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Published November 9, 2020 | Version v1
Taxonomic treatment Open

Amasa

  • 1. https: // orcid. org / 0000 - 0001 - 9697 - 3787
  • 2. URZF- Zoologie Forestière, INRAE, 2163 Avenue de la Pomme de Pin, 45075, Orléans, France.
  • 3. Department of Agronomy, Food, Natural Resources, Animals and Environment (DAFNAE), University of Padua, Viale dell'Università, 16, 35020 Legnaro, Italy.
  • 4. Department of Biology, University of Bergen, P. O. Box 7803, N- 5006 Bergen, Norway.
  • 5. ANSES, Laboratoire de la Santé des Végétaux, 755 avenue du Campus Agropolis, CS 30016, 34988 Montferrier-sur-Lez cedex, France.
  • 6. Pôle Sud-Est de la Santé des Forêts, DRAAF SRAL PACA, BP 95, 84141 Montfavet cedex, France. jean-baptiste. daubree @ agriculture. gouv. fr; https: // orcid. org / 0000 - 0002 - 5383 - 3984
  • 7. https: // orcid. org / 0000 - 0002 - 9248 - 9012

Description

- Amasa sp. near truncata (Erichson)

(Figs. 1A, 1B)

Distribution and identification. The genus Amasa is native to Asia and Australasia (Wood & Bright 1992) and comprises at least 53 species (Wood & Bright 1992; Smith et al. 2020a, 2020b). Little is known of the biology of most species, but in Australia and Malaysia most recorded hosts are in the Myrtaceae (Browne 1961; Wood & Bright 1992).

Based on photographs, Amasa specimens from France appear to belong to the same species that was collected in Spain in 2009. Furthermore, the both European populations appear to be the same as the Amasa now established in Eucalyptus plantations in New Zealand, Brazil, Uruguay and Chile (Milligan 1969; Zondag 1977; Flechtmann & Cognato 2011; Gómez et al. 2017; Kirkendall 2018). The single Spanish specimen from Cádiz was identified as the southeast Asian species A. resecta (Eggers) (Viñolas & Verdugo 2011), possibly based on photographs of said species (https://www.insectimages.org/browse/detail.cfm?imgnum=5593028). Details of the declivity differ, however. A mtDNA sequence from the COI gene of a French specimen was 100% identical to an unidentified bark beetle sequence in the BOLD database from New South Wales, Australia (M.A. Auger-Rozenberg, pers. comm.: http:// v3.boldsystems.org/index.php/Public_RecordView?processid=SBGB053-03), meaning that the French specimen is an Australian species (and morphologically it is clearly an Amasa). The New Zealand Amasa and South American populations were all identified as Amasa truncata (Erichson). This appears now to be incorrect. Bark beetle taxonomists Roger A. Beaver and Milos Knižek (both, pers. comm., April 2020) have examined the holotype, which has noticeably longer setae on the declivity and more pronounced swellings on the odd-numbered declivital interstriae. These differences can be seen in the PaDIL photographs of Amasa truncata (http://www.padil.gov.au/pests-anddiseases/pest/main/141313). Amasa sp. near truncata does not match photos or descriptions of the any of other four species of Amasa recorded from Australia, nor does the Amasa now in South America (Flechtmann & Cognato 2011), but there are at least four more undescribed species in the genus present in that country that are similar to and have been confused with A. truncata (R. A. Beaver, pers. comm., April 2020). The invasive species, then, could well be one of those undescribed cryptic species.

Many adults of an Amasa species were trapped throughout the summer 2018 in the arboretum of Villa Thuret in Antibes, then again in 2019; none were trapped in the nearby Garoupe forest although a number of similarly baited traps were deployed there. In 2019, specimens were caught on the island of Sainte Marguerite, ca. 8 km away. These data show that this species has become established in that region.

New records. ALPES-MARITIMES – Antibes, Villa Thuret, interception traps baited with ethanol 100%, (-) α-pinene and a blend of longhorn beetle pheromones: 3 ind. from 27.VI. to 18.VII.2018, 24 ind. from 19.VII. to 08.VIII.2018, 17 ind. from 29.VIII. to 19.IX.2018, and 10 ind. from 20.IX to 11.X. 2018, URZF leg.; ibidem, from 21.V. to 22.X.2019, 22 ind., URZF leg.; Cannes, Sainte- Marguerite island, interception traps baited with ethanol 100%, (-) α-pinene, and a pheromone blend for longhorn beetles, from 24.V. to 14.VI.2019, 3 ind., URZF leg .

Damage and infestation risk. Amasa species have mandibular mycangia which transport symbiotic fungi belonging to Raffaelea (previously reported as Dryadomyces), a genus that includes a number of pathogenic species (Gebhardt et al. 2005; Hulcr & Stelinski 2017). However, there are no reports yet of significant damage being caused by either A. truncata or A. sp. near truncata (reviewed in Kirkendall 2018).

Notes

Published as part of Barnouin, Thomas, Soldati, Fabien, Roques, Alain, Faccoli, Massimo, Kirkendall, Lawrence R., Mouttet, Raphaëlle, Daubree, Jean-Baptiste & Noblecourt, Thierry, 2020, Bark beetlesand pinhole borers recently ornewly introduced toFrance (Coleoptera Curculionidae, Scolytinae and Platypodinae), pp. 51-74 in Zootaxa 4877 (1) on page 55, DOI: 10.11646/zootaxa.4877.1.2, http://zenodo.org/record/4423749

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Linked records

Additional details

Biodiversity

Collection code
URZF
Event date
2018-06-27
Family
Curculionidae
Genus
Amasa
Kingdom
Animalia
Order
Coleoptera
Phylum
Arthropoda
Taxon rank
genus
Verbatim event date
2018-06-27/2019-10-22

References

  • Wood, S. L. & Bright, D. E. Jr. (1992) A catalog of Scolytidae and Platypodidae (Coleoptera), part 2: Taxonomic index. Great Basin Naturalist Memoirs, 13, 1 - 1553.
  • Smith, S. M., Beaver, R. A. & Cognato, A. I. (2020 a) Taxonomic changes for Indo-Malayan ambrosia beetles (Coleoptera: Curculionidae: Scolytinae: Xyleborini). The Coleopterists Bulletin, 74, 37 - 40. https: // doi. org / 10.1649 / 0010 - 065 X- 74.1.37
  • Smith, S. M., Beaver, R. A. & Cognato, A. I. (2020 b) A monograph of the Xyleborini (Coleoptera, Curculionidae, Scolytinae) of the Indochinese Peninsula (except Malaysia) and China. ZooKeys. [in press]
  • Browne, F. G. (1961) The biology of Malayan Scolytidae and Platypodidae. Malayan Forest Records, 22, 1 - 255.
  • Milligan, R. H. (1969) Insect damage to eucalypts. Report of the Forest Research Institute for 1 January- 31 December 1968. New Zealand Forest Service, Wellington, 60 pp.
  • Zondag, R. (1977) Xyleborus truncatus Erichson (Coleoptera: Scolytidae). Forest and Timber Insects in New Zealand, 21, 1 - 3.
  • Flechtmann, C. & Cognato, A. (2011) First report of Amasa truncata (Erichson) (Coleoptera: Curculionidae: Scolytinae) in Brazil. The Coleopterists Bulletin, 65 (4), 417 - 421. https: // doi. org / 10.1649 / 072.065.0419
  • Gomez, D., Suarez, M. & Martinez, G. (2017) Amasa truncata (Erichson) (Coleoptera: Curculionidae: Scolytinae): a new exotic ambrosia beetle in Uruguay. The Coleopterists Bulletin, 71 (4), 825 - 826.
  • Kirkendall, L. R. (2018) Invasive bark beetles (Coleoptera, Curculionidae, Scolytinae) in Chile and Argentina, including two species new for South America, and the correct identity of the Orthotomicus species in Chile and Argentina. Diversity, 10 (2), 1 - 20. https: // doi. org / 10.3390 / d 10020040
  • Vinolas, A. & Verdugo, A. (2011) Nuevas especies de coleopteros para la Peninsula Iberica. Familias Zopheridae, Corylophidae y Curculionidae. Orsis, 25, 131 - 139.
  • Gebhardt, H., Weiss, M. & Oberwinkler, F. (2005) Dryadomyces amasae: a nutritional fungus associated with ambrosia beetles of the genus Amasa (Coleoptera: Curculionidae, Scolytinae). Mycological Research, 109, 687 - 696. https: // doi. org / 10.1017 / S 0953756205002777
  • Hulcr, J. & Stelinski, L. L. (2017) The ambrosia symbiosis: from evolutionary ecology to practical management. Annual Review of Entomology, 62, 285 - 303. https: // doi. org / 10.1146 / annurev-ento- 031616 - 035105