Worldwide tests of generic attractants, a promising tool for early detection of non-native cerambycid species

A large proportion of the insects which have invaded new regions and countries are emerging species, being found for the first time outside their native range. Being able to detect such species upon arrival at ports of entry before they establish in non-native countries is an urgent challenge. The deployment of traps baited with broad-spectrum semiochemical lures at ports-of-entry and other high-risk sites could be one such early detection tool. Rapid progress in the identification of semiochemicals for cerambycid beetles during the last 15 years has revealed that aggregation-sex pheromones and sex pheromones are often conserved at global levels for genera, tribes or subfamilies of the Cerambycidae. This possibly allows the development of generic attractants which attract multiple species simultaneously, especially when such pheromones are combined into blends. Here, we present the results of a worldwide field trial programme conducted during 2018–2021, using traps baited with a standardised 8-pheromone blend, usually complemented with plant volatiles. A total of 1308 traps were deployed at 302 sites covering simultaneously or sequentially 13 European countries, 10 Chinese provinces and some regions of the USA, Canada, Australia, Russia (Siberia) and the Caribbean (Martinique). We intended to test the following hypotheses: 1) if a species is regularly trapped in significant numbers by the blend on a continent, it increases the probability that it can be detected when it arrives in other countries/continents and 2) if the blend exerts an effective, generic attraction to multiple species, it is likely that previously unknown and unexpected species can be captured due to the high degree of conservation of pheromone structures within related taxa. A total of 78,321 longhorned beetles were trapped, representing 376 species from eight subfamilies, with 84 species captured in numbers greater than 50 individuals. Captures comprised 60 tribes, with 10 tribes including more than nine species trapped on different continents. Some invasive species were captured in both the native and invaded continents. This demonstrates the potential of multipheromone lures as effective tools for the detection of ‘unexpected’ cerambycid invaders, accidentally translocated outside their native ranges. Adding new pheromones with analogous well-conserved motifs is discussed, as well as the limitations of using such blends, especially for some cerambycid taxa which may be more attracted by the trap colour or other characteristics rather than to the chemical blend.

[1]  Andrew M. Liebhold,et al.  Forest Insect Biosecurity: Processes, Patterns, Predictions, Pitfalls. , 2022, Annual review of entomology.

[2]  T. Poland,et al.  Introduced plants induce outbreaks of a native pest and facilitate invasion in the plants' native range: Evidence from the emerald ash borer , 2021, Journal of Ecology.

[3]  P. Silk,et al.  Interactions Between syn- and anti-2,3-Hexanediol Lures on Trap Catches of Woodboring Beetles and Associates in Southeastern United States , 2021, Environmental Entomology.

[4]  J. Fail,et al.  Identification of Pheromone Components of Plagionotus detritus (Coleoptera: Cerambycidae), and Attraction of Conspecifics, Competitors, and Natural Enemies to the Pheromone Blend , 2021, Insects.

[5]  J. Millar,et al.  Field Trials With Blends of Pheromones of Native and Invasive Cerambycid Beetle Species , 2021, Environmental Entomology.

[6]  R. Venette,et al.  Invasive Insect Species: Global Challenges, Strategies & Opportunities , 2021, Frontiers in Insect Science.

[7]  Jacob D. Wickham,et al.  Rapid Assessment of Cerambycid Beetle Biodiversity in a Tropical Rainforest in Yunnan Province, China, Using a Multicomponent Pheromone Lure , 2021, Insects.

[8]  J. Touroult,et al.  Nouvelles espèces et nouveaux signalements de longicornes des Petites Antilles (Coleoptera, Cerambycidae) , 2021 .

[9]  J. Goczał,et al.  Global diversity and distribution of longhorn beetles (Coleoptera: Cerambycidae) , 2021 .

[10]  H. Nahrung,et al.  Border interceptions of forest insects established in Australia: intercepted invaders travel early and often , 2021 .

[11]  J. Spaethe,et al.  Exploiting trap color to improve surveys of longhorn beetles , 2020, Journal of Pest Science.

[12]  M. Schroeder,et al.  Attraction of the cerambycid beetles Tetropium gabrieli, T. castaneum and T. fuscum to pheromones and host tree volatiles , 2020 .

[13]  J. Spaethe,et al.  Effect of Trap Color on Captures of Bark- and Wood-Boring Beetles (Coleoptera; Buprestidae and Scolytinae) and Associated Predators , 2020, Insects.

[14]  Andrew M. Liebhold,et al.  Projecting the continental accumulation of alien species through to 2050 , 2020, Global change biology.

[15]  D. Rassati,et al.  Maximizing Bark and Ambrosia Beetle (Coleoptera: Curculionidae) Catches in Trapping Surveys for Longhorn and Jewel Beetles , 2020, Journal of Economic Entomology.

[16]  J. Allison,et al.  Impact of Horizontal Edge–Interior and Vertical Canopy–Understory Gradients on the Abundance and Diversity of Bark and Woodboring Beetles in Survey Traps , 2020, Insects.

[17]  A. Vogler,et al.  Higher‐level phylogeny of longhorn beetles (Coleoptera: Chrysomeloidea) inferred from mitochondrial genomes , 2020 .

[18]  E. Russo,et al.  Biological and molecular characterization of Aromia bungii (Faldermann, 1835) (Coleoptera: Cerambycidae), an emerging pest of stone fruits in Europe , 2020, Scientific Reports.

[19]  D. Rassati,et al.  Response of native and exotic longhorn beetles to common pheromone components provides partial support for the pheromone‐free space hypothesis , 2020, Insect science.

[20]  J. Bento,et al.  Variations on a Theme: Two Structural Motifs Create Species-Specific Pheromone Channels for Multiple Species of South American Cerambycid Beetles , 2020, Insects.

[21]  Juan Shi,et al.  Are Invasive Patterns of Non-native Insects Related to Woody Plants Differing Between Europe and China? , 2020, Frontiers in Forests and Global Change.

[22]  Seunghwan Lee,et al.  Multigene Phylogeny Uncovers Oviposition-related Evolutionary History of Cerambycinae (Coleoptera: Cerambycidae). , 2019, Molecular phylogenetics and evolution.

[23]  J. Millar,et al.  A male-produced aggregation-sex pheromone of the beetle Arhopalus rusticus (Coleoptera: Cerambycidae, Spondylinae) may be useful in managing this invasive species , 2019, Scientific Reports.

[24]  D. Miller,et al.  Trap Height Affects Catches of Bark and Woodboring Beetles (Coleoptera: Curculionidae, Cerambycidae) in Baited Multiple-Funnel Traps in Southeastern United States , 2019, Journal of Economic Entomology.

[25]  Joseph C. H. Wong,et al.  The Role of Minor Pheromone Components in Segregating 14 Species of Longhorned Beetles (Coleoptera: Cerambycidae) of the Subfamily Cerambycinae , 2019, Journal of Economic Entomology.

[26]  J. Millar,et al.  (S)-Sulcatol Is a Pheromone Component for Two Species of Cerambycid Beetles in the Subfamily Lamiinae , 2019, Journal of Chemical Ecology.

[27]  D. Crook,et al.  Isolation and identification of a male-produced aggregation-sex pheromone for the velvet longhorned beetle, Trichoferus campestris , 2019, Scientific Reports.

[28]  A. Cognato,et al.  Early Detection and Rapid Response: A 10-Year Summary of the USDA Forest Service Program of Surveillance for Non-Native Bark and Ambrosia Beetles , 2019, American Entomologist.

[29]  Elizabeth A. Boyd,et al.  Pheromone identification by proxy: identification of aggregation-sex pheromones of North American cerambycid beetles as a strategy to identify pheromones of invasive Asian congeners , 2019, Journal of Pest Science.

[30]  J. Millar,et al.  Evidence of Aggregation–Sex Pheromone Use by Longhorned Beetles (Coleoptera: Cerambycidae) Species Native to Africa , 2018, Environmental Entomology.

[31]  P. Silk,et al.  Pheromone-enhanced lure blends and multiple trap heights improve detection of bark and wood-boring beetles potentially moved in solid wood packaging , 2018, Journal of Pest Science.

[32]  J. Millar,et al.  Fuscumol and Geranylacetone as Pheromone Components of Californian Longhorn Beetles (Coleoptera: Cerambycidae) in the Subfamily Spondylidinae , 2018, Environmental Entomology.

[33]  B. Strom,et al.  Trap deployment along linear transects perpendicular to forest edges: impact on capture of longhorned beetles (Coleoptera: Cerambycidae) , 2018, Journal of Pest Science.

[34]  A. Roques,et al.  Multi-component blends for trapping native and exotic longhorn beetles at potential points-of-entry and in forests , 2018, Journal of Pest Science.

[35]  Myunghee Jung,et al.  Identification of Aggregation-Sex Pheromone of the Korean Monochamus alternatus (Coleoptera: Cerambycidae) Population, the Main Vector of Pine Wood Nematode , 2018, Journal of Economic Entomology.

[36]  Víctor Sarto I Monteys,et al.  A New Alien Invasive Longhorn Beetle, Xylotrechus chinensis (Cerambycidae), Is Infesting Mulberries in Catalonia (Spain) , 2018, Insects.

[37]  T. Poland,et al.  Blends of Pheromones, With and Without Host Plant Volatiles, Can Attract Multiple Species of Cerambycid Beetles Simultaneously. , 2018, Journal of economic entomology.

[38]  T. Poland,et al.  Identifying Possible Pheromones of Cerambycid Beetles by Field Testing Known Pheromone Components in Four Widely Separated Regions of the United States , 2017, Journal of Economic Entomology.

[39]  J. Bento,et al.  Aggregation-Sex Pheromones and Likely Pheromones of 11 South American Cerambycid Beetles, and Partitioning of Pheromone Channels , 2017, Front. Ecol. Evol..

[40]  J. Millar,et al.  Novel, male-produced aggregation pheromone of the cerambycid beetle Rosalia alpina, a priority species of European conservation concern , 2017, PloS one.

[41]  Jacob D. Wickham,et al.  Identification of a male-produced sex-aggregation pheromone for a highly invasive cerambycid beetle, Aromia bungii , 2017, Scientific Reports.

[42]  P. Silk,et al.  Interactions between Ethanol, syn-2,3-Hexanediol, 3-Hydroxyhexan-2-one, and 3-Hydroxyoctan-2-one Lures on Trap Catches of Hardwood Longhorn Beetles in Southeastern United States , 2017, Journal of Economic Entomology.

[43]  Andrew M. Liebhold,et al.  Ecology of forest insect invasions , 2017, Biological Invasions.

[44]  T. Schmitt,et al.  Ecological patterns strongly impact the biogeography of western Palaearctic longhorn beetles (Coleoptera: Cerambycoidea) , 2017, Organisms Diversity & Evolution.

[45]  Ingolf Kühn,et al.  No saturation in the accumulation of alien species worldwide , 2017, Nature Communications.

[46]  D. Eyre,et al.  Invasive Cerambycid Pests and Biosecurity Measures , 2017 .

[47]  J. Millar,et al.  Synergism between Enantiomers Creates Species-Specific Pheromone Blends and Minimizes Cross-Attraction for Two Species of Cerambycid Beetles , 2016, Journal of Chemical Ecology.

[48]  Jacob D. Wickham,et al.  Likely Aggregation-Sex Pheromones of the Invasive Beetle Callidiellum villosulum, and the Related Asian Species Allotraeus asiaticus, Semanotus bifasciatus, and Xylotrechus buqueti (Coleoptera: Cerambycidae) , 2016, Journal of Economic Entomology.

[49]  J. Millar,et al.  Sex and Aggregation-Sex Pheromones of Cerambycid Beetles: Basic Science and Practical Applications , 2016, Journal of Chemical Ecology.

[50]  J. Millar,et al.  Optimizing Generic Cerambycid Pheromone Lures for Australian Biosecurity and Biodiversity Monitoring. , 2016, Journal of economic entomology.

[51]  Andrew M. Liebhold,et al.  Nonnative forest insects and pathogens in the United States: Impacts and policy options , 2016, Ecological applications : a publication of the Ecological Society of America.

[52]  R. Hofstetter,et al.  Pine Sawyers (Coleoptera: Cerambycidae) Attracted to α-Pinene, Monochamol, and Ipsenol in North America , 2016, Journal of Economic Entomology.

[53]  J. Millar,et al.  The Influence of Host Plant Volatiles on the Attraction of Longhorn Beetles to Pheromones , 2016, Journal of Chemical Ecology.

[54]  Tim M. Blackburn,et al.  Temporal and interspecific variation in rates of spread for insect species invading Europe during the last 200 years , 2016, Biological Invasions.

[55]  H. Jactel,et al.  Combining pheromone and kairomones for effective trapping of the pine sawyer beetle Monochamus galloprovincialis , 2016 .

[56]  Jacob D. Wickham,et al.  Prionic Acid: An Effective Sex Attractant for an Important Pest of Sugarcane, Dorysthenes granulosus (Coleoptera: Cerambycidae: Prioninae) , 2015, Journal of Economic Entomology.

[57]  L. Marini,et al.  Exploring the role of wood waste landfills in early detection of non-native wood-boring beetles , 2015, Journal of Pest Science.

[58]  Wolfgang Nentwig,et al.  Crossing Frontiers in Tackling Pathways of Biological Invasions , 2015 .

[59]  L. Marini,et al.  Improving the early detection of alien wood‐boring beetles in ports and surrounding forests , 2015 .

[60]  A. Roques,et al.  Taxonomic dissimilarity in patterns of interception and establishment of alien arthropods, nematodes and pathogens affecting woody plants in Europe , 2015 .

[61]  R. A. Arnold,et al.  (R)-Desmolactone Is a Sex Pheromone or Sex Attractant for the Endangered Valley Elderberry Longhorn Beetle Desmocerus californicus dimorphus and Several Congeners (Cerambycidae: Lepturinae) , 2014, PloS one.

[62]  V. Mastro,et al.  Further evidence that monochamol is attractive to Monochamus (Coleoptera: Cerambycidae) species, with attraction synergised by host plant volatiles and bark beetle (Coleoptera: Curculionidae) pheromones , 2014, The Canadian Entomologist.

[63]  P. Silk,et al.  Efficacy of semiochemical-baited traps for detection of longhorn beetles (Coleoptera: Cerambycidae) in the Russian Far East , 2014 .

[64]  Robert A. Haack,et al.  Effectiveness of the International Phytosanitary Standard ISPM No. 15 on Reducing Wood Borer Infestation Rates in Wood Packaging Material Entering the United States , 2014, PloS one.

[65]  T. Holmes,et al.  Likelihood of establishment of tree pests and diseases based on their worldwide occurrence as determined by hierarchical cluster analysis. , 2014 .

[66]  D. Rassati,et al.  Trapping wood boring beetles in Italian ports: a pilot study , 2014, Journal of Pest Science.

[67]  David Hall,et al.  2‐(Undecyloxy)‐ethanol is a major component of the male‐produced aggregation pheromone of Monochamus sutor , 2013 .

[68]  J. Millar,et al.  Field bioassays of cerambycid pheromones reveal widespread parsimony of pheromone structures, enhancement by host plant volatiles, and antagonism by components from heterospecifics , 2013, Chemoecology.

[69]  Joseph C. H. Wong,et al.  Using blends of cerambycid beetle pheromones and host plant volatiles to simultaneously attract a diversity of cerambycid species , 2012 .

[70]  Andrew M. Liebhold,et al.  Live plant imports: the major pathway for forest insect and pathogen invasions of the US , 2012 .

[71]  Joseph C. H. Wong,et al.  Fuscumol and fuscumol acetate are general attractants for many species of cerambycid beetles in the subfamily Lamiinae , 2011 .

[72]  J. Millar,et al.  cis-Vaccenyl Acetate, A Female-Produced Sex Pheromone Component of Ortholeptura valida, A Longhorned Beetle in the Subfamily Lepturinae , 2011, Journal of Chemical Ecology.

[73]  Andrew M. Liebhold,et al.  Historical Accumulation of Nonindigenous Forest Pests in the Continental United States , 2010 .

[74]  David Hall,et al.  Identification and Field Activity of a Male-Produced Aggregation Pheromone in the Pine Sawyer Beetle, Monochamus galloprovincialis , 2010, Journal of Chemical Ecology.

[75]  J. Millar,et al.  Identification and Synthesis of a Female-Produced Sex Pheromone for the Cerambycid Beetle Prionus Californicus , 2009, Journal of Chemical Ecology.

[76]  M. Obrist,et al.  Horizontal and vertical distribution of saproxylic beetles (Col., Buprestidae, Cerambycidae, Scolytinae) across sections of forest edges , 2007 .

[77]  M. Kimberley,et al.  Nationwide survey for invasive wood-boring and bark beetles (Coleoptera) using traps baited with pheromones and kairomones , 2006 .

[78]  Konrad Dettner,et al.  Enhancement of attraction and trap catches of the old-house borer, Hylotrupes bajulus (Coleoptera: Cerambycidae), by combination of male sex pheromone and monoterpenes. , 2005, Pest management science.

[79]  A. Roques,et al.  Testing multi-lure traps for surveillance of native and alien longhorn beetles (Coleoptera, Cerambycidae) at ports of entry and in forests in Austria , 2020 .

[80]  L. Marini,et al.  Developing trapping protocols for wood-boring beetles associated with broadleaf trees , 2018, Journal of Pest Science.

[81]  J. Grégoire,et al.  Monochamus species from different continents can be effectively detected with the same trapping protocol , 2018, Journal of Pest Science.

[82]  B. Richardson,et al.  Alien forest insects in a warmer world and a globalised economy: impacts of changes in trade, tourism and climate on forest biosecurity. , 2010 .