The species of Chalcidoidea (Hymenoptera) introduced to North America for biological control of the cabbage seedpod weevil, and the first recovery of Stenomalina gracilis (Chalcidoidea: Pteromalidae)

2006 ◽  
Vol 138 (3) ◽  
pp. 285-291 ◽  
Author(s):  
Gary A.P. Gibson ◽  
David R. Gillespie ◽  
Lloyd Dosdall

AbstractThe species of Pteromalidae (Chalcidoidea) introduced to British Columbia, Canada, from Europe in 1949 as Trichomalus fasciatus (Thomson, 1878), Xenocrepis pura Mayr, 1904, and Habrocytus sp. for classical biological control of Ceutorhynchus obstrictus (Marsham, 1802) (Coleoptera: Curculionidae) are shown to be misidentifications of Trichomalus perfectus (Walker, 1835), Mesopolobus morys (Walker, 1848), and Stenomalina gracilis (Walker, 1834), respectively. Species reared subsequently from seedpods of Brassica spp. (Brassicaceae) in British Columbia and reported in the literature under the first three names are shown to be misidentifications of, respectively, Trichomalus lucidus (Walker, 1835), Mesopolobus moryoides Gibson, 2005, and one or both of Pteromalus puparum (L., 1758) and T. lucidus. There is no evidence that either T. perfectus or M. morys established in North America, but S. gracilis is newly recorded from southern British Columbia based on specimens reared from Brassicaceae seedpods in 2004 and 2005.

2007 ◽  
Vol 97 (4) ◽  
pp. 387-397 ◽  
Author(s):  
H. Baur ◽  
F.J. Muller ◽  
G.A.P. Gibson ◽  
P.G. Mason ◽  
U. Kuhlmann

AbstractFour species of Mesopolobus Westwood were reared as parasitoids of Ceutorhynchinae hosts in Europe during surveys in 2000–2004. An illustrated key is given to differentiate the four species, M. gemellus Baur & Muller sp. n., M. incultus (Walker), M. morys (Walker) and M. trasullus (Walker), plus M. moryoides Gibson, a parasitoid of the cabbage seedpod weevil, Ceutorhynchus obstrictus (Marsham), in North America. Pteromalus clavicornis Walker is recognized as a junior synonym of M. incultussyn. n., and Pteromalus berecynthos Walker (also a junior synonym of M. incultus) is considered a correct original spelling. For Disema pallipes Förster (a junior synonym of Mesopolobus morys), a lectotype is designated. Mesopolobus morys is for the first time accurately associated with the seed weevil Ceutorhynchus turbatus (Schultze), a potential agent for classical biological control, of hoary cress, Lepidium draba L. (Brassicaceae), in North America. Mesopolobus gemellus is associated with another seed weevil, Ceutorhynchus typhae (=C. floralis) (Herbst), in pods of shepherd's purse, Capsella bursa-pastoris (L.) Medik. (Brassicaceae). Implications of the host–parasitoid associations are discussed relative to the introduction of species to North America for classical biological control of the cabbage seedpod weevil.


2011 ◽  
Vol 143 (4) ◽  
pp. 399-410 ◽  
Author(s):  
Franck J. Muller ◽  
Lloyd M. Dosdall ◽  
Peter G. Mason ◽  
Ulrich Kuhlmann

AbstractIn Europe, Ceutorhynchus turbatus Schultze and Ceutorhynchus typhae (Herbst) (Coleoptera: Curculionidae) feed on seeds from hoary cress and shepherd's purse (Cardaria draba (L.) Desv. and Capsella bursa-pastoris (L.) Medik.); both plants are invasive in North America. In North America, C. turbatus is a candidate for biological control of hoary cress, C. typhae is adventive, and both are sympatric with cabbage seedpod weevil (Ceutorhynchus obstrictus (Marsham)), an invasive alien pest of canola (Brassica napus L. and Brassica rapa L., Brassicaceae). We investigated host associations among C. turbatus, C. typhae, and their parasitoids in Europe. Of particular interest was host specificity of Trichomalus perfectus (Walker) and Mesopolobus morys (Walker) (Hymenoptera: Pteromalidae), candidates for biological control of C. obstrictus in North America. We found no evidence that T. perfectus attacks C. turbatus or C. typhae; however, M. morys was the most common parasitoid associated with C. turbatus.


2004 ◽  
Vol 39 (3) ◽  
pp. 350-361 ◽  
Author(s):  
Andrew S. Fox ◽  
Scott R. Shaw ◽  
Lloyd M. Dosdall ◽  
Byron Lee

Microctonus melanopus (Ruthe) were reared and dissected from adult cabbage seedpod weevil, Ceutorhynchus obstrictus (Marsham), collected in southern Alberta in 2000 and 2001, and M. melanopus females were collected near Creston, British Columbia in 2001. These collections represent the first records for this European species in Canada. Previously published records of M. melanopus in North America are from the northwestern United States. A first diagnosis for adult female M. melanopus is provided that places M. melanopus in Loan's (1969) key for Microctonus species of North America, north of Mexico. Scanning electron photomicrographs of female morphology are provided to illustrate important diagnostic characters: the mesonotal sculpture with a distinct median longitudinal carina posteriorly, and the sculpture of metasomal tergite 1 with costae distinctly converging posteriorly. It is probable that M. melanopus has long been established in the southern interior of British Columbia because its host, C. obstrictus, has occurred there for many years. The occurrence of M. melanopus in southern Alberta is likely more recent, as its host only recently dispersed to that region. Rates of parasitism of C. obstrictus by M. melanopus, with one exception, were low in southern Alberta (<10%), and only one parasitized weevil was found on spring-seeded Brassica napus L., the primary brassicaceous oilseed crop associated with the weevil on the Canadian prairies. We hypothesize that M. melanopus will not provide substantial control of C. obstrictus in the mixed grassland ecoregion of its new range.


EDIS ◽  
2017 ◽  
Vol 2017 (6) ◽  
Author(s):  
James P. Cuda ◽  
Patricia Prade ◽  
Carey R. Minteer-Killian

In the late 1970s, Brazilian peppertree, Schinus terebinthifolia Raddi (Sapindales: Anacardiaceae), was targeted for classical biological control in Florida because its invasive properties (see Host Plants) are consistent with escape from natural enemies (Williams 1954), and there are no native Schinus spp. in North America. The lack of native close relatives should minimize the risk of damage to non-target plants from introduced biological control agents (Pemberton 2000). [...]


2020 ◽  
Vol 78 ◽  
pp. 1-17
Author(s):  
Paul K. Abram ◽  
Audrey E. McPherson ◽  
Robert Kula ◽  
Tracy Hueppelsheuser ◽  
Jason Thiessen ◽  
...  

We report the presence of two Asian species of larval parasitoids of spotted wing Drosophila, Drosophila suzukii (Matsumura) (Diptera: Drosophilidae), in northwestern North America. Leptopilina japonica Novkovic & Kimura and Ganaspis brasiliensis (Ihering) (Hymenoptera: Figitidae) were found foraging near and emerging from fruits infested by D. suzukii at several locations across coastal British Columbia, Canada in the summer and fall of 2019. While G. brasiliensis was found in British Columbia for the first time in 2019, re-inspection of previously collected specimens suggests that L. japonica has been present since at least 2016. Additionally, we found a species of Asobara associated with D. suzukii in British Columbia that is possibly Asobara rufescens (Förster) (known only from the Palearctic Region) based on COI DNA barcode data. These findings add to the list of cases documenting adventive establishment of candidate classical biological control agents outside of their native ranges. The findings also illustrate the need for revisiting species concepts within Asobara, as well as host and geographic distribution data due to cryptic and/or misidentified species.


2011 ◽  
Vol 143 (2) ◽  
pp. 197-210 ◽  
Author(s):  
Franck J. Muller ◽  
Peter G. Mason ◽  
Lloyd M. Dosdall ◽  
Ulrich Kuhlmann

AbstractThe ceutorhynchine weevils Hadroplontus litura (F.) and Microplontus edentulus (Schultze) (Coleoptera: Curculionidae), are established in North America as biological control agents for Canada thistle, Cirsium arvense (L.) Scop., and scentless chamomile, Tripleurospermum perforatum (Mérat) M. Lainz (Asteraceae), respectively. In North America, both weeds occur sympatrically and in similar habitats as another ceutorhynchine, Ceutorhynchus obstrictus (Marsham) (cabbage seedpod weevil), an important pest of canola, Brassica napus L., and Brassica rapa L. (Brassicaceae). Ceutorhynchinae weevils released to control weeds in cultivated crops may serve as alternate hosts if agents released for biological control of C. obstrictus are not specific to that species. Parasitoids associated with M. edentulus and H. litura inflict similar levels of mortality on their hosts, yet a single species was associated with the latter host, whereas 13 species attacked the former. The stem-mining M. edentulus appears to be at some risk but not the root-crown feeding H. litura, should the parasitoids Trichomalus perfectus (Walker) and Mesopolobus morys (Walker) (Hymenoptera: Pteromalidae) be introduced as biological control agents of the silique-feeding C. obstrictus. These findings suggest that feeding niche may be an important criterion for developing a nontarget species test list for host-range testing of potential biological control agents.


Plant Disease ◽  
2007 ◽  
Vol 91 (7) ◽  
pp. 906-906 ◽  
Author(s):  
D. K. Berner ◽  
H. J. Dubin ◽  
E. L. Smallwood

Slender wheatgrass (Elymus trachycaulus (Link) Gould ex Shinners subsp. trachycaulus), family Poaceae, tribe Triticeae, is a native North American grass that is used as a livestock forage. Ustilago phrygica, a systemic ovary-smut fungus, is native to Turkey and West Asia and is pathogenic on Aegilops spp. and Taeniatherum caput-medusae (L.) Nevski subsp. asperum (Simonk.) Melderis (medusahead), an invasive weed in the western United States that is targeted for biological control. An isolate of the fungus (U.S. National Fungus Collections, BPI 871725; GenBank Accession No. DQ139961) was collected from medusahead in Turkey and screened for possible use in classical biological control of this weed. Screening was done in quarantine in a BSL-3 facility of the Foreign Disease-Weed Science Research Unit, USDA, ARS, Ft. Detrick, MD. The focus of screening was determination of host range of the fungus among related native and agriculturally important grasses in North America. A procedure was developed to consistently and quickly produce disease on medusahead and other grasses. Without vernalization, plants inoculated with U. phrygica will not produce smutted spikes (seedheads). Teliospores of the fungus were vacuum inoculated (1) onto caryopses (seeds) of medusahead and slender wheatgrass, which were then placed on moist germination paper in a petri dish or on moist vermiculite in plastic boxes. The dishes, sealed with Parafilm, and the boxes, covered with lids, were placed in a dark refrigerator at 3°C. After 8 weeks, all seedlings were transplanted into pots on a greenhouse bench at 22 to 25°C and 14 h light (photosynthetic photon flux density [PPFD] 620 μmol·s−1·m−2). The plants began to flower and produce smutted spikes 40 days later. These tests were repeated once. Fourteen of sixty medusahead plants from inoculated caryopses incubated on germination paper and nine of twenty-four plants from caryopses incubated on vermiculite became smutted and produced numerous smutted spikes per plant. Partial systemic infection was the norm, and all diseased plants had some spikes that were not diseased. One slender wheatgrass plant of nine plants grown from inoculated caryopses incubated on germination paper was also smutted and produced three diseased spikes. Nielsen (2) indicated susceptibility of slender wheatgrass to U. phrygica, but only as a single entry in a table under the synonym Agropyron trachycaulum (Link) Malte ex H. F. Lewis in a report on susceptibility of Aegilops spp. to U. phrygica. Because this is an obscure mention of the susceptibility of slender wheatgrass to U. phrygica, the fungus-host association does not explicitly appear in literature and is absent from relevant databases. Our tests with the fungus confirm that slender wheatgrass is susceptible to U. phrygica and lead us to conclude that the fungus would not be a good candidate for classical biological control of medusahead in North America. This formal report should establish this fungus-host association in literature and ensure reference in plant disease databases. References: (1) C. C. Allison. Univ. Minn. Agric. Exp. Stn. Tech. Bull. August:1, 1936. (2) J. Nielsen. Can. J. Bot. 70:581, 1992.


2015 ◽  
Vol 147 (3) ◽  
pp. 300-317 ◽  
Author(s):  
Leah S. Bauer ◽  
Jian J. Duan ◽  
Juli R. Gould ◽  
Roy Van Driesche

AbstractFirst detected in North America in 2002, the emerald ash borer (EAB) (Agrilus planipennis Fairmaire; Coleoptera: Buprestidae), an invasive phloem-feeding beetle from Asia, has killed tens of millions of ash (Fraxinus Linnaeus; Oleaceae) trees. Although few parasitoids attack EAB in North America, three parasitoid species were found attacking EAB in China: the egg parasitoid Oobius agrili Zhang and Huang (Hymenoptera: Encyrtidae) and two larval parasitoids Tetrastichus planipennisi Yang (Hymenoptera: Eulophidae) and Spathius agrili Yang (Hymenoptera: Braconidae). In 2007, classical biological control of EAB began in the United States of America after release of these three species was approved. In 2013, release of the larval parasitoids was approved in Canada. Research continues at study sites in Michigan, United States of America where the establishment, prevalence, and spread of O. agrili and T. planipennisi have been monitored since 2008. However, establishment of S. agrili remains unconfirmed in northern areas, and its release is now restricted to regions below the 40th parallel. In 2015, approval for release of Spathius galinae Belokobylskij (Hymenoptera: Braconidae), an EAB larval parasitoid from the Russian Far East, may be granted in the United States of America. Researchers are guardedly optimistic that a complex of introduced and native natural enemies will regulate EAB densities below a tolerance threshold for survival of ash species or genotypes in forested ecosystems.


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