2018. The number of incoming containers had increased at the top three ports – Long Beach, Los Angeles, and New York / New Jersey – between 3% and 7% since 2016.

However, APHIS told me in November 2019 that CBP reports that only about 13 million loaded containers enter the country every year by rail, truck, air, or sea. While I can’t yet explain the discrepancy, one possible explanation is that DoT counts 40-foot containers as two 20-foot containers.

(Of course, pests introduced to Canada also threaten North America’s forests. Canada received fewer than 5 million containers via maritime trade in 2016 (Asbil pers. comm. 2018).

Two decade-old estimates of the proportion of incoming containers that hold wood packaging (Haack et al. 2017, Meissner et al. 2009) allow me to estimate the risk associated with these incoming containers. Meissner et al. found that 75% of maritime containers have wood packaging. Haack et al. estimated that the wood in 0.1% of those containers was infested. Applying these two factors, I conclude that as many as 18,590 of incoming containers in maritime trade could have been transporting a woodborer in the regulated families (Cerambycids, Buprestids, Siricids). I am hesitant to apply the calculation to CBP’s estimate because I don’t know how many of the 13 million containers entered by sea. However, if I assume that the same percentage of wood packaging applied to all the CBP-counted containers, I conclude that 9,750 of those containers held infested wood packaging – still a significant number.

The actual approach rate might be less – or more! Haack et al. (2014) did not include imports from China in their calculations. Given the history of interceptions, it appears probable to me that a recalculation of the approach rate that included China would probably raise the overall proportion.

Furthermore, 11 years have passed since Haack and Meissner made their calculations. During that time, ISPM#15 has been amended to make it more effective. The most important change was restricting the size of bark remnants that may remain on the wood. I have asked several times that APHIS commission a new analysis of Agriculture Quarantine Inspection Monitoring data to determine the pest approach rate before and after the CBP action in order to determine whether the more aggressive enforcement has led to reductions in non-compliant shipments at the border.

By comparing Dr. Haack’s estimate (see above) with the CBP data, I estimate that Customs is detecting and halting the importation of 4 – 8% of the shipments that actually contain pest-infested wood. Since CBP inspects only about two percent of incoming shipments, the higher detection rate demonstrates the value of CBP’s program to target likely violators – and deserves praise. But it is obviously too low a “catch” rate to provide an adequate level of protection for our forests. 

ISPS#15 Is Not Helping to Target Inspections

So – ISPM#15 still allows too many pests to arrive at our shores. Is ISPM#15 at least helping phytosanitary agencies target inspections? No, because both U.S. and European data demonstrate that a high proportion of shipments containing infested wood pieces bore the ISPM#15 stamp. Phytosanitary agencies cannot rely on the presence or absence of the stamp to indicate the pest risk level.

U.S. data:

  • During the period 2010-2015, CBP found that an average of 95% of pest-infested shipments bore the ISPM#15 mark (Harriger). Unfortunately, CBP data from more recent years don’t provide this breakdown.
  • In the past two years, CBP inspectors have repeatedly found pests in dunnage bearing the ISPM#15 mark.
  • Krishnankutty et al. (2020b) analyzed wood packaging from 42 countries of origin intercepted by CBP over six years (April 2012 – January 2018). They found that 87% of the interceptions bore the ISPM mark.

I blogged earlier about the velvet longhorned beetle (Trichoferus (=Hesperophanes) campestris) This pest, like others, has reached our shores and entered the country both before and after implementation of ISPM#15. The predictable result is that VLB is established in three states and has been detected in 14 others plus Puerto Rico (Krishnankutty, et al. 2020a). Apparently we have been lucky that this one isn’t as damaging as so many are!

European data:

For Europe, see Eyre et al. (2018). They concluded that the ISPM-15 mark was of little value in predicting whether harmful organisms were present.

This is alarming and we need to understand the reason – How much is caused by fraud? How much is caused by failure of treatment – either intrinsic weakness or incorrect application? APHIS researchers have found that larvae from wood subjected to methyl bromide fumigationwere more likely to survive to adulthood than those intercepted in wood that had been heat treated (Nadel et al. 2016).

Krishnankutty et al. (2020b) query whether the 2009 requirement that wood be debarked might be less effective in countering insect species that require bark only in the early stages of larval development. Half of the species intercepted in hardwood shipments (e.g., Anoplophora glabripennis, Phoracantha recurva) might fit this profile. They also appear to pose a higher threat since they are polyphagous and known to infest healthy hosts. While some of the softwood-inhabiting species also require bark, they not known to infest living trees and only a quarter were classified in the high-risk group. The Mech et al. 2020 finding that no wood-borers that specialize in conifers posed a high risk appears to support these different impacts.

Krishnankutty, et al. (2020b) also note the risk from pallet recycling. The wood might occasionally be infested by dry-wood borers. One puzzling example was wood packaging shipped from Brazil and bearing a Brazilian ISPM#15 stamp that was infested with a larva of T. campestris (VLB). This is an Asian species not recorded as being present in South or Central America. The authors speculate that the pallets were recycled in Brazil after inadequate treatment in their original places of manufacture.

Of the 17 wood borer species intercepted in hardwoods, three have reproducing populations in the U.S.: A. glabripennis, Phoracantha recurva and T. campestris. Krishnankutty et al. (2020b) say that they are unaware of any of the non-native buprestids and siricids intercepted in softwood SWPM being established in the US. (One Siricid that is established, Sirex noctillio, was not detected in the wood packaging analyzed in this study.)

What Can Be Done to Slow or Eliminate this Pathway?

CBP inspectors

CBP strengthened enforcement of ISPM#15 in November 2017. CBP’s enforcement actions increased by 400% from 2017 to 2018 (John Sagle, CBP, pers. comm). CBP has also expanded its outreach to shippers and others involved in international trade with the goal of reducing all types of non-compliance – lack of documentation, pest presence, etc. in both wood packaging and shipping containers. The outreach includes awareness campaigns targetting trade, industry, affiliated associations, CBP employees, and international partners (Harriger).

Certain countries have a long-standing record of non-compliance with ISPM#15 – as seen in interception records.

  • Haack et al. 2014 – Italy was the country of origin for most wood borers intercepted 1985 – 2000.
  • Haack et al. 2014 – the top 5 countries in the 2003 – 2009 period were Mexico (33.7%), Italy (14.2%), Canada (13.4%), Netherlands (4.4%), China (4.1%).
  • APHIS’ interception database for FY2011-2016 (provided to me) showed Mexico, China, Italy, and Costa Rica had the highest numbers of interceptions.
  • Krishnankutty et al. (2020b) found the highest numbers of interceptions came from Mexico, China, and Turkey.

These numbers reflect in part the huge volumes of goods imported from both Mexico and China. But China and Italy stand out for their poor performance. (The U.S. does not regulate – or inspect! – wood packaging from our third-largest trade partner Canada.)

Officials know which individual companies within these countries have a history of non-compliance. For example, 21 of the interceptions on wood packaging made from Populus trees in China (53%) were associated with stone, ceramic, and terracotta commodities. Anoplophora glabripennis was intercepted six times in Populus originating from a single wood-treatment facility in China (Krishnankutty et al. 2020b).

How reduce risk to U.S. forests?

Over the past year or two, I have suggested the following actions:

  1. USDA APHIS join Bureau of Customs and Border Protection in penalizing violators.
  2. Citing the need for setting a higher “level of protection”, APHIS & the Canadian Food Inspection Agency (CFIA) should prepare a risk assessment to justify adopting more restrictive regulations. The new regulations should prohibit use of packaging made from solid wood – at least from the countries with records of high levels of non-compliance (listed above).
  3. USDA Foreign Agriculture Service (FAS) should assist U.S. importers to determine which suppliers reliably provide compliant wood packaging.
  4.  USDA FAS and APHIS should help importers convey their complaints about specific shipments to the exporting countries’ National Plant Protection Organizations (NPPOs; departments of agriculture).
  5. APHIS should increase pressure on foreign NPPOs and the International Plant Protection Convention more generally to ascertain the reasons ISPM#15 is failing and to fix the problems.
  6. APHIS should fund more studies and audits of wood packaging to document the current efficacy of the standard, including an urgent update of the Haack study of pest approach rate.

The international standard has demonstrably failed to provide a secure method to evaluate the pest risk associated with wood packaging accompanying any particular shipment. The presence of the stamp on pieces of wood packaging does not reliably show that the wood is pest-free.

The situation is even worse re: movement of plants for planting.

SOURCES

Asbil, W. Canadian Food Inspection Agency, pers. comm. August 2018.

Eyre, D., R. Macarthur, R.A. Haack, Y. Lu, and H. Krehan. 2018. Variation in Inspection Efficacy by Member States of SWPM Entering EU. Journal of Economic Entomology, 111(2), 2018, 707–715)

Haack, R. A., K. O. Britton, E. G. Brockerhoff, J. F. Cavey, L. J. Garrett, M. Kimberley, F. Lowenstein, A. Nuding, L. J. Olson, J. Turner, and K. N. Vasilaky. 2014. Effectiveness of the international phytosanitary standard ISPM no. 15 on reducing wood borer infestation rates in wood packaging material entering the United States. Plos One 9:e96611.

Harriger, K. Executive Director for the Agriculture Programs and Trade Liaison office, Department of Homeland Security Bureau of Customs and Border Protection (CBP), presentations to the Continental Dialogue on Non-Native Forest Insects and Diseases, over appropriate years. https://continentalforestdialogue.org/events/

Krishnankutty, S.M., K. Bigsby, J. Hastings, Y. Takeuchi, Y. Wu, S.W. Lingafelter, H. Nadel, S.W. Myers, and A.M. Ray. 2020a. Predicting Establishment Potential of an Invasive Wood-Boring Beetle, Trichoferus campestris (Coleoptera:) in the United States. Annals of the Entomological Society of America, XX(X), 2020, 1–12

Krishnankutty,  S., H. Nadel, A.M. Taylor, M.C. Wiemann, Y. Wu, S.W. Lingafelter, S.W. Myers, and A.M. Ray. 2020b. Identification of Tree Genera Used in the Construction of Solid Wood-Packaging Materials That Arrived at U.S. Ports Infested With Live Wood-Boring Insects. Commodity Treatment and Quarantine Entomology

Leung, B., M.R. Springborn, J.A. Turner, E.G. Brockerhoff. 2014. Pathway-level risk analysis: the net present value of an invasive species policy in the US. The Ecological Society of America. Frontiers of Ecology.org

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. Ecol Evol. 2019 Nov; 9(21): 12216–12230.

Meissner, H., A. Lemay, C. Bertone, K. Schwartzburg, L. Ferguson, L. Newton. 2009. Evaluation of Pathways for Exotic Plant Pest Movement into and within the Greater Caribbean Region. Caribbean Invasive Species Working Group (CISWG) and USDA APHIS Plant Epidemiology and Risk Analysis Laboratory

Nadel, H. S. Meyers, J. Molongoski, Y. Wu, S. Lingafelter, A. Ray, S. Krishnankutty, A. Taylor. 2017. Identification of Port Interceptions in Wood Packing Material Cumulative Progress Report, April 2012 – June 2017

USDA APHIS interception database – pers. comm. January 2017.

USDA APHIS press release dated September 12, 2018

U.S. Department of Agriculture, Press Release No. 0133.20, January 27, 2020

US Department of Transportation. Port Performance Freight Statistics in 2018 Annual Report to Congress 2019 https://rosap.ntl.bts.gov/view/dot/43525

Wu, Y., S.M. Krishnankutty, K.A. Vieira, B. Wang. 2020. Invasion of Trichoferus campestris (Coleoptera: Cerambycidae) into the United States characterized by high levels of genetic diversity and recurrent intros. Biological Invasions Volume 22, pages1309–1323(2020)

Yemshanov, D., F.H. Koch, M. Ducey, K. Koehler. 2012. Trade-associated pathways of alien forest insect entries in Canada. Biol Invasions (2012) 14:797–812

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.

Non-Native Pests on North American Conifers: New Overview

Fraser fir killed by balsam woolly adeligid
Clingman’s Dome, Tennessee

A recent study provides an overview of the threat non-native insects pose to conifers in North America. Unfortunately, pathogens are not included in the study. I provide a citation to the study (Mech et al., 2019) at the end of this blog.

The study’s authors based their analysis on 58 insects that specialize on conifers (trees in the families Cupressaceae, Pinaceae, and/or Taxaceae). These were derived from a list of over 500 herbivorous insects identified by Aukema et al. (2010) and Yamanaka et al.  (2015). Mech and colleagues determined that of the approximately 100 conifer species native to North America, 49 have been colonized by one or more of these 58 non-native insects. Three-quarters of the affected trees have been attacked by more than one non-native insect. One tree species was attacked by 21 non-native insects.

Looked at from the opposite perspective, one of the insects attacked 16 novel North American hosts.

Of these 58 insects, only six are causing high impacts, all in the orders Hymenoptera (i.e., sawflies) and Hemiptera (i.e., adelgids, aphids, and scales). (“High impact” is defined as causing mortality in the  localized host population, recognizing potential spread.)

These six are (1) Adelges piceae—balsam woolly adelgid; (2) Adelges tsugae—hemlock woolly adelgid; (3) Elatobium abietinum—green spruce aphid; (4) Gilpinia hercyniae—European spruce sawfly; (5) Matsucoccus matsumurae—red pine scale; and (6) Pristiphora erichsonii—larch sawfly. The high-impact pests included no wood borers, root feeders, or gall makers.

Mech and colleagues analyzed these relationships in an effort to determine factors driving bioinvaders’ impacts. They evaluated the probability of a non-native conifer specialist insect causing high impact on a novel North American host as a function of the following: (a) evolutionary divergence time between native and novel hosts; (b) life history traits of the novel host; (c) evolutionary relationship of the non-native insect to native insects that have coevolved with the shared North American host; and/or (d) the life history traits of the non-native insect.

They found that the major drivers of impact severity for those that feed on foliage and sap  (remember, they did not evaluate other feeding guilds) were:

1) Host’s evolutionary history – Divergence time in millions of years (mya) since North American species diverged from a coevolved host of the insect in its native range. The greatest probability of high impact for a leaf-feeding specialist was on a novel conifer that diverged from the native conifer host recently (~1.5–5 mya). The divergence time for peak impact was longer for sap‐feeders (~12–17 mya). The predictive power of the divergence-time factor was stronger for sap-feeders than for leaf feeders.

2) Shade tolerance and drought intolerance – A tree species with greater shade tolerance and lower drought tolerance is more vulnerable to severe impacts. This profile fits most species of Abies, Picea, and Tsuga. On the other hand, novel hosts with low shade tolerance and higher drought tolerance had a very low likelihood of suffering severe impacts.

a bad infestation of hemlock woolly adelgid

3) Insect evolutionary history – When a non-native insect shares a host with a closely related herbivore native to North America, the invader is less likely to cause severe impacts. However, this factor in isolation had relatively poor predictive performance.

None of the insect life history traits examined, singly or in combination, had predictive value. The traits evaluated were feeding guild, native region, pest status in native range, number of native host genera, voltinism (frequency of egg-laying periods), reproductive strategy, fecundity, and/or mechanism of dispersal.

See Mech et al. (2019) for a discussion of hypotheses that might explain these findings.

My Questions Answered!

The authors inform me that their project will eventually include introduced insects attacking all kinds of trees. The more than 500 insect species that utilize woody hosts have been placed into one of three categories: 1) conifer specialist (only utilizes conifer hosts), 2) hardwood/woody angiosperm specialist (only utilizes hosts in a single angiosperm family), or 3) generalists (utilizes hosts in more than one angiosperm family or both angiosperms and conifers) (Mech pers. comm.) They began with the smallest group – the conifer specialists – so that they could more easily work out kinks in their procedures.

I had asked why the brown spruce longhorned beetle (Tetropium fuscum) – which is established in Nova Scotia – was not included in this study. According to the authors, this cerambycid beetle has been reported to feed occasionally on hardwood species, so it has been placed in the third group.noted above.

SOURCES

Aukema, J.E., D.G. McCullough, B. Von Holle, A.M. Liebhold, K. Britton, & S.J. Frankel. 2010. Historical Accumulation of Nonindigenous Forest Pests in the Continental United States. Bioscience. December 2010 / Vol. 60 No. 11

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. Ecol Evol. 2019 Nov; 9(21): 12216–12230.

Yamanaka, T., Morimoto, N. , Nishida, G. M. , Kiritani, K. , Moriya, S. , & Liebhold, A. M. (2015). Comparison of insect invasions in North America, Japan and their Islands. Biological Invasions, 17, 3049–3061. 10.1007/s10530-015-0935-y [CrossRef] [Google Scholar]

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.

What the VLB Saga Tells Us About Detection Surveys

Setting Priorities for Surveillance

CBP inspects a pallet suspected for harboring an insect pest

Despite Customs and Border Protection’s heroic efforts to target inspection of wood packaging shipments, based on histories of non-compliance of specific importers’ wood packaging (which I have often praised), the majority of larvae occurring in wood packaging would probably not be intercepted by inspectors. Instead, they would be transported to the cargo’s intended destinations (Wu et al. 2020). I described these problems in the preceding blog about the velvet longhorned beetle (VLB).

As I have noted in the past, CBD detects an average of 800 shipments per year with non-compliant wood packaging. That figure is less than five percent of the 16,500 infested shipping containers that might enter the country each year, based on the estimate by Haack et al., (2014) that one tenth of one percent of incoming wood packaging might be infected.

So there is always a need to improve surveillance for pests that inspection fails to catch. We can do that in at least the following ways:

1) better target detection efforts on the most likely areas where a pest might establish

2) improve collection and use of pest-related information to determine probable hosts, pathways of movement, and potential impacts.

Discovering How the Pest Moves

Sometimes improvements must be linked to individual species – although assisted by knowledge about species with similar life histories, e.g., similar hosts or flight periods or about its close relatives (see Ray’s development of a VLB lure; full citation at end of this blog).  

Other times, improvements might result from more generalizable adjustments.

For example, the pathway analysis undertaken by Krishnankutty and colleagues is one approach to improving geographic targetting. They analyzed aspects of  the velvet longhorned beetle’s pathways of introduction: 1) the types of imports associated with VLB-infested wood packaging; 2) ports where the beetle has been detected in recent years; plus 3) the presence and calculated probable volume of imports for the types of commercial operations considered likely to transport the beetle.

This analysis required access to detailed data from many sources. They included 1) interception data revealing the types of products most often associated with infested wood and the intended destinations of intercepted cargoes; 2) the North American Industry Classification System data listing locations of businesses likely to utilize these products; 3) the beetle’s climatic requirements; and 4) the locations of actual detections of VLB as revealed by Cooperative Agricultural Pest Survey (CAPS) and other trapping programs.

Approaches to Learning More

a Lindgren funnel trap

Relying on traps to detect new pests has several advantages. These include the relative ease of scaling up to larger areas, and – sometimes — the ability to use general lures that attract a variety of insects. Some insects are attracted only, or primarily, to specific lures. Labor intensiveness (and expense) varies with how many traps must be deployed, whether the sites are easily accessible, difficulty extracting trapped insects, and the difficulty sorting the dead insects to find the species of interest.

A second approach is more labor-intensive and expensive, but it gives more information on the target species. This approach is to rear intercepted insect larvae in logs inside containers (to prevent escape) until they reach maturity and emerge. This approach facilitates determination of the species (it is difficult to identify larvae) … and allows an evaluation of feeding behavior – which translates into assessment of the damage caused to the tree.

The Canadian Food Inspection Agency (CFIA) began applying this survey method in 2006. CFIA collects logs from trees in declining health at high risk sites, such as industrial zones, current and historic landfills, and disposal facilities where large volumes of international wood packaging and dunnage are stored for extended periods of time. The logs are obtained from trees removed as part of municipal hazard tree removal programs. CFIA takes the logs to one of four research laboratories (in Toronto, Nova Scotia, Montreal, and North Vancouver), where they are placed in rearing chambers and allowed time to see what insects emerge. The logs are also dissected to reveal the type of damage caused by the insects – that is, determine whether insect was cause of tree mortality [Bullas-Appleton et al. 2014) .

The United States is applying the same approach, but less systematically.

APHIS developed a short-term project aimed at addressing two challenges: identifying larvae found in wood packaging to the species level (larvae intercepted at the border are often identified only to family); and gaining valuable information about the failure of currently required phytosanitary treatments as regards particular genera and species.

In a cooperative project begun in 2012, the DHS Bureau of Customs and Border Protection (CBP) collected live larvae of Cerambycidae and Buprestidae (and, since September of 2015, Siricidae), intercepted during inspection at initially six, later 11 U.S. ports.

mesh bags in which APHIS is rearing larvae obtained from wood packaging inspected by CBD at ports of entry
photo by USDA APHIS

These larvae were sent to an APHIS containment facility where many were reared to adults. Upon emergence, adult specimens were killed and identified by experts working for the National Identification Service. DNA barcodes of dead larvae and the reared adults were defined and compared and any  new information was added to public genetic databases. These DNA barcodes have enhanced the capacity of anyone involved in pest interception and detection to rapidly identify larval stages. In 2017, APHIS determined that it had detected almost the full range of species that might be transported in wood packaging, and stopped funding the project.

As of June 2017, the APHIS project had received 1,289 intercepted wood borers (1,052 cerambycids, 192 buprestids and 45 siricids) from 45 countries (See Nadel et. al 2017). The extensive analysis of velvet longhorned beetle described in my previous blog link was greatly assisted by the resulting data.

Cerambycid larva which was part of the study
photo USDA APHIS

Years before the APHIS project, USDA Forest Service wanted to try applying rearing techniques to aid early detection of insects in the country. At first, the scientists asked residents of Washington, D.C. to identify street trees that appeared to be infested with pests. Those trees were then cut and sections placed in rearing containers to allow scientists to determine what was causing the problem (Harvard Science).

The project was transferred in 2015 to Boston and New York. The Boston location is an arboretum; the advantage of this site is that it has 1) a diversity of tree species; 2) trained staff; and 3) detailed records of most trees on-site (Harvard Science). Project scientists now accept material from stressed, diseased, or dying trees. This material is loaded into sealed barrels and allowed two years for insects to emerge. Since 2015, project scientists have examined 8,605 beetles comprising 223 species. These studies have resulted in 16 new state records, records of some Scolytinae that are rarely collected from traditional trapping methods; documentation of  new host associations; and discovery of one previously undescribed species — Agrilus sp. 9895 (See DiGirolomo, Bohne and Dodds, 2019).

SOURCES

Bullas-Appleton, E., T. Kimoto, J.J. Turgeon. 2014. Discovery of Trichoferus campestris (Coleoptera: Cerambycidae) in Ontario, Canada and first host record in North America. Can. Entomol. 146: 111–116 (2014).

Marc DiGirolomo, Michael Bohne, Kevin Dodds. 2019. Presentation to the 19th Annual Meeting of the Continental Dialogue on Non-Native Forest Insects and Diseases https://continentalforestdialogue.files.wordpress.com/2019/12/bohne.continentaldialogue1.pdf  USFS – Durham, NH – 19th Dialogue meeting

Haack, R. A. 2006. Exotic bark- and wood-boring Coleoptera in the United States: recent establishments and interceptions. Can. J. For. Res. 36: 269–288.

Haack RA, Britton KO, Brockerhoff EG, Cavey JF, Garrett LJ, et al. (2014) Effectiveness of the International Phytosanitary Standard ISPM No. 15 on Reducing Wood Borer Infestation Rates in Wood Packaging Material Entering the United States. PLoS ONE 9(5): e96611. doi:10.1371/journal.pone.0096611

Krishnankutty, S.M., K. Bigsby, J. Hastings, Y. Takeuchi, Y. Wu, S.W. Lingafelter, H. Nadel, S.W. Myers, and A.M. Ray. 2020. Predicting Establishment Potential of an Invasive Wood-Boring Beetle, Trichoferus campestris (Coleoptera: Cerambycidae) in the United States. Annals of the Entomological Society of America, 113(2), 2020, 88-99.  https://doi.org/10.1093/aesa/saz051    

Nadel, H. S. Meyers, J. Molongoski, Y. Wu, S. Lingafelter, A. Ray, S. Krishnankutty, A. Taylor.  2017. Identification of Port Interceptions in Wood Packing Material Cumulative Progress Report, April 2012 – June 2017

Ray, A.M., J. Francese, Y. Zou, K. Watson, D.J Crook, and J.G. Millar. 2019. Isolation and identification of a male-produced aggregation sex pheromone for the velvet longhorned beetle, Trichoferus campestris. Scientific Reports 2019. 9:4459. https://doi.org/10.1038/s41598-019-41047-x

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.

Have we dodged a bullet? (more like a burst of fire from a submachine gun)

Cerambycid larva detected in wood packaging
photo by Oregon Department of Agriculture

Many highly damaging wood-borers have been introduced to North America in wood packaging.

One woodborer, a beetle in the Cerambycidae, has been introduced multiple times to the United States — both before and after implementation of ISPM#15, the international regulations designed to stop such introductions. This is the velvet longhorned beetle (VLB) (Trichoferus (=Hesperophanes) campestris). Independent scientists have recently documented how VLB is introduced and where it is established.

I first blogged about the VLB three years ago. At that time, I asked why APHIS had not undertaken a quarantine and other actions to contain or eradicate the beetle, which was clearly established in an orchard in Utah (Wu et al. 2020; full source citations appear at the end of the blog). Now, the VLB is established in three states and has been detected in many more (details below).

It appears that the VLB will not cause significant damage. I hope this proves true, because it is certainly travelling here on a regular basis. While the most detailed study of the VLB’s potential impact in North America is not yet complete, early indications are that the beetle attacks mostly dying or dead trees.

A Widespread and Adaptable Pest

The VLB is native to China, Central Asia, Japan, Korea, Mongolia, and Russia. It has also been recorded in several European countries. The risk of introduction is broader, however. VLB has established throughout the Middle East and Europe, as well as parts of South and Central America. U.S. officials have intercepted live VLB individuals in shipments originating from these introduced populations, i.e., Brazil, Italy, Mexico, and Spain (Ray et al. 2019).

Wu et al. (2020) studied the genetic diversity of VLB specimens collected by in the United States by 1) trapping at several locations and 2) by testing those intercepted in wood packaging at U.S. ports. The scientists found high levels of diversity between and even within each limited geographic population. These results indicate that VLB has been introduced numerous times via the wood packaging pathway. They also found some evidence that introduced VLB populations might be expanding so it is important to understand pathways of spread within the country (Wu et al. 2020).

Where VLB is in the United States

The VLB is now officially considered to be established in Cook and DuPage counties, IL; Salt Lake County, UT; and Milwaukee, WI. [Krishnankutty et al. 2020).

However, adults have been detected in 26 counties in 13 additional states, plus Puerto Rico, since 1992. Since a trapping survey for woodborers began in 1999, this joint federal and state Cooperative Agricultural Pest Survey (CAPS) has trapped VLB in Colorado (2013), Illinois (2009), New Jersey (2007, 2013), New York (2014, 2016–2018), Ohio (2009, 2017–2019), Pennsylvania (2016), Rhode Island (2006), and Utah (2010, 2012–2019). (Krishnankutty et al. 2020). Also, Oregon detected VLB in 2019 (Oregon Department of Agriculture 2019).

Interceptions in Wood Packaging

The velvet longhorned beetle has been detected frequently in wood packaging since at least the middle 1980s (when APHIS began recording interceptions) (Haack 2006). (Haack’s study covered 1985-2000, before implementation of the International Standard on Phytosanitary Measures (ISPM) #15.)

APHIS’ official interception database listed 60 separate interceptions of VLB in the more recent ten plus-year period June 1997 – November 2017 – which overlaps pre- and post-implementation of ISPM#15. Eighty-eight percent of these interceptions were in wood packaging. Seven percent were in wood products. The remaining seven percent were in passenger baggage or unidentified products.

As has been the case generally since ISPM#15 was adopted, a high percentage — 65.4% — of the intercepted wood packaging during this period bore the mark certifying compliance with the ISPM#15 treatment requirements. Unsurprisingly, China was the origin of 81.6% of the intercepted shipments infested by pests (Krishnankutty et al. 2020).

In the most recent data studied, all from the period after implementation of ISPM#15 — 2012 – 2017, 28 VLB were found in analyses of a sample of wood packaging (Nadel et al. 2017). (I will discuss this study and other detection tools in a separate blog.)

In agreement with earlier findings, the most high-risk imports were determined to be wood packaging for stone, cement, ceramic tile, metal, machinery, manufactured wood products (furniture, decorative items, new pallets, etc.), and wood-processing facilities (Krishnankutty et al. 2020).

These findings largely confirm what we already know about the wood packaging pathway and high levels of non-compliance with ISPM#15 by Chinese shippers. What is APHIS going to do about this well-documented problem? APHIS certainly shouldn’t ignore these findings on the grounds that this particular wood-borer is less damaging than many others. Any chink in our phytosanitary programs that allows transport and entry of VLB can – does! – allow introduction of other woodborers.

The VLB also has been found in rustic furniture – often after the furniture has been sold to consumers. I discussed a 2016 example of this pathways in my February 2017 blog. Krishnankutty et al. (2020) suggest other possible pathways are wooden decorative items and nursery stock, particularly penjing (artificially dwarfed trees and shrubs).

Krishnankutty et al. (2020) note the importance of proper disposal of wood packaging once the cargo reaches its destination. Have any state phytosanitary officials enacted regulations targetting this source of invaders?

pallet “graveyard” – Photo by Anand Prasad, Davey Tree

The Risk to North America’s Forests Is Unknown

A climate-based model described in Krishnankutty et al. (2020) suggests that climate appears to be suitable for VLB across much of the continental United States, northern Mexico, and southern Canada. Only Florida, southern Texas, and high elevation and coastal regions of the western United States and Mexico states are unlikely to support the velvet longhorned beetle, based on climate. (The study did not consider whether host trees would be present.)

Asian and European sources list a broad host range consisting of at least 40 genera of conifers, hardwoods, and fruit trees (Krishnankutty et al. 2020). Still, as noted above, new studies seem to indicate a minimal impact on healthy trees in North America. Indeed, the principal Utah outbreak is in an orchard littered with pruned material.

With so many suitable hosts across so much of the country, the potential for damage is frightening.

Setting Priorities for Surveillance

The availability of data on both port interceptions and multiple detected outbreaks provides an opportunity to test procedures for carrying out early detection surveys. Improving the efficacy of early detection is critical since – as Wu et al. (2020) note – — the majority of infesting larvae would probably not be intercepted and would subsequently be transported to the cargo’s intended destinations. This is despite CBP’s best efforts to target inspection of wood packaging shipments based on shippers’ histories of non-compliance, targeting that I strongly support.

In response to this concern, Krishnankutty et al. (2020) analyzed pathways of introduction – 1) the types of imports associated with VLB-infested wood packaging, 2) ports where the beetle has been detected in recent years, plus 3) the presence and calculated probable volume of imports of types of commercial operations considered likely to transport the beetle. These included wholesale and retail sellers of products known to be risky and businesses involved with wood fuel processing, log hauling, logging, and milling of saw lumber (Krishnankutty et al. 2020).

They could test the value of this approach by comparing the calculated “intended destination counties” declared at import to actual detections of T. campestris. VLB was detected (by CAPS or other surveys) in either the same or a neighboring county for 40% of the intended destination counties.

This seems to be a high introduction rate; detections will probably rise now that a species-specific lure is available. What could this mean for the establishment rate? Is anyone going to repeat the comparisons to track such changes? Unfortunately, we lack sufficient data to compare the VLB establishment rate (whatever it turns out to be) to the rate for other wood-borers.

Focusing on their original intentions, Krishnankutty and colleagues considered the 40% correlation between intended destinations and VLB detections to be sufficiently rewarding to be one basis for setting priorities for surveys (Krishnankutty et al. 2020).

Krishnankutty et al. (2020) say that recognition of three established populations and widespread destinations of potentially infested wood packaging to climatically suitable areas points to the need to determine whether additional populations are already established – or might soon become so. I add this need is further supported by the frequent detections of low numbers of the VLB in at least seven other states (see above). They call for enhanced surveillance to determine where the VLB is.

Improved surveillance is now facilitated by Dr. Ann Ray’s identification of a specific pheromone that can be synthesized in a lab and used to lure VLB to traps. The pheromone is much more effective in attracting VLB than previous food-like lures used by CAPS as general-purpose attractants for wood-boring insects.APHIS had provided about $50,000 over four years from the Plant Pest and Disease Management and Disaster Prevention program (which receives funding through the Farm Bill) to Dr. Ray’s search for the species-specific pheromone.

what happens when detection fails –
dead champion green ash in Michigan

I will discuss detection efforts in a separate blog.

SOURCES

Bullas-Appleton, E., T. Kimoto, J.J. Turgeon. 2014. Discovery of Trichoferus campestris (Coleoptera: Cerambycidae) in Ontario, Canada and first host record in North America. Can. Entomol. 146: 111–116 (2014).

Haack, R. A. 2006. Exotic bark- and wood-boring Coleoptera in the United States: recent establishments and interceptions. Can. J. For. Res. 36: 269–288.

Krishnankutty, S.M., K. Bigsby, J. Hastings, Y. Takeuchi, Y. Wu, S.W. Lingafelter, H. Nadel, S.W. Myers, and A.M. Ray. 2020. Predicting Establishment Potential of an Invasive Wood-Boring Beetle, Trichoferus campestris (Coleoptera:) in the United States. Annals of the Entomological Society of America, XX(X), 2020, 1–12

Nadel, H. S. Meyers, J. Molongoski, Y. Wu, S. Lingafelter, A. Ray, S. Krishnankutty, A. Taylor. 2017. Identification of Port Interceptions in Wood Packing Material Cumulative Progress Report, April 2012 – June 2017

Oregon Department of Agriculture, Plant Protection & Conservation Programs. 2019. Annual Report 2019.

 Ray, A.M., J. Francese, Y. Zou, K. Watson, D.J Crook, and J.G. Millar. 2019. Isolation and identification of a male-produced aggregation sex pheromone for the velvet longhorned beetle, Trichoferus campestris. Scientific Reports 2019. 9:4459. https://doi.org/10.1038/s41598-019-41047-x

Wu, Y., S.M. Krishnankutty, K.A. Vieira, B. Wang. 2020. Invasion of Trichoferus campestris (Coleoptera: Cerambycidae) into the United States characterized by high levels of genetic diversity and recurrent intros. Biological Invasions Volume 22, pages1309–1323(2020)

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.

SOD – questions that need answers

SOD in the nurseries

infected rhododendron
photo by Jennifer Parke
Oregon State University

As you may remember, in May 2019, we became aware of a troubling outbreak of the sudden oak death pathogen Phytophtora ramorum in the nursery trade. The discovery was made by Indiana authorities, who carefully inspected plants being sold in the state.

Briefly, 28 states initially learned that they might have received plants from the suspect sources. Later, APHIS determined that plants exposed to the pathogen had been sent to 18 states – Alabama, Arkansas, Iowa, Illinois, Indiana, Kansas, Kentucky, Michigan, Missouri, Nebraska, North Carolina, Ohio, Oklahoma, Pennsylvania, Tennessee, Texas, Virginia, and West Virginia. Of these, seven (Iowa, Illinois. Indiana, Kansas, Missouri, Nebraska, Oklahoma) plus Washington were known to have received P. ramorum-positive nursery stock. [California Oak Mortality Task Force Newsletter August 2019]

The 2019 episode was just the latest of several occasions since 2004 in which infected plants have been widely distributed by the nursery trade, despite federal and state regulations.

APHIS delays in explaining the situation and what actions it was taking led the states to complain through a letter from the National Plant Board.

For discussions of the 2019 espisode, see my earlier blog or the California Oak Mortality Task Force newsletter for February 2020.

What have we learned from this episode?

1) Three West coast states – California, Oregon, and Washington – are a usual source for the nursery trade of plant taxa that happen to host the P. ramorum pathogen plants. These states’ climates are conducive to growth of these plants and of the pathogen. After repeated nursery outbreaks over 16 years, I think it is time to question continued reliance on such a high-risk source for these plants.

2) APHIS funds the federally-mandated inspection programs in the three states through the “specialty crops” line of the agency’s annual appropriations. Funding levels have apparently remained steady in recent years (COMTF Feb 2020), despite increases in the overall funding for the “specialty crops” line in recent years. I – and some of you! – have lobbied for these increases precisely in order to address the P. ramorum threat. Why has the funding not been increased?

3) While APHIS allocated $352,945 (COMTF February 2020) from the Plant Pest and Disease Management and Disaster Prevention program to help states carry out nursery surveys in 14 states following the 2019 incident, some of the affected states were not included in the program and some states that had not received suspect plants were. States that did not get funding in Fiscal Year 2020 (2020 award report) included three where P. ramorum-positive plants were detected: Iowa, Illinois, and Indiana; and one state that had a scare – Pennsylvania received plants but none tested positive. Seven states received P. ramorum survey funds through the Plant Pest and Disease Management and Disaster Prevention program although they had not received positive plants in the 2019 incident. These were Maryland, Massachusetts, Nevada, New York, North Dakota, Rhode Island, and South Carolina.

The Plant Pest and Disease Management and Disaster Prevention program distributes $70 million annually, and is not subject to annual appropriations. Does a national crisis play any role in determining which projects get funded? Or are decisions made entirely on a proposal by proposal basis and so depend on states’ priorities and individuals’ grant-writing skills?

4) Even now, on the verge of a new plant shipping season (if one occurs given the Covid-19 virus shutdowns), I have seen no public information clarifying how the inspection systems in Washington, British Columbia, and at the U.S. border failed to detect the infested plants before they were shipped. Trace-back efforts carried out by state and U.S. authorities pointed to a nursery in British Columbia as the original source of the infested plants. However, the Canadian Food Inspection Service (CFIA) determined that no Canadian nursery shipped infected plants to the U.S. in 2018 or 2019. See the next paragraph for a description of APHIS’ efforts to resolve this discrepancy.

According to information in the Oregon Department of Agriculture report for 2019, plant imports from Canada are inspected by DHS Customs and Border Protection (CBP) agriculture specialists, not by APHIS. Apparently, CBP has been relying on rules applicable to fruits and vegetables (Q-56) rather than the more stringent provisions of the plants for planting regulation (Q-37). Alerted by Oregon to the importation of 15 Euonymus plants infested by a federally-designated quarantine pest (a thrips), the National Plant Board sent a letter to APHIS in August 2019 asking that it correct CBP’s inspection process.

In March 2020, APHIS sent a letter to the states saying it had amended its Manual and guidance to CBP agricultural inspectors to clarify that all plants for planting must be handled in accordance with the more stringent Q-37 regulations. Furthermore, APHIS is working with CFIA to clarify understanding of each other’s P. ramorum procedures. The letter states that APHIS might consider prohibiting importation of P. ramorum hosts from Canada until CFIA demonstrates that it has adopted effective management measures.

This action by APHIS demonstrates a new seriousness in addressing P. ramorum. I hope this gravitas will persist and carry through to 1) strengthening theregulatory conditions governing domestic production and sales see following section); 2) providing financial and other support to the states (see above about the “specialty crops” appropriation); 3) funding additional studies to clarify the host list and modes of transmission; and 4) using its authority under NAPPRA to curtail imports of plants from Vietnam and other areas where there are large numbers of newly detected Phytophthora species that might threaten North American plant species.  

infested plants detected by Indiana inspectors

I question sufficiency of inspection and mitigation regime

(as described in the February 2020 COMTF newsletter)

When alerted to the infected plants turning up in Indiana, in May 2019, Washington State Department of Agriculture (WSDA) began trace-back investigations. The large wholesale shipping nursery that supplied the plants appears to have acted quite responsibly – it destroy 54,000 plants, cooperated in the Critical Control Point assessment, and implemented mitigation actions. However, I am disturbed to read that the destruction of plants in the 10-meter quarantine radius from plants detected to be infected was a voluntary action. Why don’t the regulations require destruction of nearby hosts?

Descriptions of the western states’ inspection systems – those tied to this specific nursery episode and routine inspections under federal and state P. ramorum programs – indicate to me that P. ramorum is circulating in nurseries in the west coast states, but is evading detection. I cite examples from all three states.

One of the positive nurseries in California in 2019 had been found to be positive in previous years and is considered to be in compliance with quarantine regulations. Yet these measures have not been sufficient to ensure that the nursery is pathogen-free now – as illustrated by its testing positive in 2019.

In Oregon, a retail nursery found to have infected plants destroyed all host material located in the block. Is this action sufficient to ensure that the nursery is now pathogen free? What about the soil, water, cull piles, etc.?  Oregon trace-back surveys led to various suppliers that had previously not been known to be infested. This leads me to think that the pathogen is circulating below regulators’ attention.

In the wake of the 2019 crisis, Washington State Department of Agriculture (WSSA) inspected “opt-out” nurseries – those that had decided not to join APHIS’ program to ship interstate, but continued to ship within the state. WSDA relied on visual inspection only of host material; the agency collected no samples from plants or nursery soils, water, or plant waste (Feb 2020 COMTF). Given all we know about the difficulty of detecting P. ramorum, I think we need more intense inspections that do sample soils, water, and any nearby plant waste (cull piles).

Meaning of Stream Detections?

The P. ramorum pathogen continues to turn up regularly in water bodies. At a botanical garden in Washington State, plant samples have been negative since February 2016. However, water baits from a small pond were positive in 2019 and previous years. Washington’s Sammamish Riverhas been positive since 2007. In the Southeast, seven streams tested positive in 2019. Most if not all have been positive consistently or at least repeatedly for years. All these positive streams are associated with nurseries previously positive for the pathogen. However, plants in the vicinities of these streams show no symptoms.

The same is true in Vietnam: P. ramorum was found in seven out of eight high-elevation streams sampled, but none of the plants belonging to families that have proved highly vulnerable in North America and Europe had any disease symptoms (Jung et al, 2020. A Survey in Natural Forest Ecosystems of Vietnam Reveals High Diversity of both New and Described Phytophthora Taxa including P. ramorum. Forests, 2020, 11). The Jung et al. 2020 findings are discussed in the COMTF Feb. 2020 newsletter and my recent blog.

SOD in the woods

dead coast live oak in California
Joseph O’Brien, USFS

The COMTF February 2020 newsletter summarizes the worrying increase in disease in California woodlands in recent years, which followed the record wet spring of 2017. Aerial surveys documented a big increase in dead tanoak trees and affected acreages in 2018, followed by a smaller increase in 2019 – although still much higher than in 2017. [Details: in 2017, 21,000 dead trees were mapped across 18,000 acres; in 2018, 1.6 million dead trees across 106,000 acres; in 2019, 885,000 dead trees across 92,000 acres.]

California officially records as infested only those counties where infestations have been confirmed by California Department of Food and Agriculture or county Agricultural Commissioners. California currently lists 15 counties as infested. Recent observations by academics or other non-officials of Phytophthora ramorum in Del Norte and San Luis Obispo counties have not yet been confirmed by officials so neither is included in the official quarantine. I understand the need to be certain about reported detections, but we should remember that the disease is probably more widespread than official data indicate.

The newsletter reports Oregon’s treatment efforts – which have totaled 7,300 acres since 2001. I am pleased that Oregon Department of Forestry now has an Environmental Quality Incentives Program (EQIP) project with the USDA Natural Resources Conservation Service and that both the Bureau of Land Management and USDA Forest Service are treating infected areas.

treatment of SOD-infested site
in Oregon
USFS

Still, the quarantine area now covers 31% of Curry County, the EU1 lineage is established in the forest, and ODF and its partners lack sufficient resources to treat all infected areas.

Washington State doesn’t have (known) forest infestations, but it continues to find the pathogen in water bodies; the Sammamish River in King County has been positive since 2007.

In the East, seven states (Alabama, Florida, Georgia, Mississippi, North Carolina, South Carolina, and Texas) participated in the USFS Cooperative Sudden Oak Death Early Detection Stream Survey in 2019. A total of 48 streams were surveyed. P. ramorum was detected from seven streams – five in Alabama, one in Mississippi, and one in North Carolina. All positive streams were associated with nurseries previously positive for the pathogen.

Finally, the newsletter summarizes an article providing advice on managing SOD’s impacts – specifically, conservation of tanoak.

SOURCES

February 2020 issue of the California Oak Mortality Task Force newsletter http://www.suddenoakdeath.org/wp-content/uploads/2020/02/COMTF-Report-February.pdf

Oregon Department of Agriculture Plant Protection and Conservation 2019 annual report

Posted by Faith Campbell

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